Effects of Aerobic and Resistance Training on Abdominal Fat Loss

NCT ID: NCT03700827

Last Updated: 2021-10-04

Study Results

Results pending

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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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

18 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-10-01

Study Completion Date

2020-05-01

Brief Summary

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Study the effects of different exercise modes on total and regional adiposity variation in subcutaneous and visceral adipose tissue (VAT and SAT). The investigators hypothesize that total abdominal will improve for all the exercise groups compared to the control group. When comparing intervention groups: 1) no differences on the degree of improvement in total abdominal fat depots (VAT and SAT) 2) different degree of change when comparing specific sections at VAT and SAT are expected.

Detailed Description

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Conditions

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Obesity, Abdominal

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

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.

Group Type EXPERIMENTAL

Resistance Training

Intervention Type OTHER

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.

Group Type EXPERIMENTAL

Aerobic Training

Intervention Type OTHER

Aerobic Interval Training Group

Control Group

The control group must attend sessions but will not exercise.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Resistance Training

High-intensity Resistance Training Group

Intervention Type OTHER

Aerobic Training

Aerobic Interval Training Group

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 30 - 39.9 kg/m2 BMI
* White/Caucasian
* Female
* Sedentary

Exclusion Criteria

* Known cardiovascular, pulmonary, metabolic disease
* 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.)
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Washington University School of Medicine

OTHER

Sponsor Role collaborator

Southern Illinois University Edwardsville

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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United States

Other Identifiers

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16-1208-4C-2

Identifier Type: -

Identifier Source: org_study_id

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