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

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

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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