Singer 1999.
Study characteristics | ||
Methods | Randomised controlled trial; wait list control. | |
Participants | 174 parents/carers of children with a disability participated. 128 in final analysis (56 experimental/72 control). | |
Interventions | Parent‐to‐parent support. Participants were matched (following interview) to supporting parents who received training in communication skills, local services, and advocacy and support. Participants made initial call to coordinating centre to be matched; thereafter supporting parents were instructed to make a minimum of 4 phone calls to participants over 2 months. Wait‐list control. |
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Outcomes |
Primary Cognitive adaptation; empowerment; coping efficacy
Secondary Abstract mentions satisfaction measure but the qualitative analysis (of responses from a small subset of participants) was about possible mechanisms by which the intervention might provide support. See notes. Outcomes were measured at baseline and at 8 weeks following baseline. |
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Notes | Means and SDs for the empowerment outcome were sought from the author but were not available. The reported ANCOVA "suggests that initial contacts in Parent to Parent do not change parents' perceptions of empowerment". Qualitative data available 24 parents drawn from the pool of subjects who participated in Parent to Parent (12 from intervention, 12 from wait list) completed a standardised telephone interview. Transcribed interviews were coded according to identified themes. These themes pertained to how P2P makes a difference. Degree of satisfaction with intervention was not reported. |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Coin toss used |
Allocation concealment (selection bias) | Unclear risk | Allocation concealment not reported |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Unable to blind due to nature of intervention and control. |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Post‐test questionnaire asked about amount of contact with support parent, revealing group allocation. Self‐report nature of data collection means this should not have affected outcome assessments by research personnel, but may be bias from participants. |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Attrition and exclusions well reported |
Selective reporting (reporting bias) | Unclear risk | Statistical analyses reported for all outcomes, but not means and SDs for all outcomes |
Other bias | Low risk | No other sources of bias found |