Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Digital tool to enhance mental health services in Rwanda

Official title: Testing an mHealth Digital Dashboard to Improve Quality of Delivery of Evidence-based Interventions That Promote Family Mental Health and Functioning in Rwanda: A Hybrid Type 3 Study

Run by Boston College · NCT06941831 · Data updated 2026-11-12

This study is testing a new digital tool to see if it can help improve mental health and support for families with young children in Rwanda.

More Mental Health trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment1810 (estimated)
SponsorBoston College
Academic / other
Locations1 site (Kigali, Kigali)
StatusRecruiting
StartedJanuary 30, 2025
Main results expectedJune 30, 2027
Study endsMay 31, 2029
Registry record updatedMarch 27, 2026
Trial IDNCT06941831 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include primary caregivers of children aged 0-36 months living in Rwanda, particularly those categorized as Ubudehe 1 under the socio-economic classification.

Probably not a fit

Patients who do not have children within the specified age range or do not meet the socio-economic criteria may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates a technology-enabled service delivery model for the Sugira Muryango program, which aims to improve mental health and social services in Rwanda. By utilizing a digital dashboard, the program enhances data collection, visibility of performance metrics, and provides resources for continuous learning and training. The intervention targets primary caregivers of children under three years old, focusing on improving family functioning and reducing family violence. The study assesses the feasibility and impact of this digital approach in a context affected by historical trauma and ongoing mental health challenges.

Why it matters

Potential benefit: If successful, this approach could significantly improve mental health outcomes for families in Rwanda and enhance the overall quality of care provided.

How similar studies have gone: Other studies have shown success with similar technology-enabled interventions in mental health, indicating potential for positive outcomes in this context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Household inclusion criteria: Participants must be the primary caregiver to a child between birth and 36 months. Caregivers must live in the same household as the child and must be the child's legal guardian. Legal guardians may be parents, aunts, uncles, grandparents, or foster parents. Participants must be categorized as Ubudehe 1 under the socio-economic categorization of households from LODA.
* Government Official inclusion criteria: Government officials must be located at the Village, Cell, Sector and/or District level and must participate in the 1-day ECD training. Government officials must also agree to participate in the PLAY Collaborative activities throughout the course of program delivery.
* IZU interventionist inclusion criteria: IZUs must be a part of the Inshuti z'Umuryango/Friends of the Family program, must be over the age of 18, and must be literate in Kinyarwanda.
* Cell Level IZU Mentor inclusion criteria: Cell Level IZU Coordinators must be situated at the Cell Level and able to supervise at least 12 IZU interventionists, must be over 18 years of age, and must be literate in Kinyarwanda.

Exclusion Criteria:

* Household exclusion criteria: Potential participants will be excluded if they do not meet the inclusion criteria above, are experiencing an active crisis (e.g., psychosis), or have severe cognitive impairments which preclude their ability to speak to the research questions/assessments under scrutiny.
* Government Official exclusion criteria: Government officials will be excluded from participation in the PLAY Collaborative if they are not located at the Cell, Sector or District level and if they are unable to meet the demands of participation in the PLAY Collaborative.
* IZU interventionist exclusion criteria: IZUs will be excluded from participation if they do not meet the inclusion criteria above and if they are unable to meet the demands of delivering the Sugira Muryango program.
* Cell Level IZU Mentor exclusion criteria: Cell Level IZU Coordinators will be excluded if they do not meet the inclusion criteria above or are unable to meet the demands of supporting the delivery of the Sugira Muryango program.

Where it's running

  • FXB-Rwanda / 2XHQ+F2G Umerenge wa Runda, Runda, Rwanda
    Kigali, Kigali, Rwanda
    Recruiting

Study contacts

  • Principal investigator: Theresa S Betancourt, MA, Sc.D. — Boston College Research Program on Children and Adversity
  • Study coordinator: Lauren J Pisani, PhD
  • Email: pisanila@bc.edu
  • Phone: 617-552-8397

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.