- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05931640
Effects of Plyometric Training Versus Virtual Reality Among Hemiplegic Cerebral Palsy
Effects of Plyometric Training Versus Virtual Reality on Upper Limb Among Children With Hemiplegic Cerebral Palsy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Cerebral palsy is a combination of disorders that makes a child's life difficult; it mainly affects the motor abilities of the child. Cerebral palsy (CP) is a neurodevelopmental disorder characterized by abnormalities of muscle tone, movement and motor skills, and is attributed to injury to the developing brain. Children with cerebral palsy (CP) have decreased capacity to participate in play and sports activities. Reduced capacity to perform typical childhood activities contributes to low habitual physical activity and declining gross motor function in adolescence. Preceding more into this disorder there are 'hemiplegic cp'. Hemiplegic cp means that one side of the body is weak, paralyzed, it includes hand, arm, shoulder, leg of the affected side. For better treatments interventions are being invented day by day but according to my research.Plyometric therapy raises force and speeds your muscle contractions' force and speeds and strength training that leads to higher explosive power needed in sports and even everyday activities. Plyometric activities can be utilized in both the lower and upper extremities, with running, jumping, or throwing a ball and virtual reality therapy (use of virtual reality technology for psychological or occupational therapy and in affecting virtual rehabilitation.); which one is better for speedy recovery.
The tools used will be QUEST (Quality of Upper Extremity Skill Tests) and Ball & Box Test (BBT). Study will be conducted on 28 patients in two Groups. Group A will be Control Group that will be provided with Plyometric (push-ups, ball throwing, jumping, running, kicking). A protocol of 10 minutes of plyometric therapy will be given including running and jumping with ball throwing. and Group B will be Experimental Group that will be provided with Virtual Reality Therapy (VRT). A session of 12-45, twice a week, through VR goggles or VR will be given. QUEST and box & block test will be used as tools. The Control group will be administered with Plyometric therapy that includes 10 minutes of ball throwing, push-ups, jumping and hopping/skipping. At start intensity and speed is low, but will be increased gradually. Every score will be noted with the help of additional tools.The Experimental group will be administered with Virtual Reality Therapy that includes use of VR goggle, VR headset and play station if available. Virtual games like move-pro will be used for upper limb movements. A session of 12-45 minutes, twice weekly will be done. And scoring will be done with the help of additional tools.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Dr. Nosheen Manzoor, MS OPMT
- Phone Number: 03236877879
- Email: nosheen.manzoor@riphah.edu.pk
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54782
- Recruiting
- Govt. National special education centre
-
Contact:
- Naseer Khan
- Phone Number: 03076913927
-
-
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).
- Students scoring of Modified Ashworth Scale should be 3 or less than 3 out of 5 for the same muscle groups.
Exclusion Criteria:
- Low cognitive level compatible with attending a special education
- school.
- Presence of contractures in the affected upper limb.
- Surgery in the six months previously.
- Botulinum toxin in the two months previously.
- Uncontrolled epilepsy.
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: Virtual Reality
Virtual Reality Therapy that includes use of VR goggle, VR headset and play station if available.
Virtual games like move-pro will be used for upper limb movements.
A session of 12-45 minutes, twice weekly will be done.
And scoring will be done with the help of additional tools.
|
Virtual Reality Therapy that includes use of VR goggle, VR headset and play station if available.
Virtual games like move-pro will be used for upper limb movements.
A session of 12-45 minutes, twice weekly will be done.
And scoring will be done with the help of additional tools.
|
|
Experimental: Plyometric Training
Plyometric therapy that includes 10 minutes of ball throwing, push-ups, jumping and hopping/skipping.
At start intensity and speed is low, but will be increased gradually.
Every score will be noted with the help of additional tools.
|
Plyometric therapy that includes 10 minutes of ball throwing, push-ups, jumping and hopping/skipping.
At start intensity and speed is low, but will be increased gradually.
Every score will be noted with the help of additional tools.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of Upper Extremity Skill Tests
Time Frame: 4 weeks
|
Quality of Upper Extremity Skills Test (QUEST) is an outcome measure designed to evaluate movement patterns and hand function in children with cerebral palsy
|
4 weeks
|
|
Ball & Box Test
Time Frame: 4 weeks
|
The Box and Block Test (BBT) measures unilateral gross manual dexterity
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Dr. Nosheen Manzoor, MS OPMT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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/RCR&AHS/23/0724
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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