- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06736119
Effects of Task-Oriented Intervention in Children With Developmental Coordination Disorder
December 12, 2024 updated by: Riphah International University
Effects of Task-oriented Intervention of Upper Limb on Coordination and In-hand Manipulation Among Children With Developmental Coordination Disorder
physical coordination is impacted by developmental coordination disorder (DCD), commonly referred to as dyspraxia.
It makes a youngster appear to move clumsily and perform worse than expected in everyday tasks for their age.
Fine and gross motor coordination issues are a hallmark of this neurodevelopmental disorder.
Task-oriented therapies help children with DCD develop their skills, coordination, and manipulative abilities by including them in intentional, goal-directed tasks.
This is noteworthy because a child's quality of life can be greatly impacted by these skills, which are essential for everyday tasks like writing, tying shoelaces, walking, and balance.
The purpose of the research is to ascertain how task-oriented upper limb intervention affects children with impaired coordination and hand-eye coordination.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The task-oriented intervention aimed at the upper limbs will be administered to the intervention group.
For 3 months, interventions were offered 3 days a week.Over the course of 6 months, this quasi-experimental study will be carried out in Lahore.
Data will be gathered from the Harbanspura branch of The Punjab School and the Askari School System in Mughalpura.
There will be 18 students in the study.
The study's inclusion criteria will be children with developmental coordination disorders between the ages of 4 and 12 Youngsters needed to be able to comprehend and adhere to instructions, both boys and girls who scored between 15 and 57 overall on the Developmental Coordination Disorder Questionnaire 2007.Children with congenital respiratory, cardiovascular, or musculoskeletal disorders, as well as those with unstable seizures, will be excluded.
Both before and after the operation, data will be gathered.
The Movement Assessment Battery for Children (MABC-2), the Developmental Coordination Disorder Questionnaire, and the ABIL HAND KID instrument will be used to assess subjects with developmental coordination disorders.
Study Type
Interventional
Enrollment (Estimated)
18
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: Muhammad Asif Javed, MS
- Phone Number: 03224209422
- Email: a.javed@riphah.edu.pk
Study Contact Backup
- Name: IMRAN AMJAD, PhD
- Phone Number: 9233224390125
- Email: imran.amjad@riphah.edu.pk
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 5470
- Recruiting
- Askari School System, Mughalpura, The Punjab School Harbunspura baranch
-
Contact:
- Muhammad Asif Javed, MS
- Phone Number: 03224209422
- Email: a.javed@riphah.edu.pk
-
Contact:
- Amjad Imran, PHD
- Phone Number: 9233224390125
- Email: imran.amjad@riphah.edu.pk
-
Principal Investigator:
- MahNoor Fatima, MS
-
-
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:
- Developmental coordination disorder children aged 4 to 12 years old.
- Have a total score of 15-57 on the Developmental Coordination Disorder Questionnaire2007.
- Children had to be able to understand and follow instructions.
- Boys and girls both are included
Exclusion Criteria:
- Children with unstable seizures will be excluded.
- DCD children with any congenital cardio-respiratory condition, congenital musculoskeletal condition.
- DCD children with severe visual and/or hearing disability preventing them from completing exercises prescribed by either program.
- Children with behavioral difficulty making them unable to complete exercises prescribed by either 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: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Task-oriented intervention
task-oriented intervention for individual of developmental coordination disorder
|
Intervention group will recieve task oriented interventions.Throwing and catching balls of different sizes and weights will be done.
For writing, a task-oriented approach has 4 phases that will involve writing,correcting and fun writing 30-minute per session.
Interventions provided 3 days per week for 3 months.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in Motor Coordination as Measured by the DCDQ
Time Frame: 15 minutes
|
The DCDQ evaluates changes in motor coordination in children aged 4-16 years based on parent-reported outcomes.
It measures three subscales: Control During Movement, Fine Motor/Handwriting, and General Coordination.
Scores are collected at pre and post-intervention (3 months), with higher scores indicating improved motor coordination.
|
15 minutes
|
|
Changes in Manual Ability Assessed by the ABILHAND-Kids Questionnaire
Time Frame: 10 minutes
|
The ABILHAND-Kids Questionnaire evaluates changes in manual ability and bimanual coordination in daily activities among children with motor impairments.
It is a parent-reported measure assessing the ease or difficulty with which a child performs 21 bimanual tasks in their daily life.
Scores are collected at baseline (pre-intervention), and post-intervention (3 months), with higher scores indicating improved manual ability and functional performance.
|
10 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mah Noor Fatima, MS*, Riphah International University
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 (Actual)
October 28, 2024
Primary Completion (Estimated)
January 28, 2025
Study Completion (Estimated)
February 12, 2025
Study Registration Dates
First Submitted
November 3, 2024
First Submitted That Met QC Criteria
December 12, 2024
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
December 12, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR & AHS/24/0703
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.
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