Body Composition Changes During Overfeeding Plus Resistance Training

NCT ID: NCT04069351

Last Updated: 2020-05-07

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

COMPLETED

Clinical Phase

NA

Total Enrollment

32 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-09-18

Study Completion Date

2019-11-26

Brief Summary

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This study will examine the relationship between the rate and composition of mass gain during overfeeding plus resistance training, investigate the validity of multiple assessment methods for quantifying body composition changes during this period, and evaluate the effects of subject presentation on the interpretation of body composition changes.

Detailed Description

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This study will examine the relationship between the rate and composition of mass gain during overfeeding plus resistance training, investigate the validity of multiple assessment methods for quantifying body composition changes during this period, and evaluate the effects of subject presentation on the interpretation of body composition changes. For this study, resistance-trained males between the ages of 18 and 40 will be recruited. At baseline, participants will complete body composition and metabolism assessments after an overnight period of fasting and resting (i.e. standardized conditions). These baseline assessments will be repeated in the afternoon of the same day after a period of ad libitum physical activity and dietary intake (i.e. non-standardized conditions). At both visits, body composition will be evaluated by a criterion 4-compartment model, necessitating assessments via dual-energy x-ray absorptiometry, air displacement plethysmography, and bioimpedance spectroscopy. Additional assessments will be conducted using single- and multi-frequency bioelectrical impedance analysis, infrared 3-dimensional scanning, and ultrasonography. At a separate baseline session, muscular performance will be measured via 1-repetition maximum and repetitions-to-failure tests on the barbell bench press and plate-loaded hip sled. Once baseline assessments are completed, participants will commence a 6-week, 3-days/week, full-body, progressive resistance training intervention in conjunction with overfeeding. During the intervention, participants will be asked to maintain their habitual diet while also consuming a high-calorie protein/carbohydrate supplement designed to promote mass gain. Dietary recommendations to promote adequate protein intake for maximal fat-free mass accretion will also be provided. For all participants, a target mass gain of 1+ pounds per week will be implemented. However, due to known variability in the propensity to gain body mass during overfeeding and resistance training, it is expected that natural variability in the actual mass gained will be present at the conclusion of the study. After the overfeeding plus resistance training intervention is completed, participants will complete three post-intervention research visits, which will be identical to the baseline visits. Appropriate statistical methods will be used to address the specific aims of this project. These will include linear regression analysis, paired-samples t-tests, effect size calculations, and validity evaluation through metrics such as the constant error, total error, standard error of the estimate, and 95% limits of agreement.

Conditions

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Weight Gain Resistance Training Overeating

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Overfeeding Plus Resistance Training Arm

6-week overfeeding plus resistance training arm

Group Type EXPERIMENTAL

High-calorie mass gainer supplement

Intervention Type DIETARY_SUPPLEMENT

A high-calorie mass gainer supplement will be provided to all participants to promote weight gain.

Resistance Training

Intervention Type OTHER

All participants will complete a 6-week supervised resistance training program.

Interventions

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High-calorie mass gainer supplement

A high-calorie mass gainer supplement will be provided to all participants to promote weight gain.

Intervention Type DIETARY_SUPPLEMENT

Resistance Training

All participants will complete a 6-week supervised resistance training program.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Between the ages of 18 and 40
* Male
* Generally healthy (defined as an absence of any disease or medical condition which could potentially be impacted by study participation, including but not limited to cardiac, musculoskeletal, pulmonary, renal, immunological, or metabolic diseases)
* Weight-stable (defined as no change in body mass \>5 pounds \[2.3 kg\] in the past 3 months)
* Willingness to adhere to study protocol, particularly the completion of the supervised resistance training program and consumption of dietary supplements
* Desire and/or willingness to attempt to gain body mass as part of study intervention
* Resistance trained (defined as performance of resistance training on 2 to 5 days for at least 6 months prior to study initiation), as well as meeting the objective criteria below
* Maximal strength \> 1.0 x body mass on the barbell bench press exercise, executed with proper form
* Maximal strength \> 2.0 x body mass on plate-loaded hip sled, executed with proper form

* Height greater than 75.5 inches (due to height limitation of DXA scanner)
* Weight greater than 350 pounds (due to weight limitation of DXA scanner)
* Beard longer than ½ inch (and unwillingness to shave) due to the impact of facial hair on Bod Pod body volume estimates
* History of anabolic-androgenic steroid use, based on self-report
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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Dymatize Enterprises, LLC

UNKNOWN

Sponsor Role collaborator

MuscleSound

UNKNOWN

Sponsor Role collaborator

Texas Tech University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Texas Tech University

Lubbock, Texas, United States

Site Status

Countries

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United States

References

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Rodriguez C, Harty PS, Stratton MT, Siedler MR, Smith RW, Johnson BA, Dellinger JR, Williams AD, White SJ, Benavides ML, Tinsley GM. Comparison of Indirect Calorimetry and Common Prediction Equations for Evaluating Changes in Resting Metabolic Rate Induced by Resistance Training and a Hypercaloric Diet. J Strength Cond Res. 2022 Nov 1;36(11):3093-3104. doi: 10.1519/JSC.0000000000004077. Epub 2021 Jun 22.

Reference Type DERIVED
PMID: 34172636 (View on PubMed)

Other Identifiers

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IRB2019-356

Identifier Type: -

Identifier Source: org_study_id

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