Summary of findings 4. Exercise compared to pharmacological treatments for adults with depression.
Exercise compared to antidepressants for adults with depression | |||||
Patient or population: adults with depression Settings: Intervention: Exercise Comparison: antidepressants | |||||
Outcomes | Illustrative comparative risks* (95% CI) | No of Participants (studies) | Quality of the evidence (GRADE) | Comments | |
Assumed risk | Corresponding risk | ||||
Antidepressants | Exercise | ||||
Symptoms of depression | The mean symptoms of depression in the intervention groups was 0.11 standard deviations lower (0.34 lower to 0.12 higher) | 300 (4 studies) | ⊕⊕⊕⊝ moderate1,2,3 | SMD ‐0.11 (95% CI: ‐0.34 to 0.12) | |
Acceptability of treatment | Study population | 278 (3 studies) | ⊕⊕⊕⊝ moderate1 | RR 0.98 (95% CI: 0.86 to 1.12) | |
891 per 1000 | 873 per 1000 (766 to 997) | ||||
Quality of life | The mean quality of life in the intervention groups was 0 higher (0 to 0 higher) | 0 (1 study) | ⊕⊕⊕⊝ moderate1 | One trial, Brenes 2007, reported no difference in change in SF‐36 mental health and physical health components between medication and exercise groups. | |
Adverse events | See comment | See comment | 0 (3 studies) | ⊕⊕⊕⊝ moderate1 |
Blumenthal 1999 reported that 3/53 in exercise group suffered musculoskeletal injuries; injuries in the medication group were not reported. Blumenthal 2007 collected data on side effects by asking participants to rate a 36‐item somatic symptom checklist and reported that "a few patients reported worsening of symptoms"; of the 36 side effects assessed, only 1 showed a statistically significant group difference (P = 0.03), i.e. that the sertraline group reported worse post‐treatment diarrhoea and loose stools. Blumenthal 2012a assessed 36 side effects; only 2 showed a significant group difference: 20% of participants receiving sertraline reported worse post‐treatment fatigue compared with 2.4% in the exercise group and 26% reported increased sexual problems compared with 2.4% in the exercise group. |
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). CI: Confidence interval; RR: Risk ratio; | |||||
GRADE Working Group grades of evidence High quality: Further research is very unlikely to change our confidence in the estimate of effect. Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low quality: We are very uncertain about the estimate. |
1 Lack of blinding of outcome assessors probably increased effect sizes and drop‐out rates were high. Also sequence generation was considered unclear in 1 study. 2 I² = 0% and P = 0.52, indicated no heterogeneity 3 The studies included were all relevant to the review question, particularly given that all studies had to meet the criteria of the ACSM definition of exercise.