- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05026294
Plyometric Exercise With Obese Children
August 23, 2021 updated by: Hatem Allam, Taif University
Effects of Plyometric Exercises Versus Flatfoot Corrective Exercises on Postural Control and Foot Posture in Obese Children With Flexible Flatfoot
Obesity is one of the main factors that contribute to an acquired flat foot deformity which in turn impairs the balance strategies.
The purpose of the current study was to compare the effect of plyometric exercises with flatfoot corrective exercise on balance, foot posture, and functional mobility in obese children with flexible flatfoot.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
A sample of 47 male children participated in the current study.
The participants were selected from different elementary schools in Taif, Saudi Arabia.
Their age ranged from 7 to 11 years.
the sample was randomly divided into 3 groups: the experimental group I, (EGI), the experimental group II, (EGII), and the control group (CG).
The EGI received a plyometric exercise program.
The EGII received the corrective exercises 2 sessions per week for 10 weeks.
The control group did not perform any planned physical activities during the intervention period but continued in their routine physical activities.
The Prokin system was used to assess the static balance, timed up and go test was used to assess functional mobility, and Navicular drop test was used to assess the degree of flatfoot deformity, prior to and after the intervention for all groups.
Study Type
Interventional
Enrollment (Actual)
47
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, 62552
- 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
7 years to 11 years (CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Body mass index percentile equal to or greater than the 95th percentile
- All had no previous history of strength or balance training or involvement in competitive sports emphasizing muscular strength or balance.
- All participants had balance deficiency and mobile flat foot.
Exclusion Criteria:
- Previous injury to the lower limb required medical care.
- Confounding conditions, such as a deformity of or surgery in the lower limb.
- visual impairment, or neuromuscular disorders.
- engagement in obesity treatment programs, three months prior to the study.
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
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Experimental group I
The experimental group received plyometric training
|
Exercises for strength and flexibility
|
|
EXPERIMENTAL: Experimental group II
The experimental group received flat feet rehabilitation training
|
Exercises for intrinsic muscles strength
|
|
NO_INTERVENTION: Control group
The Control group didn't receive intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Foot posture
Time Frame: 10 weeks
|
condition of the medial longitudinal arch of the foot
|
10 weeks
|
|
Balance (measure 1)
Time Frame: 10 weeks
|
Perimeter area (mm).
|
10 weeks
|
|
Balance (measure 2)
Time Frame: 10 weeks
|
Ellipse area (mm2).
|
10 weeks
|
|
Balance (measure 3)
Time Frame: 10 weeks
|
Standard backward-forward deviation.
|
10 weeks
|
|
Balance (measure 4)
Time Frame: 10 weeks
|
Standard medial-lateral deviation.
|
10 weeks
|
|
Functional mobility
Time Frame: 10 weeks
|
Timed up and go test
|
10 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Hatem Allam, A.professor, Taif University
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)
December 1, 2020
Primary Completion (ACTUAL)
April 1, 2021
Study Completion (ACTUAL)
May 13, 2021
Study Registration Dates
First Submitted
August 16, 2021
First Submitted That Met QC Criteria
August 23, 2021
First Posted (ACTUAL)
August 30, 2021
Study Record Updates
Last Update Posted (ACTUAL)
August 30, 2021
Last Update Submitted That Met QC Criteria
August 23, 2021
Last Verified
August 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HAP-02-T-067- 452
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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