- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06165315
Evaluation of a Group-based Parenting Intervention for Early Childhood Development
January 2, 2024 updated by: Joshua Jeong, Harvard School of Public Health (HSPH)
This implementation research study aims to evaluate the impact and implementation of a group-based parenting program for improving early child development and caregiver outcomes.
This study is enrolling primary caregivers with children 0 to 24 months of age to promote caregiver knowledge and skills about nurturing care for young children and support caregiver psychosocial wellbeing.
Parenting groups will leverage existing community group networks and be facilitated by trained volunteers for 20 total sessions (groups will meet twice a month for 10 months).
ChildFund Kenya and its community partners will implement the program in Busia and Homabay counties.
The research study design will involve a cluster-randomized controlled trial and a qualitative implementation evaluation.
This research is being led by Emory University with funding from the Conrad N. Hilton Foundation.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
This research has two study components and aims.
First, a cluster-randomized controlled trial will be used to quantitatively estimate the effectiveness of the parenting program on early child development and caregiver outcomes.
For the research study sample, villages in Busia and Homabay counties were randomly selected and randomly assigned in each county to either the intervention or waitlist control group.
Villages in the intervention group will receive the parenting program first, while villages in the control group will receive the program after the completion of the research study.
In total, 64 villages have been selected into this study.
Then in each village, 10 primary caregivers with children 0-24 months of age will be enrolled into the study for a total of 640 caregiver-child dyads.
A caregiver survey and observational assessment of early child development skills will be administered to study participants at baseline and endline to evaluate changes in outcomes between groups over time.
Second, and following the completion of the program, qualitative in-depth interviews will be conducted with participants and various stakeholders (e.g., program participants, parenting group facilitators, community health volunteers, ChildFund program staff) to understand their roles and experiences with the parenting program as well as the challenges and successes to inform future implementation.
This qualitative implementation evaluation will seek to identify the barriers and facilitators to program impact, quality delivery, scale-up, and sustainability.
Study Type
Interventional
Enrollment (Estimated)
620
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Nairobi, Kenya
- B&M Consult
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- primary caregiver of a child aged 0-24 months at the time of enrollment
- the household resides within the geographic boundary of the village that was sampled into the research study
- primary caregiver provides informed consent for themselves and their child to participate
Exclusion Criteria:
- none
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Parenting Program
This community-based group parenting program aims improve caregiver knowledge, attitudes, and practices on nurturing care to ultimate improve early childhood development.
A secondary aim of the program is to support caregiver psychosocial wellbeing.
The curriculum covers various topics relating to responsive caregiving, early learning, child protection, maternal and child health and nutrition, and caregiver mental health.
Intervention will be delivered through existing community group networks.
Each parenting group will comprise of 10 caregivers that will be facilitated by trained volunteers.
|
Villages in the intervention group will receive the parenting program.
The parenting program consists of 20 total sessions, whereby groups will meet twice a month for 10 months.
|
|
No Intervention: Waitlist-Control
Villages in the control group will not immediately receive the parenting program.
Instead, they will receive whatever standard of care services are delivered at the community-level (e.g., routine services from community health volunteers that are primarily focused on maternal and child health and nutrition).
After endline data collection is completed for the trial, then villages in the control group will receive the parenting program.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child development
Time Frame: 10 months
|
Child development measured using the Global Scales of Early Development - Long Form (GSED-LF).
GSED-LF is based on direct administration by a research assistant.
GSED-LF provides one score for the overall development of children 0-36 months of age.
GSED scores will be age-standardized to a mean of 0 and a standard deviation of 1. Higher scores will indicate improved early developmental skills.
|
10 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child socioemotional development
Time Frame: 10 months
|
Child socioemotional development based on observational rating by a research assistant using an adapted version of the Wolke Scales (e.g., child affect, vocalization, cooperation with the research assistant).
An average score will be calculated across the items with higher scores indicating more positive child behaviors.
|
10 months
|
|
Attitudes towards parenting
Time Frame: 10 months
|
Primary caregivers will report the extent to which they agree with various statements about parental roles and engagement in nurturing care practices.
A total score will be calculated with higher scores indicating more supportive parenting attitudes.
|
10 months
|
|
Caregiving environment
Time Frame: 10 months
|
Caregiving environment will be assessed using the Home Observation for Measurement of the Environment for infants and toddlers aged 0 to 3 years (HOME-IT).
It combines caregiver-reported items and observations of parenting behaviors to assess early learning opportunities at home and responsive caregiving behaviors of primary caregiver with the child.
A total score will be calculated with higher scores indicate more responsive caregiving and enriched home learning environments.
|
10 months
|
|
Caregiver stimulation practices
Time Frame: 10 months
|
Caregiver stimulation practices reported by primary caregiver about their engagement in early learning activities with the child (e.g.
singing, telling stories).
Activities adapted from the Family Care Indicators.
A total score will be calculated with higher scores indicating more engagement in stimulation activities.
|
10 months
|
|
Caregiver disciplinary practices
Time Frame: 10 months
|
Caregiver disciplinary practices reported by primary caregivers in terms of harsh punishment (e.g., shook the child, shouted at child) and positive disciplinary practices (e.g., explained why the behavior was wrong) used towards the child.
Items adapted from Child Discipline Module of Multiple Indicator Cluster Survey.
Separate indicators will be created for use of any harsh disciplinary practices or any positive disciplinary practices.
|
10 months
|
|
Infant and young child feeding practices
Time Frame: 10 months
|
Infant and young child feeding (IYCF) practices including caregiver-reported breastfeeding and exclusive breastfeeding practices and child dietary diversity score (number of food groups the child consumed in previous 24 hours) based on WHO guidelines.
|
10 months
|
|
Parenting stress
Time Frame: 10 months
|
Parenting distress reported by the primary caregiver using the Parenting Stress Index-Short Form, Parental Distress subscale.
Higher total scores indicate greater parenting distress.
|
10 months
|
|
Depressive symptoms
Time Frame: 10 months
|
Depressive symptoms reported by the primary caregiver using the Centre for Epidemiological Studies Depression Scale-10 items (CESD-10).
Caregivers report on the frequency of depressive symptoms in the previous week.
Items are summed to create an overall depression score, with higher scoring indicating greater depressive symptoms.
|
10 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Joshua Jeong, ScD, Harvard School of Public Health (HSPH)
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2023
Primary Completion (Estimated)
October 30, 2024
Study Completion (Estimated)
October 30, 2024
Study Registration Dates
First Submitted
December 2, 2023
First Submitted That Met QC Criteria
December 2, 2023
First Posted (Actual)
December 11, 2023
Study Record Updates
Last Update Posted (Estimated)
January 3, 2024
Last Update Submitted That Met QC Criteria
January 2, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- ISERC/JOOTRH/736/23
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Child Development
-
SangathUNICEFCompletedChild Development | Child Nutrition and Early Child DevelopmentIndia
-
Yale UniversityRobinhood Foundation; Adelphi University; Docs for TotsCompletedSocial Skills | Child Behavior | Child Development | Infant DevelopmentUnited States
-
International Care Ministries, PhilippinesCompassion International, United States of AmericaNot yet recruitingChild Development | Child Nutrition, Child Neurobehavioral Development | Academic Attainment | Household and Family | Financial Wellbeing
-
University of Southern CaliforniaSafe Water and AIDS Project; Early Childhood Development Network for Kenya...Active, not recruitingChild Behavior | Child Development | Language, ChildKenya
-
Windward Islands Research and Education FoundationGrand Challenges Canada; St. George's University; GRENCASECompletedDevelopment, Child | Behavior, Child | Neurocognition, ChildGrenada
-
London School of Hygiene and Tropical MedicineInternational Centre for Diarrhoeal Disease Research, Bangladesh; University... and other collaboratorsActive, not recruitingChild Development | Child Development DisorderBangladesh, Tanzania, Nepal
-
Children's Hospital of PhiladelphiaNational Institute on Minority Health and Health Disparities (NIMHD)CompletedDevelopment Delay | Development, ChildUnited States
-
University of WashingtonRecruitingChild Behavior | Child DevelopmentUnited States
-
The Hospital for Sick ChildrenAga Khan University; March of DimesCompletedChild Development | Child Mortality | Child Morbidity | Child BehaviourPakistan
-
Universidade Federal de PernambucoCoordination for the Improvement of Higher Education PersonnelNot yet recruitingChild Development | Music Education | Early Child Development | Adaptive Behavior | Preschool EducationBrazil
Clinical Trials on Parenting program
-
University of North Carolina, Chapel HillNational Heart, Lung, and Blood Institute (NHLBI)Completed
-
The University of Hong KongCompletedMindfulness | Parent Management Training | Mindful Parenting TrainingHong Kong
-
Svenja TaubnerUniversity of Geneva, Switzerland; Vilnius University; University of La Rioja; CHANSE... and other collaboratorsNot yet recruitingWell-being | Mental HealthGermany, Lithuania, Spain, Switzerland
-
McGill UniversityMbarara University of Science and TechnologyCompletedDepression | Child DevelopmentUganda
-
Özlem TekeUskudar UniversityRecruiting
-
University of TulsaCompletedParenting | Military FamilyUnited States
-
Florida International UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development...CompletedParenting | Behavior ProblemUnited States
-
NYU Langone HealthCompletedAttention Deficit Hyperactivity DisorderUnited States
-
Université Catholique de LouvainCompleted
-
Arizona State UniversityDepartment of Health and Human ServicesRecruitingEvaluation of the Parenting in the Moment Online Program for Forcibly Displaced Families (PIMonline)Trauma | Parenting | Post Traumatic Stress Disorder | Mental Health | Emotional Regulation | Child Maltreatment | Child Wellbeing | Adjustment | Child Safety | CoercionUnited States