Triple P forADHD Children's Mothers, Education of Behavioral Problems, and Change in Mothers' Attitude
(ADHD)
Positive Parenting Program for Attention Deficit Hyperactivity Disorder: Maternal Perspective Shifts and Child Behavior Problems Reduction in a Clinical Trial
1 other identifier
interventional
67
1 country
1
Brief Summary
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jul 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 25, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 30, 2024
CompletedFirst Submitted
Initial submission to the registry
June 21, 2025
CompletedFirst Posted
Study publicly available on registry
July 17, 2025
CompletedResults Posted
Study results publicly available
January 29, 2026
CompletedJanuary 29, 2026
January 1, 2026
1.1 years
June 21, 2025
July 23, 2025
January 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
SDQ: Strengths and Difficulties Questionnaire SDQ
The Strengths and Difficulties Questionnaire (SDQ) is a validated behavioral screening tool that assesses emotional and behavioral difficulties in children through 25 items grouped into five subscales: Emotional Symptoms, Conduct Problems, Hyperactivity/Inattention, Peer Relationship Problems, and Prosocial Behavior. Each subscale includes 5 items scored from 0 to 2, resulting in subscale scores ranging from 0 to 10. Higher scores on the first four subscales indicate greater difficulties, while higher scores on the Prosocial Behavior subscale reflect better social functioning. A Total Difficulties Score (the lowest is 0 and the highest is 40) is calculated by summing the four difficulties subscales, with higher scores indicating more behavioral problems. Scores are reported as mean ± standard deviation, with higher total or subscale scores indicating worse outcomes for difficulties and better outcomes for prosocial behavior (Goodman, 1997; Stone et al., 2010)
Pre (Baseline) intervention and Post (12 months)
Secondary Outcomes (2)
Parenting Scale
"Pre (Baseline)"intervention and "Post (12 months)")
PSOC: Parenting Sense of Competence PSOC Scale
"Pre (Baseline)"intervention and "Post (12 months)")
Study Arms (2)
Mothers of children with ADHD and with children with ADHD aged 6-12 years
EXPERIMENTALHad the Triple P sessions
control
NO INTERVENTIONDid not receive triple p
Interventions
An evidence-based program with self-agency strategies enhances trust and confidence in managing children's ADHD behaviors
Eligibility Criteria
You may qualify if:
- having a child aged 6 - 13 years with an ADHD diagnosis
- attending a child mental health clinic
- No participation with another professional agency to receive parental support for mothers.
- having a child with ADHD combined with neurological disorders
- known medical conditions, severe aggression, intellectual disability, psychosis, and bipolar disorder.
- children with ADHD older than 12 or younger than 6 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Child Mental Health Clinic
Hebron, Palestinian Territories
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Limitations and Caveats
First, the study used a pre-post design with no long-term follow-up, limiting insight into sustained effects. Second, the sample size was modest, affecting generalizability. Third, intervention delivery by a single researcher may have introduced social desirability bias. Lastly, data collection occurred during the Gaza conflict and lockdowns. Early termination leading to small numbers of subjects analyzed; Technical problems with measurement leading to unreliable or uninterpretable data.
Results Point of Contact
- Title
- Latifa Dardas
- Organization
- PPU
Study Officials
- PRINCIPAL INVESTIGATOR
Nadia A Amro, phd
AAUP
- PRINCIPAL INVESTIGATOR
Nadia A Amro, phd
Palestine Polytechnic University
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- D Nadia Amro,lecturer at Palestine Polytechnique university
Study Record Dates
First Submitted
June 21, 2025
First Posted
July 17, 2025
Study Start
July 25, 2023
Primary Completion
August 30, 2024
Study Completion
August 30, 2024
Last Updated
January 29, 2026
Results First Posted
January 29, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, ICF
- Time Frame
- one year
- Access Criteria
- any way of contact
the whole process sesign prtocol ,data collection can be siscussed