- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03898518
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
Status
Completed
Conditions
Intervention / Treatment
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.
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 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
Additional Relevant MeSH Terms
Other Study ID Numbers
- UNOVRLJRSE
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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