The Effects of a Jump Rope Exercise Program on Body Composition and Self-efficacy in Obese Adolescent Girls

October 30, 2020 updated by: Won-mok son, Pusan National University

The Effects of a 12-week Jump Rope Exercise Program on Body Composition, Insulin Sensitivity, and Academic Self-efficacy in Obese Prehypertensive Adolescent Girls

The purpose of this study was to examine the impact of a 12-week jump rope exercise program on body composition, blood pressure, insulin resistance, and academic self-efficacy in prehypertensive adolescent obese girls. Forty-eight prehypertensive adolescent obese girls participated in this study. The girls were randomly divided into the jump rope exercise intervention group (EX, n=24) and control group (CON, n=24). The EX group performed a jump rope training program at 40-70% of their heart rate reserve (HRR) 5 days/week for 12 weeks (sessions 50 minutes in duration). The CON group did not participate in any structure or unstructured exercise protocol. Blood pressure, body fat percentage, waist circumference, blood glucose and insulin, homeostatic model assessment - insulin resistance, and Academic Self-Efficacy were measured before and after the 12-weeks study.

Study Overview

Study Type

Interventional

Enrollment (Actual)

48

Phase

  • Not Applicable

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

12 years to 14 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • prehypertensive
  • sedentary (no regular exercise training or physical activity within the last year)
  • no weight loss diet during the last six months
  • obese

Exclusion Criteria:

  • pregnancy
  • chronic disease
  • daily medication use

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control Group
The control group was in the facility for all jump rope exercise sessions but did not participate in the exercise intervention.
Experimental: Experimental Group
The experimental group performed the jump rope exercise intervention.
Each jump rope exercise session of the program was performed for 50 minute, with a 5 minute warm-up and cool-down. Sessions were performed once a day, 5 days a week, for 12 weeks. The program consisted of various main jump rope exercises (1 line 2 jump, jumping feet together, running jumping, open side jump, open back and forth jump, rock paper scissor jump). The warm-up and cool-down consisted of static stretching, walking, and jogging. Intensity of exercise was gradually increased form 40-50% heart rate reserve (HRR) in weeks 1-4 and 60-70% HRR in weeks 9-12. Each training session was supervised by the researchers. Ever subject wore a heart rate monitor during the whole training session in order to maintain the designated training intensity.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lean Body Mass
Time Frame: 12 weeks
Lean body mass (kg) was determined using a bioelectrical impedance-meter.
12 weeks
Body Fat
Time Frame: 12 weeks
Body fat percentage was measured to the nearest 0.1%.
12 weeks
Blood Pressure
Time Frame: 12 weeks
Blood pressure was measured in duplicate using an automated sphygmomanometer. The average of the was recorded as the resting blood pressure. Both systolic and diastolic blood pressure were recorded.
12 weeks
Body Mass
Time Frame: 12 weeks
Body mass was measured to nearest 0.1kg.
12 weeks
Height
Time Frame: 12 weeks
Height was measured to the nearest 1 cm.
12 weeks
Waist Circumference
Time Frame: 12 weeks
Waist circumference as measured at midpoint between the lower rib and the iliac crest at the end of a normal expiration using a tap measure.
12 weeks
Glucose
Time Frame: 12 weeks
Blood glucose concentrations were assessed with a glucose reagent kit.
12 weeks
Insulin
Time Frame: 12 weeks
Serum insulin was evaluated using an enzyme-linked immunosorbent assay (ELISA) kit.
12 weeks
Homeostatic Model Assessment - Insulin Resistance
Time Frame: 12 weeks
Homeostatic model assessment - insulin resistance was calculated from the fasting plasma blood glucose and insulin levels according to previously established models.
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this 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)

October 3, 2010

Primary Completion (Actual)

February 23, 2011

Study Completion (Actual)

December 6, 2011

Study Registration Dates

First Submitted

March 29, 2019

First Submitted That Met QC Criteria

March 29, 2019

First Posted (Actual)

April 2, 2019

Study Record Updates

Last Update Posted (Actual)

November 3, 2020

Last Update Submitted That Met QC Criteria

October 30, 2020

Last Verified

October 1, 2020

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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