Skip to main content
Springer logoLink to Springer
. 2021 Dec 6;272(4):643–677. doi: 10.1007/s00406-021-01360-x

Aerobic exercise in severe mental illness: requirements from the perspective of sports medicine

Peter Falkai 1, Andrea Schmitt 1,2, Christian P Rosenbeiger 1, Isabel Maurus 1,, Lisa Hattenkofer 1, Alkomiet Hasan 3, Berend Malchow 4, Pascale Heim-Ohmayer 5, Martin Halle 5,6, Melanie Heitkamp 5
PMCID: PMC9095557  PMID: 34873635

Abstract

Major depression, bipolar disorder, and schizophrenia are severe mental illnesses. Despite receiving psychopharmacological and psychosocial treatments, about half of patients develop a chronic course with residual cognitive and negative symptoms and have a high risk for cardiovascular disease and reduced life expectancy. Therefore, add-on innovative treatment approaches are needed to improve outcome. Aerobic exercise interventions have been shown to improve global functioning, cognition, and negative and depressive symptoms in these patients. The basic mechanism of these exercise-related changes has been reported to be improved brain plasticity, e.g., increased volume of disease-related brain regions such as the hippocampus. The optimal type, duration, and frequency of exercise have not yet been determined and need to be addressed in supervised physical exercise studies. Because of the low physical activity levels, lack of drive related to negative and depressive symptoms, and high prevalence of cardiovascular comorbidities in patients with severe mental illness, besides aiming to improve symptoms of mental illness, exercise interventions should also aim to increase cardiorespiratory fitness, which they should comprehensively assess by direct measurements of maximal oxygen uptake. Based on the recommendations for developing cardiorespiratory fitness by the American College of Sports Medicine, 150 min moderate-intensity training per week or vigorous-intensity exercise training for 75 min per week are appropriate. Most studies have had relatively short intervention periods, so future studies should focus on long-term adherence to exercise by implementing motivational strategies supported by telemedicine and by identifying and targeting typical barriers to exercise in this patient population.

Keywords: Major depression, Bipolar disorder, Schizophrenia, Aerobic exercise, Physical activity, Cardiorespiratory fitness, Neuroplasticity

Introduction

In 2010, more than 25% of the population in Europe was diagnosed with a mental illness [1]. Among mental illnesses, major depression (MDD), bipolar disorder (BD) and schizophrenia (SZ) belong to the 20 most burdensome disorders and result in annual costs of 207 billion euro in Europe. Thus, besides cardiovascular diseases [2, 3], mental disorders—especially MDD—are one of the leading illness-related causes of years lived with disability worldwide [4]. Furthermore, more than 50% of patients in Europe with a mental illness, equivalent to about 25 million Europeans, develop a relapsing, chronic course of their illness with residual symptoms, which are associated with poor functional outcome [5].

Epidemiological research showed that in the last 100 years the long-term outcome of SZ has remained relatively stable [6], despite the introduction of psychotropic medications 70 years ago. Furthermore, psychotropic medications also have not improved outcome dimensions like cognition or negative symptoms. Overall, about 20% of patients with SZ have a good outcome and are able to participate in the primary job market, maintain a stable partnership and have longer phases with no need for psychopharmacological support [7, 8]; about 30% of patients will have a good prognosis but will need to take long-term psychotropic medication, which can have burdensome side effects, especially related to metabolic syndrome [9]; and about 50% of patients will develop a chronic course (defined as continuous symptoms over a period of at least 2 years) with different degrees of residual symptoms and disability [5]. Residual symptoms include cognitive dysfunction, impaired mood, reduced drive, and reduced ability to cope with stress. These individuals have an unfavorable long-term social outcome, meaning that they have difficulties finding a long-term job on the primary job market or maintaining a stable partnership [8].

Besides having a direct influence on functional outcome, environmental risk factors also affect mortality: The mortality rate from physical causes, including suicide is 20-fold higher in patients with unipolar depression than in the general population, 15-fold higher in patients with BD, and 12-fold higher in patients with SZ [1013]. Another important cause is the high incidence of medical comorbidities due to unhealthy lifestyle habits, such as high rates of cigarette smoking and low levels of physical activity. Estimates indicate that together suicides and lifestyle-related factors reduce life expectancy by nearly 10 to 20 years compared with the general population [14, 15].

A meta-analysis of data from 29 countries on 6 continents confirmed that people with mental disorders have a significantly higher mortality rate and that, in 65 studies, the highest mortality rate (relative risk 2.54; 95% CI 2.35–2.75) was among patients with psychosis [1518]. People with severe mental illness have a higher risk of developing coronary heart disease than controls (adjusted hazard ratio 1.54; 95% CI 1.30–1.82) and a higher rate of autonomic nervous system dysfunction, including diminished heart rate variability, hypertension, alterations of the QT interval, and lipid pattern abnormalities [19]. Unfortunately, the currently available psychopharmacological and psychosocial treatments do not ameliorate or improve these symptoms significantly and therefore do not help to improve functional outcome or increase life expectancy.

Surprisingly few studies have examined whether aerobic exercise combined with diet and psychosocial interventions can reduce the mortality gap between patients with mental disorders and the general population, and the studies included only small samples of patients [20]. The seminal paper by the Lancet Commission [21] identified an unhealthy diet and a sedentary lifestyle as major risk factors for the physical illness burden of patients with MDD, BD, and SZ, diseases that are also collectively referred to as affective and nonaffective psychoses. The paper gives recommendations to influence these modifiable risk factors, e.g., including regularly exercise in treatment programs.

This qualitative review will outline the effects of aerobic exercise on clinical outcome in patients with MDD, BD, and SZ and will evaluate the quality of intervention studies on the basis of the requirements of modern sports medicine.

Physical activity, physical fitness, and medical health outcome in patients with MDD, BD, and SZ

Low physical activity levels and poor cardiorespiratory fitness (CRF) are associated with a high risk of cardiovascular disease and all-cause mortality [22]. Exercise and good CRF play an important role in mitigating cardiovascular disease risk factors, such as metabolic syndrome, which is defined as a combination of increased waist circumference; elevated fasting glucose, triglycerides, and low high-density lipoprotein cholesterol; and high blood pressure [23, 24]. A meta-analysis determined that the risk of metabolic syndrome was elevated in all patients with affective and nonaffective psychoses (32.6%, 95% CI 30.8–34.3%) and that the prevalence did not differ between patients with MDD, BD, or SZ [25].

Another meta-analysis found that patients with MDD had lower levels of physical activity (standardized mean differenc, − 30; 95% CI − 0.40 to 0.21) and higher levels of sedentary behavior (standardized mean difference 0.99; 95% CI 0.01–0.18) than healthy controls [26]. Therefore, researchers concluded that less physically active patients might benefit from specific aerobic exercise interventions aimed at increasing physical fitness [27]. An important aspect to consider in this context is that low physical activity is related to negative symptoms such as amotivation [28], so aerobic exercise interventions must be supervised by experienced sports scientists to ensure that patients adhere to the intervention [29].

Physical fitness and physical activity are low not only in patients with MDD, but also in those with BD [30]. However, this diagnostic group is highly underrepresented in physical activity studies.

A study in patients with SZ showed that low physical fitness was associated with a higher prevalence of metabolic syndrome and more severe cognitive, negative, and positive symptoms [27]. The exercise capacity (measured by the distance covered in the 6-min walking test) of patients with SZ and prediabetes was reduced and the body mass index was increased; in addition, patients with SZ and manifest type 2 diabetes were less physically active [31].

Previous aerobic exercise studies showed the feasibility of endurance training in patients with SZ, and adaptations to aerobic endurance training in patients were comparable to those in healthy controls, as assessed by physical working capacity and maximal achieved power. However, differences were detected in changes of performance at a lactate concentration of 3 mmol/L, i.e., patients with SZ showed an impaired increase in lactate [29].

Different types of interventions have been evaluated that aim to improve physical health in patients with mental illness. A meta-analysis of 47,231 patients with SZ summarized and compared the effects of pharmacological and nonpharmacological interventions [32]. The authors showed that the most effective interventions for weight reduction were individual lifestyle counseling and exercise interventions, followed by psychoeducation, augmentation with the atypical antipsychotic aripiprazole, topiramate add-on therapy, and dietary interventions. The best efficacy in reducing glucose levels was found for a switch from olanzapine (the atypical antipsychotic with the highest risk for metabolic syndrome) to aripiprazole and add-on medication with metformin. Efficacy was also shown for treatment with glucagon-like peptide-1-receptor agonists, dietary interventions, and aripiprazole augmentation. Insulin resistance improved best followed by metformin treatment. Metformin also had the greatest effects on total cholesterol and high-density lipoprotein cholesterol. The best effect on triglycerides and low-density lipoprotein cholesterol was achieved with topiramate. Importantly, only exercise interventions increase exercise capacity [32]. Recent efforts to increase the efficacy of exercise include the use of high-intensity interval training (HIIT). In a randomized controlled HIIT study, compliant patients with overweight and SZ showed improvement in waist circumference, negative symptoms, and psychosocial functioning [33]. HIIT may be a feasible and effective way to improve CRF and metabolic parameters and has been established as such in physical disorders. It may also have more beneficial effects on the metabolic state than more moderate and continuous endurance training methods [20].

Effects of aerobic exercise on symptoms of MDD

Aerobic exercise, often revered to as “endurance exercise”, is defined as physical activity with a predominant metabolic pathway that uses oxygen to meet energy demands (oxidative phosphorylation) and leads to only low blood lactate levels [34]. In practice, aerobic exercise is usually characterized by repeated sequences of physical activity in a light to moderate intensity for extended periods of time. Aerobic exercise improves especially CRF and includes typically activities such as walking, swimming or cycling [35]. Contrastingly, anaerobic exercise refers to short-term high-intensity efforts with a preponderance of metabolic pathways not using oxygen (phosphagens metabolic pathway and glycolytic pathway) [36]. In most studies, the term "anaerobic training" is used to describe high-intensity exercise intervals with a duration of up to several minutes that result in increased lactate levels.

Aerobic exercise studies addressing MDD are summarized in Table 1. An aerobic exercise training study of 12 × 75-min sessions over a period of 4 weeks in patients with SZ and MDD revealed improvements in cognition, which were more pronounced in the patients with SZ; however, the patients with MDD showed a greater reduction in depressive symptoms and anxiety [37]. Aerobic exercise studies in MDD showed that exercise improves working memory and psychosocial functioning and reduces depressive symptoms [38, 39]. In particular, one study provided evidence for an effect of aerobic exercise on remission in MDD by showing that 29.5% of patients with unremitted MDD remitted after 3 months of aerobic exercise treatment [40].

Table 1.

Aerobic exercise studies in major depressive disorder, including study design, methodology, and clinical outcome

Year Publication Study design and diagnosis Sample size, n Intervention Control Measurement of CRF and PA Intervention duration /follow-up Outcome
IG CG
2019 Asthon et al. 2020 [52]

Exploratory subanalysis of an RCT (145 of 181 who reported data on PA)

Bipolar depression

(A) 50

(B) 46

49

(A) N-acetylcysteine alone

(B) N-acetylcysteine with a combination of nutraceuticals

Placebo

MADRS at week 16

IPAQ-SF at week 4

MADRS at week 16

And others

16 weeks

PA was unrelated to change in depression symptoms across study duration

In patients receiving combination treatment, total PA significantly predicted changes in bipolar depression symptoms

2019 Gujral et al. 2019 [97]

RCT, double blind

Pilot study

Major depressive episode

7 8

Venlafaxine XR AND

supervised exercise

Sessions: individualized, 3x/week, 1 h

Moderate intensity (60–75% of age-based HR for ~ 45 min on a treadmill and/or cycle ergometer)

Supervised: yes

Venlafaxine XR

CRF: submaximal VO2 test

PA: Body Media Sensewear armband, triaxial accelerometer

12 weeks

No significant changes in fitness in the exercise group

Significant reduction of depressive symptoms in both groups

Association between improvement in fitness and increased cortical thickness in the anterior cingulate cortex

2018 Gerber et al. 2019 [98]

Secondary analysis of RCT

MDD

53

Randomization: n.a

(A) Sprint interval training: 25 repetitions of 30 s high-intensity burst at 80% of max. power output, followed by 30 s of total rest

(B) Continuous aerobic exercise training: 20 min continuous aerobic exercise on a bicycle ergometer with an intensity level of 60% of the maximal power output

Both sessions: 3x/week, 35 min

Intensity: prescribed individually to

each participant

Supervised by an experienced exercise coach

n.a

CRF: VO2max, bicycle ergometer

Fitness Questionnaire, not specified

4 weeks

Improvements in VO2max were associated with fewer depressive symptoms, better mental wellbeing, and better sleep post-intervention

Improvements in perceived fitness were associated with less depression symptoms and better sleep higher mental wellbeing post-intervention

Improvements in VO2max and perceived fitness were associated with favorable changes in depressive symptoms, mental wellbeing, and sleep

2018 Minghetti et al. 2018 [48]

RCT

MDD

(A) 30

(B) 29

(A) Continuous aerobic exercise training [108]: 20 min continuous exercise at a power output corresponding to 60% of the maximal power output

(B) Sprint interval training (SIT): 25 repetitions of 30 s high-intensity bursts at 80% of maximal power output followed by 30 s of total rest (remaining seated on the bicycle)

Sessions: 3x/week, 35 min

Supervised by an experienced exercise coach

Medication was counterbalanced in both intervention arms

n.a

CRF: exhausting incremental exercise test, bicycle ergometer

Beck Depression Inventory-II

4 weeks

BDI-II scores substantially decreased in both groups, while submaximal and maximal variables improved in both groups

Short-term SIT leads to similar results as CAT in patients with MDD

2018 Patten et al. 2019 [44]

Pilot Study

Depressive symptoms

18 18

Free membership in fitness center for 12 weeks AND

Six 30-min individually tailored sessions with an exercise counselor; included aerobic exercise, strength training, stretching, and recommendations to exercise regularly

Exercise at the fitness center and at home were both encouraged, but no supervised exercise was provided

Free membership in fitness center for 12 weeks but no additional intervention

CRF: 6–12-min submaximal cardiorespiratory test, cycle ergometer

PA: evaluation of trunk flexibility, resting heart rate, blood pressure and body composition measured by bioelectrical impedance

Questionnaires: Stage of change for exercise, IPAQ, Beck Depression Inventory-II

12 weeks No group differences were found in IPAQ or BDI-II scores at week 12. Increases from baseline in IPAQ moderate/vigorous activity minutes were associated with decreases in BDI-II scores at week 12
2017 Rethorst et al. 2017 [40]

Randomized, secondary analysis

MDD

Two exercise doses:

 (A) 4 kcal/kg/week

 (B) 16 kcal/kg/week

Exercise intensity was self-selected and monitored with an HR monitor

Supervised: yes (complete dose in week 1, two in week 2, and 1 in week 3–12; rest unsupervised)

12 weeks Predictors of remission were higher levels of brain-derived neurotrophic factor (BDNF) and Interleukin-1B, greater depressive symptom severity, and higher post-exercise positive affect. Predictors of treatment non-response were low cardiorespiratory fitness, lower levels of IL-6 and BDNF, and lower post-exercise positive affect. Models including these predictors resulted in predictive values greater than 70% (true predicted remitters/all predicted remitters) with specificities greater than 25% (true predicted remitters/all remitters)
2015 Carneiro et al. 2015 [41]

RCT; only women

Clinical depression

13 13

Aerobic exercise group: indoor/outdoor natural circuit workouts AND

Pharmacotherapy

Sessions: 45–50 min/week; 3x/week

Intensity: based on baseline fitness. First month: at least 65% of %HRmax; second month: to 70%; third month: 80%. Diverse

Supervised: yes

Motivational strategies (e.g., multidisciplinary teams; Facebook page; outings in the sunlight and in pleasant settings; etc.)

Pharmacotherapy only

Physical functioning:

 Distance walked in 6 min

 Number of times they could sit and stand from a chair in 30 s

 A seated medicine ball throw

4 months

Decrease in BDI-II and DASS-21 total score scales in exercise group. Relative to DASS-21, a significant decrease in anxiety and stress is found

Improvement in relation to physical functioning parameters in exercise group

Anthropometric parameters only significant different between groups in fat mass percentage

No differences between groups in weight, body mass index, waist circumference, and self-esteem

2015 Doose et al. 2015 [42]

RCT

Unipolar depression

30 16

Walking/running aerobic exercise program at a local sports club

Sessions 3x/week, 60 min, outside

Intensity: self-selected exercise intensity according to perceived exertion

Supervised by teams of coaches and medical students

Wait list

CRF: Fitness Index,

VO2max as estimated or UKK 2 km Walk Test

8 weeks Large reduction of depressive symptoms in HRSD-17 scores. BDI-II, FI scores, and VO2 max did not change significantly
2015 Kerling et al. 2015 [92]

Randomized Pilot trial

Inpatient

Moderate to severe depression

22 20

Exercise training

3x/week, 45 min: 25 min bicycle and 20 min cross trainer, stepper, arm ergometer, treadmill, etc. as preferred

Moderate intensity: 50% of maximum workload from incremental test; above the VAT and below anaerobic lactate threshold

Supervised by physicians, group format

Treatment as usual

CRF: VO2peak, VAT, Watts, lactate on bicycle ergometer

MetS

6 weeks Cardiorespiratory fitness (VO2peak, VAT, Watts), waist circumference and HDL cholesterol significantly improved in exercise group. Treatment response (expressed as ≥ 50% MADRS reduction) was more frequent in the exercise group
2014 Danielsson et al. 2014 [47]

RCT

MDD

(A) Aerobic exercise: Training in the rehab center (e.g., cross trainer, jumping ropes, stationary bikes, etc.)

Intensity: intervals with higher perceived intensity

(B) Basic body awareness therapy: body scanning and stretch-release movements, postural stability, movement flow, and free breathing

Both programs: 2 sessions/week, 1 h during which 5–8 participants trained at the same time

Supervised by experienced physical therapists

Single consultation with advice on PA CRF: VO2max, submaximal bicycle test 10 weeks Improvements in MADRS score and cardiovascular fitness in the exercise group. Per-protocol analysis confirmed the effects of exercise and indicated that BBAT has an effect on self-rated depression
2014 Krogh et al. 2014 [84]

RCT

MDD

41 38

Aerobic exercise intervention on stationary bikes

Sessions: 3x/week, 45 min

Intensity: 80% of their maximal heart rate

Supervised: yes

Attention CG CRF: VO2max, bicycle cardiopulmonary exercise test 12 weeks

Post-intervention the mean VO2max increased with 3.90 ml/kg/min in the aerobic exercise group and 0.95 ml/kg/min in the control group

The hippocampal volume, BDNF, VEGF, or IGF-1 did not differ between the two groups

Positive association found post hoc between change in hippocampal volume and verbal memory and change in hippocampal volume and depressive symptoms

2014 Oertel-Knöchel et al., 2014 [37]

??

MDD and SZ

(A) 16

(B) 17

18

(A) CT combined with aerobic physical exercise: boxing, circuit training

Intensity: 60–70% of individual HRmax (calculated from HRmax from ECG)

Supervised by a trained physical exercise instructor

(B) CT combined with relaxation training (no yoga or PMR, just breathing, “enjoy exercises”)

Both 3x/week, 75 min: 30 min CT and 45 min training

CT and relaxation conducted by an exercise instructor

Waiting list CG

Complete physical examination, ECG, blood investigation

Validated questionnaires

4 weeks

Increase in cognitive performance in visual learning, working memory and speed of processing

Increase in subjective quality of life between pre- and post-testing

Significant reduction in depressive symptoms and state anxiety

The effects in SZ patients compared with MDD patients were stronger for cognitive performance, whereas there were stronger effects in MDD patients than in SZ patients in individual psychopathology values

2012 Krogh et al. 2012 [93]

Outpatient

RCT

MDD

56 59

Aerobic exercise

3x/week: cycle ergometer

Intensity: first 4 weeks: at least 65% of maximal capacity (VO2max), progressing to 70% and 80% during the second and third month, respectively

Supervised by a physiotherapist

Stretching, low intensity CRF: estimated VO2max, bicycle cardiopulmonary exercise test 12 weeks

After the intervention, the mean difference between groups was 20.78 points on the HAM-D17

At follow-up, higher VO2max and visuospatial memory on Rey’s Complex Figure Test and lower blood glucose levels and waist circumference in aerobic exercise group compared with stretching exercise group

2010 Oeland et al. 2010 [94]

Controlled clinical study

Panic disorder, generalized anxiety disorder, mild and moderate depression, mild and moderate recurrent depressive disorder

27 21

Group exercise: aerobic training (30 min) as circuit training

Intensity: high intensity, at least 65–75% of maximum aerobic capacity AND

Non-aerobic weightlifting with five basic exercises for muscles in legs, chest, abdomen, and lower and upper back: 8–10 repetitions with an intensity of 10 RM AND

The instructor encouraged the participants to exercise once a week on their own initiative, at least 30 min; they were free to choose intensity and type of exercise

2x/week, 90 min

Supervised: yes

Yes, but n.a

Aerobic capacity: submaximal bicycle ergometer test

Muscle strength: Senior Fitness Test

Questionnaires

20 weeks

12 weeks’ follow-up

Increase of physical activity and VO2max in intervention group

VO2max increase was maintained after a 12-week follow-up period

2009 Krogh et al. 2009 [49]

RCT, outpatient

Unipolar depression

(A) 55

(B) 55

55

(A) Strength group: circuit training with 6 machine exercises for large muscle groups

Intensity: Initially 12 repetitions of 50% of RM 2 or 3 times per exercise. As the patients progressed, the numbers of repetitions were reduced to 10 and 8, and RM was increased to 75%

(B) Aerobic group program: 10 different aerobic exercises for large muscle groups: cycling, running, stepping, etc

Intensity: During the first 8 sessions, each exercise was done twice for 2 min at an intensity level of 70% of maximal heart rate and followed by a 2-min rest. This gradually increased to a level during the last 8 sessions at which each exercise was done for 3 min at an intensity level of 89%, with a 1-min rest

Sessions: 2x/week, 1.5 h

Supervised by a physiotherapist

Relaxation group

CRF: VO2max, bicycle ergometry;

RM

4 months

6 months’ follow-up

Increase of strength measured by 1 RM in strength training group compared to relaxation group at month 4

Increase of VO2max in aerobic group compared to relaxation group at month 4

No statistically significant effect on cognitive abilities

2009 Hoffman et al. 2008 [95]

RCT

MDD

(A) 51

(B) 53

(C) 49

49

(A) Supervised aerobic exercise: 3x/week; individual training ranges equivalent to 70–85% HR reserve, calculated from the HRmax achieved during initial treadmill test

(B) Home-based aerobic exercise: one initial training and 2 follow-up sessions with an exercise physiologist

A and B: individual training ranges equivalent to 70–85% HR reserve, calculated from the HRmax achieved during initial treadmill test

(C) Sertraline

Placebo pill Aerobic capacity: VO2peak, graded treadmill exercise testing 16 weeks

Higher levels of VO2peak and longer treadmill times in supervised exercise patients than in those who exercised at home

No differences in neuropsychological tests between groups

Better performance on tests of executive function but not on tests of verbal memory or verbal fluency/working memory in exercise group

2007 Legrand and Heuze 2007 [43]

Pilot study, randomized

Depression

(A) 8

(B) 8

7

(A) High-frequency exercise: 3–5 sessions/week, within their THR on a motorized treadmill, a stationary bicycle, or a rowing ergometer

(B) High-frequency exercise AND group-based intervention: 3–5 sessions/week AND group support: e.g., collective training sessions, asking participants to wear group T-shirts, encouraging participants to chat and to cheer each other on

Supervision by first author of the study

Low-frequency exercise: 30 min/week of one aerobic exercise

Reaction to group intervention: participants’ scores of perceived cohesions

Questionnaire sur l’Ambiance du Groupe

8 weeks

Lower depression scores in high-frequency aerobic exercise group than in CG at week 4 and 8

Alleviation in depressive symptoms was not found to be greater in those participants who received a group-based intervention

2002 Penninx et al. 2002 [112]

RCT, single blind

Knee arthritis plus depression

(A) 112 low dep: 34 high

(B) 115 low; 28 high

113 (36 high-dep)

(A) Resistance exercise: facility-based program, 3x/week, 1 h AND a 15-month home-based program. Repetitions of various upper and lower body exercises with dumbbells and cuff weights

Supervised: yes

(B) Aerobic exercise: indoor track; walking at an intensity equivalent to 50–70% of the HRR (determined from a screening exercise treadmill test). In months 4–6, the exercise leader visited participants four times and called them six times to offer assistance and support in the development of a walking exercise program in their home environment

Health education Self-reported disability, 6-min walking speed, knee pain

3 months

15 months’ home-based follow-up

Significant decrease of depressive symptoms in aerobic exercise group compared to control group

No such effect was observed for resistance exercise

Reduction of depressive symptoms in both participants: with initially high and low depressive symptomatology

Significant decrease of disability and pain and increase of walking speed in aerobic and resistance exercise group

1999 Blumenthal et al. 1999 [96]

RCT

MDD

(A) 53

(B) 48

(C) 55

(A) Aerobic exercise session: 10 min warm up, 30 min continuous walking or jogging, 5 min cool down

(B) Medication: antidepressants: Sertraline hydrochloride

(C) Exercise + medications combined

Sessions 3x/week

Intensity: 70–85% of HRR calculated from HRmax

Supervised: yes

n.a Symptom-limited graded exercise treadmill test under continuous electrocardiographic recording 16 weeks

No statistical difference in groups on HAM-D or BDI scores

Patients in the exercise and combination groups showed significant improvements in aerobic capacity, whereas patients in the medication group did not

1989 Martinsen et al. 1989 [45]

RCT

Inpatient

Depression

51 47

Aerobic exercise: Brisk walks and jogging

Intensity: corresponding to approximately 70% of maximum aerobic capacity

3x/week, 1 h, 5–10 persons/group

Supervision by an experienced instructor

Non-aerobic, low intensity, muscular strength training CRF: VO2max, submaximal bicycle ergometer test 8 weeks

Significant increase of VO2max in the aerobic group

No change in the non-aerobic group

Significant reduction of depression scores in both scores during the study

Correlation between increase in physical fitness and reduction in depression scores was low

BBAT basic body awareness therapy, BDI-II Beck Depression Inventory-II, BDNF brain-derived neurotrophic factor, CAT continuous aerobic exercise training, CG control group, CRF cardiorespiratory fitness, CT cognitive training, DASS-21 Depression Anxiety and Stress Scale-21, ECG electrocardiogram, FI-Score fitness Index Score, HAM-D17 Hamilton Depression Scale-17, HRmax heart rate maximum, HRR heart rate reserve, HRSD-17 Hamilton Rating Scale for Depression-17, IG Intervention Group, IGF-1 insulin-like growth factor 1, IPAQ International Physical Activity Questionnaire, IPAQ-SF International Physical Activity Questionnaire–Short Form, MADRS Montgomery Asberg Depression Rating Scale, MDD Major depressive disorder, MetS Metabolic Syndrome, n.a. not applicable, PA Physical activity, PMR Progressive muscle relaxation, RCT randomized controlled trial, RM Repetition maximum, SIT sprint interval training, THR target heart rate, UKK 2 km Urho Kaleka Kekkonen 2-km Walk Test, VAT Ventilatory anaerobic threshold, VEGF vascular endothelial growth factor, VO2max maximal oxygen uptake, VO2peak peak oxygen uptake

In a randomized, controlled trial, 50 min’ add-on supervised aerobic exercise training 3 times a week for 4 months decreased symptoms of depression, anxiety, and stress compared with pharmacotherapy with antidepressants [41]. After an 8-week walking or running aerobic exercise program in local sports clubs, patients with MDD showed a large reduction in depressive symptoms compared with patients on a waiting list [42]. Moreover, an 8-week study found that high-frequency exercise was superior to low-frequency exercise with respect to depressive symptoms [43]. In an unsupervised study of physical activity in patients with MDD given access to fitness center resources, an increase in moderate-to-vigorous activity was associated with improvements in depressive symptoms [44]. In an 8-week study both aerobic and non-aerobic training methods had favorable effects on depression scores [45].

Different types of exercise have been studied in the last decade. A meta-analysis revealed small effects of aerobic exercise and yoga in outpatients with MDD, whereas the effects of Tai Chi were insufficient to enable conclusions to be drawn [46]. Additionally, aerobic exercise was superior to basic body awareness therapy with respect to depressive symptoms and cardiovascular fitness [47]. In patients with MDD randomized to 4 weeks’ sprint interval training or continuous aerobic exercise training, improvements in CRF were observed in both groups and were associated with improved depressive symptoms, emotional wellbeing, and sleep [48]. In contrast, another study found no improvements in depression score in the Hamilton Rating Scale for Depression after a 4-month strength and aerobic exercise training in patients with MDD [49]. Using mendelian randomization methods on genomic and phenotypic data from the UK biobank, beneficial effects of exercise were detected in depression but not in SZ [50, 51] (Table 1).

Effects of physical activity on symptoms of BD

No interventional studies have examined the effects of exercise in patients with BD. However, in a study examining the effects of N-acetylcysteine treatment, physical activity was not related to improvements in depressive symptoms, although those participants who engaged in higher levels of physical activity had greater improvements in social and occupational functioning [52].

Aerobic exercise training improves cognition and symptoms in patients with SZ

Several studies have demonstrated beneficial effects of physical exercise on symptoms of SZ (Table 2). For example, a well-cited meta-analysis showed that in patients with SZ aerobic exercise improves negative, positive, and depressive symptoms and global functioning, as measured by the Global Assessment of Functioning (GAF) score [53]. In addition, another meta-analysis focusing on cognition demonstrated improved global cognition, working memory, social cognition, and attention after aerobic exercise in patients with SZ [54]. A recent meta-analysis of randomized controlled trials found that aerobic exercise had small beneficial effects on negative symptoms in patients with SZ [55]. Across aerobic exercise studies, symptom improvement was seen in interventions consisting of 90 min of moderate exercise per week [56]. This finding is in line with our own work, which showed that 3 × 30 min of aerobic exercise per week alleviated negative symptoms and significantly improved global functioning and short-term memory in patients with SZ [57, 58]. Moreover, we found preliminary evidence that the improvements in level of functioning might be sustained even after exercise cessation [59].

Table 2.

Aerobic exercise studies in schizophrenia, including methodology, cardiorespiratory fitness measurements, and clinical outcome

Year Publication Study design and diagnosis Sample size, n Intervention Control Measurement of CRF and PA Intervention duration /follow-up Outcome
IG CG
2021 Kimhy et al. 2021 [105]

Single-blind RCT

SZ

16 17

Aerobic exercise program with 2 active-play video games (Xbox 360 Kinect) and traditional aerobic exercise equipment (treadmill, bike)

Sessions: 3x/week, 1 h

Moderate intensity: activities that expend 3.0–5.9 times the energy expended at rest; 60% of HRmax in week 1, 65% in week 2, 70% in week 3, and 75% in weeks 4–12

Supervision by a BSc in Science of Therapeutic Recreation

UC CRF: VO2peak, cycle ergometer 12 weeks

↑ In VO2max by 18.0% vs. 0.5%

Improvements in VO2max significantly predicted enhancement in SF as indexed by self-, informant-, and clinician-reported measures, predicting 47%, 33%, and 25% of the variance, respectively

Significant improvement in SF (23.0% vs. − 4.2%)

2020 Andersen et al. 2020 [99]

RCT

SZ

21 26

HIIT

Walking/running on a treadmill,

Sessions: 2x/week, 45 min

Intensity: 4 × 4 min 85–95% of HRmax, active breaks consisting of 3 min of ~ 70% of HRmax

Supervision by mental health care providers with or without PA competence (half of the participants, respectively)

PC gaming skills (Nintendo Wii sports console), supervised

CRF: VO2max (treadmill, maximum exercise session, mod. Balke protocol)

PA: Actigraph GT3X + accelerometer

12 weeks

No significant within-group differences in CRF

↑ Workload in 61% of HIIT

↑ In VO2max when adding PA competence of the mental health care providers

No significant effect on PA level or body composition

2020 Dubreucq et al. 2020 [113]

Quasi experimental trial

SZ

57 30

Exercise-enriched integrated social cognitive remediation intervention

Sessions: 1x/week, 2 h

Intensity: not defined

Supervised by two facilitators

Active CG practicing Touch Rugby

12 × 2-h sessions

Supervised by specialized sport scientists

12 weeks

6 months’ follow-up

Moderate to large improvements in social function, symptom severity, verbal abstraction, aggression bias, and self-stigma that were specific to the IG and were not observed in participants playing only Touch Rugby. Effects were persistent over time and even larger between post-treatment and follow-up
2020 Korman et al. 2020 [102]

Single arm, prospective feasibility study

SMI; 92% SZ

42 No CG

Mixed aerobic and resistance training: circuit training, combined with a dietary intervention (six individual and group sessions)

Sessions: 3x/week, 1 h

Intensity: Moderate from week 3. (RPE at 2–3 for the first 2 weeks, then increased to a minimum RPE of 4/10 by week 3 and further increased as per individual participant's capacity)

Supervised by exercise physiology students

No CG

Functional exercise capacity: 6 MWT

PA: questionnaire SIMPAQ

Motivation towards exercise: BREQ

10 weeks

Significant improvements in functional exercise capacity, volume of exercise, general psychiatric symptoms, and negative psychotic symptoms

No change in anthropometric and metabolic blood markers

2020 Massa et al. 2020 [101]

RCT

Outpatient

SZ

21 17

Aerobic exercise on a stationary bicycle, groups of about 5 participants

Sessions: 3x/week, initially 20 min to 45 min (increasing 5 min each week)

Intensity began at low levels (50% of maximal HRR) to 80% of HRmax (increased by 5% every week)

Supervised by at least one qualified instructor

Stretching and balance training for same amount of time, groups of about 5 participants 400 m walk test → Estimate VO2max

12 weeks

8 weeks’ follow-up

Subjects in both groups were slower at the 400 m walk in week 12 compared with baseline, but the IG had significantly less slowing than the CG

Between week 12 and week 20, the aerobic exercise group had a significantly greater change score on the Composite and Visual Learning Domain of the MATRICS Consensus Cognitive Battery

2019 Brobakken et al. 2019 [100]

RCT

Feasibility study

SZ

25 23

Aerobic interval training in groups, walking/running on a treadmill

Sessions: 2x/week, 35 min

Intensity: 4 × 4 min 85–95% of HRpeak, active pauses consisting of 3 min of ~ 70% of HRpeak

Supervised by experienced healthcare professionals

Two aerobic interval training sessions and encouragement to exercise on their own CRF: VO2peak 12 weeks

VO2peak by 10%, no change in the CG

No intergroup difference in weight, body mass index (BMI), waist circumference, blood pressure, lipids, or glucose at posttest

↑Weight and BMI in the CG, no change in the IG

2019 Hallgren et al. 2019 [60]

Single-arm feasibility study

First-episode psychosis; majority SZ

91 No CG

Circuit training: high-volume resistance exercises, aerobic training, and stretching

Sessions: at least 3x/week, 1 h

Supervised by exercise science graduates and exercise physiologist

No CG 12 weeks Significant post-intervention improvements for processing speed, visual learning, and visual attention; all with moderate effect sizes
2019 Larsen et al. 2019 [114]

RCT, Feasibility study

First-episode psychosis, SZ, Schizotypal and delusional disorder, and other non-organic psychotic disorders

13 12

Cross-fit-oriented training

Session: 3x/week, 1 h

Moderate to high intensity

Supervised by two instructors (undergraduate students)

Waiting list CG 8 weeks Three main themes and ten subthemes emerged during the analysis: (1) motivation and expectations for enrollment (subthemes: routines and structure, social obligation, goal setting and self-worth); (2) new demands and opportunities (subthemes: practicalities of the training, an understanding exercise setting, and alone and together); and (3) looking ahead—reflections on impact (subthemes: restored sleep and circadian rhythm, energy and sense of achievement, changed everyday life, and hope of finding a new path)
2019 Shimada et al. 2019 [62]

Pilot RCT

SZ

(A) 16 15

(A) Aerobic exercise: individual and group programs

Sessions: 2x/week, 1 h

Intensity: individually calibrated at 60–80% of aerobic capacity. Patients were required to participate in a minimum of 75% of each session

Supervised by occupational therapists

UC n.a 12 weeks IG and CG patients showed significant improvements in cognition, intrinsic motivation, psychiatric symptoms, and interpersonal relations
2017 Bhatia et al. 2017 [115]

Single-blind RCT

SZ

A) 104

(B) 90

92

(A) Yoga training (postures and breathing)

(B) Physical exercise training: brisk walks, jogging, and directed aerobic exercises

Sessions: 5x/week, 1 h

Supervised by qualified instructors

UC n.a

21 days

6 months’ follow-up (provided with a yoga training booklet, compliance charts)

Speed index of attention domain in group (A) showed greater improvement than group (B) at 6 month follow-up

In group (B), accuracy index of attention domain showed greater improvement than UC alone at 6-month follow-up

For several other cognitive domains, significant improvements were observed with (A) or (B) compared with UC alone

2017 Cheng et al. 2017 [107]

RCT

SZ

26 28

Aerobic dance program

Sessions: 2x/week, 60 min

Intensity: 60–79% of predicted HRmax

Supervised by professional instructor

UC Muscular endurance (1-min flexed leg sit-up), flexibility (sit-and-reach test), cardiorespiratory endurance (3-min step test; HR)

8 weeks

4 weeks’ follow-up

Significant between-group differences at posttest and in the follow-up for all of the health-related fitness outcomes with the exception of muscular endurance
2017 Curcic et al. 2017 [63]

RCT

SZ

40 40

Individual training: Walking/running 2–4 km outside

Sessions: 4x/week, 45 min

Intensity: 65–75% HRmax

Supervised by a fitness trainer

UC CRF: VO2max 12 weeks

After 12 weeks, patients in IG showed a significant increase of VO2max and significantly higher level of VO2max compared to the CG

Significant differences on PANSS general psychopathology subscale and on PANSS total score. The pharmacotherapy and exercise had influence on PANSS general psychopathology and PANSS total score

2016 Duncan et al. 2016 [116]

Randomized cross-over study

SZ

28

Bout of exercise: walking on the treadmill

Intensity: moderate (64–76% of the calculated HRmax)

1 × 10 min

Passive sitting for 14 min Mean HR, percent maximum HR, Borg RPE 10-min post-tests after 14 and 24 min Significant differences between pleasure at baseline, both immediately after task and 10 min after task. No other main effects or interactions
2016 Ho et al. 2016 [68]

RCT

Chronic SZ

(A) 51

(B) 51

49

(A) Tai Chi: 22 simple movements

(B) Moderate aerobic exercise routine to achieve 50–60% of maximal oxygen consumption

Both groups: 1x/week, 60 min AND 2x/week, 45 min

Supervised by mental health professionals

Wait list control

UC; they were offered the Tai chi or exercise class on a voluntary basis after the 3-month post-intervention follow-up assessment

Heart rate

12 weeks

3 months’ follow-up

Compared with CG, the Tai-chi group showed significant decreases in motor deficits and increases in backward digit span and mean cortisol, while the exercise group displayed significant decreases in motor deficits, negative and depression symptoms and increases in forward digit span, daily living function, and mean cortisol

No significantly different therapeutic effects of the two interventions, except for fewer symptom manifestations in the exercise group

2016 Kang et al. 2016 [67]

RCT

Chronic SZ

118 126

Community-based integrated intervention = Tai Chi Intervention AND Social Skills Training

Sessions 2x/month, 120 min: 45 min social skill training, 45 min Tai Chi, 30 min break

Supervised by three full-time psychiatrists and one assistant

Both groups received medication maintenance treatment to prevent relapse

Medical treatment alone 12 months Compared with the medical treatment alone group, the community-based integrated intervention group had lower scores on PANSS and negative symptoms, a lower risk for aggressive behavior, and a greater improvement in adherence to medication after 1 year of intervention
2016 Keller-Varady et al. 2016 [29]

Controlled interventional study

SZ

(A) 22

(B) 21

22 healthy controls

(A) Endurance group: dynamic aerobic endurance training on bicycle ergometers

Sessions: 3x/week, 30 min

Intensity: set according to the individual results of a baseline assessment of endurance capacity, equivalent to blood lactate concentrations of 2 mmol/l

Supervised by sport scientist

(B) Table soccer group: table soccer

Sessions: 3x/week, 30 min

Supervision: n.a

All participants continued with their usual medication

Healthy control in endurance group

Endurance capacity by ergometer stress test

Standardized questionnaire, specially developed for measuring PA

12 weeks

3 and 6 months’ follow-up

Improvements of endurance capacity in (A), but not in (B)

Patients and healthy controls showed comparable adaptations to endurance training, as assessed by physical working capacity and maximal achieved power

Differences in changes of performance at a lactate concentration of 3 mmol/l

2016 Malchow et al. 2016 [88]

RCT

SZ

2021 healthy controls 19

Endurance training on bicycle ergometers

Sessions: 3x/week, 30 min

Intensity: individually defined intensity, gradually increased according to blood lactate concentrations of approximately 2 mmol/l, HR, Borg Scale

Supervised by sports scientists

From week 6, the computer-assisted training program COGPACK was added as an intervention in each group to train cognitive performance

Table soccer in groups (2–4 players)

Endurance capacity (PWC130) by maximal exercise stress test

PA was monitored throughout the study, not defined

6 weeks

3 months

No significant increases in the volumes of the hippocampus or hippocampal substructures in SZ patients or healthy controls

Increased volume of the left superior, middle, and inferior anterior temporal gyri compared with baseline in SZ patients after the endurance training, whereas patients playing table soccer showed increased volumes in the motor and anterior cingulate cortices. After the additional training-free period, the differences were no longer present

Improvements of endurance capacity in exercising patients and healthy controls

No change in psychopathological symptoms

2016 Su et al. 2016 [61]

3-month follow-up study, single blind, randomized

SZ

30 27

Aerobic exercise: individually tailored for each participant because exercise prescriptions were based on each individual's age-adjusted HRmax

Sessions: at least 3x/week, 40 min

One-on-one supervision throughout the sessions

Stretching and toning control group, individually conducted, own pace

Same social interactions as those in aerobic exercise group

Estimated VO2max

12 weeks

3 months’ follow-up

No significant difference between the two groups in any cognitive outcome measured at follow-up; improvement over time was noted in certain cognitive domains in the IG

No significant between-group differences in aerobic fitness at posttest and follow-up

Fitness level was not related to changes in cognitive performance

2016 Yoon et al. 2016 [108]

Single-arm pilot study

SZor schizoaffective disorder

24 No CG

Exercise intervention: group-based outdoor cycling

1x/week, at least 40 min

Individual performance (average speed, distance, and duration) and heart rate, were monitored by individual supervising staff during every session.)

Supervised by two professional cyclists and other staff: medical doctors, nurses, and social workers

No CG Cardiorespiratory function test (step test): 3-min YMCA step test

3 months

6 months’ follow-up

Significant increase in participant’s self-esteem, positive relationship, global function, and quality of life

CRF significantly improved after 3 months

At the 9-month follow-up, 6 months after program completion, only in interpersonal relationship change the improved effects were maintained

2015 Kaltsatou et al. 2015 [69]

RCT, outpatient

SZ

16 15

Greek traditional dancing program

Sessions: 3x/week, 60 min

Intensity: 60–70% of individual HRmax (220-age)

Supervised by a PA instructor

Sedentary CG, Patients were asked to refrain from any other form of organized PA during study period

6 MWT

Sit-to-stand test, 10 times

Lower limb strength testing

Hand-grip strength

8 months ↑ Walking distance in the 6 MWT, sit-to-stand test, Berg Balance Scale score, lower limbs maximal isometric force, Positive and Negative Syndrome Scale total score, Global Assessment of Functioning scale total score, and Quality of Life total score
2015 Kimhy et al. 2015 [117]

Single-blind RCT, inpatient

SZ

16 17

Aerobic exercise program utilizing 2 active-play video games (Xbox 360 Kinect) and traditional aerobic exercise equipment (treadmill, bike)

Sessions: 3x/week, 1 h

Intensity: moderate intensity, minimal aerobic exercise intensity was set to 60% of HRmax in week 1, 65% in week 2, 70% in week 3, and 75% in weeks 4–12

Supervised by a BSc in Science of Therapeutic Recreation

UC CRF: VO2peak 12 weeks

VO2peak by 18.0% in the IG vs a − 0.5% decline in the CG

Improvement of neurocognition by 15.1% vs − 2.0%

CRF and increases in BDNF predicted 25.4% and 14.6% of the neurocognitive improvement variance, respectively

2015 Loh et al. 2015 [118]

RCT, inpatient

SZ

52 52

Structured, organized walking intervention, 3x/week, supervised

3x/week, the first month: 20-min walking exercise, second month: 30-min walking exercise, third month: 40-min walking

HR was monitored before and after the exercise to prevent overexertion

Supervised by ward staff nurses and assistant medical officers

Treatment as usual IPAQ-M

12 weeks

3 months’ follow-up

At 3-month follow-up, significant within-group differences in QOL (SF-36), psychiatric symptoms (PANSS), and personal and social performance (PSP)

Increase in the median SF-36 scores, with increases shown in physical functioning, physical role limitations, social functioning

Reduction of median PANSS in positive and negative symptom, and general psychopathology scales

Increase in the median PSP score

Between-group differences at post-intervention (favoring intervention) were significant for PANSS positive and SF-36

2015 Malchow et al. 2015 [58]

RCT

SZ

2223 healthy controls 21

Endurance training on bicycle ergometers

Sessions: 3x/week, 30 min

Intensity: individually defined intensity, gradually increased according to blood lactate concentrations of approximately 2 mmol/l, HR, Borg Scale

Supervised by sports scientists

From week 6, the computer-assisted training program COGPACK was added as an intervention in each group to train cognitive performance

Table soccer in groups (2–4 players) Endurance capacity (PWC130) by a maximal exercise test on a bicycle ergometer

6 weeks

3 months

6 months’ follow-up

After 3 months, improvement in GAF and SAS-II social/leisure activities and household functioning adaptation in the endurance training augmented with cognitive remediation, but not in the table soccer augmented with cognitive remediation group

Significant improvements in the severity of negative symptoms and performance in the VLMT and WCST in the endurance training augmented with cognitive remediation group from week 6 to the end of the 3-month training period

2015 Masa-Font et al. 2015 [111]

RCT

Severe mental illness; 67% SZ

169 163

Educational program AND

PA program based on different stages → 24 sessions 2x/week over 3 months: The first 8 sessions (40 min) consisted of making first contact with PA. The other 16 sessions (60 min) aimed to increase the number of daily steps taken to reach 10,000 steps per day on routes adapted to the physical condition of the participants

AND Dietary intervention → 16 sessions 2x/week, 20 min to provide basic knowledge on healthy dietary habits

Supervised by professionals

No intervention, usual program of regular check-ups with their reference psychiatrist

All the participants in both the IG and CG kept up their usual visits with their reference mental health professional and continued the usual treatment for their disease

PA: IPAQ, METs expended per week

3 months

12 months’ follow-up

↑ Average weekly walking METs in the IG

BMI decreased significantly more in the CG

No significant differences in the waist circumference

2015 Silva et al. 2015 [70]

RCT “blind”

SZ

(A) 12

(B) 9

13

(A) Resistance: progressive resistance training

Intensity: from 40% 1RM in week 1 up to 85% 1RM in week 20

(B) Concurrent exercise: endurance training and strength resistance training

Intensity: from 40% VO2max in week 1 up to 75% VO2max in week 20

Sessions: 2x/week, 60 min

Supervised by professional physical educators

Control: equipment load was kept at a minimum, treadmill speed remained at 4 km/h CRF: VO2max 20 weeks

A significant time-by-group interaction was found for (A) and (B) on the Positive and Negative Syndrome Scale total score for disease symptoms, positive symptoms, and on the arm extension one-repetition maximum test

Improvements in (A) on negative symptoms, on the role-physical domain of the Short Form-36 Health Survey, and on the chest press 1RM test

2015 Svatkova et al. 2015 [90]

RCT

SZ

(A) 16

(B) 17

(A) 24

(B) 24 healthy controls

(A) Aerobic and anerobic exercise. Aerobic exercise: bicycle ergometer, rowing machine, cross trainer, treadmill and muscle strength exercises (6 exercises per week, 3 times). Anaerobic exercise: working with weights

2x/week, 1 h: 40 min aerobic training, 20 min anaerobic training

Intensity: n.a

Supervision: n.a

(B) No exercise = life-as-usual

(A) exercise

(B) no exercise = life- as-usual

Healthy controls

CRF: VO2peak

Structured questionnaire to assess the level of daily life physical activities at baseline

Brain scans

6 months

Irrespective of diagnosis, regular physical exercise of an overlearned skill, such as bicycling, significantly increases the integrity, especially of motor functioning-related white matter fiber tracts, whereas life-as-usual leads to a decrease in fiber integrity

Significant differences in the exercise and non-exercise group from the first to the second measurement in Wpeak and VO2peak

2014 Oertel-Knöchel et al. 2014 [37] MDD (n = 22) and SZ (n = 29)

(A) 16

(B) 17

18

(A) Cognitive training combined with aerobic physical exercise: boxing, circuit training

Intensity: 60–70% of individual HRmax (calculated from HRmax from ECG)

Supervised by a trained physical exercise instructor

(B) CT combined with relaxation training (no yoga or PMR, just breathing, “enjoy exercises”)

CT and relaxation conducted by instructors

Both sessions: 3x/week, 75 min (30 min CT and 45 min training)

Waiting list CG 4 weeks

Increase in cognitive performance in the domains visual learning, working memory and speed of processing; decrease in state anxiety; and increase in subjective quality of life in the total group of patients

The effects in SZ patients compared with MDD patients were stronger for cognitive performance, whereas there were stronger effects in MDD patients compared with SZ patients in individual psychopathology values. MDD

Reductions in depressive symptoms and state anxiety values in patients

Reduction of negative symptoms severity in SZ patients

2014 Vancampfort et al. 2014 [119]

Pilot Study cross-sectional

SZ

88 No intervention

Spirometry: 2 spirometry attempts while seated, conducted by trained technicians

CRF: 6-min walk test

PA: IPAQ

Screening: 6 months

Patients with MetS had a reduced predicted forced expiratory volume for 1 s and predicted forced vital capacity

Significantly more patients with MetS were diagnosed with restrictive lung dysfunction

SZ patients with restrictive lung dysfunction had a significantly larger waist circumference, were less physically active and walked less on the 6 MWT than patients without

2013 Scheewe et al. 2013 [64]

RCT

SZ

31 32

Exercise therapy:

 Muscle strength exercises (six exercises/week, 3 × 10 to 15 RM for biceps, triceps, abdominal, quadriceps, pectoral, and deltoid muscles). 2x/week, 1 h

Intensity: increased stepwise: week 1–3, 45%; week 4–12, 65%; week 13–26, 75% of HR reserve based on baseline CPET data

Supervised by a psychomotor therapist

Occupational therapy creative and recreational activities CRF: VO2peak and Wpeak 6 months

Wpeak in IG compared with CG

Exercise therapy reduced symptoms of SZ, depression, need of care, and increased VO2peak in the IG compared with CG

No effect for MetS factors

2013 Scheewe et al. 2013 [85]

RCT

SZ

(A) 18

(B) 14

(A) 25

(B) 27

(A) Exercise therapy intervention: upright and recumbent bicycle ergometer, rowing machine, cross trainer, and treadmill AND muscle strength exercises (for biceps, triceps, abdominal, quadriceps, pectoral, deltoid muscles)

1 h of exercise consisting of both cardiovascular exercises (40 min) and muscle strength exercises (20 min) twice weekly

Supervised by a psychomotor therapist specialized in psychiatry

(B) Occupational therapy by an occupational therapist 1 h/twice weekly: Occupational therapy comprised creative and recreational activities, no physical activity

(A) Exercise therapy

(B) Life as usual

More details n.a

CRF: VO2peak 6 months

Significantly smaller baseline cerebral (gray) matter, and larger third ventricle volumes, and thinner cortex in most areas of the brain in patients versus controls

No changes in global brain and hippocampal volume or cortical thickness

CRF improvement was related to increased cerebral matter volume and lateral and third ventricle volume decrease in patients and to thickening in the left hemisphere in large areas of the frontal, temporal and cingulate cortex irrespective of diagnosis

1–2 h of exercise therapy did not elicit significant brain volume changes in patients or controls

CRF improvement attenuated brain volume changes

2012 Scheewe et al. 2012 [106]

RCT

SZ

(A) Exercise therapy 31//

Healthy controls 27

(B) Occupational therapy 32

28

Exercise therapy:

 (A) Muscle strength exercises (six exercises weekly; three times 10–15 RM for biceps, triceps, abdominal, quadriceps, pectoral, and deltoid muscles)

Sessions: 2x/week, 1 h

 Intensity was increased stepwise (week 1–3, 45%; week 4–12, 65%; week 13–26, 75% of HRR based on baseline CPET data

 Supervised by a psychomotor therapist

(B) Patients not randomized to exercise therapy were offered occupational therapy 2x/week, 1 h: creative and recreational activities

Life as usual, not allowed to incorporate moderate physical activity more than 1 h weekly CRF: VO2peak and Wpeak 6 months

Patients had higher resting HR and lower peak HR, peak systolic blood pressure, relative VO2peak, Wpeak, RER, minute ventilation and HR recovery than controls

In patients, exercise therapy increased relative VO2peak compared with decreased relative VO2peak after occupational therapy

In controls, relative VO2peak increased after exercise therapy and to a lesser extent after life-as-usual

Exercise therapy increased Wpeak in patients and controls compared with decreased Wpeak in nonexercising patients and controls

2012 Takahashi et al. 2012 [87]

??

SZ

13 10

Program including exercise, nutrition education and medication counseling

Exercise module: aerobic exercise (walking and jogging), muscle-stretching exercise and sports exercise (basketball). The exercise module was 30–60 min long, and was delivered twice a day (a total of 60–120 min per day) from Monday to Saturday

For each participant, the exercise intensity level was set at 11–13 (fairly light to somewhat hard) on the Borg scale

Supervised by a group of professionals from diverse disciplines (physical therapists, psychiatric nurses, psychiatrists, nutritionists, and pharmacists)

All patients received antipsychotics, and their medications remained unchanged during this study

Attended the day-hospital unit but not the program 3 months

Body mass index and general psychopathology scale of PANSS were significantly reduced in the program group but not in the control group after a 3-month interval

Compared with baseline, activation of the body-selective extrastriate body area [23] in the posterior temporal-occipital cortex during observation of sports-related actions was increased in the program group. In this group, increase in EBA activation was associated with improvement in the general psychopathology scale of PANSS

Sports participation had a positive effect not only on weight gain but also on psychiatric symptoms in schizophrenia

2011 Heggelund et al. 2011 [104]

RCT

SZ

12 7

HIIT

Sessions: 3 days/week, 36 min: 4 × 4 min

Intensity: 4 min 85–95%, 3 min 70% HRpeak

Supervised by an exercise physiologist

Played PC (Tetris) games; 3 days/week, 36 min

Supervised by the same exercise physiologist

CRF: VO2peak 8 weeks

The HIIT group improved VO2peak by 12% compared with the CG group

Net mechanical efficiency of walking improved 12% in the HIIT group compared with the CG group

No significant changes in PANSS, CDSS or SF-36 in either group

2011 Methapatara and Srisurapanont 2011 [120]

RCT

SZ

32 32

Pedometer walking AND motivational interviewing program → 5 × 1-h sessions:

 First session: individual motivational interviewing with a focus on obesity/overweight and motivation for adequate daily walking

 Second session: group education on nutrition, exercise, warming up, cooling down, and implementation of pedometer

 Third session: specific, measurable, acceptable, realistic, and timed criteria were used to set an individual goal, the first goal of daily walking was set at a minimum of 3000 steps per day

 Forth session: group practicing of pedometer walking under supervision

 Fifth session: therapist gave feedback on the patients’ practice, informed about self-regulation principles to cope with lapses and relapse

Control patients received the usual care only and no pedometer 12 weeks

Bodyweight of intervention group decreased more than that of the control group at week 4, 8, and 12

BMI at week 12 was significantly different between groups

The decreases of waist circumference were significantly more in the intervention group for all three time-points of assessment

2011 Vancampfort et al. 2011 [65]

Pilot study

SZ

(A) 40

(B) 40

40

(A) One single 30-min yoga session, trained by a physiotherapist

(B) One single 20-min aerobic exercise session, performed on an electronically braked ergometer; consisted of cycling for 20 min at self-selected intensity with heart rate feedback. A physiotherapist was present during exercise

No exercise, participants sat quietly in a room for 20 min and were allowed to read. A physiotherapist was also present n.a One single event After single sessions of yoga and aerobic exercise, individuals with SZ or schizoaffective disorder showed significantly decreased state anxiety, decreased psychological stress, and increased subjective wellbeing compared to a no-exercise control condition. The magnitude of the changes did not differ significantly between yoga and aerobic exercise
2010 Pajonk et al. 2010 [57]

RCT, day-hospital/outpatient

SZ

88 healthy control 8

Aerobic exercise training (cycling)

Sessions: 3x/week, 30 min

Intensity: heart rate (± 10 beats/min) corresponding to a blood lactate concentration of about 1.5–2 mmol/l (14–18 mg/dl) derived from the results of the pretest

Supervised by one of the investigators

Played table football

The comparison group of patients played tabletop football for 30 min, 3 times per week, in a setting with comparable levels of stimulation to those provided for aerobic exercise. Tabletop football enhances coordination and concentration but does not improve aerobic fitness

CRF: VO2max 3 months

After exercise training, relative hippocampal volume increased significantly in patients (12%) and healthy individuals (16%), with no change in the non-exercise group of patients

Changes in hippocampal volume in the exercise group were correlated with improvements in aerobic fitness measured by change in maximum oxygen consumption

In the SZ exercise group, change in hippocampal volume was associated with a 35% increase in the N-acetylaspartate to creatine ratio in the hippocampus

Improvement in test scores for short-term memory in the combined exercise and non-exercise SZ group was correlated with change in hippocampal volume

BDNF brain-derived neurotrophic factor, BMI body mass index, BREQ Behavioral Regulation In Exercise Questionnaire, CDSS Calgary Depression Scale for Schizophrenia, CG control group, CPET cardiopulmonary exercise testing, CRF cardiorespiratory fitness, CT cognitive training, EBA extrastriate body area, GAF Global Assessment of Functioning, HIIT high-intensity interval training, HR heart rate, HRmax heart rate maximum, HRpeak peak hear rate, HRR Heart rate reserve, IG Intervention group, IPAQ International Physical Activity Questionnaire, IPAQ-M International Physical Activity Questionnaire, Malay version, MATRICS Measurement and Treatment Research to Improve Cognition in Schizophrenia, MDD Major depressive disorder, MET metabolic equivalent, MetS Metabolic Syndrom, MWT Minute walk test, n.a. not applicable, PA Physical activity, PANSS Positive and Negative Syndrome Scale, PMR progressive muscle relaxation, PSP personal and social performance, PWC130 Physical Working Capacity 130, QoL Quality of Life, RCT Randomized controlled trial, RER respiratory exchange ratio, RM Repetition maximum, RPE Rating of perceived exertion, SAS II Social Adjustment Scale-II, SF-36 Short-Form-36, SIMPAQ Simple Physical Activity Questionnaire, SZ schizophrenia, UC usual care, VLMT verbal learning memory test, VLMT verbal learning memory test, VO2max maximal oxygen uptake, VO2peak Peak oxygen uptake, WCST Wisconsin Card Sorting Test, Wpeak Watt peak, WSCT Wisconsin Card Sorting Test, YT Yoga Training

Effects of aerobic exercise on cognition have been observed also in patients with first-episode SZ. After a 12-week supervised circuit-training program, improvement was seen in processing speed, visual learning, and visual attention domains [60]. In 75 patients with SZ randomized to 12 weeks of either moderate-intensity treadmill exercise or stretching and toning exercise, aerobic exercise improved processing speed and attention [61]. However, in a pilot randomized controlled trial in a small sample, group aerobic exercise over 12 weeks showed similar improvements in cognition and symptoms as treatment as usual [62]. After patients with SZ performed 12 weeks of treadmill training, their general and psychopathology and total score on the Positive and Negative Symptom Scale (PANSS) and aerobic capacity improved [63]. In a 6-month randomized study comparing aerobic exercise with occupational therapy in patients with SZ, exercise reduced symptoms, depression, and need of care and increased cardiovascular fitness [64]. In contrast, after a single session of aerobic exercise and yoga, patients from both groups showed only decreased anxiety and psychological stress and increased subjective wellbeing [65]. In meta-analyses of meditation-based mind–body interventions, small effect sizes have been observed for yoga in SZ [66]. Besides yoga, other exercise interventions such as Tai Chi have been applied in SZ patients and led to improvements in PANSS score, negative symptoms, and aggressive behavior [67]. A study that compared a 12-week Tai Chi program with aerobic exercise showed improved negative and depression symptoms [68]. In a randomized 8-month study of a Greek traditional dancing program, the dancing group showed improved positive and negative symptoms, GAF score, and quality of life compared with a sedentary group [69]. Finally, resistance training was studied in patients with SZ and improved negative symptoms [70] and level of functioning assessed with the GAF [71] (Table 2).

Neuroplasticity effects of aerobic exercise

Animal models and basic research in humans clearly show that aerobic exercise has favorable neurobiological effects. These effects may involve epigenetic alterations, synaptic plasticity, differentiation of glial cells and neurogenesis, the hypothalamus–pituitary–adrenal axis, growth factors, immune-related mechanisms, neurotransmitters, and the endocannabinoid system [72]. In 2103 adults from the general population, CRF, measured as peak oxygen uptake (VO2peak), was related to higher gray matter volume and showed a strong association with gray matter volume of the left middle temporal gyrus, right hippocampus, left orbitofrontal cortex, and bilateral cingulate cortex [73]. A meta-analysis of hippocampal volume in 737 voluntary participants revealed significant positive effects of aerobic exercise on left hippocampal volume but not on total hippocampus volume [74]. These results may be relevant for MDD, BD, and SZ because these brain disorders have been repeatedly shown to involve structural and functional alterations in the hippocampal formation [75, 76]. Moreover, a 7-Tesla magnetic resonance imaging study in older adults found a prominent volume increase in the left cornu ammonis (CA) subregions of the hippocampus and a trend for a volume increase in the left CA4/dentate gyrus after physical activity [77].

Deficits in both episodic and working memory are related to hippocampal abnormalities and are hallmarks of an unfavorable outcome in MDD [78] and SZ [79]. Our first study to investigate the effects of aerobic endurance training in a small sample of patients with multi-episode SZ showed a significant 10% increase in hippocampal volume after 3 months [57]. In our subsequent study in 20 patients, which combined 3 months of aerobic endurance training with cognitive remediation, we found no changes in hippocampal volume in the exercise group [58], but we did find a significant correlation between exercise-related volume increases in the CA4/dentate gyrus subregion of the hippocampus and the SZ polygenic risk score (SZ-PRS, [80]). Using cell-specific PRS, we found that this volume effect in CA4 was also caused by oligodendrocyte precursor cell-related pathways [81], which is also in line with our post-mortem finding of reduced oligodendrocyte number in the CA4 subregion [82]. In SZ and MDD it has been hypothesized that metabolic coupling may link oligodendrocyte to interneuron pathology [83]. Other studies found no changes in total hippocampal volume after aerobic exercise in MDD [84] or SZ [85]. However, after a 12-week aerobic exercise training, hippocampal volume in the CA1 subregion increased in SZ patients, whereas hippocampal vascular volume was unchanged, indicating no effect of aerobic exercise on blood vessels [86]. Additionally, a study that compared aerobic exercise training with table soccer in patients with SZ and healthy controls showed an increased volume of the right entorhinal cortex compared with baseline after 6 weeks’ training [87] and of the left superior, middle, and inferior anterior temporal gyri after 3 months’ training; but patients with SZ who played table soccer showed increased volumes in the motor and anterior cingulate cortices [88]. After 6 weeks’ aerobic exercise training, a magnetic resonance spectroscopy study in patients with SZ found increased N-acetyl-aspartate/total creatine levels in the left dorsolateral prefrontal cortex in both the aerobic exercise and table soccer groups [89], indicating improved neuronal viability. Additionally, a 6-month aerobic exercise program improved the integrity of motor function-related white matter fiber tracts compared with a life-as-usual condition [90].

Taken together, these results indicate that in SZ exercise has neuroplastic effects in brain regions that are affected by the disease itself. The effects of aerobic exercise on brain volume changes and underlying mechanisms warrant further study, not only in patients with SZ but also in those with MDD and BD.

Improvements of CRF in patients with severe mental illness

CRF is an important marker of cardiovascular health and should be comprehensively assessed in both clinical studies and clinical practice [22]. Especially in patients with severe mental illness and negative symptoms such as reduced drive and motivation, CRF serves as a control for the efficacy of an exercise intervention. Because of the above-mentioned low activity levels and high prevalence of cardiovascular comorbidities in patients with severe mental illness, besides aiming to improve symptoms of mental illness exercise interventions should also aim to increase CRF [91].

Several studies have focused on changes of CRF in patients with MDD [42, 45, 4749, 84, 9298] (Table 1) and SZ (e.g. [99103]) (Table 2). Some studies directly measured maximal oxygen uptake (referred to as VO2max or VO2peak) to test changes in CRF in patients with MDD [45, 48, 49, 92, 95, 97, 98] and SZ [57, 63, 64, 85, 90, 99, 100, 103106]. These tests are considered the gold standard, but other tests indirectly assessing CRF have been applied. For example, rather than being directly measured by cardiopulmonary exercise testing, VO2max can be estimated by data from a maximal or submaximal stress test. This approach of estimating CRF was used in a few studies in MDD [42, 47, 84, 93] and one in SZ [61]. Submaximal proxy measures can also be used to estimate CRF, e.g., the 6-min walking test, 400-m walking test, and 3-min step test; some studies in SZ have used such tests [69, 101, 102, 107, 108]. Aerobic capacity or endurance capacity can also be measured by an exercise stress test without assessing oxygen uptake, an approach used in studies in MDD [96] and SZ [29, 58, 88].

Besides using different measurement methods, studies differ regarding the training modalities. To date, the effects of anaerobic exercise interventions have been investigated only scarcely. However, there are studies that combined aerobic and anaerobic training elements [90]. In addition, there is a growing body of studies investigating HIIT [33, 47, 98100, 104], which is typically characterized by high-intensity exercise at 4 × 4 min intervals (85–95% of maximum heart rate [HRmax]), with active breaks consisting of 3 min of moderate-intensity exercise (approximately 70% of HRmax). HIIT was shown to be effective in improving CRF in patients with SZ. A small, 8-week study showed that VO2peak increased by 12% in the HIIT group (n = 12) but did not increase in the PC gaming group (n = 7) [104]. These results were confirmed by a recent randomized controlled trial on the effects of 12 weeks’ HIIT on VO2max in 21 patients with SZ. Like the study by Heggelund et al. [104], in this study the control group (n = 26) practiced their PC gaming skills. Although more than half of the patients in the HIIT group showed a significant increase in workload, a significant within-group difference in VO2max was only observed when the physical activity competence of the health care providers was added into the statistical model. This result underlines the importance of professional and experienced supervision when aiming to successfully improve CRF in patients with SZ [99]. The study findings are supported by a similar study in which the training group (n = 25) performed aerobic interval training and received professional adherence support twice a week over the 12-week intervention period. The patients’ VO2peak improved by 10%, while no change was observed in the control group (n = 23), who performed two supervised exercise sessions at the beginning of the study and were subsequently encouraged to continue exercising on their own [100].

To the best of our knowledge, only two studies have evaluated a form of interval training in patients with MDD. Gerber et al. [98] found associations between an increase in VO2max and improvements of symptoms in patients who performed a sprint interval training consisting of 25 repetitions of 30-s high-intensity bursts at 80% of maximal power output, followed by 30 s of total rest. Danielsson et al. [47] reported a significant increase of CRF in the intervention group, which performed intervals of exercise at higher perceived intensity during the aerobic exercise program, although training intensity was not strictly defined.

Exercise training of moderate intensity can also be effective in improving maximal oxygen consumption in patients with MDD [45, 92, 97] and SZ [29, 57, 63, 85, 105]. For example, in the most recent study in SZ, VO2max improved by 18% in patients after a 12-week aerobic exercise program with intensities ranging from 60 to 75% of HRmax (n = 16) but decreased by − 0.5% in the usual care group (n = 17) [105].

Mixed programs consisting of aerobic training combined with resistance training may also have the potential to improve CRF in patients with MDD [49, 94] and SZ [85, 102]. Although three studies measured CRF directly by cardiopulmonary exercise testing [49, 85, 94, 106], Korman et al. [102] used a submaximal test (they assessed functional exercise capacity, a submaximal proxy measure of CRF, as the distance walked during the 6-min walking test). Moreover, two studies that evaluated the effect of dancing programs in SZ showed improvements in performance during the 6-min walking test [69] or the 3-min step test [107]. Overall, little evidence is available on the effects of mixed programs, so further studies are needed that use clearly defined exercise programs and high-quality CRF measurements.

In summary, in patients with severe mental illness aerobic exercise, especially endurance training, has shown beneficial effects on global functioning, cognition, and negative and depressive symptoms. It stimulates synaptic and brain plasticity and affects the volume of specific brain regions, with genetic risk (SZ-PRS) influencing the results. However, despite the growing body of literature, the type, duration, and frequency of exercise needed for beneficial effects in the long term have yet to be determined before aerobic exercise will be used widely in general practice [109]. Some recommendations for further studies can be given from the perspective of sports medicine:

  • The American College of Sports Medicine recommends that adults engage in moderate-intensity cardiorespiratory exercise training for ≥ 30 min/day on ≥ 5 days/week for a total of ≥ 150 min/week, or vigorous-intensity cardiorespiratory exercise training for ≥ 20 min/day on ≥ 3 days/week for a total of ≥ 75 min/week [110].

  • Further studies are needed to identify the most effective exercise interventions (type, duration, frequency).

  • Because most studies were conducted over a relatively short intervention period of 3 to 4 months, were supervised and did not include a follow-up, future studies should focus on long-term adherence to exercise (e.g., by implementing motivational strategies supported by telemedicine and apps and by identifying and targeting typical barriers to exercise in this patient population).

  • This patient group has a high prevalence of cardiovascular disease, so researchers should consider measuring the associated risk factors when performing exercise intervention studies.

  • CRF should be comprehensively assessed in both clinical studies and clinical practice by direct measurements of maximal oxygen uptake.

  • Exercise interventional studies in patients with BD need to be conducted because this patient group is underrepresented.

Acknowledgements

This research was funded by the grants Klinische Forschergruppe (KFO) 241 and PsyCourse (FA241/16–1) to P. Falkai from the Deutsche Forschungsgemeinschaft (DFG). Further funding was received from the German Federal Ministry of Education and Research (BMBF) through the research network on psychiatric diseases ESPRIT (grant number 01EE1407E) to P. Falkai, A. Hasan, A. Schmitt. The authors thank Jacquie Klesing, BMedSci (Hons), Board-certified Editor in the Life Sciences (ELS), for editing assistance with the manuscript; Ms. Klesing received compensation for her work from the LMU Munich, Germany.

Funding

Open Access funding enabled and organized by Projekt DEAL.

Declarations

Conflict of interest

C.P. Rosenbeiger, I. Maurus, B. Malchow, L. Hattenkofer, P. Heim-Ohmayer, M. Halle, and M. Heitkamp report no conflicts of interest. A. Hasan has been invited to scientific meetings by Lundbeck, Janssen, and Pfizer, and he received paid speakerships from Janssen, Otsuka, and Lundbeck. He was member of Roche, Otsuka, Lundbeck, and Janssen advisory boards. A. Schmitt was an honorary speaker for TAD Pharma and Roche and a member of Roche advisory boards. P. Falkai has been an honorary speaker for AstraZeneca, Bristol Myers Squibb, Lilly, Essex, GE Healthcare, GlaxoSmithKline, Janssen Cilag, Lundbeck, Otsuka, Pfizer, Servier, and Takeda and has been a member of the advisory boards of Janssen-Cilag, AstraZeneca, Lilly, and Lundbeck.

References

  • 1.Wittchen HU, Jacobi F, Rehm J, Gustavsson A, Svensson M, Jonsson B, Olesen J, Allgulander C, Alonso J, Faravelli C, Fratiglioni L, Jennum P, Lieb R, Maercker A, van Os J, Preisig M, Salvador-Carulla L, Simon R, Steinhausen HC. The size and burden of mental disorders and other disorders of the brain in Europe 2010. Eur Neuropsychopharmacol. 2011;21:655–679. doi: 10.1016/j.euroneuro.2011.07.018. [DOI] [PubMed] [Google Scholar]
  • 2.Collaborators GDaIIaP Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet. 2017;390:1211–1259. doi: 10.1016/s0140-6736(17)32154-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Gustavsson A, Svensson M, Jacobi F, Allgulander C, Alonso J, Beghi E, Dodel R, Ekman M, Faravelli C, Fratiglioni L. Cost of disorders of the brain in Europe 2010. Eur Neuropsychopharmacol. 2011;21:718–779. doi: 10.1016/j.euroneuro.2011.08.008. [DOI] [PubMed] [Google Scholar]
  • 4.Collaborators GDaI Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet. 2020;396:1204–1222. doi: 10.1016/s0140-6736(20)30925-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Kessler RC, Angermeyer M, Anthony JC, De Graaf R, Demyttenaere K, Gasquet I, De Girolamo G, Gluzman S, Gureje O, Haro JM. Lifetime prevalence and age-of-onset distributions of mental disorders in the World Health Organization's World Mental Health Survey Initiative. World Psychiatry. 2007;6:168. [PMC free article] [PubMed] [Google Scholar]
  • 6.Kahn RS, Keefe RS. Schizophrenia is a cognitive illness: time for a change in focus. JAMA Psychiat. 2013;70:1107–1112. doi: 10.1001/jamapsychiatry.2013.155. [DOI] [PubMed] [Google Scholar]
  • 7.Schennach R, Riedel M, Obermeier M, Spellmann I, Musil R, Jäger M, Schmauss M, Laux G, Pfeiffer H, Naber D. What are residual symptoms in schizophrenia spectrum disorder? Clinical description and 1-year persistence within a naturalistic trial. Eur Arch Psychiatry Clin Neurosci. 2015;265:107–116. doi: 10.1007/s00406-014-0528-2. [DOI] [PubMed] [Google Scholar]
  • 8.Häfner H, der Heiden W. schizophrenia. Oxford: Blackwell Science; 2003. Course and outcome of schizophrenia; pp. 101–141. [Google Scholar]
  • 9.Hasan A, Falkai P, Wobrock T, Lieberman J, Glenthoj B, Gattaz WF, Thibaut F, Möller H-J, Schizophrenia WTfoTGf World Federation of Societies of Biological Psychiatry (WFSBP) guidelines for biological treatment of schizophrenia, part 2: update 2012 on the long-term treatment of schizophrenia and management of antipsychotic-induced side effects. World J Biol Psychiatry. 2013;14:2–44. doi: 10.3109/15622975.2012.739708. [DOI] [PubMed] [Google Scholar]
  • 10.Lawrence D, Hancock KJ, Kisely S. The gap in life expectancy from preventable physical illness in psychiatric patients in Western Australia: retrospective analysis of population based registers. BMJ. 2013;346:f2539. doi: 10.1136/bmj.f2539. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Laursen TM, Munk-Olsen T, Gasse C. Chronic somatic comorbidity and excess mortality due to natural causes in persons with schizophrenia or bipolar affective disorder. PLoS ONE. 2011;6:e24597. doi: 10.1371/journal.pone.0024597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Jia H, Zack MM, Gottesman II, Thompson WW. Associations of smoking, physical inactivity, heavy drinking, and obesity with quality-adjusted life expectancy among US adults with depression. Value Health. 2018;21:364–371. doi: 10.1016/j.jval.2017.08.002. [DOI] [PubMed] [Google Scholar]
  • 13.Hällgren J, Ösby U, Westman J, Gissler M. Mortality trends in external causes of death in people with mental health disorders in Sweden, 1987–2010. Scand J Public Health. 2019;47:121–126. doi: 10.1177/1403494818758912. [DOI] [PubMed] [Google Scholar]
  • 14.Ringen PA, Engh JA, Birkenaes AB, Dieset I, Andreassen OA. Increased mortality in schizophrenia due to cardiovascular disease—a non-systematic review of epidemiology, possible causes, and interventions. Front Psychiatry. 2014;5:137. doi: 10.3389/fpsyt.2014.00137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Walker ER, McGee RE, Druss BG. Mortality in mental disorders and global disease burden implications: a systematic review and meta-analysis. JAMA Psychiat. 2015;72:334–341. doi: 10.1001/jamapsychiatry.2014.2502. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Kessing LV, Vradi E, Andersen PK. Life expectancy in bipolar disorder. Bipolar Disord. 2015;17:543–548. doi: 10.1111/bdi.12296. [DOI] [PubMed] [Google Scholar]
  • 17.Laursen TM, Wahlbeck K, Hällgren J, Westman J, Ösby U, Alinaghizadeh H, Gissler M, Nordentoft M. Life expectancy and death by diseases of the circulatory system in patients with bipolar disorder or schizophrenia in the Nordic countries. PLoS ONE. 2013;8:e67133. doi: 10.1371/journal.pone.0067133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Laursen TM, Musliner KL, Benros ME, Vestergaard M, Munk-Olsen T. Mortality and life expectancy in persons with severe unipolar depression. J Affect Disord. 2016;193:203–207. doi: 10.1016/j.jad.2015.12.067. [DOI] [PubMed] [Google Scholar]
  • 19.De Hert M, Detraux J, Vancampfort D. The intriguing relationship between coronary heart disease and mental disorders. Dialogues Clin Neurosci. 2018;20:31–40. doi: 10.31887/DCNS.2018.20.1/mdehert. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Schmitt A, Maurus I, Rossner MJ, Roh A, Lembeck M, von Wilmsdorff M, Takahashi S, Rauchmann B, Keeser D, Hasan A, Malchow B, Falkai P. Effects of aerobic exercise on metabolic syndrome, cardiorespiratory fitness, and symptoms in schizophrenia include decreased mortality. Front Psychiatry. 2018;9:690. doi: 10.3389/fpsyt.2018.00690. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Firth J, Siddiqi N, Koyanagi A, Siskind D, Rosenbaum S, Galletly C, Allan S, Caneo C, Carney R, Carvalho AF. The lancet psychiatry commission: a blueprint for protecting physical health in people with mental illness. Lancet Psychiatry. 2019;6:675–712. doi: 10.1016/S2215-0366(19)30132-4. [DOI] [PubMed] [Google Scholar]
  • 22.Ross R, Blair SN, Arena R, Church TS, Després J-P, Franklin BA, Haskell WL, Kaminsky LA, Levine BD, Lavie CJ. Importance of assessing cardiorespiratory fitness in clinical practice: a case for fitness as a clinical vital sign: a scientific statement from the American Heart Association. Circulation. 2016;134:e653–e699. doi: 10.1161/CIR.0000000000000461. [DOI] [PubMed] [Google Scholar]
  • 23.Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, Franklin BA, Gordon DJ, Krauss RM, Savage PJ, Smith SC., Jr Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute scientific statement. Circulation. 2005;112:2735–2752. doi: 10.1161/CIRCULATIONAHA.105.169404. [DOI] [PubMed] [Google Scholar]
  • 24.Alberti KGMM, Zimmet P, Shaw J. Metabolic syndrome—a new world-wide definition. A consensus statement from the international diabetes federation. Diabet Med. 2006;23:469–480. doi: 10.1111/j.1464-5491.2006.01858.x. [DOI] [PubMed] [Google Scholar]
  • 25.Vancampfort D, Stubbs B, Mitchell AJ, De Hert M, Wampers M, Ward PB, Rosenbaum S, Correll CU. Risk of metabolic syndrome and its components in people with schizophrenia and related psychotic disorders, bipolar disorder and major depressive disorder: a systematic review and meta-analysis. World Psychiatry. 2015;14:339–347. doi: 10.1002/wps.20252. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Schuch F, Vancampfort D, Firth J, Rosenbaum S, Ward P, Reichert T, Bagatini NC, Bgeginski R, Stubbs B. Physical activity and sedentary behavior in people with major depressive disorder: a systematic review and meta-analysis. J Affect Disord. 2017;210:139–150. doi: 10.1016/j.jad.2016.10.050. [DOI] [PubMed] [Google Scholar]
  • 27.Vancampfort D, Probst M, Scheewe T, De Herdt A, Sweers K, Knapen J, van Winkel R, De Hert M. Relationships between physical fitness, physical activity, smoking and metabolic and mental health parameters in people with schizophrenia. Psychiatry Res. 2013;207:25–32. doi: 10.1016/j.psychres.2012.09.026. [DOI] [PubMed] [Google Scholar]
  • 28.Vancampfort D, De Hert M, Vansteenkiste M, De Herdt A, Scheewe TW, Soundy A, Stubbs B, Probst M. The importance of self-determined motivation towards physical activity in patients with schizophrenia. Psychiatry Res. 2013;210:812–818. doi: 10.1016/j.psychres.2013.10.004. [DOI] [PubMed] [Google Scholar]
  • 29.Keller-Varady K, Hasan A, Schneider-Axmann T, Hillmer-Vogel U, Adomssent B, Wobrock T, Schmitt A, Niklas A, Falkai P, Malchow B. Endurance training in patients with schizophrenia and healthy controls: differences and similarities. Eur Arch Psychiatry Clin Neurosci. 2016;266:461–473. doi: 10.1007/s00406-015-0651-8. [DOI] [PubMed] [Google Scholar]
  • 30.Vancampfort D, Stubbs B, Sienaert P, Wyckaert S, De Hert M, Soundy A, Probst M. A comparison of physical fitness in patients with bipolar disorder, schizophrenia and healthy controls. Disabil Rehabil. 2016;38:2047–2051. doi: 10.3109/09638288.2015.1114037. [DOI] [PubMed] [Google Scholar]
  • 31.Vancampfort D, De Hert M, Sweers K, De Herdt A, Detraux J, Probst M. Diabetes, physical activity participation and exercise capacity in patients with schizophrenia. Psychiatry Clin Neurosci. 2013;67:451–456. doi: 10.1111/pcn.12077. [DOI] [PubMed] [Google Scholar]
  • 32.Vancampfort D, Firth J, Correll CU, Solmi M, Siskind D, De Hert M, Carney R, Koyanagi A, Carvalho AF, Gaughran F. The impact of pharmacological and non-pharmacological interventions to improve physical health outcomes in people with schizophrenia: a meta-review of meta-analyses of randomized controlled trials. World Psychiatry. 2019;18:53–66. doi: 10.1002/wps.20614. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Romain AJ, Fankam C, Karelis AD, Letendre E, Mikolajczak G, Stip E, Abdel-Baki A. Effects of high intensity interval training among overweight individuals with psychotic disorders: a randomized controlled trial. Schizophr Res. 2019;210:278–286. doi: 10.1016/j.schres.2018.12.021. [DOI] [PubMed] [Google Scholar]
  • 34.Hargreaves M, Spriet LL. Skeletal muscle energy metabolism during exercise. Nat Metab. 2020;2:817–828. doi: 10.1038/s42255-020-0251-4. [DOI] [PubMed] [Google Scholar]
  • 35.WHO . Global recommendations on physical activity for health. World Health Organization; 2010. [PubMed] [Google Scholar]
  • 36.Chamari K, Padulo J. ‘Aerobic’and ‘Anaerobic’terms used in exercise physiology: a critical terminology reflection. Sports Medicine-Open. 2015;1:1–4. doi: 10.1186/s40798-015-0012-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Oertel-Knochel V, Mehler P, Thiel C, Steinbrecher K, Malchow B, Tesky V, Ademmer K, Prvulovic D, Banzer W, Zopf Y, Schmitt A, Hansel F. Effects of aerobic exercise on cognitive performance and individual psychopathology in depressive and schizophrenia patients. Eur Arch Psychiatry Clin Neurosci. 2014;264:589–604. doi: 10.1007/s00406-014-0485-9. [DOI] [PubMed] [Google Scholar]
  • 38.Toups M, Carmody T, Greer T, Rethorst C, Grannemann B, Trivedi MH. Exercise is an effective treatment for positive valence symptoms in major depression. J Affect Disord. 2017;209:188–194. doi: 10.1016/j.jad.2016.08.058. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Greer TL, Trombello JM, Rethorst CD, Carmody TJ, Jha MK, Liao A, Grannemann BD, Chambliss HO, Church TS, Trivedi MH. Improvements in psychosocial functioning and health-related quality of life following exercise augmentation in patients with treatment response but nonremitted major depressive disorder: results from the TREAD study. Depress Anxiety. 2016;33:870–881. doi: 10.1002/da.22521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Rethorst CD, South CC, Rush AJ, Greer TL, Trivedi MH. Prediction of treatment outcomes to exercise in patients with nonremitted major depressive disorder. Depress Anxiety. 2017;34:1116–1122. doi: 10.1002/da.22670. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Carneiro LS, Fonseca AM, Vieira-Coelho MA, Mota MP, Vasconcelos-Raposo J. Effects of structured exercise and pharmacotherapy vs. pharmacotherapy for adults with depressive symptoms: a randomized clinical trial. J Psychiatr Res. 2015;71:48–55. doi: 10.1016/j.jpsychires.2015.09.007. [DOI] [PubMed] [Google Scholar]
  • 42.Doose M, Ziegenbein M, Hoos O, Reim D, Stengert W, Hoffer N, Vogel C, Ziert Y, Sieberer M. Self-selected intensity exercise in the treatment of major depression: a pragmatic RCT. Int J Psychiatry Clin Pract. 2015;19:266–275. doi: 10.3109/13651501.2015.1082599. [DOI] [PubMed] [Google Scholar]
  • 43.Legrand F, Heuze JP. Antidepressant effects associated with different exercise conditions in participants with depression: a pilot study. J Sport Exerc Psychol. 2007;29:348–364. doi: 10.1123/jsep.29.3.348. [DOI] [PubMed] [Google Scholar]
  • 44.Patten CA, Vickers KS, Lewis BA, Finnie SB, Wheeldon TJ, Decker PA, Stevens S, Hathaway JC, Reese MM, Seime RJ. Feasibility trial of an unsupervised, facility-based exercise programme for depressed outpatients. Psychol Health Med. 2019;24:320–332. doi: 10.1080/13548506.2018.1499944. [DOI] [PubMed] [Google Scholar]
  • 45.Martinsen EW, Hoffart A, Solberg Ø. Comparing aerobic with nonaerobic forms of exercise in the treatment of clinical depression: a randomized trial. Compr Psychiatry. 1989;30:324–331. doi: 10.1016/0010-440X(89)90057-6. [DOI] [PubMed] [Google Scholar]
  • 46.Seshadri A, Adaji A, Orth SS, Singh B, Clark MM, Frye MA, Fuller-Tyszkiewicz M, and McGillivray J (2020) Exercise, yoga, and tai chi for treatment of major depressive disorder in outpatient settings: a systematic review and meta-analysis. Prim Care Companion CNS disord 23 [DOI] [PubMed]
  • 47.Danielsson L, Papoulias I, Petersson E-L, Carlsson J, Waern M. Exercise or basic body awareness therapy as add-on treatment for major depression: a controlled study. J Affect Disord. 2014;168:98–106. doi: 10.1016/j.jad.2014.06.049. [DOI] [PubMed] [Google Scholar]
  • 48.Minghetti A, Faude O, Hanssen H, Zahner L, Gerber M, Donath L. Sprint interval training (SIT) substantially reduces depressive symptoms in major depressive disorder (MDD): a randomized controlled trial. Psychiatry Res. 2018;265:292–297. doi: 10.1016/j.psychres.2018.04.053. [DOI] [PubMed] [Google Scholar]
  • 49.Krogh J, Saltin B, Nordentoft M. The DEMO trial: a randomized, parallel-group, observer-blinded clinical trial of strength versus aerobic versus relaxation training for patients with mild to moderate depression. J Clin Psychiatry. 2009;70:790–800. doi: 10.4088/JCP.08m04241. [DOI] [PubMed] [Google Scholar]
  • 50.Choi KW, Chen CY, Stein MB, Klimentidis YC, Wang MJ, Koenen KC, Smoller JW. Assessment of bidirectional relationships between physical activity and depression among adults: a 2-sample mendelian randomization study. JAMA Psychiat. 2019;76:399–408. doi: 10.1001/jamapsychiatry.2018.4175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Papiol S, Schmitt A, Maurus I, Rossner MJ, Schulze TG, Falkai P. Association between physical activity and schizophrenia: results of a 2-sample Mendelian randomization analysis. JAMA Psychiat. 2021;78:441–444. doi: 10.1001/jamapsychiatry.2020.3946. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Ashton MM, Mohebbi M, Turner A, Marx W, Berk M, Malhi GS, Ng CH, Cotton SM, Dodd S, Sarris J. Physical activity as a predictor of clinical trial outcomes in bipolar depression: a subanalysis of a mitochondrial-enhancing nutraceutical randomized controlled trial. Can J Psychiatry. 2020;65:306–318. doi: 10.1177/0706743719889547. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Dauwan M, Begemann MJ, Heringa SM, Sommer IE. Exercise improves clinical symptoms, quality of life, global functioning, and depression in schizophrenia: a systematic review and meta-analysis. Schizophr Bull. 2016;42:588–599. doi: 10.1093/schbul/sbv164. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Firth J, Stubbs B, Rosenbaum S, Vancampfort D, Malchow B, Schuch F, Elliott R, Nuechterlein KH, Yung AR. Aerobic exercise improves cognitive functioning in people with schizophrenia: a systematic review and meta-analysis. Schizophr Bull. 2017;43:546–556. doi: 10.1093/schbul/sbw115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Sabe M, Kaiser S, Sentissi O. Physical exercise for negative symptoms of schizophrenia: Systematic review of randomized controlled trials and meta-analysis. Gen Hosp Psychiatry. 2019;62:13–20. doi: 10.1016/j.genhosppsych.2019.11.002. [DOI] [PubMed] [Google Scholar]
  • 56.Firth J, Cotter J, Elliott R, French P, Yung AR. A systematic review and meta-analysis of exercise interventions in schizophrenia patients. Psychol Med. 2015;45:1343–1361. doi: 10.1017/s0033291714003110. [DOI] [PubMed] [Google Scholar]
  • 57.Pajonk FG, Wobrock T, Gruber O, Scherk H, Berner D, Kaizl I, Kierer A, Muller S, Oest M, Meyer T, Backens M, Schneider-Axmann T, Thornton AE, Honer WG, Falkai P. Hippocampal plasticity in response to exercise in schizophrenia. Arch Gen Psychiatry. 2010;67:133–143. doi: 10.1001/archgenpsychiatry.2009.193. [DOI] [PubMed] [Google Scholar]
  • 58.Malchow B, Keller K, Hasan A, Dorfler S, Schneider-Axmann T, Hillmer-Vogel U, Honer WG, Schulze TG, Niklas A, Wobrock T, Schmitt A, Falkai P. Effects of endurance training combined with cognitive remediation on everyday functioning, symptoms, and cognition in multiepisode schizophrenia patients. Schizophr Bull. 2015;41:847–858. doi: 10.1093/schbul/sbv020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Falkai P, Maurus I, Schmitt A, Malchow B, Schneider-Axmann T, Röll L, Papiol S, Wobrock T, Hasan A, Keeser D. Improvement in daily functioning after aerobic exercise training in schizophrenia is sustained after exercise cessation. Eur Arch Psychiatry Clin Neurosci. 2021;271:1201–1203. doi: 10.1007/s00406-021-01282-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Hallgren M, Skott M, Ekblom Ö, Firth J, Schembri A, Forsell Y. Exercise effects on cognitive functioning in young adults with first-episode psychosis: FitForLife. Psychol Med. 2019;49:431–439. doi: 10.1017/S0033291718001022. [DOI] [PubMed] [Google Scholar]
  • 61.Su CY, Wang PW, Lin YJ, Tang TC, Liu MF, Chen MD. The effects of aerobic exercise on cognition in schizophrenia: a 3-month follow-up study. Psychiatry Res. 2016;244:394–402. doi: 10.1016/j.psychres.2016.08.011. [DOI] [PubMed] [Google Scholar]
  • 62.Shimada T, Ito S, Makabe A, Yamanushi A, Takenaka A, Kobayashi M. Aerobic exercise and cognitive functioning in schizophrenia: a pilot randomized controlled trial. Psychiatry Res. 2019;282:112638. doi: 10.1016/j.psychres.2019.112638. [DOI] [PubMed] [Google Scholar]
  • 63.Curcic D, Stojmenovic T, Djukic-Dejanovic S, Dikic N, Vesic-Vukasinovic M, Radivojevic N, Andjelkovic M, Borovcanin M, Djokic G. Positive impact of prescribed physical activity on symptoms of schizophrenia: randomized clinical trial. Psychiatr Danub. 2017;29:459–465. doi: 10.24869/psyd.2017.459. [DOI] [PubMed] [Google Scholar]
  • 64.Scheewe TW, Backx FJ, Takken T, Jorg F, van Strater AC, Kroes AG, Kahn RS, Cahn W. Exercise therapy improves mental and physical health in schizophrenia: a randomised controlled trial. Acta Psychiatr Scand. 2013;127:464–473. doi: 10.1111/acps.12029. [DOI] [PubMed] [Google Scholar]
  • 65.Vancampfort D, De Hert M, Knapen J, Wampers M, Demunter H, Deckx S, Maurissen K, Probst M. State anxiety, psychological stress and positive well-being responses to yoga and aerobic exercise in people with schizophrenia: a pilot study. Disabil Rehabil. 2011;33:684–689. doi: 10.3109/09638288.2010.509458. [DOI] [PubMed] [Google Scholar]
  • 66.Vancampfort D, Stubbs B, Van Damme T, Smith L, Hallgren M, Schuch F, Deenik J, Rosenbaum S, Ashdown-Franks G, Mugisha J. The efficacy of meditation-based mind-body interventions for mental disorders: a meta-review of 17 meta-analyses of randomized controlled trials. J Psychiatr Res. 2020;134:181–191. doi: 10.1016/j.jpsychires.2020.12.048. [DOI] [PubMed] [Google Scholar]
  • 67.Kang R, Wu Y, Li Z, Jiang J, Gao Q, Yu Y, Gao K, Yan Y, He Y. Effect of community-based social skills training and tai-chi exercise on outcomes in patients with chronic schizophrenia: a randomized, one-year study. Psychopathology. 2016;49:345–355. doi: 10.1159/000448195. [DOI] [PubMed] [Google Scholar]
  • 68.Ho RT, Fong TC, Wan AH, Au-Yeung FS, Wong CP, Ng WY, Cheung IK, Lo PH, Ng S, Chan CL. A randomized controlled trial on the psychophysiological effects of physical exercise and Tai-chi in patients with chronic schizophrenia. Schizophr Res. 2016;171:42–49. doi: 10.1016/j.schres.2016.01.038. [DOI] [PubMed] [Google Scholar]
  • 69.Kaltsatou A, Kouidi E, Fountoulakis K, Sipka C, Theochari V, Kandylis D, Deligiannis A. Effects of exercise training with traditional dancing on functional capacity and quality of life in patients with schizophrenia: a randomized controlled study. Clin Rehabil. 2015;29:882–891. doi: 10.1177/0269215514564085. [DOI] [PubMed] [Google Scholar]
  • 70.Andrade e Silva B, Cassilhas RC, Attux C, Cordeiro Q, Gadelha AL, Telles BA, Bressan RA, Ferreira FN, Rodstein PH, Daltio CS. A 20-week program of resistance or concurrent exercise improves symptoms of schizophrenia: results of a blind, randomized controlled trial. Rev Bras Psiquiatr. 2015;37:271–279. doi: 10.1590/1516-4446-2014-1595. [DOI] [PubMed] [Google Scholar]
  • 71.Maurus I, Mantel C, Keller-Varady K, Schmitt A, Lembeck M, Röh A, Papazova I, Falkai P, Schneider-Axmann T, Hasan A. Resistance training in patients with schizophrenia: concept and proof of principle trial. J Psychiatr Res. 2020;120:72–82. doi: 10.1016/j.jpsychires.2019.09.015. [DOI] [PubMed] [Google Scholar]
  • 72.Maurus I, Hasan A, Röh A, Takahashi S, Rauchmann BS, Keeser D, Malchow B, Schmitt A, Falkai P. Neurobiological effects of aerobic exercise, with a focus on patients with schizophrenia. Eur Arch Psychiatry Clin Neurosci. 2019;269:1–17. doi: 10.1007/s00406-019-01025-w. [DOI] [PubMed] [Google Scholar]
  • 73.Wittfeld K, Jochem C, Dörr M, Schminke U, Gläser S, Bahls M, Markus MRP, Felix SB, Leitzmann MF, Ewert R, Bülow R, Völzke H, Janowitz D, Baumeister SE, Grabe HJ. Cardiorespiratory fitness and gray matter volume in the temporal, frontal, and cerebellar regions in the general population. Mayo Clin Proc. 2020;95:44–56. doi: 10.1016/j.mayocp.2019.05.030. [DOI] [PubMed] [Google Scholar]
  • 74.Firth J, Stubbs B, Vancampfort D, Schuch F, Lagopoulos J, Rosenbaum S, Ward PB. Effect of aerobic exercise on hippocampal volume in humans: a systematic review and meta-analysis. Neuroimage. 2018;166:230–238. doi: 10.1016/j.neuroimage.2017.11.007. [DOI] [PubMed] [Google Scholar]
  • 75.Adriano F, Caltagirone C, Spalletta G. Hippocampal volume reduction in first-episode and chronic schizophrenia: a review and meta-analysis. Neuroscientist. 2012;18:180–200. doi: 10.1177/1073858410395147. [DOI] [PubMed] [Google Scholar]
  • 76.Wise T, Radua J, Via E, Cardoner N, Abe O, Adams TM, Amico F, Cheng Y, Cole J, Périco CdAM. Common and distinct patterns of grey-matter volume alteration in major depression and bipolar disorder: evidence from voxel-based meta-analysis. Mol Psychiatry. 2017;22:1455–1463. doi: 10.1038/mp.2016.72. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Rosano C, Guralnik J, Pahor M, Glynn NW, Newman AB, Ibrahim TS, Erickson K, Cohen R, Shaaban CE, MacCloud RL. Hippocampal response to a 24-month physical activity intervention in sedentary older adults. Am J Geriatr Psychiatry. 2017;25:209–217. doi: 10.1016/j.jagp.2016.11.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Gotlib IH, Joormann J. Cognition and depression: current status and future directions. Annu Rev Clin Psychol. 2010;6:285–312. doi: 10.1146/annurev.clinpsy.121208.131305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Green MF. Impact of cognitive and social cognitive impairment on functional outcomes in patients with schizophrenia. J Clin Psychiatry. 2016;77(Suppl 2):8–11. doi: 10.4088/JCP.14074su1c.02. [DOI] [PubMed] [Google Scholar]
  • 80.Papiol S, Popovic D, Keeser D, Hasan A, Schneider-Axmann T, Degenhardt F, Rossner MJ, Bickeböller H, Schmitt A, Falkai P. Polygenic risk has an impact on the structural plasticity of hippocampal subfields during aerobic exercise combined with cognitive remediation in multi-episode schizophrenia. Transl Psychiatry. 2017;7:e1159. doi: 10.1038/tp.2017.131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Papiol S, Keeser D, Hasan A, Schneider-Axmann T, Raabe F, Degenhardt F, Rossner MJ, Bickeböller H, Cantuti-Castelvetri L, Simons M. Polygenic burden associated to oligodendrocyte precursor cells and radial glia influences the hippocampal volume changes induced by aerobic exercise in schizophrenia patients. Transl Psychiatry. 2019;9:1–8. doi: 10.1038/s41398-019-0618-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Falkai P, Malchow B, Wetzestein K, Nowastowski V, Bernstein H-G, Steiner J, Schneider-Axmann T, Kraus T, Hasan A, Bogerts B. Decreased oligodendrocyte and neuron number in anterior hippocampal areas and the entire hippocampus in schizophrenia: a stereological postmortem study. Schizophr Bull. 2016;42:S4–S12. doi: 10.1093/schbul/sbv157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Schmitt A, Simons M, Cantuti-Castelvetri L, Falkai P. A new role for oligodendrocytes and myelination in schizophrenia and affective disorders? Springer; 2019. [DOI] [PubMed] [Google Scholar]
  • 84.Krogh J, Rostrup E, Thomsen C, Elfving B, Videbech P, Nordentoft M. The effect of exercise on hippocampal volume and neurotrophines in patients with major depression—a randomized clinical trial. J Affect Disord. 2014;165:24–30. doi: 10.1016/j.jad.2014.04.041. [DOI] [PubMed] [Google Scholar]
  • 85.Scheewe TW, van Haren NE, Sarkisyan G, Schnack HG, Brouwer RM, de Glint M, Pol HEH, Backx FJ, Kahn RS, Cahn W. Exercise therapy, cardiorespiratory fitness and their effect on brain volumes: a randomised controlled trial in patients with schizophrenia and healthy controls. Eur Neuropsychopharmacol. 2013;23:675–685. doi: 10.1016/j.euroneuro.2012.08.008. [DOI] [PubMed] [Google Scholar]
  • 86.Woodward M, Gicas K, Warburton D, White R, Rauscher A, Leonova O, Su W, Smith G, Thornton A, Vertinsky A. Hippocampal volume and vasculature before and after exercise in treatment-resistant schizophrenia. Schizophr Res. 2018;202:158–165. doi: 10.1016/j.schres.2018.06.054. [DOI] [PubMed] [Google Scholar]
  • 87.Takahashi S, Keeser D, Rauchmann B-S, Schneider-Axmann T, Keller-Varady K, Maurus I, Dechent P, Wobrock T, Hasan A, Schmitt A. Effect of aerobic exercise combined with cognitive remediation on cortical thickness and prediction of social adaptation in patients with schizophrenia. Schizophr Res. 2020;216:397–407. doi: 10.1016/j.schres.2019.11.004. [DOI] [PubMed] [Google Scholar]
  • 88.Malchow B, Keeser D, Keller K, Hasan A, Rauchmann BS, Kimura H, Schneider-Axmann T, Dechent P, Gruber O, Ertl-Wagner B, Honer WG, Hillmer-Vogel U, Schmitt A, Wobrock T, Niklas A, Falkai P. Effects of endurance training on brain structures in chronic schizophrenia patients and healthy controls. Schizophr Res. 2016;173:182–191. doi: 10.1016/j.schres.2015.01.005. [DOI] [PubMed] [Google Scholar]
  • 89.Rauchmann BS, Ghaseminejad F, Keeser D, Keller-Varady K, Schneider-Axmann T, Takahashi S, Karali T, Helms G, Dechent P, Maurus I, Hasan A, Wobrock T, Ertl-Wagner B, Schmitt A, Malchow B, Falkai P. The impact of endurance training and table soccer on brain metabolites in schizophrenia. Brain Imaging Behav. 2019 doi: 10.1007/s11682-019-00198-1. [DOI] [PubMed] [Google Scholar]
  • 90.Svatkova A, Mandl RC, Scheewe TW, Cahn W, Kahn RS, Hulshoff Pol HE. Physical exercise keeps the brain connected: biking increases white matter integrity in patients with schizophrenia and healthy controls. Schizophr Bull. 2015;41:869–878. doi: 10.1093/schbul/sbv033. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Vancampfort D, Kimbowa S, Basangwa D, Smith L, Stubbs B, Van Damme T, De Hert M, Mugisha J. Test-retest reliability, concurrent validity and correlates of the two-minute walk test in outpatients with psychosis. Psychiatry Res. 2019;282:112619. doi: 10.1016/j.psychres.2019.112619. [DOI] [PubMed] [Google Scholar]
  • 92.Kerling A, Tegtbur U, Gützlaff E, Kück M, Borchert L, Ates Z, von Bohlen A, Frieling H, Hüper K, Hartung D, Schweiger U, Kahl KG. Effects of adjunctive exercise on physiological and psychological parameters in depression: a randomized pilot trial. J Affect Disord. 2015;177:1–6. doi: 10.1016/j.jad.2015.01.006. [DOI] [PubMed] [Google Scholar]
  • 93.Krogh J, Videbech P, Thomsen C, Gluud C, Nordentoft M. DEMO-II trial. Aerobic exercise versus stretching exercise in patients with major depression—a randomised clinical trial. PLoS ONE. 2012;7:e48316. doi: 10.1371/journal.pone.0048316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 94.Oeland AM, Laessoe U, Olesen AV, Munk-Jørgensen P. Impact of exercise on patients with depression and anxiety. Nord J Psychiatry. 2010;64:210–217. doi: 10.3109/08039480903511373. [DOI] [PubMed] [Google Scholar]
  • 95.Hoffman BM, Blumenthal JA, Babyak MA, Smith PJ, Rogers SD, Doraiswamy PM, Sherwood A. Exercise fails to improve neurocognition in depressed middle-aged and older adults. Med Sci Sports Exerc. 2008;40:1344–1352. doi: 10.1249/MSS.0b013e31816b877c. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Blumenthal JA, Babyak MA, Moore KA, Craighead WE, Herman S, Khatri P, Waugh R, Napolitano MA, Forman LM, Appelbaum M, Doraiswamy PM, Krishnan KR. Effects of exercise training on older patients with major depression. Arch Intern Med. 1999;159:2349–2356. doi: 10.1001/archinte.159.19.2349. [DOI] [PubMed] [Google Scholar]
  • 97.Gujral S, Aizenstein H, Reynolds CF, III, Butters MA, Grove G, Karp JF, Erickson KI. Exercise for depression: a feasibility trial exploring neural mechanisms. Am J Geriatr Psychiatry. 2019;27:611–616. doi: 10.1016/j.jagp.2019.01.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 98.Gerber M, Minghetti A, Beck J, Zahner L, Donath L. Is improved fitness following a 12-week exercise program associated with decreased symptom severity, better wellbeing, and fewer sleep complaints in patients with major depressive disorders? A secondary analysis of a randomized controlled trial. J Psychiatr Res. 2019;113:58–64. doi: 10.1016/j.jpsychires.2019.03.011. [DOI] [PubMed] [Google Scholar]
  • 99.Andersen E, Bang-Kittilsen G, Bigseth TT, Egeland J, Holmen TL, Martinsen EW, Stensrud T, Engh JA. Effect of high-intensity interval training on cardiorespiratory fitness, physical activity and body composition in people with schizophrenia: a randomized controlled trial. BMC Psychiatry. 2020;20:425. doi: 10.1186/s12888-020-02827-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Brobakken MF, Nygård M, Güzey IC, Morken G, Reitan SK, Heggelund J, Wang E, Vedul-Kjelsaas E. Aerobic interval training in standard treatment of out-patients with schizophrenia: a randomized controlled trial. Acta Psychiatr Scand. 2019;140:498–507. doi: 10.1111/acps.13105. [DOI] [PubMed] [Google Scholar]
  • 101.Massa N, Alrohaibani A, Mammino K, Bello M, Taylor N, Cuthbert B, Fargotstein M, Coulter MM, Boatright JH, Nocera J, Duncan E. The effect of aerobic exercise on physical and cognitive outcomes in a small cohort of outpatients with schizophrenia. Brain Plast. 2020;5:161–174. doi: 10.3233/bpl-200105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102.Korman N, Fox H, Skinner T, Dodd C, Suetani S, Chapman J, Parker S, Dark F, Collins C, Rosenbaum S, Siskind D. Feasibility and acceptability of a student-led lifestyle (diet and exercise) intervention within a residential rehabilitation setting for people with severe mental illness, GO HEART (Group Occupation, Health, Exercise And Rehabilitation Treatment) Front Psychiatry. 2020;11:319. doi: 10.3389/fpsyt.2020.00319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Scheewe TW, Jörg F, Takken T, Deenik J, Vancampfort D, Backx FJG, Cahn W. Low physical activity and cardiorespiratory fitness in people with schizophrenia: a comparison with matched healthy controls and associations with mental and physical health. Front Psychiatry. 2019;10:87. doi: 10.3389/fpsyt.2019.00087. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104.Heggelund J, Nilsberg GE, Hoff J, Morken G, Helgerud J. Effects of high aerobic intensity training in patients with schizophrenia: a controlled trial. Nord J Psychiatry. 2011;65:269–275. doi: 10.3109/08039488.2011.560278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105.Kimhy D, Tay C, Vakhrusheva J, Beck-Felts K, Ospina LH, Ifrah C, Parvaz M, Gross JJ, Bartels MN. Enhancement of aerobic fitness improves social functioning in individuals with schizophrenia. Eur Arch Psychiatry Clin Neurosci. 2021;271:367–376. doi: 10.1007/s00406-020-01220-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Scheewe TW, Takken T, Kahn RS, Cahn W, Backx FJ. Effects of exercise therapy on cardiorespiratory fitness in patients with schizophrenia. Med Sci Sports Exerc. 2012;44:1834–1842. doi: 10.1249/MSS.0b013e318258e120. [DOI] [PubMed] [Google Scholar]
  • 107.Cheng SL, Sun HF, Yeh ML. Effects of an 8-week aerobic dance program on health-related fitness in patients with schizophrenia. J Nurs Res. 2017;25:429–435. doi: 10.1097/jnr.0000000000000200. [DOI] [PubMed] [Google Scholar]
  • 108.Yoon S, Ryu JK, Kim CH, Chang JG, Lee HB, Kim DH, Roh D. Preliminary effectiveness and sustainability of group aerobic exercise program in patients with schizophrenia. J Nerv Ment Dis. 2016;204:644–650. doi: 10.1097/nmd.0000000000000534. [DOI] [PubMed] [Google Scholar]
  • 109.Schmitt A, Reich-Erkelenz D, Hasan A, Falkai P. Aerobic exercise in mental disorders: from basic mechanisms to treatment recommendations. Eur Arch Psychiatry Clin Neurosci. 2019;269:483–484. doi: 10.1007/s00406-019-01037-6. [DOI] [PubMed] [Google Scholar]
  • 110.Garber CE, Blissmer B, Deschenes MR, Franklin BA, Lamonte MJ, Lee IM, Nieman DC, Swain DP. American College of Sports Medicine position stand. Quantity and quality of exercise for developing and maintaining cardiorespiratory, musculoskeletal, and neuromotor fitness in apparently healthy adults: guidance for prescribing exercise. Med Sci Sports Exerc. 2011;43:1334–1359. doi: 10.1249/MSS.0b013e318213fefb. [DOI] [PubMed] [Google Scholar]
  • 111.Font RM, Sanmartín MIF, López LMM, Tabueña NO, Canet SO, Echevarría LSE, Jato MI, Múgjica BD, Tejón SG, and Cabrera LV (2015) The effectiveness of a program of physical activity and diet to modify cardiovascular risk factors in patients with severe mental illness (CAPiCOR study). Int Arch Med 8
  • 112.Penninx BW, Rejeski WJ, Pandya J, Miller ME, Di Bari M, Applegate WB, Pahor M. Exercise and depressive symptoms: a comparison of aerobic and resistance exercise effects on emotional and physical function in older persons with high and low depressive symptomatology. J Gerontol B Psychol Sci Soc Sci. 2002;57:P124–P132. doi: 10.1093/geronb/57.2.P124. [DOI] [PubMed] [Google Scholar]
  • 113.Dubreucq J, Gabayet F, Ycart B, Faraldo M, Melis F, Lucas T, Arnaud B, Bacconnier M, Bakri M, and Cambier G (2020) Improving social function with real-world social-cognitive remediation in schizophrenia: results from the RemedRugby quasi-experimental trial. Eur Psychiatry 63 [DOI] [PMC free article] [PubMed]
  • 114.Larsen LQ, Schnor H, Tersbøl BP, Ebdrup BH, Nordsborg NB, Midtgaard J. The impact of exercise training complementary to early intervention in patients with first-episode psychosis: a qualitative sub-study from a randomized controlled feasibility trial. BMC Psychiatry. 2019;19:1–12. doi: 10.1186/s12888-019-2179-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115.Bhatia T, Mazumdar S, Wood J, He F, Gur RE, Gur RC, Nimgaonkar VL, Deshpande SN. A randomised controlled trial of adjunctive yoga and adjunctive physical exercise training for cognitive dysfunction in schizophrenia. Acta Neuropsychiatrica. 2017;29:102–114. doi: 10.1017/neu.2016.42. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Duncan MJ, Smith M, Clarke ND, Eyre EL, Wright SL. Dual task performance in older adults: examining visual discrimination performance whilst treadmill walking at preferred and non-preferred speeds. Behav Brain Res. 2016;302:100–103. doi: 10.1016/j.bbr.2016.01.020. [DOI] [PubMed] [Google Scholar]
  • 117.Kimhy D, Vakhrusheva J, Bartels MN, Armstrong HF, Ballon JS, Khan S, Chang RW, Hansen MC, Ayanruoh L, Lister A. The impact of aerobic exercise on brain-derived neurotrophic factor and neurocognition in individuals with schizophrenia: a single-blind, randomized clinical trial. Schizophr Bull. 2015;41:859–868. doi: 10.1093/schbul/sbv022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 118.Loh SY, Abdullah A, Bakar AKA, Thambu M, Jaafar NRN. Structured walking and chronic institutionalized schizophrenia inmates: a pilot RCT study on quality of life. Global J Health Sci. 2016;8:238. doi: 10.5539/gjhs.v8n1p238. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 119.Vancampfort D, Probst M, Stubbs B, Soundy A, De Herdt A, De Hert M. Metabolic syndrome and lung function in schizophrenia: a pilot study. Psychiatry Res. 2014;220:58–62. doi: 10.1016/j.psychres.2014.06.008. [DOI] [PubMed] [Google Scholar]
  • 120.Methapatara W, Srisurapanont M. Pedometer walking plus motivational interviewing program for Thai schizophrenic patients with obesity or overweight: a 12-week, randomized, controlled trial. Psychiatry Clin Neurosci. 2011;65:374–380. doi: 10.1111/j.1440-1819.2011.02225.x. [DOI] [PubMed] [Google Scholar]

Articles from European Archives of Psychiatry and Clinical Neuroscience are provided here courtesy of Springer

RESOURCES