Summary of findings 2. Hypnotherapy compared with control for children and adolescents with recurrent abdominal pain.
Hypnotherapy compared with control for children and adolescents with recurrent abdominal pain | ||||||
Patient or population: children and adolescents with recurrent abdominal pain Settings: mixed Intervention: hypnotherapy Comparison: usual care or wait‐list control | ||||||
Outcomes | Probable outcome with control or usual care | Probable outcome with hypnotherapy | OR (95% CI) | Number of participants (studies) | Quality of the evidence (GRADE) | Comments |
Treatment success: postintervention | 136 per 1000 | 525 per 1000 | Pooled OR 6.78 (2.41 to 19.07) | 146 (4) | ⊕⊕⊝⊝ 1 Low | 2 studies defined treatment success or remission as > 80% decrease in pain intensity. 1 study used the definition of "4 or less days of pain per month and no missed activities" and 1 study as "> 50% reduction in API" (Walker 1997). |
Pain intensity: postintervention Lower score equals less pain. |
The pain intensity score in the hypnotherapy groups was, on average, 1.01 SDs lower (95% CI ‐1.41 to ‐0.61) than in the usual care or wait‐list control groups. | — | 146 (4) | ⊕⊕⊝⊝ 1 Low | As a rule of thumb, 0.2 SD represents a small difference, 0.5 SD a moderate difference, and 0.8 SD a large difference. 1.3 represents a large effect difference. Pain intensity measured by 2 different scales (the FACES Pain Scale and the API (Bieri 1990; Walker 1997)). |
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Pain frequency: postintervention Lower score equals less pain. |
The pain frequency score in the hypnotherapy groups was, on average, 1.28 SDs lower (95% CI ‐1.84 to ‐0.72) than in the usual care or wait‐list control groups. | — | 146 (4) | ⊕⊕⊝⊝ 1 Low | As a rule of thumb, 0.2 SD represents a small difference, 0.5 SD a moderate difference, and 0.8 SD a large difference. 1.50 SD represents a large effect difference. Pain frequency measured by different scales (bespoke pain diary recording the number of days; daily scale ranging from 0 to 3, summed over 7 days; and API, range 1 to 8 (Walker 1997)). |
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API: Abdominal Pain Index; CI: confidence interval; OR: odds ratio; SD: standard deviation | ||||||
GRADE Working Group grades of evidence High quality: Further research is very unlikely to change our confidence in the estimate of effect. Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low quality: We are very uncertain about the estimate. |
1Downgraded two levels: a high risk of bias across the studies in study design and outcome assessment (unblinded allocation and assessment, wait‐list control) and a low number of participants included in the analysis or low number of events.