- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05951543
Effects of Plyometric Exercises on Static and Dynamic Balance of Children With Down,s Syndrome.
November 9, 2023 updated by: Riphah International University
Effects of Plyometric Exercises on Static and Dynamic Balance in Children With Down,s Syndrome
Down syndrome is a condition in which a person has an extra chromosome.
Typically, a baby is born with 46 chromosomes.
Down syndrome is a genetic condition that causes mild to serious physical and developmental problems.
Symptoms associated with the syndrome include mental retardation, distinctive facial characteristics, and increased risk for heart defects and digestive problems, which can range from mild to severe.. Early treatment programs can help improve skills.
They may include speech, physical, occupational, and/or educational therapy.
The aim of the the current study is to determine the effects of plyometric exercise on static and dynamic balance in children with Down syndrome
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This will be a randomized controlled trail.
After approval from ethical committee, data will be collected from rising sun institute of special education, Lahore.
Total sample size will be 20 and there will be two groups.
Group A will be given with Standard Physical therapy treatment twice a week for 8 weeks.
While group B will be given with plyometric exercises along with standard physical therapy treatment twice a week for 8 weeks.
Patients will be evaluated before and after the intervention on Pediatric balance scale, time up and go test, five times sit to stand.
Data will be analyzed on SPSS 26.0 and necessary analysis will be done after checking the normality of data.
Study Type
Interventional
Enrollment (Actual)
20
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
-
-
Punjab
-
Lahore, Punjab, Pakistan
- Riphah International 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:
- 6 to 12 years of age both genders will be included.
- Children with medical diagnosis of DS.
- Able to follow the command
Exclusion Criteria:
- Recent injury to lower extremities.
- Children with cerebral palsy and other neuromuscular disease will be excluded.
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: plyometric group
Experimental group will be given baseline exercises along with plyometric exercises such as Vertical jump, run and jump, drop jump (jump height between 40 and 50 cm) drop jump and horizontal jump with same height from 3rd week.particepents
perform exercises carrying medicine balls.
Participants will place their hands on the wall and performed foot stretches with the feet apart, 30 to 50 cm from the wall.
Side row, biceps stretch and frontal row.
Throwing and receiving, with a distance between 3 to 4 m.
|
Experimental group will be given baseline exercises along with plyometric exercises such as Vertical jump, run and jump, drop jump (jump height between 40 and 50 cm) drop jump and horizontal jump with same height from 3rd week.particepents
perform exercises carrying medicine balls.
Participants will place their hands on the wall and performed foot stretches with the feet apart, 30 to 50 cm from the wall.
Side row, biceps stretch and frontal row.
Throwing and receiving, with a distance between 3 to 4 m.
Other Names:
|
|
Other: dynamic balance group control group
Control group will be given with the standard physical therapy intervention that includes progressive resistance training that will be performed using weights, two sets of 10 repetitions will be given for each muscle group, resistance will be increased by ½ Kg as children are able to complete without undue stresses); balance exercises (stand on a balance board, one-leg stance, heal-to-toes stance, walking on balance board, walking on a balance beam, walking on a line, and walking on the inclined surface); flexibility exercises
|
Control group will be given with the standard physical therapy intervention that includes progressive resistance training that will be performed using weights, two sets of 10 repetitions will be given for each muscle group, resistance will be increased by ½ Kg as children are able to complete without undue stresses); balance exercises (stand on a balance board, one-leg stance, heal-to-toes stance, walking on balance board, walking on a balance beam, walking on a line, and walking on the inclined surface); flexibility exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Balance and standing
Time Frame: 8 weeks
|
Paediatric berg balance scale
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ayesha Khalid, 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)
May 23, 2023
Primary Completion (Actual)
August 31, 2023
Study Completion (Actual)
September 15, 2023
Study Registration Dates
First Submitted
June 6, 2023
First Submitted That Met QC Criteria
July 18, 2023
First Posted (Actual)
July 19, 2023
Study Record Updates
Last Update Posted (Estimated)
November 13, 2023
Last Update Submitted That Met QC Criteria
November 9, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS/23/0709
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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