Adverse events post‐intervention Number of people reporting an adverse event before completing the intervention · patients with fibromyalgia
It is very uncertain whether movement therapies changes adverse events post‐intervention Number of people reporting an… compared with usual care (very low certainty).
1 finding from 1 review
Functioning as assessed post‐intervention Fibromyalgia Impact Questionnaire. Scale from: 0 to 100 · patients with fibromyalgia
1 finding from 1 review
Pain as assessed post‐intervention Short Form ‐ McGill Pain Questionnaire Total Score. Scale from: 0 to 78 · patients with fibromyalgia
1 finding from 1 review
Mood · patients with fibromyalgia
1 finding from 1 review
All cause attrition post‐intervention Number of people withdrawing from the study before completing the intervention · patients with fibromyalgia
It is very uncertain whether relaxation changes all cause attrition post‐intervention Number of people withdrawing… compared with usual care (very low certainty).
1 finding from 1 review
Adverse events post‐intervention ‐ not reported · patients with fibromyalgia
The review found no eligible studies for this question.
1 finding from 1 review
Anxiety (state) · patients with fibromyalgia
1 finding from 1 review
All cause attrition post‐intervention Number of people withdrawing from the study before completing the intervention · patients with fibromyalgia
It is very uncertain whether psychological therapies changes all cause attrition post‐intervention Number of people withdrawing… compared with usual care (very low certainty).
1 finding from 1 review
Adverse events post‐intervention Number of people reporting an adverse event before completing the intervention · patients with fibromyalgia
Psychological therapies showed no clear difference in adverse events post‐intervention Number of people reporting an… compared with usual care (low certainty).
1 finding from 1 review
Functioning as assessed post‐intervention Fibromyalgia Impact Questionnaire. Scale from: 0 to 100 · patients with fibromyalgia
1 finding from 1 review
Patient‐reported pain intensity or pain relief (VAS, NRS or categorical scale) · patients with fibromyalgia
1 finding from 1 review
Mood as assessed post‐intervention The Symptom Checklist‐90 Revised. Scale from: 0 to 90 · patients with fibromyalgia
1 finding from 1 review
All cause attrition post‐intervention Number of people withdrawing from the study before completing the intervention · patients with fibromyalgia
It is very uncertain whether biofeedback changes all cause attrition post‐intervention Number of people withdrawing… compared with usual care (very low certainty).
1 finding from 1 review
Intervention not reported
ACR 50% improvement ‐ not measured · patients with treating rheumatoid arthritis
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Participants (n) reported adverse events ( · patients with Rheumatoid arthritis
The intervention showed no clear difference in participants (n) reported adverse events ( (low certainty).
1 finding from 1 review
Intervention not reported
Change in radiographic progression ‐ not measured · patients with Rheumatoid arthritis
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Achievement of low disease state (DAS 28) ‐ not measured · patients with Rheumatoid arthritis
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Pain Visual Analogue Scale. Scale from: 0 to 100. ( · patients with treating rheumatoid arthritis
1 finding from 1 review
Intervention not reported
Disability (HAQ score) percent change. Scale from: 0 to 100. ( · patients with treating rheumatoid arthritis
1 finding from 1 review
Intervention not reported
Participants (n) reported adverse events ( · patients with treating rheumatoid arthritis
The intervention showed no clear difference in participants (n) reported adverse events ( (moderate certainty).
1 finding from 1 review