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Body Composition Changes During Overfeeding Plus Resistance Training

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04069351
Enrollment
32
Registered
2019-08-28
Start date
2019-09-18
Completion date
2019-11-26
Last updated
2020-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overeating, Resistance Training, Weight Gain

Brief summary

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

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.

Interventions

DIETARY_SUPPLEMENTHigh-calorie mass gainer supplement

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

OTHERResistance Training

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

Sponsors

Dymatize Enterprises, LLC
CollaboratorUNKNOWN
MuscleSound
CollaboratorUNKNOWN
Texas Tech University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Body mass6 weeksBody mass in kilograms
Rate of Body Mass Gain6 weeksRate of body mass gained calculated in kilograms gained per week.
Fat-free mass6 weeksFat-free mass in kilograms, assessed via multiple methods.
Fat mass6 weeksFat mass in kilograms, assessed via multiple methods.
Skeletal muscle size6 weeksMuscle thickness in centimeters.
Resting metabolism6 weeksResting metabolism in kcal/day.
Proportion of Body Mass Gained as Fat-Free Mass6 weeksCalculated as change in fat-free mass (in kilograms) divided by change in body mass (in kilograms).

Secondary

MeasureTime frameDescription
Muscular Endurance (repetitions until failure)6 weeksMuscular endurance in repetitions (i.e. repetitions until failure) using a sub-maximal load.
Skeletal Muscle Quality via Ultrasonography6 weeksSkeletal muscle quality via ultrasonography (e.g. echo intensity in arbitrary units).
Estimated Skeletal Muscle Glycogen6 weeksEstimated muscle glycogen as assessed via ultrasound, in arbitrary units.
Estimated Skeletal Muscle Intramuscular Fat6 weeksEstimated intramuscular fat as assessed via ultrasound, in arbitrary units
Muscular Strength (1-repetition maximum test)6 weeksMaximal muscular strength in kilograms as assessed by 1-repetition maximum test.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026