- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06759792
Physical Activity on Eye Hand Coordination Post Strabismus Surgery
April 18, 2025 updated by: Amany Refaat Mohamed Abdel Wahid
Effect of Physical Activity on Eye Hand Coordination in Patient With Strabismus Amblyopia Post Surgery
The aim of this study is to determine the effect of physical activity on eye hand coordination in patient with amblyopia after strabismus surgery.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Eye hand coordination is essential to many of everyday activities.
Strabismus not only affect vision but also affect eye hand activities and coordination.
Through this study the patients will apply physical therapy sessions to improve eye hand coordination for strabismus amblyopic patient.
Study Type
Interventional
Enrollment (Actual)
60
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 Locations
-
-
-
Giza, Egypt, 11432
- Cairo University
-
-
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
No
Description
Inclusion Criteria:
- Patients are both males and females.
- Their age will range from (10-14) years.
- Patients received strabismus operation.
- Patients are suffering from strabismic amblyopia
- Patients are suffering from eye hand coordination problems
- Patients will begin the training program after 2 months of operation.
- All types of strabismus surgery will be included.
Exclusion Criteria:
- Patient who didn't complete the physiotherapy training program for 3 months.
- Muscular disorders that will impair performance during training.
- Any organic lesion in the eye.
- Neurological disorders.
- Malignant conditions.
- Psychiatric illness, severe behavior or cognitive disorders.
- Children who can't understand the therapist's instructions and orders
- Amblyopia which is not related to strabismus condition .
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: eye hand coordination exercise
this group will receive therapeutic exercises to improve eye hand coordination post strabismus surgery
|
exercises to improve eye hand coordination post strabismus surgery
|
|
No Intervention: traditional eye observation
this group will receive traditional eye observation post strabismus surgery
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Eye Hand Coordination Test
Time Frame: From enrollment to the end of treatment at 12 weeks
|
|
From enrollment to the end of treatment at 12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Amany R M Abdel Wahid, Doctoral degree, Lecturer at faculty of physical therapy, Cairo 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)
July 15, 2024
Primary Completion (Actual)
March 15, 2025
Study Completion (Actual)
April 15, 2025
Study Registration Dates
First Submitted
December 29, 2024
First Submitted That Met QC Criteria
December 29, 2024
First Posted (Actual)
January 6, 2025
Study Record Updates
Last Update Posted (Actual)
April 20, 2025
Last Update Submitted That Met QC Criteria
April 18, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/005409
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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