Integrating Evidence-based Approaches to Prevent Child Maltreatment in Kyrgyzstan
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-74
SponsorThe University of Texas at Arlington
About this trial
The goal of this clinical trial is to learn if a family-based prevention program works to prevent child maltreatment risk and other adverse childhood experiences (ACEs) among families in Kyrgyzstan. It will also learn about the safety, feasibility, and acceptability of the program. The main questions it aims to answer are: (1) Does the integrated family and economic empowerment program improve children's self-regulation, behavioral adjustment, and school adaptation? (2) Is the program feasible and acceptable for families and schools in Kyrgyzstan?
Researchers will compare the integrated prevention program to bolstered standard school services to see if the program improves child and family outcomes. Participants will: (a) Be randomly assigned to either the prevention program or bolstered standard school services; (b) Attend weekly group sessions for 16 weeks (if assigned to the prevention program); (c) Complete surveys at baseline, immediately after the 16-week program, and at the end of the school year; and (d) Provide information about child behavior, (co)parenting, family relationships, and financial well-being.
Results from this pilot study will inform a future larger trial.
Eligibility criteria
Qualifiers
Two adult caregivers (≥18 years old) who identify as co-parents or primary caregivers of a target child
Target child aged 6-9 years enrolled in one of the participating schools in Bishkek, Kyrgyzstan
Both caregivers identify each other as family members responsible for the care of the child (e.g., parents, grandparents, or other adult caregivers)
Both caregivers report feeling safe participating together in a family-based program
Disqualifiers
Report of severe physical or sexual intimate partner violence between caregivers within the past 12 months, as assessed during screening
Either caregiver is unable to provide informed consent
Either caregiver has a cognitive impairment or a severe mental health condition that would preclude participation in group sessions
Family plans to relocate outside the study area during the intervention period
Trial design
Treatments tested in this trial
- Integrated Family and Economic Empowerment Program
Treatment groups
396 Participants
are divided into 2 treatment groupsSponsors and collaborators
The University of Texas at Arlington
Lead sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborator
Source ClinicalTrials.gov