Triple P for ADHD Children's Mothers, Education of Behavioral Problems, and Change in Mothers' Attitude

NCT ID: NCT07069621

Last Updated: 2025-07-20

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

COMPLETED

Clinical Phase

NA

Total Enrollment

64 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-07-25

Study Completion Date

2024-08-30

Brief Summary

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

The goal of this clinical trial is to investigate whether the Triple P program will reduce behavioral problems for ADHD children, improve mothers' sense of competency, and improve their attitudes

The main questions it aims to answer are:

1 . What is the feasibility and cultural acceptability of implementing the Triple P program within the Palestinian context? 2. Does the Triple P program promote positive attitudes towards managing ADHD among mothers in Palestine? 3. How does the Triple P program affect the maternal sense of competency among mothers in Palestine? 4. Does the Triple P program delivery affect reducing children's ADHD behavioural symptoms?

Participants :

took the triple p strategies, and the control will not Outcome measures will be evaluated pre- and post-intervention

Detailed Description

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

Mothers of children with ADHD are included; children with other mental health disorders or combined types of autism are excluded. The sample was taken from mental health clinics with children diagnosed with ADHD, aged 6-12 years old.

Conditions

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

ADHD, Predominantly Hyperactive - Impulsive Behavior Problems, Child ADHD - Attention Deficit Disorder With Hyperactivity Healthy Adult Females Competence Positive Parenting

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

One group received the Triple P program
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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

Mothers of children with ADHD and with children with ADHD aged 6-12 years

Had the Triple P sessions

Group Type EXPERIMENTAL

Triple p level parenting program

Intervention Type BEHAVIORAL

An evidence-based program with self-agency strategies enhances trust and confidence in managing children's ADHD behaviors

control

Did not receive triple p

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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

Triple p level parenting program

An evidence-based program with self-agency strategies enhances trust and confidence in managing children's ADHD behaviors

Intervention Type BEHAVIORAL

Eligibility Criteria

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

Inclusion Criteria

1. having a child aged 6 - 13 years with an ADHD diagnosis
2. attending a child mental health clinic
3. No participation with another professional agency to receive parental support for mothers.

The exclusion criterion

1-having a child with ADHD combined with neurological disorders, or known medical conditions, severe aggression, intellectual disability, psychosis, and bipolar disorder.

children with ADHD older than 12 or younger than 6 years
Minimum Eligible Age

6 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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

Palestine Polytechnic University

OTHER

Sponsor Role lead

Responsible Party

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

Nadia Amro

D Nadia Amro,lecturer at Palestine Polytechnique university

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Nadia Abed Amro, phd

Role: PRINCIPAL_INVESTIGATOR

AAUP

Nadia Abed Amro, phd

Role: PRINCIPAL_INVESTIGATOR

Palestine Polytechnic University

Locations

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

Child Mental Health Clinic

Hebron, , Palestinian Territories

Site Status

Countries

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

Palestinian Territories

Provided Documents

Download supplemental materials such as informed consent forms, study protocols, or participant manuals.

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

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

R-2024/A/131/N

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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

Triple P With Pediatric Residents
NCT01946958 COMPLETED NA
Caregiver Implementation Strategies Field Pre-Test
NCT06770036 ACTIVE_NOT_RECRUITING NA