- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07786532
Effect of Sports Based Structured Cognitive Therapy Program on Attention, Memory and Behavior for School Going Children
August 25, 2026 updated by: Riphah International University
Effect of a Sports-Based Structured Cognitive Therapy Program on Attention, Memory, and Behavior in School-Going Children: A Randomized Controlled Trial
This randomized controlled trial will evaluate the effect of a sports-based structured cognitive therapy program on attention, memory, and behavior in school-going children aged 8-12 years with mild to moderate attention or behavioral difficulties.
A total of 52 participants will be randomly allocated to either an experimental group receiving an 8-week sports-based structured cognitive therapy program or a control group receiving conventional physical activity.
The intervention will be delivered three times per week.
Outcomes will be assessed at baseline, Week 4, and Week 8 using the Stroop Test, Teacher Report Form (TRF), and Behavior Rating Scale to determine changes in attention, memory, and behavior
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
This randomized controlled trial aims to evaluate the effectiveness of a sports-based structured cognitive therapy program on attention, memory, and behavior in school-going children aged 8-12 years with mild to moderate attention or behavioral difficulties.
The primary objective is to determine whether participation in an 8-week sports-based structured cognitive therapy program improves attention, memory, and behavior compared with conventional physical activity.
Attention will be assessed using the Stroop Test, behavioral and academic functioning using the Teacher Report Form (TRF), and behavior using the Behavior Rating Scale.
Study Type
Interventional
Enrollment (Estimated)
52
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 Contact
- Name: Zobia Naseem, MS
- Phone Number: +923321963584
- Email: zobia.naseem@riphah.edu.pk
Study Contact Backup
- Name: noreen khan, Phd
- Phone Number: 03369687196
Study Locations
-
-
Kpk
-
Chak Six Hundred Twenty-four, Kpk, Pakistan, 25000
- Recruiting
- Gghss Sarai Naimat Khan Haripur
-
-
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
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- School-going children aged 8-12 years.
- Children with mild to moderate attention or behavioral difficulties.
- Children enrolled in participating primary or secondary schools in Haripur District.
- Written informed consent obtained from a parent or legal guardian.
Exclusion Criteria:
- Children diagnosed with severe neurological or psychiatric disorders.
- Children with physical disabilities that prevent participation in sports-based activities.
- Children currently participating in another structured cognitive or physical 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
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Sports-Based Structured Cognitive Therapy
Participants assigned to the experimental group will receive an 8-week Sports-Based Structured Cognitive Therapy Program delivered three sessions per week, with each session lasting 45-60 minutes.
The intervention integrates structured physical activities with cognitive tasks targeting attention, memory, executive function, and behavioral regulation.
Activities include aerobic exercises, attention drills, memory exercises, and behavior-regulation games delivered at moderate to vigorous intensity.
|
Participants will receive an 8-week Sports-Based Structured Cognitive Therapy Program delivered three times per week.
The program combines structured physical activities with cognitive tasks designed to improve attention, memory, executive function, and behavioral regulation through attention drills, memory exercises, and behavior-regulation games.
|
|
Active Comparator: Conventional Physical Activity
Participants assigned to the control group will receive conventional physical activity consisting of routine exercise-based activities supervised by a licensed physical therapist.
Sessions will be conducted three times per week for 45-60 minutes over 8 weeks and will include warm-up exercises, stretching, balance activities, classroom games, and cool-down exercises without structured cognitive-sports integration.
|
Participants will receive conventional physical activity consisting of routine exercise-based activities including warm-up exercises, stretching, balance activities, classroom games, and cool-down exercises for 45-60 minutes per session, three sessions per week for 8 weeks, without structured cognitive training.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stroop Interference Score
Time Frame: Baseline, Week 4, and Week 8
|
The Stroop Test will be used to assess selective attention and inhibitory control.
The outcome will be measured using the Stroop Interference Score.
Lower interference scores indicate better inhibitory control and attention.
|
Baseline, Week 4, and Week 8
|
|
Teacher Report Form (TRF) T-score
Time Frame: Baseline, Week 4, and Week 8
|
The Teacher Report Form (TRF) will be used to assess behavioral, emotional, and academic functioning in the school environment.
The outcome will be summarized using the standardized TRF T-score according to the scoring procedures of the instrument.
|
Baseline, Week 4, and Week 8
|
|
Behavior Rating Scale Total Score
Time Frame: Baseline, Week 4, and Week 8
|
The Behavior Rating Scale will be used to assess behavioral functioning in children.
The outcome will be summarized using the total score obtained according to the scoring procedures of the scale.
|
Baseline, Week 4, and Week 8
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Movement-Sequence Recall Score
Time Frame: Baseline, Week 4, and Week 8
|
Memory performance will be assessed using a movement-sequence recall task.
The outcome will be summarized as the number of movement sequences correctly recalled.
|
Baseline, Week 4, and Week 8
|
|
Number Recall Score
Time Frame: Baseline, Week 4, and Week 8
|
Memory performance will be assessed using a number-recall task.
The outcome will be summarized as the number of numerical sequences correctly recalled.
|
Baseline, Week 4, and Week 8
|
|
Word Recall Score
Time Frame: Baseline, Week 4, and Week 8
|
Memory performance will be assessed using a word-recall task.
The outcome will be summarized as the number of words correctly recalled.
|
Baseline, Week 4, and Week 8
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Zobia Naseem, MS, Riphah International University
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)
August 16, 2026
Primary Completion (Estimated)
October 1, 2026
Study Completion (Estimated)
October 30, 2026
Study Registration Dates
First Submitted
August 5, 2026
First Submitted That Met QC Criteria
August 25, 2026
First Posted (Actual)
August 26, 2026
Study Record Updates
Last Update Posted (Actual)
August 26, 2026
Last Update Submitted That Met QC Criteria
August 25, 2026
Last Verified
August 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Aqsa Imtiaz
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.