- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01107691
Comparison of 1 vs 3 Sets of Resistance Training on Muscular Hypertrophy
Resistance Training Energy Balance & Weight Management
This study is designed to investigate the effects of two levels of resistance weight training on body composition, energy expenditure, and energy intake in men and women. The weight training will take about one hour to complete. Participants will perform the training 3 days per week for 9 months in a private exercise room equipped with state of the art equipment and a personal trainer to help guide you through the exercises.
The project lasts 21 months total with one follow-up visit 1-year from your last training date. You will be required to stay in the Lawrence area and train 3 day/week over the summer & holidays.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Kansas
-
Lawrence, Kansas, United States, 66045
- Energy Balance Lab, The University of Kansas
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- BMI 22-<30
- 18- 30 years old
- sedentary
- no medications
- weight stable for at least 3 months
Exclusion Criteria:
- Tobacco/Drug user
- metabolism altering medication
- gain/lost 10lbs in the last 3 months
- current exerciser
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Resistance training
1 set of progressive resistance training per session
|
to determine the impact of the volume (1 vs. 3 sets) of a progressive resistance training protocol for inducing muscular hypertrophy
|
|
Experimental: 3 sets per session
3 sets of progressive resistance training per session
|
to determine the impact of the volume (1 vs. 3 sets) of a progressive resistance training protocol for inducing muscular hypertrophy
|
|
No Intervention: Control
Non exercise control group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body Composition
Time Frame: 21 Months
|
Changes in body composition will be evaluated by measuring the change in percent body fat, total fat mass, and total lean mass by dual energy x-ray absorptiometry (DEXA).
|
21 Months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Resting Metabolic Rate
Time Frame: 9 months
|
Resting metabolic rate as measured by indirect calorimetry as kcal/day will be evaluated.
Also, substrate oxidation (fat and carbohydrate oxidation) will be evaluated at these time points.
|
9 months
|
|
Muscular Strength
Time Frame: 9 months
|
One rep max strength will be measured on the chest and leg press.
|
9 months
|
|
Daily Energy Expenditure
Time Frame: 9 months
|
Total daily energy expenditure over a 14 day period will be measured using doubly labeled water.
|
9 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Richard A Washburn, PhD, University of Kansas
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- HSCL17623
- NIDDKRO180832 (Other Grant/Funding Number: National Institues of Health)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.