Actively Recruiting
Implementing the Adapted Parenting Program SafeCare Kenya to Build Community Health Volunteers' Capacity and Support Parents With Young Children
Led by Pacific University · Updated on 2025-04-18
369
Participants Needed
1
Research Sites
17 weeks
Total Duration
On this page
Sponsors
P
Pacific University
Lead Sponsor
E
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to evaluate the adapted parenting program SafeCare Kenya, designed to improve skills and knowledge of parents with children aged 18 months to 5 years. The study will assess whether SafeCare Kenya improves outcomes for children and parents, compare virtual versus in-person delivery methods, and determine if community health volunteers can effectively deliver the program. The trial is sponsored by Pacific University and focuses on child maltreatment and parenting support. Community health volunteers will be randomly assigned to either continue their usual services or be trained to deliver SafeCare Kenya. Families enrolled will then be randomized to receive the SafeCare Kenya program either virtually or in person, with the curriculum consistent across both methods. Usual care involves monthly visits focused on physical health needs, while SafeCare Kenya adds structured support in parent-child interactions, child health, and home safety. Mothers will participate by completing assessments at baseline, 6 months, and 18 months. Researchers will measure changes in parenting skills, knowledge about child safety and health, child abuse potential, child behavior, injuries, parenting stress, and quality of life for both child and parent. The study includes ongoing monitoring of these outcomes to evaluate the program's impact over time.
CONDITIONS
Brief Title
Building Community Health Volunteers' Capacity to Support Parents With Young Children With SafeCare Kenya
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female primary caregiver
- At least 18 years old
- Has at least one child between 18 months and 5 years old
- Resides in Kibera
- Able to participate in English or Swahili
- Owns a smartphone to participate virtually
- Community health volunteers must be female, 18 or older, affiliated with project agencies in Kibera, able to participate in English or Swahili, and own a smartphone
- Trainers must be 18 or older, able to participate in English and Swahili, and trained as SafeCare trainers
- Stakeholders must be 18 or older, able to participate in English, and involved as project stakeholders
You will not qualify if you...
- Younger than 18 years old
- Unable to participate in English or Swahili
- Does not own a smartphone to participate virtually
- Community health volunteers who are male, not affiliated with project agencies, or do not meet language and technology requirements
- Trainers not trained as SafeCare trainers or unable to participate in required languages
- Stakeholders not involved in the project or unable to participate in English
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit
Duration - Up to 18 months
Participants whose community health volunteer is assigned to the SafeCare Kenya program receive the program either in-person at their home or virtually via a virtual platform. Community Health Volunteers trained in SafeCare Kenya deliver this behavioral parenting program that focuses on parent-child interactions, child health, and home safety. Participants in the Care as Usual group continue to receive their usual monthly community health volunteer support focused on physical health needs.
Monthly visits for Care as Usual group; visits as scheduled by Community Health Volunteers for SafeCare Kenya program delivery
Duration - Up to 18 months after baseline
Participants complete follow-up assessments at 6 months and 18 months after baseline to evaluate changes in parenting skills, child safety, and child well-being.
2 assessment visits (at 6 months and 18 months)
Trial Site Locations
Total: 1 location
1
Africa Institute of Mental and Brain Health
Nairobi, Kenya
Actively Recruiting
Research Team
J
Jenelle R. Shanley, PhD
L
Lisa P. Armistead, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
3
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