Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
NCT07574567

Familia Imara: A Parenting Program to Reduce Family Violence in Tanzania

Led by Saini Das · Updated on 2026-05-08

6216

Participants Needed

1

Research Sites

100 weeks

Total Duration

On this page

Sponsors

S

Saini Das

Lead Sponsor

E

Emory University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This cluster-randomized controlled trial will evaluate the effectiveness, implementation, and scalability of Familia Imara, a group-based, couples-focused, community health worker (CHW)-delivered parenting program, on reducing intimate partner violence (IPV), harsh discipline, and improving child development and nutrition outcomes in the Mara and Geita regions of Tanzania. Villages will be randomly assigned to either an intervention or control arm. The study will be implemented in two sequential cohorts. In Cohort 1, a traditional randomized controlled trial will compare intervention villages receiving the program to control villages receiving no intervention (waitlist control), with delivery supported primarily by implementing partners in collaboration with government supervisors. In Cohort 2, the same villages will retain their original assignment. Intervention villages will receive the program under a government-led delivery model to assess scalability and integration into existing systems, while control villages will transition from waitlist to receive the intervention. Evidence generated will inform policy and practice for preventing family violence and promoting early childhood development at scale.

CONDITIONS

Official Title

Familia Imara: A Parenting Program to Reduce Family Violence in Tanzania

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • The household has a child aged 0-24 months at enrollment
  • The child has a primary female caregiver (mother) and a primary male caregiver (father) who are in a partnered relationship
  • Primary female caregiver, primary male caregiver, and child all live together in the same household
  • Both caregivers provide written informed consent for themselves and their child to participate in the study
Not Eligible

You will not qualify if you...

  • Does not meet the inclusion criteria
  • Plans to relocate within the next year

AI-Screening

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Trial Site Locations

Total: 1 location

1

National Institute for Medical Research (NIMR)

Dar es Salaam, Tanzania

Actively Recruiting

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Research Team

J

Joshua Jeong, ScD

CONTACT

G

Gerry Mshana, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

2

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