Parenting for Lifelong Health Program in Kuwait

NCT ID: NCT06875713

Last Updated: 2025-03-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-03-04

Study Completion Date

2025-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Parenting interventions play a crucial role in promoting positive parent-child interactions, which are fundamental to fostering child well-being. Over the years, substantial progress has been made in understanding the importance of these interactions, particularly in the context of early childhood development. Positive parent-child interactions lay the groundwork for various aspects of child development, including socioemotional skills, academic performance, and mental health. Evidence-based parenting programs have demonstrated strong effectiveness in promoting positive parenting and preventing child maltreatment. The Parenting for Lifelong Health (PLH) program has yielded positive outcomes in many countries. This project aims to culturally adapt the PLH program and conduct a randomized controlled trial (RCT) to assess its feasibility and effectiveness in Kuwait.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Child Development Parenting Behavior Parenting Intervention Child Mental Health

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

intervention group

The intervention group will participate in eight in-person sessions of the PLH program, supplemented by the use of a digital parenting program (ParentApp) aimed at enhancing positive parenting behaviours.

Group Type EXPERIMENTAL

Parenting for Lifelong Health Program (DAYEM)

Intervention Type BEHAVIORAL

This intervention consists of the Parenting for Lifelong Health (PLH) program, delivered through eight in-person sessions, supplemented by a digital parenting program (ParentApp). The intervention aims to enhance positive parenting behaviors and reduce child maltreatment.

control group

The control group will receive education on adult nutrition over the same period.

Group Type ACTIVE_COMPARATOR

Adult nutrition

Intervention Type BEHAVIORAL

The control group will receive education on adult nutrition over the same period.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Parenting for Lifelong Health Program (DAYEM)

This intervention consists of the Parenting for Lifelong Health (PLH) program, delivered through eight in-person sessions, supplemented by a digital parenting program (ParentApp). The intervention aims to enhance positive parenting behaviors and reduce child maltreatment.

Intervention Type BEHAVIORAL

Adult nutrition

The control group will receive education on adult nutrition over the same period.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* A primary caregiver of children aged 2-9 years
* Over the age of 18.
* Kuwaiti
* Lives in Kuwait
* Speaks Arabic

Exclusion Criteria

* Non-Arabic speakers
* Non-Kuwaitis
* Parent whose co-parent is participating in study
* Not resident of Kuwait
* Target child has mental disability or special needs
* Facilitator, supervisor, or caregiver contributor in the DAYEM program
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ministry of Health, Kuwait

OTHER_GOV

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Hind Almazeedi

Head of Research Unit and Prevention Programs Unit at CPO

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Child Protection Office - Ministry of Health

Safat, Safat, Kuwait

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Kuwait

Related Links

Access external resources that provide additional context or updates about the study.

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2024/2735

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Promoting Healthy Children and Youth
NCT06977438 NOT_YET_RECRUITING PHASE4