Integrating Evidence-based Approaches to Prevent Child Maltreatment in Kyrgyzstan

Recruiting now · Not applicable

Conditions studied: Parent-Child Relationships, Child Maltreatment

In brief

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.

Key facts

Study ID

NCT07712822

Run by

The University of Texas at Arlington

People needed

396

Starts

2026-09-01

Expected to finish

2027-12-31

Last updated by the study team

2026-07-20

Who can join

Age: 6 and older, up to 74. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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
• Both caregivers are fluent in either Russian or Kyrgyz
• Both caregivers are able and willing to provide informed consent
• Child is able to provide assent and participate in age-appropriate assessments.
• Family is willing to participate in study procedures, including random assignment and completion of assessments at baseline, post-intervention (16 weeks), and end-of-school-year follow-up.

You may not qualify if…

• 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
• Child has a severe developmental or medical condition that would prevent participation in assessments
• Inability to communicate in Russian or Kyrgyz.

Where it is running

• Republican Institute for Advanced Studies and Teacher Training under the Ministry of Education of the Kyrgyz Republic — Bishkek, Kyrgyzstan (enrolling)

Full record on ClinicalTrials.gov

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