The Effects of a Jump Rope Exercise Program on Body Composition and Self-efficacy in Obese Adolescent Girls
The Effects of a 12-week Jump Rope Exercise Program on Body Composition, Insulin Sensitivity, and Academic Self-efficacy in Obese Prehypertensive Adolescent Girls
1 other identifier
interventional
48
0 countries
N/A
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2010
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 3, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 23, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
December 6, 2011
CompletedFirst Submitted
Initial submission to the registry
March 29, 2019
CompletedFirst Posted
Study publicly available on registry
April 2, 2019
CompletedNovember 3, 2020
October 1, 2020
5 months
March 29, 2019
October 30, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (9)
Body Fat
Body fat percentage was measured to the nearest 0.1%.
12 weeks
Blood Pressure
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
Body mass was measured to nearest 0.1kg.
12 weeks
Height
Height was measured to the nearest 1 cm.
12 weeks
Waist Circumference
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
Lean Body Mass
Lean body mass (kg) was determined using a bioelectrical impedance-meter.
12 weeks
Glucose
Blood glucose concentrations were assessed with a glucose reagent kit.
12 weeks
Insulin
Serum insulin was evaluated using an enzyme-linked immunosorbent assay (ELISA) kit.
12 weeks
Homeostatic Model Assessment - Insulin Resistance
Homeostatic model assessment - insulin resistance was calculated from the fasting plasma blood glucose and insulin levels according to previously established models.
12 weeks
Study Arms (2)
Control Group
NO INTERVENTIONThe control group was in the facility for all jump rope exercise sessions but did not participate in the exercise intervention.
Experimental Group
EXPERIMENTALThe experimental group performed the jump rope exercise intervention.
Interventions
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.
Eligibility Criteria
You may qualify if:
- prehypertensive
- sedentary (no regular exercise training or physical activity within the last year)
- no weight loss diet during the last six months
- obese
You may not qualify if:
- pregnancy
- chronic disease
- daily medication use
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Pusan National Universitylead
- Chonnam National Universitycollaborator
- University of Nebraskacollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 29, 2019
First Posted
April 2, 2019
Study Start
October 3, 2010
Primary Completion
February 23, 2011
Study Completion
December 6, 2011
Last Updated
November 3, 2020
Record last verified: 2020-10
Data Sharing
- IPD Sharing
- Will not share