- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05221268
Effect of Downhill Training on Ankle Joint
January 22, 2022 updated by: Hatem Allam, Taif University
Effect of Repeated Downhill Walking Bouts on Ankle Isokinetic Parameters in Children With Obesity
Downhill training help to improve musculoskeletal condition.
Applying downhill training could help obese children by improving their muscular strength.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
the current study aimed to find the effect of downhill training on the ankle isokinetic parameters of obese children.
There were two experimental groups, the first received level walking while the second received downhill training.
The ankle isokinetic parameters were assessed pre and post-intervention for 6 weeks.
Study Type
Interventional
Enrollment (Actual)
32
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
-
-
Mecca
-
Taif, Mecca, Saudi Arabia, 2425
- College of Applied Medical Sciences
-
-
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
8 years to 12 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Body mass index percentile 95% or more
- age ranged from 8-12 year
- student in one of Taif's elementary schools
Exclusion Criteria:
- suffering from any musculoskeletal problem or chronic disease.
- engaged in regular sports activities during the last 6 months
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: downhill
Received downhill walking training.
|
treadmill exercise with -20 inclination
|
|
Experimental: Level -walking
Received level walking training.
|
treadmill exercise with 0 inclination
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Isokinetic eccentric plantarflexion tourque
Time Frame: 6 weeks
|
Eccentric plantarflexion normalized peak tourque N.M/kg
|
6 weeks
|
|
Isokimetic Concentric plantarflexion tourque
Time Frame: 6 weeks
|
Concentric dorsiflexion normalized peak tourque N.M/kg
|
6 weeks
|
|
Isokinetic Eccentric dorsiflexion tourque
Time Frame: 6 weeks
|
Eccentric dorsiflexion normalized peak tourque N.M/kg
|
6 weeks
|
|
Isokinetic Concentric dorsiflexion tourque
Time Frame: 6 weeks
|
Concentrc dorsiflexion normalized peak tourque N.M/kg
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
October 11, 2021
Primary Completion (Actual)
December 5, 2021
Study Completion (Actual)
December 10, 2021
Study Registration Dates
First Submitted
December 20, 2021
First Submitted That Met QC Criteria
January 22, 2022
First Posted (Actual)
February 2, 2022
Study Record Updates
Last Update Posted (Actual)
February 2, 2022
Last Update Submitted That Met QC Criteria
January 22, 2022
Last Verified
January 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 646
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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