Effects of Aerobic and Resistance Training on Abdominal Fat Loss
NCT ID: NCT03700827
Last Updated: 2021-10-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
18 participants
INTERVENTIONAL
2017-10-01
2020-05-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Resistance Training Group
Resistance training will consist of 3 whole body circuits per week for 3 weeks lasting approximately 1 hour per session. All major muscle groups will be involved (leg press, bent-over-row, bench press, back squat, dumbbell jump squats, dead-lifts, and weighted abdominal crunches). Each participant will go through each circuit three times with 30 seconds between each exercise and 2 minutes between each set.
Resistance Training
High-intensity Resistance Training Group
Aerobic Training Group
Aerobic interval training will consist of 3 sessions/week for 3 weeks for approximately 45-50 minutes per session depending on exercise energy expenditure. There will be two periods of intervals. The first period will be 3 minutes of high-intensity activity and the second period will be reduced to moderate-intensity for 2 minutes. The speed/incline will change depending on the participants perception or Borg's rating of perceived exertion. Intensity will be measured using Lactate levels after each session.
Aerobic Training
Aerobic Interval Training Group
Control Group
The control group must attend sessions but will not exercise.
No interventions assigned to this group
Interventions
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Resistance Training
High-intensity Resistance Training Group
Aerobic Training
Aerobic Interval Training Group
Eligibility Criteria
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Inclusion Criteria
* White/Caucasian
* Female
* Sedentary
Exclusion Criteria
* Pregnant females
* Any excluded criteria with MRI scans (i.e. certain metal implants, recent tattoos)
* Diabetic
* Hypertension
* Cigarette smoking
* MRI related contraindications (metal, no removable devices, etc.)
18 Years
35 Years
FEMALE
Yes
Sponsors
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Washington University School of Medicine
OTHER
Southern Illinois University Edwardsville
OTHER
Responsible Party
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Principal Investigators
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Maria Fernandez del Valle, PhD
Role: PRINCIPAL_INVESTIGATOR
Southern Illinois University of Edwardsville
Locations
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Southern Illinois University of Edwardsville
Edwardsville, Illinois, United States
Countries
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Other Identifiers
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16-1208-4C-2
Identifier Type: -
Identifier Source: org_study_id
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