- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06407895
Effects of Lower Limb Fitness Program in Children With DS
Effects of Lower Limb Fitness Program in Children With Down Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Group A: Experimental group:
Group A will receive Range of motion for 5 minutes involving movements that stretch and strengthen the muscles and improve the stability. Proprioceptive training for 5 minutes which involve Single-leg balance Start with 20-30 seconds per leg and gradually increase to 1 minute 2-3 sets per leg. Weight bearing exercises on an uneven surface (such as Bosu ball or stability disc) and jumping rope 5-10 minutes/session. All proprioceptive training done firstly with eyes open and then with close eyes. Squat-to-stand training proprioceptive training lower extremity. This intervention aims to get the muscles ready before the actual intervention and improve proprioceptive ability. Exercises will be given three times a week for 6 weeks with session conducting 45 minutes per sessions which involve Squat-to-stand training will repeat 30 times 3 sets for 20 min. 2minute break after 1 set.. Balance training which involves standing activities with support, progressing to unsupported as tolerated for 10 minutes/session.
Group B: Control group:
In control group routine therapy will be given 3 times a week for 6 weeks with session conducting 45 minutes per sessions which involve standing balance exercises, sitting from chair to stand, heal to toe stand will be performed.
Data will be assessed by assessor at baseline by single leg stance test and at the end of 6th session of treatment (Pre and post).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Punjab
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Lahore, Punjab, Pakistan, 54000
- Riphah International University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 6-12 years
- Both Genders.
- Single leg stance Test: If unable to stand for 5 seconds or less client at greater risk of injury from fall.
- Ability to understand and follow basic instructions.
- Deficits in Balance
Exclusion Criteria:
- Children who are unable to engage in a structured fitness program due to behavioral or physical limitations.
- Children who have undergone lower limb surgery or experienced significant lower limb injuries in the past six months
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: Lower Limb Fitness Program
Group A will receive Range of motion for 5 minutes involving movements that stretch and strengthen the muscles and improve the stability.
Proprioceptive training for 5 minutes which involve Single-leg balance Start with 20-30 seconds per leg and gradually increase to 1 minute 2-3 sets per leg.
Weight bearing exercises on an uneven surface (such as Bosu ball or stability disc) and jumping rope 5-10 minutes/session.
All proprioceptive training done firstly with eyes open and then with close eyes.
Squat-to-stand training proprioceptive training lower extremity.
|
the stability of the core area can help to improve dynamic balance, coordinate the upper and lower trunk muscles, and reduce muscles' damage and abnormalities.
Physiotherapy had a role in programming training for Down Syndrome children, for example, using squat to stand training that seemed to improving lower extremity muscle power.
Squat-to-stand training will stimulate the proprioceptive stimulation on the trunk and lower extremity
|
|
Active Comparator: Routine Therapy
In control group routine therapy will be given 3 times a week for 6 weeks with session conducting 45 minutes per sessions which involve standing balance exercises, sitting from chair to stand, heal to toe stand will be performed.
|
In control group routine therapy will be given 3 times a week for 6 weeks with session conducting 45 minutes per sessions which involve standing balance exercises, sitting from chair to stand, heal to toe stand will be performed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Timed up and go test
Time Frame: 6 weeks
|
The TUG test assesses the participant's mobility by timing how quickly they can complete the test and dynamic balance by assessing their ability to sit-to-stand, stand-to-sit, walk, and their ability to change directions.
The participant stood up from a chair (46 cm seat height) with no armrests, walked 10 feet, turned around, walked back to the chair, and sat back down as quickly as possible
|
6 weeks
|
|
Pediatric Balance scale
Time Frame: 6 weeks
|
Pediatric version of balance scale is used to evaluate static and dynamic balance in children aged 3-15 years with mild-to-moderate motor impairment.
The scale comprises 14 items including sitting balance, standing balance, sitting to standing/standing to sitting, transfers, stepping, reaching forward with outstretched arm, retrieving object from floor, turning, and placing foot on stool items.
Each item is scored from 0 points (lowest function) to 4 points (highest function) with a maximum score of 56 points
|
6 weeks
|
|
Modified Clinical Test of Sensory Interaction in Balance (CTSIB-M)
Time Frame: 6 weeks
|
This test is designed to assess how well an older adult is using sensory inputs when one or more sensory systems are compromised.
In condition one, all sensory systems (i.e., vision, somatosensory, and vestibular) are available for maintaining balance.
In condition two, vision has been removed and the older adult must rely on the somatosensory and vestibular systems to balance
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6 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Aqdas Javaid, MS*, Riphah International University
Publications and helpful links
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/RCR&AHS/23/0786
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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