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Recruiting NCT07712822

NCT07712822 Integrating Evidence-based Approaches to Prevent Child Maltreatment in Kyrgyzstan

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Clinical Trial Summary
NCT ID NCT07712822
Status Recruiting
Phase —
Sponsor The University of Texas at Arlington
Condition Parent-Child Relationships
Study Type INTERVENTIONAL
Enrollment 396 participants
Start Date 2026-09-01
Primary Completion 2027-08-31

Eligibility & Interventions

Sex All sexes
Min Age 6 Years
Max Age 74 Years
Study Type INTERVENTIONAL
Interventions
Integrated Family and Economic Empowerment Program

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 396 participants in total. It began in 2026-09-01 with a primary completion date of 2027-08-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

Inclusion Criteria: * 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. Exclusion Criteria: * 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.

Contact & Investigator

Central Contact

Associate Professor, PhD

✉ saltanat.childress@uta.edu

📞 608-422-9771

Frequently Asked Questions

Who can join the NCT07712822 clinical trial?

This trial is open to participants of all sexes, aged 6 Years or older, up to 74 Years, studying Parent-Child Relationships. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07712822 currently recruiting?

Yes, NCT07712822 is actively recruiting participants. Contact the research team at saltanat.childress@uta.edu for enrollment information.

Where is the NCT07712822 trial being conducted?

This trial is being conducted at Bishkek, Kyrgyzstan.

Who is sponsoring the NCT07712822 clinical trial?

NCT07712822 is sponsored by The University of Texas at Arlington. The trial plans to enroll 396 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology