- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02402556
Mother and Child Education Program in Palestinian Refugee Camps
December 1, 2016 updated by: Yale University
Implementation and Impact Evaluation of the Mother and Child Education Program (MOCEP) Among Children and Families in Palestinian Refugee Camps in Beirut, Lebanon
The purpose of the Mother Child Education Program (MOCEP)-a group-based early childhood development parenting education program-is to provide school-readiness and parenting skills to mothers of young children who do not have access to preschool education services.
The MOCEP intervention also provides a setting in which caregivers can model pro-social behaviors and practice conflict resolution techniques directly with young children.
Study Overview
Detailed Description
The purpose of the evaluation study is to rigorously evaluate the impact of MOCEP on child and parent outcomes among Palestinian refugees in Beirut, Lebanon.
This evaluation employs an innovative, mixed-methods bio-behavioral approach to investigate the associations among social contexts; maternal, child and family functioning; and reduction in violence through the promotion of harmonious family relationships.
The results of this study have implications for improving the lives of and reducing violence for the hundreds of thousands of families with young children living in fragile contexts.
We hypothesize that when MOCEP is implemented with fidelity (i.e., delivered as intended by design), participating families will experience reduced violence in their homes and have better individual and intra-family outcomes than families who do not participate in the program.
Study Type
Interventional
Enrollment (Actual)
106
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
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Beirut, Lebanon
- Bourj el-Barajneh refugee camp
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Beirut, Lebanon
- Charila
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Beirut, Lebanon
- Mar Elias Refugee Camp
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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
3 years to 6 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Child must be between 3 and 6 years of age (children age 7 may be accepted under special circumstances)
- Mother must be able to read and write in Arabic (although skills may not be well-developed)
- Mothers must commit to participate in the 25-week MOCEP Intervention program
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
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: MOCEP
MOCEP is implemented over a period of 25 weeks, through weekly group meetings that last approximately three hours.
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Through parent support and an evidence-based curriculum, MOCEP uses education to reduce risk factors that hinder children's health and wellbeing.
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Active Comparator: Waitlist Control Group
For ethical reasons, no one recruited will be excluded from the opportunity to benefit from the intervention.
MOCEP group will be the primary intervention group and the second group will act as the wait-listed control group.
Although the families in the wait-listed control group will start out as a control group (not receiving the intervention), they will have the opportunity to participate in the intervention in a later round of implementation, after the intervention group has completed the program.
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Through parent support and an evidence-based curriculum, MOCEP uses education to reduce risk factors that hinder children's health and wellbeing.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Disciplinary Style Questionnaire
Time Frame: 25 weeks
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Parent report measure of parental disciplinary style assesses the frequency with which parents engage in seven forms of discipline when dealing with children's undesirable behavior
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25 weeks
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Better Parenting Questionnaire
Time Frame: 25 weeks
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11 Item questionnaire that measures parental knowledge, attitudes and practices regarding education and learning, child development and discipline / child rearing.
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25 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Socio-Emotional Status: Strengths and Difficulties Questionnaire (child assessment)
Time Frame: 25 weeks
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Parent report measure assesses children's emotional and conduct problems, hyperactivity, and peer relations.
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25 weeks
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Parental Stress Index
Time Frame: 25 weeks
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Assessment of maternal stress
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25 weeks
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Duke Social Support Index
Time Frame: 25 weeks
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Addresses social support in two domains: social interaction and subjective support
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25 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
May 1, 2014
Primary Completion (Actual)
September 1, 2016
Study Completion (Actual)
September 1, 2016
Study Registration Dates
First Submitted
March 25, 2015
First Submitted That Met QC Criteria
March 27, 2015
First Posted (Estimate)
March 30, 2015
Study Record Updates
Last Update Posted (Estimate)
December 2, 2016
Last Update Submitted That Met QC Criteria
December 1, 2016
Last Verified
December 1, 2016
More Information
Terms related to this study
Other Study ID Numbers
- 1403013605
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.
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