Completed

Body Composition Changes During Overfeeding Plus Resistance Training: Influence of Rate of Mass Gain, Assessment Method, and Participant Standardization

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What is being tested

High-calorie mass gainer supplement

+ Resistance Training

Dietary SupplementOther
Who is being recruted

Body Weight+4

+ Body Weight Changes

+ Hyperphagia

From 18 to 40 Years
See all eligibility criteria
How is the trial designed

Other Study

Interventional
Study Start: September 2019
See protocol details

Summary

Principal SponsorTexas Tech University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 18, 2019

Actual date on which the first participant was enrolled.

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.

Official TitleBody Composition Changes During Overfeeding Plus Resistance Training: Influence of Rate of Mass Gain, Assessment Method, and Participant Standardization
NCT04069351
Principal SponsorTexas Tech University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

32 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other Study

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Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Male

Biological sex of participants that are eligible to enroll.

From 18 to 40 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Body WeightBody Weight ChangesHyperphagiaSigns and SymptomsSigns and Symptoms, DigestivePathological Conditions, Signs and SymptomsWeight Gain

Criteria

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 Exclusion Criteria: * Failing to meet any of the aforementioned inclusion criteria * 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

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
6-week overfeeding plus resistance training arm

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Texas Tech University

Lubbock, United StatesOpen Texas Tech University in Google Maps
CompletedOne Study Center