- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06292416
Mirror Therapy With Sensory Motor Training in Children With CP
Effects of Mirror Therapy With Sensory Motor Training on Upper Limb Functions and Quality of Movement in Children With Hemiplegic Cerebral Palsy
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan
- Eliya care Centre Faisalabad
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged between 6 and 12 years
- Lack of use of the affected upper limb
- Level I-III of the Manual Ability Classification System (MACS)
- Level I-III in the Gross Motor Function Classification System (GMFCS)
Exclusion Criteria:
- Disease not associated with congenital hemiplegia
- Presence of contractures in the affected upper limb affecting the functional movement
- Surgery in the six months previously to the treatment
- Botulinum toxin in the two months previously to or during the intervention
- Pharmacologically uncontrolled epilepsy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mirror therapy with sensory motor training.
The child will be seated on a chair and a 30*30 cm mirror will set up on a table in front of them. The affected hand will be placed behind the mirror so that the image of a healthy hand can be seen clearly |
Block design, finding shapes in pictures, puzzles, matching geometric shapes and letters, numbers, and classification. Pointing to the body parts, life-size drawing, turning left and right side and awareness of the body parts through touch. feeling various textures, touching boards, and feeling shapes. Ocular-pursuit training, moving ball and pegboard activities During the sessions, subjects were asked to try and do the same movement with the paretic hand simultaneously The patients will be asked to repeat each movement 20 times per set for three sets, with a 2-minute break between sets. Session will last for 45 mins |
|
Experimental: Mirror Therapy with motor training.
supination-pronation, wrist flexion-extension, finger flexion-extension, abduction, adduction, opposition
|
the participant is asked to perform a forearm movement sting on the paretic side while the subjects look into the mirror, watching the image of their non-involved hand and thus seeing the reflection of the hand movement projected over the involved hand.
During the sessions subjects were asked to try and do the same movement with the paretic hand simultaneously.
movement was repeated 20 times per set for three sets, with a 2-minute break between sets
|
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Other: Motor Training
|
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Melbourne Assessment of Unilateral Upper Limb Function (Melbourne Assessment)
Time Frame: Assessment will be done at 6th week by outcome measuring tool
|
It is an evaluation tool that objectively measures upper-extremity function in children with cerebral palsy.
The total score is 122, which is the maximum, whereas the minimum score is 0. It is Reported as a percentage, with higher scores reflecting greater quality of upper-limb movement
|
Assessment will be done at 6th week by outcome measuring tool
|
|
Jebsen Taylor Hand dysfunction test
Time Frame: 6 weeks
|
It measures the fine and gross motor function of the hands.
The results are measured by timing the time taken to accomplish each task.
|
6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Huma Saleem, MS NMPT*, Riphah International Univerisity
- Principal Investigator: Ammara Abbas, tDPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- REC/0257Huma Saleem
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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