| Literature DB >> 30866431 |
Lijuan Guo1, Zhaowei Kong2, Yanjie Zhang3.
Abstract
This current meta-analysis review was conducted to examine the effectiveness of Qigong-based therapy on individuals with major depressive disorder. Six electronic databases (PubMed, PsycINFO, Cochrane Library, and Web of Science, Chinese National Knowledge Infrastructure, and Wangfang) were employed to retrieve potential articles that were randomized controlled trials. The synthesized effect sizes (Hedges' g) were computerized to explore the effectiveness of Qigong-based therapy. Additionally, a moderator analysis was performed based on the control type. The pooled results indicated that Qigong-based therapy has a significant benefit on depression severity (Hedges' g = -0.64, 95% CI -0.92 to -0.35, p < 0. 001, I² = 41.73%). Specifically, Qigong led to significantly reduced depression as compared to the active control groups (Hedges' g = -0.47, 95% CI -0.81 to -0.12, p = 0.01, I² = 22.75%) and the passive control groups (Hedges' g = -0.80, 95% CI -1.23 to -0.37, p < 0.01, I² = 48.07%), respectively. For studies which reported categorical outcomes, Qigong intervention showed significantly improved treatment response rates (OR = 4.38, 95% CI 1.26 to 15.23, p = 0.02) and remission rates (OR = 8.52, 95% CI 1.91 to 37.98, p = 0.005) in comparison to the waitlist control group. Conclusions: Qigong-based exercises may be effective for alleviating depression symptoms in individuals with major depressive disorder. Future well-designed, randomized, controlled trials with large sample sizes are needed to confirm these findings.Entities:
Keywords: Qigong; Tai Chi; emotion dysfunction; mental disorder; mind–body exercise
Mesh:
Year: 2019 PMID: 30866431 PMCID: PMC6427394 DOI: 10.3390/ijerph16050826
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390
Figure 1The process of study identification, screening, and selection.
Characteristics of the eligible randomized controlled trials.
| Reference | Characteristics of Participants | Intervention Protocol | Outcome Measured | Study Quality | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Patients Diagnostic Criteria, % of MDD, | Total Sample Size (DR), Female (%), | Age: | Training Prescription | Total Training Min | Grp or Ind | Co-intervention | Outcomes | Concealed Allocation | Intention to Treat Analysis | Blinded | |
| Yeung et al. (2017) [ | DSM-IV (psychiatrist), | 67 (25.3%), 72% female, | 54 (13) | Q: 2 × 60 min/week, 12 weeks | 1440 | Grp | None | Remission rate, response rate, depression severity | No | Yes | No |
| Chan et al. (2012) [ | DSM-IV-TR (psychiatrist), | 75 (33.3%), 80% female, 100% Chinese | Q: 47.1 (9.5) | Q:1 × 90 min/week 10 weeks | 900 | Grp | Antidepressants | Depression severity | Yes | No | Yes |
| Yeung et al. (2012) [ | DSM-IV (psychiatrist), | 39 (5.1%), 77% female, | 55(10) | Q: 2 × 60 min/week, 12 weeks | 1440 | Grp | Antidepressants allowed | Remission rate, response rate, | Yes | Yes | Yes |
| Lavretsky et al. (2011) [ | DSM-IV (psychiatrist), | 73 (6.8%), 61.6% female, | Q: 69.1 (7.0) | Q: 1 × 120 min/week, 10 weeks | 1200 | Grp | Escitalopram/lorazepam: 10–20 mg/day | Depression severity (HAM-D24) | Yes | Yes | Yes |
| Chou et al. (2004) [ | DSM-IV (psychiatrist), | 14 (0%), 50% female, | 72.6 (4.2) | Q: 3 × 45 min/week, 12 weeks | 1620 | Grp | Antidepressants or psychotherapy | Depression severity | No | Yes | Yes |
| Costa et al. (2016) [ | DSM-IV (psychiatrist), | 40 (7.5%), 74% female, | Q: 39 (1.2) | Q: 1 × 60min/week (Grp) + | 240 | Mixed | Antidepressants | Depression severity (BDI) | Yes | No | No |
| Fissler et al. (2016) [ | DSM-IV (a psychiatrist), | 74 (8.1%), 56% female, | 42 (12.5) | Q: 7 × 50 min/week, 2 weeks | 700 | Grp | Antidepressants | Depression severity | Yes | No | No |
Note: MDD = major depressive disorder; DR = dropout rate; FU = follow-up period; AE = adverse event; SD = standard deviation; Q = Qigong group; C = control group; HK = Hong Kong; DSM-IV = Diagnostic and Statistical Manual of Mental Disorders; Grp = group based practice; Ind = individual practice; CES-D = Epidemiological Studies Depression Scale; HAM-D17 = 17-item Hamilton Depression Rating Scale; BDI = Beck Depression Inventory; HAM-D24 = 24-Item Hamilton Depression Rating Scale; Remission rate = HAM-D17 scores ≤ 7; Response rate = ≥ 50% improvement on the HAM-D17 score; CBT = cognitive behavioral therapy.
Moderator analysis for Qigong versus control group.
| Categorical Moderator | Outcome | Level | No. of Studies/ | Hedges’ g | 95% CI | I2 % | Test for Between-Group | ||
|---|---|---|---|---|---|---|---|---|---|
| df ( | |||||||||
| Control Type | Depression | Active | 4 | −0.47 | −0.81 to −0.12 | 22.75% | 1.41 | 1 | 0.23 |
| Passive | 5 | −0.80 | −1.23 to −0.37 | 48.07% | |||||
| Qigong Type | Depression | Movement | 7 | −0.62 | −0.96 to −0.28 | 41.62% | 0.02 | 1 | 0.9 |
| Static | 2 | −0.67 | −1.38 to 0.04 | 67.84% | |||||
Figure 2Effects of Qigong on depression severity. Note: HAM-D24 = 24-item Hamilton Depression Rating Scale, HAM-D17 = 17-item Hamilton Depression Rating Scale, CES-D = Epidemiological Studies Depression Scale, BDI = Beck Depression Inventory. HE = heath education, WL = waitlist, CBT = cognitive behavioral therapy, GI = guided imagery, RM = rest and music.