Skip to main content
BMC Sports Science, Medicine and Rehabilitation logoLink to BMC Sports Science, Medicine and Rehabilitation
. 2026 Jan 7;18:66. doi: 10.1186/s13102-025-01432-8

Effect of different types of exercise in fibromyalgia syndrome: a network meta-analysis

Wen Yuan 1,2,#, Pengfei Wan 3,#, Hui Wang 4, MingZhu Suo 1, Pingping Xie 1,
PMCID: PMC12882235  PMID: 41501867

Abstract

Background

Patients with fibromyalgia syndrome (FMS) often exhibit poor health and reduced physical function. Exercise interventions can effectively alleviate symptoms and improve function. This study aims to systematically evaluate and compare the efficacy of different exercise interventions on the key clinical outcomes to identify the most effective modality and inform evidence-based exercise recommendations for patients with FMS.

Methods

This study conducted a systematic search of four databases: PubMed, Embase, the Cochrane Library, and Web of Science. The primary outcome measures included health status, pain intensity, the number of tender points (TP), and aerobic capacity. Stata 15.0 and R software were used for network meta-analysis (NMA), and the effect size and its 95% confidence interval were calculated using a random-effects model. The methodological quality of the included studies was assessed using the Cochrane RoB 2.0 tool and the TESTEX scale.

Results

Stretching combined with balance training resulted in the greatest improvement in health status (MD = − 25.13; 95% CI [− 33.81, − 16.44]). For other symptom-related outcomes, aerobic exercise (AE) combined with strength and stretching showed the highest probability of alleviating pain intensity (MD = − 3.61; 95% CI [− 4.40, − 2.82]). AE alone was most effective in reducing the number of tender points (MD = − 2.28; 95% CI [− 3.57, − 1.00]), while whole-body vibration (WBV) produced the largest enhancement in aerobic capacity (MD = 55.0; 95% CI [26.14, 83.75]).

Conclusions

Stretching combined with balance training was found to be most effective in improving health status. AE combined with strength training and stretching demonstrated the greatest efficacy in reducing pain intensity, while AE was most effective in decreasing the number of tender points. WBV appeared to provide the largest improvement in aerobic capacity in patients with FMS. These findings suggest that healthcare providers should combine AE, strength, stretching, balance, WBV, and other exercises based on the individual circumstances of patients with FMS, while further high-quality RCTs are warranted to confirm these results and to standardize exercise protocols.

Trial registration

CRD420251036473.

Supplementary Information

The online version contains supplementary material available at 10.1186/s13102-025-01432-8.

Keywords: Exercise, Fibromyalgia syndrome, Health status, Pain

Background

FMS is a chronic, widespread, and non-inflammatory musculoskeletal disorder that profoundly affects patients’ quality of life and relationships [1, 2]. It is characterized by widespread musculoskeletal pain, accompanied by fatigue, cognitive dysfunction, sleep disturbances, decreased concentration and memory, negative mood, and a variety of somatic symptoms [3]. The etiology of the disease is currently unknown, and it is typically characterized as a disorder affecting the musculoskeletal and connective tissue systems [4]. Some studies attribute its origin to central sensitization processes [5], inflammation [6], or small fiber neuropathy [7]. It is the third most common musculoskeletal disorder, following low back pain and osteoarthritis, with a prevalence ranging from 3% to 10% in the global population [8]. It affects women more frequently than men [9], particularly those aged between 30 and 60 years [10], and it leads to significant disability and a substantial healthcare burden, either directly or indirectly [11]. There are no specific therapies for treating FMS patients. Instead, multimodal pharmacological and non-pharmacological treatments are recommended, each with its own potential risks and side effects. Only 10% to 25% of patients with FMS who receive medication experience a reduction in pain intensity of at least 50%. Many patients also fear addiction or adverse effects from the medication [12]. This inadequate treatment not only necessitates efficient healthcare services but also imposes a significant economic burden [13]. A Canadian study estimated the annual healthcare expenditure per individual to be approximately CAD 3800 [14]. Therefore, for both medical and economic reasons, incorporating exercise therapy into treatment programs is essential.

Regular exercise training is recommended as an effective treatment strategy to improve pain, quality of life, physical functioning, sleep, depression, and anxiety in patients with FMS [15]. Regimens for FMS typically include aerobic, resistance, and stretching exercises. Numerous studies have examined the effects of AE [16], stretching exercise [17], resistance exercise [18], AE combined with strengthening exercise [19], traditional Chinese exercise [20], and AE combined with resistance exercise [21] on patients with FMS, using pain symptoms as an outcome indicator in meta-analyses. A recent study analyzed the effect of different exercise doses of intervention based on frequency, intensity, type, and duration [22]. One study compared the efficacy of pool-based and land-based aerobic exercise interventions [23].

In recent years, some network meta-analyses have compared pain intensity in female FMS patients; their focus has mainly been on pain as a single outcome, and the interventions included have been limited [24]. Other systematic reviews and meta-analyses tend to use pairwise meta-analysis methods [15], which means they cannot be compared directly in the same model. Furthermore, there is still insufficient systematic evaluation of other key outcomes (e.g., health status, aerobic capacity) beyond pain.

Therefore, this study aims to construct an NMA framework that encompasses multiple forms of exercise interventions and compares their effects on improving health status, reducing pain intensity and the number of tender points, and enhancing aerobic capacity. This approach will provide FMS patients with more comprehensive evidence-based treatment recommendations and address the limitations of existing studies in terms of the scope of interventions and outcome dimensions.

Methods

Registration

This study follows the Preferred Reporting Items (PRISMA) statement for systematic reviews and meta-analyses [25]. The study is registered with PROSPERO under registration number CRD420251036473. The PRISMA checklist is provided in Supplementary Material 1.

Search strategy

Articles were obtained from PubMed, Embase, the Cochrane Library, and Web of Science through a systematic electronic search. The searches were performed on February 7, 2025, using a combination of subject terms and free-text keywords. Specific search strategies for each database are detailed in Supplementary Material 2.

Inclusion criteria

The inclusion criteria follow the PICOS (Participants, Intervention, Comparison, Outcome, Study Design) strategy.

  1. Study design

    Randomized controlled trials are included, with no restrictions on blinding method or allocation concealment method. Only English language studies are included.

  2. Population

    Inclusion criteria: adults (≥18 years old) with FMS, diagnosed according to the American College of Rheumatology (ACR) criteria; no restriction on disease duration; exclusion of patients with severe cardiovascular, respiratory, or neuromuscular diseases, or other diseases affecting physical function.

  3. Intervention

    Any form of therapeutic exercise (TE), including single-mode (e.g., AE, strength training, stretching, balance training, WBV, exergame) or pre-defined fixed-combination mode (e.g., AE+ strength + stretching, AE + stretching, stretching + balance, resistance + stretching), with the content of the intervention clearly described in the study, including the elements of training, frequency, intensity, duration of each session, and intervention cycle.

  4. Control group

    Conventional care, placebo intervention, no intervention, or other exercise intervention modes (used for comparing nodes in network meta-analyses). The type of control must be clearly stated in the included studies and categorized uniformly in the analysis.

  5. Result indicators

    Health status (Fibromyalgia Impact Questionnaire, FIQ), pain intensity (Visual Analogue Scale, VAS), number of tender points (Tender Points, TP), and aerobic capacity (6-minute walk test, 6MWT).

Exclusion criteria

  1. Repeatedly published studies, review articles, conference abstracts, animal experiments, laboratory-based research, and case reports.(1) Repeatedly published studies, review articles, conference abstracts, animal experiments, laboratory-based research, and case reports.

  2. Studies that combine physical intervention with other interventions (e.g., educational therapy, psychological intervention) and cannot be analyzed separately for physical intervention effects.

  3. Studies in which both the experimental and control groups only received the same form of AE intervention, making it impossible to perform group comparisons.

  4. Studies where the outcome was not reported or where the necessary data could not be extracted.

  5. Studies where the intervention measures were not clearly described in terms of training elements (frequency, intensity, duration, cycle), making it impossible to assess the intervention.

Data extraction

Two researchers conducted a thorough review of the literature, adhering to predefined inclusion and exclusion criteria, and independently extracted all relevant data. In cases of disagreement, the involved parties resolved their differences and reached a consensus through discussion, negotiation, or consultation with an additional researcher. The information extracted from the included studies encompassed essential details such as the first author’s name, publication year, country of study, sample size, gender distribution, age range, type of intervention employed, and outcome indicators assessed.

In cases where essential information was unavailable, the corresponding authors of the included studies were contacted via email to request the missing data.

Risk of bias assessment

Two researchers independently assessed the methodological quality of the included studies using the RoB 2.0 tool and the TESTEX scale. In cases of disagreement, the reviewers reached a consensus through discussion, and a third researcher was consulted to arbitrate when necessary.

The RoB 2.0 tool primarily assesses the risk of bias across five domains: randomization process, deviation from the intended intervention, missing outcome data, outcome measurement, and selective reporting. The results are categorized as ‘low risk’, ‘some concerns’, or ‘high risk’. The TESTEX scale scores the quality of study design (5 items) and reporting quality (10 items) in exercise intervention studies, with a total score of 15 points. A higher score indicates better methodological quality and reporting quality. Ultimately, the credibility of the study results will be determined by considering both the RoB 2.0 bias risk assessment and the TESTEX scale score.

Certainty of evidence

This study applied the GRADE (Grading of Recommendations Assessment, Development and Evaluation) framework to evaluate the quality of evidence for the primary outcome measures. The GRADE system evaluates evidence systematically across five domains: risk of bias, inconsistency, indirectness, imprecision, and publication bias, and classifies the quality of evidence into four levels: high, moderate, low, and very low. Two researchers independently conducted the assessments, and any disagreements were resolved through discussion or consultation with a third expert.

Statistical analysis

A Bayesian NMA of multiple trials was conducted using a priori random-effects random effects model with R software. Markov chain Monte Carlo methods were employed to derive the best combined estimates and probabilities for each treatment regimen. Trajectory plots and Brooks-Gelman-Rubin plots were utilized to assess model convergence, with the results presented as posterior mean differences (MD) and their corresponding 95% confidence intervals (CI). The percentage area under the cumulative ranking curve (SUCRA) was calculated to estimate the probability of the optimal intervention. Network and funnel plots were generated using Stata 15.0, while cumulative probability plots were created using the ggplot2 package.

Results

Study selection

A total of 3,169 potentially eligible articles were identified through an initial database search. After removing 1,029 duplicates, 2,140 records remained for screening, of which 2,049 were excluded after title and abstract review. After re-reading the full text and obtaining it again, a further 26 articles were removed, leaving 65 articles for quantitative synthesis. The flow diagram of the study selection process is presented in Fig. 1.

Fig. 1.

Fig. 1

PRISMA flow diagram of the study process. PRISMA, Preferred Reporting Items for Systematic review and Meta-analysis

Study characteristics

This NMA included 65 randomized controlled trials published between 2001 and 2024, covering a variety of exercise interventions [2687, 90]. The studies were conducted in Spain (21), Brazil (13), Turkey (10), the United States (8), Canada (3), Sweden (3), Italy (2), the United Kingdom (1), China (1), South Korea (1), the Netherlands (1), and Romania (1). A total of 52 studies reported FIQ as an outcome, 29 reported VAS, 18 reported TP, and 14 reported 6MWT. A total of ten studies included both male and female participants, while the remaining fifty-five studies focused exclusively on female subjects. In total, 3,764 patients diagnosed with FMS were randomly assigned to either the exercise group (n = 2,420) or the non-exercise group (n = 1,344). Among these participants, there were 3,707 females and 57 males, with a mean age ranging from 30 to 60 years.

The experimental group received a single exercise or a combination of multiple forms of exercise, while the control group received routine care or active treatment. This NMA compared eleven types of exercise interventions: AE, AE combined with strength and stretching, AE combined with stretching, exergaming, resistance training, resistance training combined with stretching, strength training, stretching, stretching combined with balance training, WBV, and balance training. Detailed characteristics of the included studies are presented in Table 1.

Table 1.

Key characteristics and intervention details of studies included in the Meta-Analysis

Study Year Country Sample size Gender(M/F) Age(years) Intervention Outcomes
Gowans 2001 Canada

Aerobi:16

Control:15

3/28

Aerobi:46.7

Control:49.1

30 min

3times

23weeks

F1

F3

F4

Jones 2002 American

Strength:14

Stretch:14

0/28

Strength:49.2

Stretch:49.2

60 min

2times

12weeks

F1

F3

King 2002 Canada

Aerobic:46

Control:39

0/85

Aerobic:45.2

Control:47.3

40 min

3times

12weeks

F1

F3

F4

Richards 2002 Britain

Aerobic:69

Stretch:67

10/126

Aerobic:48

Stretch:45

60 min

2times

12weeks

F1

F3

Schachter 2003 Canada

Aerobic:51

Control:36

0/87

Aerobic:41.3

Control:42.5

60 min 4times

16weeks

F2
Valim 2003 Brazil

Aerobic:38

Stretch:38

0/76

Aerobic:46.05

Stretch:47.57

45 min

3times

20weeks

F2

F3

Altan 2004 Turkey

Aerobic:24

Control:22

0/46

Aerobic:43.1

Control:43.9

35 min

3times

12weeks

F1

F2

F3

Sencan 2004 Turkey

Aerobic:20

Control:20

0/40

Aerobic:35.4

Control:35.55

40 min

3times

6weeks

F2
Izquierdo 2007 Spain

Aerobic:29

Control:24

0/53

Aerobic:50

Control:46

60 min

3times

16weeks

F3
Rooks 2007 American

Aerobic_Stretch:35

Aerobic_Strength_Stretch:35

0/70

Aerobic_Stretch:48

Aerobic_Strength_Stretch:50

60 min

1times

16weeks

F1

F4

Carus 2007 Spain

Aerobic:17

Control:17

0/34

Aerobic:51

Control:51

60 min 3times

12weeks

F1
Tomas 2007 Spain

Aerobic:17

Control:17

0/34

Aerobic:51

Control:51

60 min 3times

12weeks

F1
Bircan 2008 Turkey

Aerobic:13

Strength:13

0/26

Aerobic:48.3

Strength:46.0

30 min 3times

6weeks

F2

F3

F4

Jones 2008 American

Aerobic:39

Control:41

2/78

Aerobic:49.62

Control:49.78

60 min 3times

24weeks

F2
Izquierdo 2008 Spain

Aerobic:29

Control:24

0/53

Aerobic:50

Control:46

60 min 3times

16weeks

F3
Altan 2009 Turkey

Aerobic:25

Control:24

0/49

Aerobic:48.2

Control:50

60 min

3times

24weeks

F1

F2

F3

Valencia 2009 Spain

Stretch:10

Control:10

0/20

Stretch:54.1

Control:56.4

60 min

2times

12weeks

F1

F3

Carson 2010 American

Aerobic:25

Control:28

0/53

Aerobic:51.4

Control:55.8

120 min

1times

8weeks

F1

F3

Wang 2010 American

Aerobic:33

Control:33

9/57

Aerobic:49.7

Control:50.5

60 min

2times

12weeks

F1

F2

F4

Sanudo 2011 Spain

Aerobic_Strength_Stretch:18

Control:20

0/38

Aerobic_Strength_Stretch:55.48

Control:56.15

60 min

2times

24weeks

F1
Hooten 2012 American

Strength:36

Aerobic:36

7/65

Strength:47.3

Aerobic:45.8

50 min

2times

3weeks

F1

F3

Baptista 2012 Brazil

Aerobic:40

Control:40

0/80

Aerobic:49.5

Control:49.1

45 min

2times

16weeks

F2

F4

Martinez 2012 Spain

Aerobic_Strength_Stretch:14

Control:14

0/28

Aerobic_Strength_Stretch:59.3

Control:58.6

60 min

2times

15weeks

F1
Jones 2012 American

Aerobic:51

Control:47

7/91

Aerobic:53

Control:54.8

90 min

2times

12weeks

F1
Rodriguez 2012 Spain

Aerobic:35

Stretch:35

0/70

Aerobic:55.41

Stretch:55.41

60 min

2times

12weeks

F1

F2

Sanudo 2012 Spain

Aerobic_Strength_Stretch:21

Control:20

0/41

Aerobic_Strength_Stretch:58.6

Control:58.6

60 min

2times

24weeks

F1

F4

Hustings 2013 Netherlands

Aerobic:47

Control:48

0/95

Aerobic:43.9

Control:42.9

60 min

2times

12weeks

F1
Gavi 2014 Brazil

Strength:35

Stretch:31

0/66

Strength:44.34

Stretch:48.65

45 min

2times

16weeks

F1
Genc 2015 Turkey

Aerobic:27

Stretch:27

0/54

Aerobic:35.1

Stretch:36.9

50 min

3times

6weeks

F1
Kibar 2015 Turkey

Stretch_Balance:28

Stretch:29

3/54

Stretch_Balance:48.11

Stretch:48.17

20 min

5times

4weeks

F1
Larsson 2015 Sweden

Resistance:67

Control:63

0/130

Resistance:50.81

Control:52.1

60 min

2times

15weeks

F1

F4

Ericsson 2016 Sweden

Resistance:67

Control:63

0/130

Resistance:50.81

Control:52.1

60 min

2times

15weeks

F1
Bongi 2016 Italy

Aerobic:22

Control:22

0/44

Aerobic:50.36

Control:54.3

60 min

2times

16weeks

F1

F3

Paolucci 2016 Italy

Aerobic:19

Control:20

0/39

Aerobic:50.4

Control:51.3

60 min

2times

5weeks

F1
Mateo 2017 Spain

Exergame:42

Control:41

0/83

Exergame:52.52

Control:52.47

60 min

2times

8weeks

F1
Ekici 2017 Turkey

Aerobic:15

Control:21

0/36

Aerobic:37.13

Control:36.86

60 min

2times

4weeks

F1

F2

Assumpcao 2018 Brazil

Stretch:14

Resistance:16

Control:14

0/44

Stretch:47.9

Resistance:45.7

Control:46.9

40 min

2times

12weeks

F1

F2

F3

Ernberg 2018 Sweden

Resistance:49

Control:43

0/92

Resistance:48.2

Control:48.2

2times

15weeks

F1

F4

Andrade 2019 Brazil

Resistance:25

Control:21

0/46

Resistance:52.0

Control:50.6

60 min

3times

4weeks

F1
AndradeS 2019 Brazil

Aerobic:27

Control:27

0/54

Aerobic:48

Control:47

16weeks

F1

F2

Fernandes 2019 Brazil

Resistance:41

Stretch:41

0/82

Resistance:47.8

Stretch:55.0

45 min

2times

14weeks

F2
Jiao 2019 China

Aerobic:31

Control:31

8/54

Aerobic:48.9

Control:53.5

60 min

2times

12weeks

F1

F3

Silva 2019 Brazil

Resistance:30

Control:30

0/60

Resistance:44.93

Control:49.40

40 min

2times

12weeks

F2

F4

Villafaina 2019 Spain

Exergame:28

Control:27

0/55

Exergame:54.04

Control:52.72

60 min

2times

24weeks

F1
Atan 2020 Turkey

Aerobic_Strength_Stretch:20

Aerobic_Strength_Stretch:20

Control:20

0/60

Aerobic_Strength_Stretch:46.57

Aerobic_Strength_Stretch:47.36

Control:52.7

60 min

5times

6weeks

F1

F2

Carvalho 2020 Brazil

Exergame:16

Control:19

0/35

Exergame:55.64

Control:47.70

60 min

3times

7weeks

F1
Alventosa 2020 Spain

Aerobic:16

Control:16

0/32

Aerobi:53.3

Control:53.3

60 min

2times

8weeks

F1

F2

F4

Sarmento 2020 American

Aerobic:10

Control:10

0/20

Aerobic:42.6

Control:56.1

25 min

7times

10weeks

F2
Valmana 2020 Spain

Aerobic:23

Control:25

0/48

Aerobic:55.01

Control:52.96

90 min

2times

12weeks

F1

F2

Villafaina 2020 Spain

Exergame:22

Control:15

0/37

Exergame:54.27

Control:53.44

60 min

2times

24weeks

F1

F4

Ardila 2021 Spain

Strength:36

Control:33

0/69

Strength:56.06

Control:54.39

13weeks

F1

F2

Garijo 2021 Spain

Aerobic:17

Control:17

0/34

Aerobic:51.81

Control:55.06

50 min

2times

15weeks

F1

F2

F3

F4

Alventosa 2021 Spain

Aerobic:16

Control:16

0/32

Aerobic:53.06

Control:55.13

60 min

2times

8weeks

F1

F2

Park 2021 Korea

Strength:20

Stretch:20

2/38

Strength:52.8

Stretch:50.5

30 min

2times

4weeks

F1
Patru 2021 Romania

Aerobic:34

Control:32

0/66

Aerobic:55.3

Control:56.3

60 min

3times

12weeks

F1
Mansilla 2021 Spain

Aerobic:29

Aerobic:33

Control:31

0/93

Aerobic:52.24

Aerobic:52.24

Control:52.24

45 min

2times

4weeks

F1

F2

Ribeiro 2021 Brazil

Whole-body vibration:17

Control:15

0/32

Whole-body vibration:56

Control:54

3times

6weeks

F1

F2

F4

Fernandez 2022 Spain

Aerobic:40

Control:40

6/74

Aerobic:50.6

Control:50.7

2weeks F1
Lorena 2022 Brazil

Stretch:19

Control:21

0/40

Stretch:46.47

Control:46.38

90 min

1times

10weeks

F1

F2

Kolak 2022 Turkey

Aerobic_Stretch:13

Resistance_Stretch:13

Stretch:15

0/41

Aerobic_Stretch:48.3

Resistance_Stretch:46

Stretch:45.9

40 min

3times

12weeks

F1

F2

Marcen 2023 Spain

Aerobic:33

Control:31

0/64

Aerobic:46.9

Control:48.7

60 min

3times

16weeks

F1
Mansilla 2023 Spain

Aerobic:31

Control:29

0/60

Aerobic:52.24

Control:52.24

45 min

2 times

4weeks

F1
Yavuz 2023 Turkey

Aerobic:26

Balance:25

0/51

Aerobic:38.12

Balance:41

3times

6 weeks

F2
Fernandes 2024 Brazil

Resistance:41

Stretch:41

0/82

Resistance:47.8

Stretch:55

45 min

2 times

14 weeks

F2
Schulze 2024 Brazil

Stretch:13

Control:12

0/25

Stretch:45.92

Control:45.17

45 min

1times

8weeks

F1

F2

F3

F1:FIQ(Fibromyalgia lmpact Questionnaire)

F2:VAS(a 10 mm visual analog scale)

F3:TP(tender point)

F4:6MWT(6-minute walk)

Quality assessment

The RoB 2.0 results indicated that most studies had a low risk of bias concerning the randomization process and missing outcome data, but raised some concerns regarding blinding. Due to the unique nature of exercise interventions, nearly all studies were unable to implement blinding for participants and researchers, resulting in a high risk across this dimension. Overall, the methodological quality of the included studies was moderate, with some limitations remaining. Detailed assessment results for each study are provided in Supplementary Material 3.

The TESTEX evaluation results showed that the scores ranged from 9 to 13 points, with an average score of 10.37 points, indicating overall quality ranging from moderate to high. Most studies clearly defined inclusion criteria and ensured comparability between baseline groups, and all reported intergroup comparisons, point estimates, and variability measures. Additionally, they provided relatively thorough descriptions of the intensity, volume, and energy expenditure of the exercise interventions. Detailed assessment results for each study are provided in Supplementary Material 4.

Pairwise meta-analysis

In the pairwise meta-analysis, different exercise intervention methods demonstrated varying degrees of effectiveness compared to the control group across multiple outcome measures. Overall results indicated that certain exercise interventions significantly improved FIQ, VAS, and 6MWT, while the improvement in TP was relatively limited. The combined effect results for each outcome measure are presented in Supplementary Material 5.

Additionally, we conducted a publication bias analysis using Egger’s test for the primary outcomes. The results indicated significant publication bias for FIQ (P = 0.000) and VAS (P = 0.002), while no obvious publication bias was observed for TP (P = 0.288) and 6MWT (P = 0.354).

Network meta-analysis

Each circle in the diagram represents an exercise intervention, with the size of the circle corresponding to the number of patients involved. Lines connecting the nodes signify direct comparisons between two interventions. Thicker lines denote studies that were more frequently used for direct comparisons. The global inconsistency test revealed no significant inconsistency in the network (P > 0.05). A network diagram comparing various exercise interventions across four outcome measures is presented in Fig. 2.

Fig. 2.

Fig. 2

Network plot of different exercise interventions for key outcomes in patients with fibromyalgia syndrome

The network diagram forms a closely connected loop, with the control group at its center. However, when the FIQ was employed as the outcome index for the NMA, we observed notable differences in the results of direct comparisons, indirect comparisons, and network comparisons between the strength and control groups, as well as between the stretch and control groups (P < 0.05). In contrast, when VAS and TP were employed as outcome indicators, the local inconsistency test yielded non-significant results, indicating that no data exhibited inconsistencies between direct and indirect comparisons (P > 0.05). Furthermore, since the network diagram using 6MWT as an outcome index did not form a closed loop, a local inconsistency test was deemed unnecessary. Local consistency test results for all outcomes are presented in Supplementary Material 6.

At the same time, we used the GRADE framework to grade the certainty of evidence for the primary outcome measures. The results showed that the evidence quality for FIQ was moderate, while that for TP, VAS, and 6MWT was low. This implies that while our conclusions have certain reference significance, they should be interpreted with caution and verified through further high-quality clinical trials. Detailed GRADE assessments for all primary outcomes are provided in Supplementary Material 7.

Efficacy outcomes

The findings indicate that FIQ, AE [MD = −10.23, 95% CI (−11.28, −9.19)], AE and Strength and Stretch [MD = −17.23, 95% CI (−20.93, −13.53)], AE and Stretch [MD = −15.92, 95% CI (−22.48, −9.31)], Exergame [MD = −6.80, 95% CI (−10.81, −2.78)], Resistance [MD = −6.90, 95% CI (−10.18, −3.62)], resistance and stretch [MD = −23.65, 95% CI (−34.43, −12.90)], Strength [MD = −15.87, 95% CI (−18.23,−13.51)], Stretch [MD = −12.44, 95% CI (−13.83, −11.05)], stretch and balance [MD = −25.13, 95% CI (−33.81, −16.44)], and WBV [MD = −23.70, 95% CI (−34.91,−12.47)] were found to be significantly more effective than the control group according to the results of the consistency NMA. Overall, all exercise interventions significantly improved the FIQ, with stretching combined with balance training, whole-body vibration training, and resistance combined with stretching showing the largest effect sizes, suggesting these interventions may represent the most effective exercise options.

For VAS, AE [MD = −1.26, 95% CI (−1.52, −1.01)], AE and Strength and Stretch [MD = −3.61, 95% CI (−4.40, −2.82)], AE and Stretch [MD = −2.71, 95% CI (−3.80, −1.62)], Balance [MD = −1.52, 95% CI (−2.58, −0.46)], Resistance [MD = −1.73, 95% CI (−2.35, −1.11)], resistance and stretch [MD = −3.12, 95% CI (−3.98, −2.26)], Stretch [MD = −1.12, 95% CI (−1.39, − 0.85)], and WBV [MD = − 2.45, 95%CI (–4.11, − 0.80)] were found to be more effective than the control group based on the results of a consistent NMA. In contrast, strength training alone [MD = −0.65, 95% CI (−1.47, 0.17)] did not show a significant difference. Overall, composite interventions (e.g., AE and strength and stretch, resistance and stretch) demonstrated superior effects compared with single-modality interventions.

For TP, AE showed a statistically significant advantage over the control group [MD = −2.28, 95% CI (−3.57, −1.00)]. In contrast, Resistance [MD = −1.00, 95% CI (−6.46, 4.47)], Strength [MD = −2.29, 95% CI (−4.59, 0.01)], and Stretch [MD = −1.83, 95% CI (−3.89, 0.28)] did not show statistically significant differences compared to the control group. Overall, AE was most effective in improving the number of tender points, while single resistance, strength, or stretching training did not show significant advantages.

For 6MWT, AE [MD = 53.18, 95% CI (35.01, 71.29)], Resistance [MD = 46.97, 95% CI (31.50, 62.49)], and WBV [MD = 55.00, 95% CI (26.14, 83.75)] were found to be more effective than the control group. In comparison, AE and Strength and Stretch [MD = 24.49, 95% CI (−18.72, 67.72)], AE and Stretch [MD = 5.62, 95% CI (−49.13, 60.12)], Exergame [MD = 18.08, 95% CI (−48.50, 84.52)], and Strength [MD = 44.30, 95% CI (−20.79, 108.93)] did not reach statistical significance compared to the control group. Overall, AE, resistance training, and WBV training were the most effective in improving patients’ exercise endurance. The meta-analysis effect sizes of various exercise movement types on post-intervention efficacy in patients with FMS are displayed in Tables 2, 3, 4 and 5.

Table 2.

Network Meta-Analysis matrix of Post-Intervention effects on health status (FIQ) across different exercise interventions in patients with FMS

MD95%CI
AE
6.99(3.16,10.84)* AE_Strength_Stretch
5.68(−1.01,12.32) −1.33(−7.26,4.6) AE_Stretch
−10.23(−11.28,−9.19)* −17.23(−20.93,−13.53)* −15.92(−22.48,−9.31)* Control
−3.44(−7.59,0.72) −10.43(−15.91,−5)* −9.11(−16.82,−1.4)* 6.8(2.78,10.81)* Exergame
−3.34(−6.79,0.1) −10.33(−15.28,−5.39)* −9(−16.36,−1.64)* 6.9(3.62,10.18)* 0.1(−5.08,5.31) Resistance
13.42(2.63,24.22)* 6.42(−4.58,17.49) 7.74(−3.51,19.06) 23.65(12.9,34.43)* 16.83(5.37,28.35)* 16.77(5.52,28.03)* Resistance_Stretch
5.64(3.18,8.09)* −1.35(−5.73,3.02) −0.05(−6.94,6.92) 15.87(13.51,18.23)* 9.07(4.42,13.74)* 8.98(4.93,13.01)* −7.78(−18.68,3.13) Strength
2.21(0.6,3.82)* −4.77(−8.7,−0.88)* −3.47(−10.12,3.22) 12.44(11.05,13.83)* 5.64(1.39,9.9)* 5.54(1.99,9.11)* −11.21(−21.94,−0.5)* −3.43(−5.55,−1.3)* Stretch
14.9(6.18,23.59)* 7.89(−1.54,17.3) 9.22(−1.64,20.12) 25.13(16.44,33.81)* 18.33(8.78,27.9)* 18.23(8.94,27.47)* 1.48(−12.23,15.16) 9.26(0.42,18.08)* 12.7(4.09,21.26)* Stretch_Balance
13.46(2.21,24.74)* 6.46(−5.32,18.23) 7.8(−5.22,20.84) 23.7(12.47,34.91)* 16.9(4.99,28.8)* 16.81(5.17,28.47)* 0.04(−15.52,15.56) 7.81(−3.63,19.28) 11.25(−0.04,22.55) −1.45(−15.54,12.71) WBV

*meansP < 0.05

Table 3.

Network Meta-Analysis matrix of Post-Intervention effects on pain intensity (VAS) across different exercise interventions in patients with FMS

MD95%CI
AE
2.35(1.51,3.18)* AE_Strength_Stretch
1.45(0.33,2.56)* −0.89(−2.25,0.44) AE_Stretch
0.26(−0.77,1.29) −2.09(−3.41,−0.76)* −1.19(−2.7,0.33) Balance
−1.26(−1.52,−1.01)* −3.61(−4.4,−2.82)* −2.71(−3.8,−1.62)* −1.52(−2.58,−0.46)* Control
0.47(−0.2,1.13) −1.88(−2.88,−0.88)* −0.98(−2.2,0.23) 0.21(−1.02,1.43) 1.73(1.11,2.35)* Resistance
1.86(0.96,2.75)* −0.49(−1.65,0.68) 0.41(−0.71,1.54) 1.6(0.23,2.96)* 3.12(2.26,3.98)* 1.39(0.37,2.41)* Resistance_Stretch
−0.62(−1.45,0.22) −2.96(−4.1,−1.82)* −2.07(−3.42,−0.69)* −0.88(−2.2,0.45) 0.65(−0.17,1.47) −1.08(−2.1,−0.05)* −2.47(−3.67,−1.28)* Strength
−0.14(−0.51,0.22) −2.49(−3.32,−1.65)* −1.59(−2.65,−0.54)* −0.4(−1.5,0.69) 1.12(0.85,1.39)* −0.61(−1.21,−0.01)* −2(−2.82,−1.18)* 0.47(−0.4,1.33) Stretch
1.19(−0.49,2.87) −1.15(−3,0.68) −0.26(−2.26,1.73) 0.93(−1.04,2.9) 2.45(0.8,4.11)* 0.72(−1.05,2.49) −0.67(−2.54,1.21) 1.8(−0.05,3.66) 1.33(−0.35,3.02) WBV

*meansP < 0.05

Table 4.

Network Meta-Analysis matrix of Post-Intervention effects on number of tender points (TP) across different exercise interventions in patients with FMS

MD95%CI
AE
−2.28(−3.57,−1)* Control
−1.28(−6.91,4.33) 1(−4.47,6.46) Resistance
0.02(−2.19,2.21) 2.29(−0.01,4.59) 1.29(−4.63,7.24) Strength
−0.44(−2.55,1.59) 1.83(−0.28,3.89) 0.83(−5.02,6.65) −0.46(−3.02,2.05) Stretch

*meansP < 0.05

Table 5.

Network Meta-Analysis matrix of Post-Intervention effects on aerobic capacity (6MWT) across different exercise interventions in patients with FMS

MD95%CI
AE
28.63(−18.26,75.55) AE_Strength_Stretch
47.59(−9.94,105.4) 18.98(−14.46,52.25) AE_Stretch
53.18(35.01,71.29)* 24.49(−18.72,67.72) 5.62(−49.13,60.21) Control
35.06(−33.76,104.07) 6.52(−72.41,85.87) −12.47(−98.53,73.5) −18.08(−84.52,48.5) Exergame
6.16(−17.65,30.09) −22.38(−68.39,23.54) −41.41(−98.32,15.22) −46.97(−62.49,−31.5)* −28.93(−97.31,39.41) Resistance
8.77(−53.34,71.3) −19.73(−97.22,58.06) −38.68(−123.49,45.64) −44.3(−108.93,20.79) −26.3(−119.42,66.74) 2.61(−63.83,69.55) Strength
−1.83(−35.8,32.24) −30.41(−82.5,21.41) −49.32(−111.21,12.36) −55(−83.75,−26.14)* −36.91(−109.51,35.28) −8.03(−40.73,24.53) −10.68(−82.07,60.09) WBV

*meansP < 0.05

Rank probability

The rankings based on SUCRA values for FIQ are as follows: stretch and balance (SUCRA = 90.43%) > resistance and stretch (SUCRA = 85.86%) > WBV (SUCRA = 85.35%) > AE and Strength and Stretch (SUCRA = 67.05%) > Strength (SUCRA = 59.54%) > AE and Stretch (SUCRA = 58.72%) > Stretch (SUCRA = 42.01%) > AE (SUCRA = 29.90%) > Resistance (SUCRA = 15.58%) > Exergame (SUCRA = 15.54%) > Control (SUCRA = 0.01%).

For VAS, the rankings are: AE and Strength and Stretch (SUCRA = 95.42%) > resistance and stretch (SUCRA = 85.63%) > AE and Stretch (SUCRA = 75.66%) > WBV (SUCRA = 68.78%) > Resistance (SUCRA = 53.07%) > Balance (SUCRA = 44.17%) > AE (SUCRA = 35.46%) > Stretch (SUCRA = 26.59%) > Strength (SUCRA = 14.49%) > Control (SUCRA = 0.73%).

For TP, the rankings are: AE (SUCRA = 71.06%) > Strength (SUCRA = 70.07%) > Stretch (SUCRA = 56.13%) > Resistance (SUCRA = 42.10%) > Control (SUCRA = 10.64%).For 6MWT, the rankings are: WBV (SUCRA = 78.59%) > AE (SUCRA = 77.58%) > Resistance (SUCRA = 67.18%) > Strength (SUCRA = 62.41%) > AE and Strength and Stretch (SUCRA = 43.07%) > Exergame (SUCRA = 36.68%) > AE and Stretch (SUCRA = 21.05%) > Control (SUCRA = 13.43%). The comparative efficacy of various interventions in enhancing pain relief and exercise capacity among patients with FMS is illustrated in Fig. 3.

Fig. 3.

Fig. 3

Cumulative ranking probability plots of exercise interventions for improving outcomes in patients with fibromyalgia syndrome

Sensitivity analysis

To assess the robustness of the results, we conducted sensitivity analyses and heterogeneity tests for each outcome measure. Overall, the sensitivity analysis results showed that the effect sizes varied only slightly across different models and methods, and did not substantially alter the relative ranking of exercise interventions, suggesting that the findings of this study are highly robust.

Regarding heterogeneity, the I² values varied significantly across different outcomes and comparison pairs. The FIQ results indicated that some comparisons exhibited high heterogeneity, such as Control vs. AE (pairwise 36.6%, network 37.8%) and Stretch vs. Control (pairwise 20.4%, network 87.3%), suggesting substantial differences in effect sizes between exercise modalities. In the VAS results, Control vs. AE (pairwise 67.6%, network 65.7%) and Stretch vs. Control (pairwise 56.8%, network 75.0%) also exhibited moderate to high heterogeneity. In the TP results, heterogeneity was significant for Control vs. AE (pairwise 86.7%, network 85.9%) and Stretch vs. Strength (network 91.2%). Some comparisons (e.g., Strength vs. Control, Resistance vs. Control) demonstrate low heterogeneity (I² = 0%). In the 6MWT metric, most comparisons showed low heterogeneity (e.g., Resistance vs. Control, I² = 0%), suggesting relatively stable conclusions. Detailed results of heterogeneity tests are shown in Supplementary Material 8.

Overall, although some outcome metrics and comparisons exhibited high heterogeneity, sensitivity analysis results indicated that these differences did not affect the overall conclusions or intervention rankings, validating the robustness of this NMA.

Publication bias

Based on the symmetry criterion and visual inspection, the majority of studies were distributed symmetrically about the center line in the funnel plot, suggesting the robustness of the research findings, with no significant publication bias observed (Fig. 4).

Fig. 4.

Fig. 4

Comparison-adjusted funnel plot illustrating potential publication bias across exercise intervention studies

Discussion

Main findings

Exercise therapy has become one of the most commonly used and popular rehabilitation methods for patients with FMS [90]. To our knowledge, this is the first and largest NMA to date, incorporating 65 randomized controlled trials involving 3,764 participants. It systematically compared the effects of 11 different exercise interventions on FMS, covering functional status (FIQ), pain intensity (VAS), tender point count (TP), and aerobic capacity (6MWT). This study used an NMA to simultaneously compare the effects of single and combined exercise interventions and rank multiple intervention measures, thereby providing a more comprehensive reference for clinical practice. Due to the limited number of studies for some interventions and the heterogeneity of the included populations, caution is warranted when interpreting these results. The results showed that in terms of the FIQ metric, stretching combined with balance training was the most effective intervention, followed by resistance combined with stretching, with WBV ranking third. In terms of the VAS metric, combined aerobic, strength, and stretching exercises were the most effective, followed by resistance combined with stretching and aerobic combined with stretching. In terms of the TP metric, AE performed best, with no significant differences observed among other exercise forms. On the 6MWT metric, WBV ranked first, followed by AE and resistance exercise in second and third place, respectively. Overall, composite training and WBV demonstrated a strong advantage in improving multiple core outcomes.

The risk of bias varied across the included studies, with the primary risk stemming from limitations in the implementation of blinding. Sensitivity analyses further supported the robustness of the study’s conclusions.

Effects of different exercise types on health status

Current research indicates that FMS patients often experience a significant decline in health status [91]. Previous meta-analyses suggest that aerobic, resistance, and stretching exercises can significantly improve FMS symptoms (P < 0.05), but no statistically significant differences were observed between different types of exercise [15]. Additionally, neither aerobic nor resistance exercise alone can fully counteract all the negative effects of FMS [92]. Another meta-analysis demonstrated that a combination of exercises significantly improves FMS-related sleep, whereas individual aerobic or strength exercises do not have a positive effect [93]. However, these studies were limited in the types of exercise examined and focused mainly on outcomes such as quality of life, sleep, and mood, failing to cover all types of exercise interventions. In contrast, this study incorporated a more comprehensive range of exercise intervention forms and introduced additional metrics such as TP, VAS, and 6MWT, highlighting the innovative nature of this research. The results showed that all included exercise forms significantly improved the FIQ of FMS patients; however, the ranking results suggested that stretching combined with balance training may be the most effective approach for enhancing the health status of FMS patients, consistent with the positive effects reported in previous studies [55]. Related studies have found that stretching combined with balance training is more advantageous than stretching alone in improving health status. A meta-analysis indicated that stretching exercises can significantly improve FIQ scores [17, 94], while the effects of balance training are considered comparable to those of AE [87]. The underlying mechanisms may include the following: stretching can increase the joint range of motion in FMS patients [95, 96], and by activating the descending pain-inhibitory system, promoting the release of endogenous opioids, and regulating descending pain pathways, it can suppress pain and improve health status [9799]. Therefore, the combination of stretching and balance training holds potential advantages in FMS intervention.

In addition to widespread pain, loss of balance is also a common complaint in FMS patients, with 45%−68% of FMS cases experiencing balance issues [87]. Current evidence suggests that the severity of FMS symptoms is closely associated with balance disorders, making the incorporation of balance training into rehabilitation programs clinically valuable [100]. Balance training not only improves postural control and stability, reducing the risk of falls, but may also further improve patients’ quality of life by improving motor function and self-efficacy [55]. Future studies may further explore the combined effects of balance training and other forms of exercise to provide more comprehensive treatment strategies for patients with FMS.

Therefore, it is reasonable to assume that combining stretching exercises with balance training may help improve the health status of patients with FMS. However, the evidence supporting this view is currently limited to a single study reporting such benefits, and the underlying physiological mechanisms remain unclear. More high-quality research is needed to confirm these findings and support their clinical application.

Effects of different exercise types on pain intensity and number of painful areas

Our research found that combined aerobic, strength, and stretching exercises may be the most effective way to relieve pain, consistent with the conclusions of Altan et al. [70]. Studies have shown that a combination of AE and yoga can significantly improve pain levels in patients with FMS, with better results than AE alone [101]. Additionally, Kolak et al. noted that a combination of AE with stretching or resistance training was more effective than stretching alone in reducing VAS scores [102]. In contrast, Park et al. found no significant changes in VAS scores in the strength training group, but a noticeable improvement in the stretching group [103]. An increasing number of studies suggest that combined interventions involving multiple forms of exercise are more effective than single-modality exercise in alleviating FMS-related pain [48]. The mechanisms of action may include: AE or strength training can enhance muscle oxygenation, reduce peripheral and central sensitivity, thereby improving clinical pain [104]; combining AE with strength training may alleviate pain by releasing neurotransmitters through the central nervous system and promoting local muscle adaptation; stretching exercises can reduce tender point sensitivity, increase joint range of motion, and alleviate movement fear, thereby further alleviating pain [62, 105].

This study found that AE was most effective in reducing the number of tender points in patients with FMS. Although resistance training and stretching exercises also showed improvement trends, they did not reach statistically significant differences. Previous studies have also suggested that aerobic mind-body exercises such as Ba Duan Jin and Tai Chi are highly effective in improving FMS symptoms [58, 67]. Some studies have reported that yoga can reduce the number of TP [43]. It is worth noting that traditional Chinese medicine exercise therapies (such as Ba Duan Jin and Tai Chi) can effectively reduce the perception of pain in multiple areas by harmonizing the mind and body and improving central nervous system function [20]. Compared with conventional aerobic exercises (e.g., running, swimming, or cycling), traditional mind-body exercises emphasize mind-body integration and deep relaxation, potentially conferring unique benefits in alleviating pain in patients with FMS [106].

Effects of different exercise types on aerobic capacity

Patients with FMS often experience insufficient physical activity, which can exacerbate symptoms and lead to a decline in physical fitness levels [81]. The results of this study suggest that WBV training may be the most effective form of exercise for improving aerobic capacity in FMS patients. WBV has been recommended in recent years as a time-saving, feasible, well-tolerated, and low-risk intervention method [107]. It works by mechanically stimulating muscles and the nervous system through vibration, thereby improving muscle contraction efficiency and blood circulation. This leads to enhanced aerobic capacity [108], reduced visceral fat, optimized body composition [109], increased muscle strength [110], improved balance [111, 112], and enhanced flexibility [113]. These physiological and functional improvements may collectively contribute to enhanced exercise endurance in FMS patients.

Limitations

This study still has some limitations. First, due to the difficulty of implementing blinding for participants and researchers in exercise intervention studies, the majority of included studies have a risk of bias in this dimension. Second, the limited number of studies available for certain outcome measures may lead to small-sample effects and potential publication bias, thereby affecting the robustness of the results. In this study, the results of Egger’s test suggest a possible publication bias for FIQ and VAS, while TP and 6MWT showed no obvious bias. Small-sample studies are more likely to report positive results, potentially leading to an overestimation of intervention effects. As SUCRA rankings are based on effect estimates from network meta-analyses, the presence of publication bias or small-sample effects may affect the stability of rankings for different exercise interventions. For example, in studies with limited sample sizes, fluctuations in effect values may lead to certain exercise forms (such as combined training) being overestimated in SUCRA rankings. Therefore, while SUCRA provides a relative ranking of different interventions, its results should be interpreted cautiously in light of the potential influence of publication bias and small-sample effects. Third, according to the GRADE evidence grading system, this study found that the evidence quality was moderate for FIQ. In contrast, the evidence quality for VAS, TP, and 6MWT was low, indicating that there remains uncertainty regarding the evidence for pain intensity, tender point count, and exercise endurance. Fourth, the NMA itself has methodological limitations. The reliability of NMA depends on the transitivity assumption, which states that differences in participant characteristics, interventions, and outcome measures across studies should be as comparable as possible. However, the included studies exhibited heterogeneity in intervention frequency, intensity, and duration, which may affect the robustness of the results. Although consistency tests suggested overall consistency between direct and indirect evidence, some comparisons relied primarily on indirect evidence and should be interpreted with caution. Additionally, most data for certain outcomes originate from small-sample studies, which increases indirectness and uncertainty. In summary, the conclusions of this study should be applied cautiously in clinical settings. Further large-sample, high-quality, long-term randomized controlled trials are needed to confirm these findings.

Conclusion

This systematic review and NMA indicate that stretching combined with balance training is most effective in improving the overall health status of FMS patients; AE and strength training combined with stretching are significantly effective in alleviating pain intensity; AE performs best in reducing the number of pain points; and WBV training has advantages in enhancing aerobic exercise capacity. Overall, compared to single exercise modalities, combined training may offer unique advantages in improving multidimensional outcomes for patients with FMS.

Based on the current evidence, stretching and balance training can be prioritized as adjunctive therapies for patients with FMS. However, the limited number of randomized controlled trials on combined interventions, coupled with significant variations in intervention forms, duration, and intensity, restricts the comparability and generalizability of results. Future studies should focus on conducting large-scale, high-quality, long-term randomized controlled trials to establish the comparative efficacy of various exercise modalities and guide evidence-based clinical exercise prescriptions.

Supplementary Information

Acknowledgements

Not applicable.

Abbreviations

FMS

Fibromyalgia Syndrome

WBV

Whole-Body Vibration

AE

Aerobic Exercise

NMA

Network Meta-Analysis

TP

Tender Points

Authors’ contributions

(1) Wen Yuan: Literature retrieval, data extraction, data analysis, quality evaluation, article writing; (2) Pengfei Wan: Literature retrieval, data extraction, data analysis; (3) Hui Wang: data extraction, quality evaluation; (4) MingZhu Suo: data extraction, quality evaluation; (5) Pingping Xie: Writing – review & editing.

Funding

Not applicable.

Data availability

All data generated or analyzed during this study are included in this published article and its supplementary information files.

Declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Wen Yuan and Pengfei Wan contributed equally to this work and should be considered co-first authors.

References

  • 1.Srivastava S, et al. Global mapping of physical activity promotion strategies in Fibromyalgia- A comprehensive methodological scoping review protocol. MethodsX. 2025;14:103234. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Triviño Martínez Á, Solano Ruiz MC, Siles J, González. La Cronicidad de La fibromialgia: Una revisión de La literatura. Enfermería Global. 2014;13(35):273–92.
  • 3.Elsaid NY. Understanding fibromyalgia: A comprehensive review of the literature. Egypt Rheumatologist. 2025;47(2):90–7. [Google Scholar]
  • 4.Pavillon G, Maguin P. The 10th revision of the international classification of diseases. Rev Epidemiol Sante Publique. 1993;41(3):253–5. [PubMed] [Google Scholar]
  • 5.Yunus MB. Fibromyalgia and overlapping disorders: the unifying concept of central sensitivity syndromes. Semin Arthritis Rheum. 2007;36(6):339–56. [DOI] [PubMed] [Google Scholar]
  • 6.Benlidayi IC. Role of inflammation in the pathogenesis and treatment of fibromyalgia. Rheumatol Int. 2019;39(5):781–91. [DOI] [PubMed] [Google Scholar]
  • 7.Martinez-Lavin M. Fibromyalgia and small fiber neuropathy: the plot thickens! Clin Rheumatol. 2018;37(12):3167–71. [DOI] [PubMed] [Google Scholar]
  • 8.Pastor-Mira M-a et al. Motivational determinants of objective physical activity in women with fibromyalgia who attended rehabilitation settings. J Clin Med, 2021;10(23):5547. [DOI] [PMC free article] [PubMed]
  • 9.Wolfe F et al. Fibromyalgia diagnosis and biased assessment: Sex, prevalence and bias. PLoS ONE, 2018;13(9):e0203755. [DOI] [PMC free article] [PubMed]
  • 10.Rasulova K et al. Mitochondrial MiRNAs and fibromyalgia: new biomarker candidates. Mol Biol Rep. 2025;52(1):16. [DOI] [PubMed]
  • 11.Lee LK, et al. Humanistic and economic burden of fibromyalgia in Japan (9, Pg 967, 2016). J Pain Res. 2016;9:p1161–1161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Giorgi V, et al. Pharmacological treatment of fibromyalgia syndrome: A Practice-Based review. Curr Pain Headache Rep. 2024;28(12):1349–63. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Climent-Sanz C, et al. Fibromyalgia pain management effectiveness from the patient perspective: a qualitative evidence synthesis. Disabil Rehabil. 2024;46(20):4595–610. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Lacasse A, Bourgault P, Choiniere M. Fibromyalgia-related costs and loss of productivity: a substantial societal burden. BMC Musculoskelet Disord. 2016;17(1):168. [DOI] [PMC free article] [PubMed]
  • 15.Couto N et al. Effect of different types of exercise in adult subjects with fibromyalgia: a systematic review and meta-analysis of randomised clinical trials. Sci Rep. 2022;12(1):10391. [DOI] [PMC free article] [PubMed]
  • 16.Casanova-Rodriguez D et al. Aerobic exercise prescription for pain reduction in fibromyalgia: A systematic review and Meta-Analysis. Eur J Pain. 2025;29(2):e4783. [DOI] [PMC free article] [PubMed]
  • 17.Mao S, et al. Effects of traditional Chinese martial arts and stretching exercises on symptoms of fibromyalgia: A systematic review and Meta-Analysis. Percept Mot Skills. 2024;131(6):2244–75. [DOI] [PubMed] [Google Scholar]
  • 18.Wang J-J, et al. Effect of resistance exercises on function and pain in fibromyalgia. Am J Phys Med Rehabil. 2024;103(4):275–83. [DOI] [PubMed] [Google Scholar]
  • 19.Correyero-Leon M, et al. Effectiveness of aquatic training based on aerobic and strengthening exercises in patients with fibromyalgia: systematic review with meta-analysis. Explore-the J Sci Healing. 2024;20(1):27–38. [DOI] [PubMed] [Google Scholar]
  • 20.Wang X, Luo H. Effects of traditional Chinese exercise therapy on pain scores, sleep quality, and anxiety-depression symptoms in fibromyalgia patients: a systematic review and meta-analysis. BMC Musculoskelet Disord. 2024;25(1):99. [DOI] [PMC free article] [PubMed]
  • 21.Chen J, Han B, Wu C. On the superiority of a combination of aerobic and resistance exercise for fibromyalgia syndrome: A network meta-analysis. Front Psychol. 2022;13:949256. [DOI] [PMC free article] [PubMed]
  • 22.Niu G et al. Effects of exercise dosage on the treatment of fibromyalgia: A meta-analysis of randomised controlled trials. Musculoskelet Care. 2024;22(3)e1918. [DOI] [PubMed]
  • 23.Li M D H. The Effects of Pool-Based Aerobic Exercise Versus Land-Based Aerobic Exercise on Pain for Adults with Fibromyalgia: A Meta-Analysis. California State University, Fresno, 2017.
  • 24.Rodríguez-Domínguez Á. The most effective therapeutic exercises for pain intensity in women with fibromyalgia: A systematic review and network meta-analysis. Braz J Phys Ther. 2025;29(4):101226. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Hutton B, et al. The PRISMA extension statement for reporting of systematic reviews incorporating network Meta-analyses of health care interventions: checklist and explanations. Ann Intern Med. 2015;162(11):777–84. [DOI] [PubMed] [Google Scholar]
  • 26.Gowans SE, et al. Effect of a randomized, controlled trial of exercise on mood and physical function in individuals with fibromyalgia. Arthritis Rheum. 2001;45(6):519–29. [DOI] [PubMed] [Google Scholar]
  • 27.Jones KD, et al. A randomized controlled trial of muscle strengthening versus flexibility training in fibromyalgia. J Rheumatol. 2002;29(5):1041–8. [PubMed] [Google Scholar]
  • 28.King SJ, et al. The effects of exercise and education, individually or combined, in women with fibromyalgia. J Rheumatol. 2002;29(12):2620–7. [PubMed] [Google Scholar]
  • 29.Richards SC, Scott DL. Prescribed exercise in people with fibromyalgia: parallel group randomised controlled trial. BMJ (Clinical research ed.), 2002. 325(7357): p. 185. [DOI] [PMC free article] [PubMed]
  • 30.Schachter CL, et al. Effects of short versus long bouts of aerobic exercise in sedentary women with fibromyalgia: a randomized controlled trial. Phys Ther. 2003;83(4):340–58. [PubMed] [Google Scholar]
  • 31.Valim V, et al. Aerobic fitness effects in fibromyalgia. J Rheumatol. 2003;30(5):1060–9. [PubMed] [Google Scholar]
  • 32.Altan L, et al. Investigation of the effects of pool-based exercise on fibromyalgia syndrome. Rheumatol Int. 2004;24(5):272–7. [DOI] [PubMed] [Google Scholar]
  • 33.Sencan S, et al. A study to compare the therapeutic efficacy of aerobic exercise and Paroxetine in fibromyalgia syndrome. J Back Musculoskelet Rehabil. 2004;17(2):57–61. [Google Scholar]
  • 34.Munguía-Izquierdo D, Legaz-Arrese A. Exercise in warm water decreases pain and improves cognitive function in middle-aged women with fibromyalgia. Clin Exp Rheumatol. 2007;25(6):823–30. [PubMed] [Google Scholar]
  • 35.Rooks DS, et al. Group exercise, education, and combination self-management in women with fibromyalgia: a randomized trial. Arch Intern Med. 2007;167(20):2192–200. [DOI] [PubMed] [Google Scholar]
  • 36.Tomas-Carus P, et al. The fibromyalgia treatment with physical exercise in warm water reduces the impact of the disease on female patients’ physical and mental health. Reumatologia Clin. 2007;3(1):33–7. [DOI] [PubMed] [Google Scholar]
  • 37.Tomas-Carus P, et al. Aquatic training and detraining on fitness and quality of life in fibromyalgia. Med Sci Sports Exerc. 2007;39(7):1044–50. [DOI] [PubMed] [Google Scholar]
  • 38.Bircan C, et al. Effects of muscle strengthening versus aerobic exercise program in fibromyalgia. Rheumatol Int. 2008;28(6):527–32. [DOI] [PubMed] [Google Scholar]
  • 39.Jones KD, et al. A six-month randomized controlled trial of exercise and pyridostigmine in the treatment of fibromyalgia. Arthritis Rheum. 2008;58(2):612–22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Munguía-Izquierdo D, Legaz-Arrese A. Assessment of the effects of aquatic therapy on global symptomatology in patients with fibromyalgia syndrome: a randomized controlled trial. Arch Phys Med Rehabil. 2008;89(12):2250–7. [DOI] [PubMed] [Google Scholar]
  • 41.Altan L, et al. Effect of pilates training on people with fibromyalgia syndrome: a pilot study. Arch Phys Med Rehabil. 2009;90(12):1983–8. [DOI] [PubMed] [Google Scholar]
  • 42.Valencia M, et al. Effects of 2 physiotherapy programs on pain perception, muscular flexibility, and illness impact in women with fibromyalgia: a pilot study. J Manip Physiol Ther. 2009;32(1):84–92. [DOI] [PubMed] [Google Scholar]
  • 43.Carson JW, et al. A pilot randomized controlled trial of the yoga of awareness program in the management of fibromyalgia. Pain. 2010;151(2):530–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Wang C, et al. A randomized trial of Tai Chi for fibromyalgia. N Engl J Med. 2010;363(8):743–54. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Sañudo B, et al. Effects of a prolonged exercise program on key health outcomes in women with fibromyalgia: a randomized controlled trial. J Rehabil Med. 2011;43(6):521–6. [DOI] [PubMed] [Google Scholar]
  • 46.Baptista AS, et al. Effectiveness of dance in patients with fibromyalgia: a randomized, single-blind, controlled study. Clin Exp Rheumatol. 2012;30(6 Suppl 74):18–23. [PubMed] [Google Scholar]
  • 47.García-Martínez AM, De Paz JA, Márquez S. Effects of an exercise programme on self-esteem, self-concept and quality of life in women with fibromyalgia: a randomized controlled trial. Rheumatol Int. 2012;32(7):1869–76. [DOI] [PubMed] [Google Scholar]
  • 48.Hooten MW, et al. Effects of strength vs aerobic exercise on pain severity in adults with fibromyalgia: a randomized equivalence trial. Pain. 2012;153(4):915–23. [DOI] [PubMed] [Google Scholar]
  • 49.Jones KD, et al. A randomized controlled trial of 8-form Tai Chi improves symptoms and functional mobility in fibromyalgia patients. Clin Rheumatol. 2012;31(8):1205–14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.López-Rodríguez MM, et al. Comparison between aquatic-biodanza and stretching for improving quality of life and pain in patients with fibromyalgia. Atencion primaria /, vol. 44. Sociedad Espanola de Medicina de Familia y Comunitaria; 2012. p. 641–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Sañudo B, et al. Effects of exercise training and detraining in patients with fibromyalgia syndrome: a 3-yr longitudinal study. Am J Phys Med Rehabil. 2012;91(7):561–9. quiz 570‐3. [DOI] [PubMed] [Google Scholar]
  • 52.van Eijk-Hustings Y, et al. Challenges in demonstrating the effectiveness of multidisciplinary treatment on quality of life, participation and health care utilisation in patients with fibromyalgia: a randomised controlled trial. Clin Rheumatol. 2013;32(2):199–209. [DOI] [PubMed] [Google Scholar]
  • 53.Gavi MB, et al. Strengthening exercises improve symptoms and quality of life but do not change autonomic modulation in fibromyalgia: a randomized clinical trial. PLoS ONE. 2014;9(3):e90767. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Genc A, et al. Does aerobic exercise affect the hypothalamic-pituitary-adrenal hormonal response in patients with fibromyalgia syndrome? J Phys Therapy Sci. 2015;27(7):2225–31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Kibar S, et al. New approach in fibromyalgia exercise program: A preliminary study regarding the effectiveness of balance training. Arch Phys Med Rehabil. 2015;96(9):1576–82. [DOI] [PubMed] [Google Scholar]
  • 56.Larsson A, et al. Resistance exercise improves muscle strength, health status and pain intensity in fibromyalgia–a randomized controlled trial. Arthritis Res Therapy. 2015;17(1):161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Ericsson A, et al. Resistance exercise improves physical fatigue in women with fibromyalgia: a randomized controlled trial. Arthritis Res Therapy. 2016;18:176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Maddali Bongi S, et al. Efficacy of rehabilitation with Tai Ji Quan in an Italian cohort of patients with fibromyalgia syndrome. Complement Ther Clin Pract. 2016;24:109–15. [DOI] [PubMed] [Google Scholar]
  • 59.Paolucci T, et al. A new rehabilitation tool in fibromyalgia: the effects of perceptive rehabilitation on pain and function in a clinical randomized controlled trial. Evidence-based Complement Altern Medicine: eCAM. 2016;2016:p7574589. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Collado-Mateo D, et al. Exergames for women with fibromyalgia: a randomised controlled trial to evaluate the effects on mobility skills, balance and fear of falling. PeerJ. 2017;5(4):e3211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Ekici G, et al. Effects of active/passive interventions on pain, anxiety, and quality of life in women with fibromyalgia: randomized controlled pilot trial. Women Health. 2017;57(1):88–107. [DOI] [PubMed] [Google Scholar]
  • 62.Assumpção A, et al. Muscle stretching exercises and resistance training in fibromyalgia: which is better? A three-arm randomized controlled trial. Eur J Phys Rehabil Med. 2018;54(5):663–70. [DOI] [PubMed] [Google Scholar]
  • 63.Ernberg M, et al. Plasma cytokine levels in fibromyalgia and their response to 15 weeks of progressive resistance exercise or relaxation therapy. Mediat Inflamm. 2018;2018:p3985154. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Andrade A, Sieczkowska SM, Vilarino GT. Resistance training improves quality of life and associated factors in patients with fibromyalgia syndrome. PM R: J Injury Function Rehabilitation. 2019;11(7):703–9. [DOI] [PubMed] [Google Scholar]
  • 65.Andrade CP, et al. Effects of aquatic training and detraining on women with fibromyalgia: controlled randomized clinical trial. Eur J Phys Rehabil Med. 2019;55(1):79–88. [DOI] [PubMed] [Google Scholar]
  • 66.Fernandes G, et al. A functional exercise program improves pain and health related quality of life in patients with fibromyalgia: a randomized controlled trial. Arthritis Rheumatol. 2019;71:350. [DOI] [PubMed] [Google Scholar]
  • 67.Jiao J, et al. Ba-Duan-Jin alleviates pain and fibromyalgia-related symptoms in patients with fibromyalgia: results of a randomised controlled trial. Clin Exp Rheumatol. 2019;37(6):953–62. [PubMed] [Google Scholar]
  • 68.Silva HJA, et al. Sophrology versus resistance training for treatment of women with fibromyalgia: a randomized controlled trial. J Bodyw Mov Ther. 2019;23(2):382–9. [DOI] [PubMed] [Google Scholar]
  • 69.Villafaina S, et al. Benefits of 24-Week exergame intervention on Health-Related quality of life and pain in women with fibromyalgia: A Single-Blind, randomized controlled trial. Games Health J. 2019;8(6):380–6. [DOI] [PubMed] [Google Scholar]
  • 70.Atan T, Karavelioğlu Y. Effectiveness of High-Intensity interval training vs Moderate-Intensity continuous training in patients with fibromyalgia: a pilot randomized controlled trial. Arch Phys Med Rehabil. 2020;101(11):1865–76. [DOI] [PubMed] [Google Scholar]
  • 71.Carvalho MS, et al. Effects of exergames in women with fibromyalgia: A randomized controlled study. Games Health J. 2020;9(5):358–67. [DOI] [PubMed] [Google Scholar]
  • 72.Izquierdo-Alventosa R et al. Low-Intensity physical exercise improves pain catastrophizing and other psychological and physical aspects in women with fibromyalgia: A randomized controlled trial. Int J Environ Res Public Health. 2020;17(10):3634 . [DOI] [PMC free article] [PubMed]
  • 73.Sarmento CVM, et al. The therapeutic efficacy of qigong exercise on the main symptoms of fibromyalgia: a pilot randomized clinical trial. Integr Med Res. 2020;9(4):100416. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Sauch Valmaña G, et al. Effects of a physical exercise program on patients affected with fibromyalgia. J Prim Care Community Health. 2020;11:2150132720965071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Villafaina S, et al. Effects of exergames on heart rate variability of women with fibromyalgia: a randomized controlled trial. Sci Rep. 2020;10(1):5168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Garrido-Ardila EM et al. Effects of physiotherapy vs. Acupuncture in quality of life, pain, stiffness, difficulty to work and depression of women with fibromyalgia: a randomized controlled trial. J Clin Med. 2021;10(17):3765. [DOI] [PMC free article] [PubMed]
  • 77.Hernando-Garijo I et al. Immediate effects of a telerehabilitation program based on aerobic exercise in women with fibromyalgia. Int J Environ Res Public Health. 2021;18(4):2075. [DOI] [PMC free article] [PubMed]
  • 78.Izquierdo-Alventosa R et al. Effectiveness of High-Frequency transcranial magnetic stimulation and physical exercise in women with fibromyalgia: a randomized controlled trial. Phys Ther. 2021;101(10):159. [DOI] [PubMed]
  • 79.Park HK, et al. Comparison of core muscle strengthening exercise and stretching exercise in middle-aged women with fibromyalgia: A randomized, single-blind, controlled study. Med (Baltim). 2021;100(50):e27854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Patru S et al. Influence of multidisciplinary therapeutic approach on fibromyalgia patients. Experimental Therapeutic Med. 2021;21(5):528. [DOI] [PMC free article] [PubMed]
  • 81.Ribeiro VGC et al. Efficacy of Whole-Body Vibration Training on Brain-Derived Neurotrophic Factor, Clinical and Functional Outcomes, and Quality of Life in Women with Fibromyalgia Syndrome: A Randomized Controlled Trial. Journal of Healthcare Engineering, 2021. [DOI] [PMC free article] [PubMed]
  • 82.Arroyo-Fernández R, et al. Effectiveness of transcranial direct current stimulation combined with exercising in people with fibromyalgia: A randomized Sham-Controlled clinical trial. Arch Phys Med Rehabil. 2022;103(8):1524–32. [DOI] [PubMed] [Google Scholar]
  • 83.de Lorena SB, et al. Effects of a physical self-care support program for patients with fibromyalgia: a randomized controlled trial. J Back Musculoskelet Rehabil. 2022;35(3):495–504. [DOI] [PubMed] [Google Scholar]
  • 84.Kolak E, Ardıç F, Fındıkoğlu G. Effects of different types of exercises on pain, quality of life, depression, and body composition in women with fibromyalgia: A three-arm, parallel-group, randomized trial. Archives of rheumatology. 2022;37(3):444. [DOI] [PMC free article] [PubMed]
  • 85.Estrada-Marcén NC et al. Can an aerobic exercise programme improve the response of the growth hormone in fibromyalgia patients? A randomised controlled trial. Int J Environ Res Public Health. 2023;20(3):2261. [DOI] [PMC free article] [PubMed]
  • 86.Rodriguez-Mansilla J et al. Effects of an exercise for Well-Being and physical training programme on muscle Strength, range of Movement, respiratory capacity and quality of life in women with fibromyalgia: a randomized controlled trial. J Clin Med. 2023;12(3):774. [DOI] [PMC free article] [PubMed]
  • 87.Yavuz H, et al. A Comparison of the effects of balance- proprioception and aerobic exercises on functional status, Pain, and balance in patients with fibromyalgia syndrome- a randomized controlled study. J Istanbul Fac Medicine-Istanbul Tip Fakultesi Dergisi. 2023;86(4):368–75. [Google Scholar]
  • 88.Fernandes G, et al. A functional exercise program improves pain and health related quality of life in patients with fibromyalgia: a randomized controlled trial. Adv Rheumatol (London England). 2024;64(1):p81. [DOI] [PubMed] [Google Scholar]
  • 89.Schulze NBB, et al. The effect of myofascial release of the physiological chains on the pain and health status in patients with fibromyalgia, compared to passive muscle stretching and a control group: a randomized controlled clinical trial. Disabil Rehabil. 2024;46(16):3629–42. [DOI] [PubMed] [Google Scholar]
  • 90.Rodríguez-Mansilla J, Mejías-Gil A, Garrido-Ardila EM, et al. Effects of non-pharmacological treatment on pain, flexibility, balance and quality of life in women with fibromyalgia: a randomised clinical trial. Journal of Clinical Medicine. 2021;10(17):3826. [DOI] [PMC free article] [PubMed]
  • 91.Larsson A, et al. Resistance exercise improves muscle strength, health status and pain intensity in fibromyalgia-a randomized controlled trial. Arthritis Research & Therapy. 2015;17(1):161. [DOI] [PMC free article] [PubMed]
  • 92.Bidonde J et al. Aerobic exercise training for adults with fibromyalgia. Cochrane Database Syst Reviews, 1996;2017(6). [DOI] [PMC free article] [PubMed]
  • 93.Cuenca-Martinez F et al. Exercise-based interventions on sleep quality in patients with fibromyalgia syndrome: an umbrella and mapping review with meta-analysis. Semin Arthritis Rheum, 2023 ; 61:152216. [DOI] [PubMed]
  • 94.Stove MP, et al. The effectiveness of stretching exercises in patients with fibromyalgia: A systematic review. Clin Rheumatol. 2024;43(10):3039–53. [DOI] [PubMed] [Google Scholar]
  • 95.da Costa BO et al. Effects of a telehealth stretching exercise program on Pain, Sleep, Depression, and functionality of women with fibromyalgia during the COVID-19 pandemic: A randomized clinical trial. Sustainability, 2023 ;15(3):2604.
  • 96.Konrad A, et al. Chronic effects of stretching on range of motion with consideration of potential moderating variables: A systematic review with meta-analysis. J Sport Health Sci. 2024;13(2):186–94. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97.Stove MP et al. The effect of six-week regular stretching exercises on regional and distant pain sensitivity: an experimental longitudinal study on healthy adults. Bmc Sports Sci Med Rehabilitation, 2024 ; 16(1):202 . [DOI] [PMC free article] [PubMed]
  • 98.Stove MP, Hirata RP, Palsson TS. Regional and widespread pain sensitivity decreases following stretching in both men and women - Indications of stretch-induced hypoalgesia. J Bodyw Mov Ther. 2024;39:32–7. [DOI] [PubMed] [Google Scholar]
  • 99.Tompra N, van Dieen JH, Coppieters MW. Central pain processing is altered in people with Achilles tendinopathy. Br J Sports Med. 2016;50(16):1004–U79. [DOI] [PubMed] [Google Scholar]
  • 100.Navarrete DS, et al. Association between balance Disorders, fibromyalgia Severity, and balance confidence: an observational study on fibromyalgia. Rev Med Chil. 2024;152(7):776–86. [DOI] [PubMed] [Google Scholar]
  • 101.Sevgin O et al. Efficacy of different exercises in women with fibromyalgia syndrome: a randomised controlled trial. Clinical and experimental rheumatology, 2025. [DOI] [PubMed]
  • 102.Kolak E, Ardic F, Findikoglu G. Effects of different types of exercises on pain, quality of life, depression, and body composition in women with fibromyalgia: A three-arm, parallel-group, randomized trial. Archives Rheumatol. 2022;37(3):444–55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Park H-K et al. Comparison of core muscle strengthening exercise and stretching exercise in middle-aged women with fibromyalgia: A randomized, single-blind, controlled study. Medicine, 2021;100(50): e27854. [DOI] [PMC free article] [PubMed]
  • 104.Bidonde J et al. Mixed exercise training for adults with fibromyalgia. Cochrane Database Syst Reviews, 1996; 2019(5). [DOI] [PMC free article] [PubMed]
  • 105.Matsutani LA, et al. Effectiveness of muscle stretching exercises with and without laser therapy at tender points for patients with fibromyalgia. Clin Exp Rheumatol. 2007;25(3):410–5. [PubMed] [Google Scholar]
  • 106.Zhang H et al. Effects of traditional Chinese exercises in fibromyalgia syndrome: A meta-analysis of randomized controlled trials. Complement Ther Med, 2024. 80. [DOI] [PubMed]
  • 107.Angel Garcia D, Martinez Nicolas I, Saturno Hernandez PJ. Clinical approach to fibromyalgia: synthesis of Evidence-based recommendations, a systematic review. Reumatologia Clin. 2016;12(2):65–71. [DOI] [PubMed] [Google Scholar]
  • 108.Mingorance JA, et al. The therapeutic effects of Whole-Body vibration in patients with Fibromyalgia. A randomized controlled trial. Frontiers in Neurology; 2021. p. 12. [DOI] [PMC free article] [PubMed]
  • 109.dos Santos JM et al. Whole-Body vibration training on oxidative stress Markers, Irisin Levels, and body composition in women with fibromyalgia: A randomized controlled trial. Bioengineering-Basel, 2023 ; 10(2):260 . [DOI] [PMC free article] [PubMed]
  • 110.Sanudo B, et al. The effect of a 6-week exercise programme and whole body vibration on strength and quality of life in women with fibromyalgia: a randomised study. Clin Exp Rheumatol. 2010;28(6):S40–5. [PubMed] [Google Scholar]
  • 111.Sanudo B, et al. Effect of Whole-Body vibration exercise on balance in women with fibromyalgia syndrome: A randomized controlled trial. J Altern Complement Med. 2012;18(2):158–64. [DOI] [PubMed] [Google Scholar]
  • 112.Adsuar JC, et al. Whole body vibration improves the single-leg stance static balance in women with fibromyalgia: a randomized controlled trial. J Sports Med Phys Fitness. 2012;52(1):85–91. [PubMed] [Google Scholar]
  • 113.de Hoyo M, et al. Incidencia Del ejercicio físico y El Entrenamiento vibratorio sobre La amplitud de movimiento de mujeres Con fibromialgia. Revista Andaluza De Med Del Deporte. 2013;6(2):52–6. [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Data Availability Statement

All data generated or analyzed during this study are included in this published article and its supplementary information files.


Articles from BMC Sports Science, Medicine and Rehabilitation are provided here courtesy of BMC

RESOURCES