Intervention not reported
Quality of life (SF‐36 mental score) short term · patients with chronic neck pain (pain for more than 90 days)
1 finding from 1 review
Intervention not reported
Disability (NPQ) short term · patients with chronic mechanical neck pain (pain for more than 90 days)
1 finding from 1 review
Intervention not reported
Disability (NDI) short term · patients with chronic mechanical neck pain (pain for more than 90 days)
1 finding from 1 review
Intervention not reported
Quality of life (SF‐36) short term · patients with chronic mechanical neck pain (pain for more than 90 days)
1 finding from 1 review
Intervention not reported
Pain intensity (VAS) short term · patients with chronic neck pain (pain for more than 90 days)
1 finding from 1 review
Intervention not reported
Pain pressure threshold short term · patients with chronic neck pain (pain for more than 90 days)
1 finding from 1 review
Intervention not reported
Disability (NDI) short term Function (NPQ) short term · patients with chronic neck pain (pain for more than 90 days)
1 finding from 1 review
Intervention not reported
Quality of life (SF‐36, Functional Component) short term · patients with chronic neck pain (pain for more than 90 days)
1 finding from 1 review
Intervention not reported
Pain intensity (VAS) short term · patients with chronic neck pain (pain for more than 90 days)
1 finding from 1 review
Intervention not reported
Adverse effects: Acupressure versus placebo , no treatment or active controls · women with primary dysmenorrhoea
The review found no eligible studies for this question.
1 finding from 1 review
Intervention not reported
Pain: Acupressure versus sham or placebo control · women with primary dysmenorrhoea
1 finding from 1 review
Intervention not reported
Pain: Acupressure versus NSAIDs · women with primary dysmenorrhoea
It is very uncertain whether the intervention changes pain: Acupressure versus NSAIDs (very low certainty).
1 finding from 1 review
Intervention not reported
Pain score: Acupressure versus no treatment · women with primary dysmenorrhoea
It is very uncertain whether the intervention changes pain score: Acupressure versus no treatment (very low certainty).
1 finding from 1 review
Pain1 Not measured · men and women with end‐stage kidney disease
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Beck Depression Inventory (BDI); higher score means more depression · men and women with end‐stage kidney disease
1 finding from 1 review
Quality of sleep · men and women with end‐stage kidney disease
1 finding from 1 review
Fatigue · men and women with end‐stage kidney disease
1 finding from 1 review
Nausea · People at risk of postoperative nausea and vomiting
Acupoint PC6 stimulation may leads to lower nausea ‐ All trials compared with sham (low certainty).
1 finding from 1 review
Vomiting · People at risk of postoperative nausea and vomiting
It is very uncertain whether acupoint PC6 stimulation and antiemetic combination changes vomiting compared with antiemetic (very low certainty).
1 finding from 1 review
Rescue antiemetic · People at risk of postoperative nausea and vomiting
Acupoint PC6 stimulation and antiemetic combination may leads to lower rescue antiemetic compared with antiemetic (low certainty).
1 finding from 1 review