- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05192993
Effect of Oculomotor Exercise on Writing Capabilities on Autism
Effect of Oculomotor and Gaze Stability Exercise on Writing Capabilities on Autism
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Cairo, Egypt, P.O. Box:77
- Misr University for Science and Technology
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Mild autism (score 55-71) on Gilliam Autism Rating Scale (GARS-3).
- Intelligence quotient (IQ) score 70-100.
- Writing difficulties
Exclusion Criteria:
- Middle ear disorders
- Physical or mental conditions that may affect handwriting (e.g., seizures)
- Uncorrected visual or hearing impairments.
Study Plan
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: visual motor integration group
participants in the experimental group will receive visual motor integration program
|
Oculomotor exercises as follow:(1) Eye follow with a stationary head 2)Saccadic eye movements 3) Gaze stability 4)Eye/head co-ordination 5)Balancing exercises
|
|
Active Comparator: Handwriting intervention group
participants in the experimental group will receive handwriting intervention program.
|
(1)Eye motor coordination (2)position in space(3)coping-figure ground(4)spatial relationship(5)visual closure(6)constancy of shapes(7)far and near coping
|
|
Active Comparator: visual motor integration and Handwriting intervention group
participants in the group will receive visual motor integration program and handwriting intervention program.
|
Oculomotor exercises as follow:(1) Eye follow with a stationary head 2)Saccadic eye movements 3) Gaze stability 4)Eye/head co-ordination 5)Balancing exercises 6)Eye motor coordination (7)position in space(8)coping-figure ground(9)spatial relationship(10)visual closure(11)constancy of shapes(12)far and near coping Hand writing intervention as follow (1)Eye motor coordination (2)position in space(3)coping-figure ground(4)spatial relationship(5)visual closure(6)constancy of shapes(7)far and near coping |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
gaze stability
Time Frame: 6 weeks
|
Rating scale of gaze stability 0= negative Gaze stable smooth well coordinated,percise and fast movement of the head,fluent change of head movement direction
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
eye head coordination
Time Frame: 6 weeks
|
Rating scale of sequential head and eye movements 0= negative Clear,regular ,smooth, dissociated movements,of head and eyes.
|
6 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
saccadic eye movement
Time Frame: 6 weeks
|
0= negative Smooth, percise, fast eye movements,fast change of gaze direction,head remain stable
|
6 weeks
|
Collaborators and Investigators
Investigators
- Principal Investigator: Samah M Sheha, PhD, Misr University for Science and Technology
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/003283
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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