Jang 2015.
Study characteristics | ||
Methods |
Study design: RCT Recruitment period: not reported Recruitment mode: an orthopaedist had diagnosed people with acute LBP Statistical analysis: a paired t‐test was carried out to examine changes according to the intervention, and an independent t‐test was used to compare the 2 groups Sample size calculation: not reported |
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Participants |
Sample size: total: 30; EG1: 15; EG2: 15 Setting: not reported Country: Republic of Korea Baseline characteristics
Duration LBP: ≤ 3 weeks, otherwise not specified Inclusion criteria
Exclusion criteria
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Interventions |
EG1: Tai chi
EG2
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Outcomes |
Note: outcomes were not designated as major or minor outcomes. Pain: VAS (0–10; converted to a 0–100 scale)
Others: muscle activity, balance Adverse events: not reported |
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Notes |
Authors' results and conclusions: according to the results of this study, Tai Chi is considered an appropriate exercise program to reduce acute LBP in females in their 20s. It is effective in decreasing pain. Review authors' note: only a minimal difference was detected that was not clinically relevant Funding: no funding sources reported Declaration of interest: no official disclosure regarding potential conflicts of interest |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Equally and randomly divided, randomisation not described. |
Allocation concealment (selection bias) | Unclear risk | Not described. |
Blinding All outcomes ‐ Participants | High risk | No mention of any attempts to blind participants to the other intervention or their perceptions of the potential effectiveness of the different interventions. |
Blinding All outcomes ‐ Healthcare providers | High risk | No mention of any attempts to blind care providers to the other group. |
Blinding All outcomes ‐ outcome assessors | High risk | The outcome measures were self‐reported and participants were unblinded. |
Influence of co‐interventions | Unclear risk | Study did not mention if co‐interventions were allowed, or similar in both groups. |
Group similarity at baseline | Low risk | Baseline pain scores similar, and all participants were women in their 20s. |
Compliance | Unclear risk | Not reported. |
Timing of outcome assessments | Low risk | Pre‐and post‐treatment. |
Incomplete outcome data (attrition bias) Dropouts – all outcomes | Unclear risk | No data provided, only group means of outcomes reported. |
Intention‐to‐treat‐analysis | Unclear risk | Not reported, an independent t‐test was used to compare the 2 groups. |
Selective reporting (reporting bias) | High risk | Function not reported; no published protocol available. |
Other bias | Unclear risk | No funding sources reported. No official disclosure regarding potential conflicts of interest. |