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Recruiting NCT06363695

Building Community Health Volunteers' Capacity to Support Parents With Young Children With SafeCare Kenya

No phase Interventional Child Maltreatment Parenting

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: SafeCare Kenya, Care as Usual by Community Health Volunteers.
Who it may be relevant to
Registry conditions: Child Maltreatment, Parenting. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Kenya
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Implementing the Adapted Parenting Program, SafeCare Kenya, to Reduce Noncommunicable Disease Burden: Building Community Health Volunteers' Capacity to Support Parents With Young Children

Overview

The goal of this clinical trial is to implement and examine the impact of SafeCare Kenya, an adapted parenting program, to improve parents' skills and knowledge related to the care of their children between the ages of 18 months and 5 years old. The main questions it aims to answer are: * Will SafeCare Kenya improve child and parent outcomes? * Is virtual delivery as effective as in-person delivery of SafeCare Kenya? * Is SafeCare Kenya feasible to deliver by community health volunteers? Mothers will: * Complete study assessments at three timepoints: baseline, 6 months and 18 months * Mothers in the SafeCare Kenya group will receive the program from their community health volunteer Researchers will compare SafeCare Kenya to care as usual by community health volunteers to see if SafeCare Kenya families show improvements in parent interaction skills, safety and health knowledge, potential for child abuse, child behavior problems, child injuries, parenting stress, and child and parent quality of life.

Detailed description

After being informed about the study and potential risks, all community health volunteers consented to the study will be randomized to continue their usual services with families or be trained to deliver SafeCare Kenya to add to their usual services with families. All community health volunteers will inform their eligible families about the study and share with the research team mothers who express interest in the study. After being informed about the study and potential risks, all mothers giving informed consent will complete a baseline assessment, along with a 6 month and 18 month follow up assessment. Mothers whose community health volunteer is assigned to the SafeCare Kenya program will receive the program from their community health volunteers. All SafeCare Kenya mothers will be randomized to receive the program either in-person or virtually. Trainers and Stakeholders will provide information about their involvement in the project.

Interventions

  • Behavioral SafeCare Kenya
    Adapted from SafeCare, this is a strengths-based program for parents with children ages 18 months through age 5, teaching parents skills and knowledge in three areas: 1) parent-child interactions, 2) child health, and 3) home safety.
  • Other Care as Usual by Community Health Volunteers
    Community Health Volunteers support families with children up to age 5 around the physical health needs of family members, including delivering key health messages (e.g., importance of immunizations); treating minor injuries and illnesses; identifying/treating/referring common childhood illnesses (e.g., diarrhea, malaria); conducting home visits to evaluate the home environment and discuss improvements; and encouraging care at home and appropriate health seeking behaviors. These support services

Primary outcome measures

  • Change from Baseline in score on Child Planned Activities Training (cPAT) at 6 months [Time frame: Baseline and 6 months]
  • Change from Baseline in score on Child Planned Activities Training (cPAT) at 18 months [Time frame: Baseline and 18 months]
  • Change from Baseline in scores on Parenting Young Children (PARYC) at 6 months [Time frame: Baseline and 6 months]
  • Change from Baseline in scores on Parenting Young Children (PARYC) at 18 months [Time frame: Baseline and 18 months]
  • Change from Baseline in score on How to Keep your Child Safe and Healthy Quiz at 6 months [Time frame: Baseline and 6 months]
  • Change from Baseline in score on How to Keep your Child Safe and Healthy Quiz at 18 months [Time frame: Baseline and 18 months]
  • Change from Baseline in score on Brief Child Abuse Potential Inventory (BCAPI) at 6 months [Time frame: Baseline and 6 months]
  • Change from Baseline in score on Brief Child Abuse Potential Inventory (BCAPI) at 18 months [Time frame: Baseline and 18 months]
Secondary outcome measures (10)
  • Change from Baseline in score on Child Behavior Checklist (CBCL) at 6 months [Time frame: Baseline and 6 months]
  • Change from Baseline in score on Child Behavior Checklist (CBCL) at 18 months [Time frame: Baseline and 18 months]
  • Change from Baseline in scores on Parenting Stress Index at 6 months [Time frame: Baseline and 6 months]
  • Change from Baseline in scores on Parenting Stress Index at 18 months [Time frame: Baseline and 18 months]
  • Change from Baseline in score on Childhood injuries at 6 months [Time frame: Baseline and 6 months]
  • Change from Baseline in score on Childhood injuries at 18 months [Time frame: Baseline and 18 months]
  • Change from Baseline in score on Child Quality of Life at 6 months [Time frame: Baseline and 6 months]
  • Change from Baseline in score on Child Quality of Life at 18 months [Time frame: Baseline and 18 months]
  • Change from Baseline in score on Parent Quality of Life at 6 months [Time frame: Baseline and 6 months]
  • Change from Baseline in score on Parent Quality of Life at 18 months [Time frame: Baseline and 18 months]

Eligibility criteria

Parents Inclusion Criteria:

  • being the female primary caregiver
  • at least 18 years old of age
  • at least one child between 18 months and age 5
  • reside in Kibera
  • have ability to participate virtually (i.e., owns a smart phone) in English or Swahili.

Parent Exclusion Criteria:

  • younger than 18 years old
  • unable to participate in English or Swahili
  • does not own smart phone to participate in virtual sessions.

CHV Inclusion Criteria:

  • 18 years or older
  • able to participate in English or Swahili
  • has ability to participate virtually (i.e., owns a smart phone)
  • female community health volunteer who is affiliated with one of the project's agencies in Kibera

CHV Exclusion Criteria:

  • younger than 18 years old
  • not able to participate in English or Swahili
  • does not have a smart phone
  • is not female
  • is not a community health volunteer affiliated with one of the project's agencies

Trainer Inclusion Criteria:

  • 18 years or older
  • able to participate in English and Swahili
  • trained as a SafeCare trainer

Trainer Exclusion Criteria:

  • younger than 18 years old
  • not able to participate in English and Swahili
  • not trained as a SafeCare Trainer

Stakeholder Inclusion Criteria:

  • 18 years or older
  • able to participate in English
  • involved in the project as a stakeholder

Stakeholder Exclusion Criteria:

  • younger than 18 years old
  • not able to participate in English
  • not a stakeholder for this project

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Prevention

Study locations

Kenya · 1 center
  • Africa Institute of Mental and Brain Health — Nairobi

Identifiers

NCT: NCT06363695 · 131-22 · 1R01HD112043-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗