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Completed NCT05943132

MISC-CBO to Improve the Mental Health of OVC in South Africa

Conditions: Mental Disorder, Child

Sex: All
Ages: 7 Years – 11 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 792
Sponsor: University of Houston

Location: University of the Free State Bloemfontein Free State

Summary

The goal of this cluster randomized control clinical trial is to evaluate the effectiveness of the Mediational Intervention for Sensitizing Caregivers for Community-based Organizations (MISC-CBO) in reducing mental health problems in orphan and vulnerable children in South Africa. Aim 1 will evaluate the direct effects of MISC-CBO on video-coded CBO caseworker caregiving quality (affiliation and attachment) and children's mental health outcomes over a 24 month period. 24 CBOs (360 children and 72 caseworkers) will be recruited using existing Non-Governmental Organization (NGO) partner (Childline) in two districts in the Free State, South Africa (SA). CBOs will be randomly assigned to receive either one year of bi-weekly MISC-CBO or Treatment as Usual (TAU). The investigators hypothesize that MISC-CBO will be associated with comparative increases in caseworker caregiving quality and reductions in mental health problems in Orphans and Vulnerable Children (OVC). Aim 2a,will test the hypothesis that caregiving quality at end-of-intervention (12 months) accounts for intervention effects on child mental health at 18 and 24 months. Aim 2b will evaluate the moderating effects of orphan status and the quality of the home environment, expecting that OVC who are maternal and double orphans, and from impoverished home environments will show reduced response to intervention compared to children without these risk factors. Aim 3a will use World Health Organization metrics to test the hypothesis that MISC-CBO is cost-effective in terms of disability-adjusted life years (DALYs) averted. Aim 3b will use qualitative methodology to test the hypothesis that community stakeholders deem the climate favorable and ready for the implementation of MISC-CBO, and that additional barriers and facilitators for scale-up and implementation will be identified. The proposed work extends the investigators' formative work to now fully test the real-world effectiveness, mechanisms of action, cost-effectiveness and implementation readiness of MISC-CBO during the critical developmental window of at-risk children aging into adolescence, consistent with National Institute of Mental Health's strategic objectives.

Eligibility Criteria

Inclusion Criteria: 1. Status as OVC. 2. Children will be 7-11 years old 3. Resident in the CBO catchment area 4. Child has a legal guardian Exclusion Criteria: 1. Children with a medical history of serious birth complications 2. Children with a medical history severe malnutrition 3. Children with a neurological disability

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05943132). StuddyBuddy aggregates publicly available trial information.