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dc.contributor.authorBaerecke, Lauren
dc.contributor.authorOrnellas, Abigail
dc.contributor.authorSomefun, Oluwaseyi
dc.date.accessioned2024-08-14T06:46:47Z
dc.date.available2024-08-14T06:46:47Z
dc.date.issued2024
dc.identifier.citationBaerecke, L., Ornellas, A., Wamoyi, J., Wambura, M., Klapwijk, J., Chetty, A.N., Simpson, A., Janowski, R., de Graaf, K., Stern, D. and Clements, L., 2024. A hybrid digital parenting programme to prevent abuse of adolescents in Tanzania: study protocol for a pragmatic cluster-randomised controlled trial. Trials, 25(1), p.119.en_US
dc.identifier.urihttps://doi.org/10.1186/s13063-023-07893-x
dc.identifier.urihttp://hdl.handle.net/10566/9424
dc.description.abstractBackground- Evidence-based parenting programmes have strong evidence in preventing and mitigating violence, but in-person programmes are challenging to deliver at scale. ParentApp is an open-source, offline-first app-based adaptation of the Parenting for Lifelong Health for Parents and Teens programme to promote playful and positive parenting, reduce risks for sexual violence victimisation, and prevent violence against adolescents. This study aims to evaluate the effectiveness and cost-effectiveness of ParentApp compared to an attention-control group. Methods- This study is a two-arm pragmatic cluster-randomised controlled trial to test whether ParentApp reduces adolescent physical abuse, emotional abuse, and sexual violence risks and victimisation at 1 month and 12 months post-intervention. Caregivers of adolescents aged 10–17 years and their adolescent children (N=2400 caregiver-adolescent dyads) will be recruited in urban and peri-urban communities in the Mwanza region of Tanzaniaen_US
dc.language.isoenen_US
dc.publisherBioMed Central Ltden_US
dc.subjectChild abuseen_US
dc.subjectParentingen_US
dc.subjectAdolescentsen_US
dc.subjectDigitalen_US
dc.subjectViolence against childrenen_US
dc.titleA hybrid digital parenting programme to prevent abuse of adolescents in Tanzania: study protocol for a pragmatic cluster-randomised controlled trialen_US
dc.typeArticleen_US


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