Table 6.
Quality Assessment | Summary of Findings, SMD (95% CI) | |||||||
---|---|---|---|---|---|---|---|---|
Number of Participants (Studies), Follow-Up Period | Risk of Bias | Inconsistency | Indirectness | Imprecision | Publication Bias | Sham | rTMS | Certainty of Evidence |
228 (9), immediately post-intervention | No serious limitation a | Serious limitation b | No serious limitation c | Serious limitation d | Undetectable | −0.383 (−0.597, −0.170) e | −1.165 (−1.492, −0.837) f | Low ⨁⨁◯◯ |
139 (6), 2 weeks to 1 month after the last session | No serious limitation a | No serious limitation b | No serious limitation c | Serious limitation d | Undetectable | −0.387 (−0.719, −0.055) g | −1.157 (−1.579, −0.735) h | Moderate ⨁⨁⨁◯ |
CI: confidence interval; FIQ: Fibromyalgia Impact Questionnaire; FIQR: Revised Fibromyalgia Impact Questionnaire; rTMS: repetitive transcranial magnetic stimulation; SMD: standardized mean difference. a Most studies included scored low risk of bias during assessment. b The I2 was over 50% during the first follow-up and below 50% at the second follow-up. c No indirectness was detected in this outcome. d The upper and lower limit of 95% CI ranged from large to small effect size. e This was calculated by pooling the sham group of the 11 comparisons included in the primary outcome, comparing the FIQ/FIQR score before and after treatment. f This was calculated by pooling the rTMS group of the 11 comparisons included in the primary outcome, comparing the FIQ/FIQR score before and after treatment. g This was calculated by pooling the rTMS group of the 5 studies included in the primary outcome and provided baseline data, comparing the FIQ/FIQR score before and 2 weeks to 1 month after treatment. h This was calculated by pooling the rTMS group of the 5 studies included in the primary outcome and provided baseline data, comparing the FIQ/FIQR score before and 2 weeks to 1 month after treatment.