Terminé

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

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Ce qui est testé

High-calorie mass gainer supplement

+ Resistance Training

Complément alimentaireAutre
Qui peut participer

Poids Corporel+4

+ Changements de Poids Corporel

+ Hyperphagie

De 18 à 40 ans
Voir tous les critères d'éligibilité
Comment se déroule l'étude

Autre étude

Interventionnel
Date de début : septembre 2019
Voir le détail du protocole

Résumé

Sponsor principalTexas Tech University
Dernière mise à jour : 28 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Date de début de l'étude : 18 septembre 2019

Date à laquelle le premier participant a commencé l'étude.

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.

Titre officielBody Composition Changes During Overfeeding Plus Resistance Training: Influence of Rate of Mass Gain, Assessment Method, and Participant Standardization
NCT04069351
Sponsor principalTexas Tech University
Dernière mise à jour : 28 janvier 2026
Issu d'une base de données validée par les autorités. Revendiquer en tant que partenaire

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design

32 participants à inclure

Nombre total de participants que l'essai clinique vise à recruter.

Autre

Cette catégorie concerne les études qui ne relèvent d'aucune des catégories précédentes. Cela peut inclure des recherches innovantes, de nouvelles technologies ou des domaines émergents de la santé.



Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères

Homme

Le sexe biologique des participants éligibles à s'inscrire.

De 18 à 40 ans

Tranche d'âge des participants éligibles à participer.

Volontaires sains autorisés

Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.

Conditions

Pathologie

Poids CorporelChangements de Poids CorporelHyperphagieSignes et symptômesSignes et symptômes digestifsConditions pathologiques, signes et symptômesPrise de Poids

Critères

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

Plan de l'étude

Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.
Groupes de traitement
Objectifs de l'étude

Un seul groupe d'intervention est désigné dans cette étude

Cette étude ne comporte pas de groupe placebo. 

Groupes de traitement

Groupe I

Expérimental
6-week overfeeding plus resistance training arm

Objectifs de l'étude

Objectifs principaux

Objectifs secondaires

Centres d'étude

Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.

Cette étude comporte 1 site

Suspendu

Texas Tech University

Lubbock, United StatesOuvrir Texas Tech University dans Google Maps
Terminé1 Centres d'Étude