The Effect of Breakfast Consumption on Afternoon Resistance Training Performance

August 8, 2022 updated by: Texas Tech University

The Effect of Breakfast Consumption on Afternoon Resistance Training Performance in Habitual Breakfast Consumers and Non-Consumers

This study is a randomized crossover trail examining the effect of breakfast consumption or omission on afternoon resistance training performance. Resistance-trained adults will complete a resistance training workout comprised of barbell back squat, barbell bench press, and barbell conventional deadlift following either consuming breakfast and lunch, or the same amount of food consumed solely at lunch. For each testing session the participants will be provided with all food to consume prior to arriving at the laboratory. Major performance outcomes will be total repetition volume completed for each exercise (i.e. bench press, squat, and deadlift) and the entire workout (each individual trial), along with barbell kinematics for each exercise.

Study Overview

Detailed Description

OVERVIEW

This study is a randomized crossover trail examining the effect of breakfast consumption or omission on afternoon resistance training performance. Resistance-trained adults will complete a resistance training workout comprised of barbell back squat, barbell bench press, and barbell conventional deadlift following either consuming breakfast and lunch, or the same amount of food consumed solely at lunch. For each testing session the participants will be provided with all food to consume prior to arriving at the laboratory. Major performance outcomes will be total repetition volume completed for each exercise (i.e. bench press, squat, and deadlift) and the entire workout (each individual trial), along with barbell kinematics for each exercise.

Participants will report to the laboratory on three separate occasions, with 3 to 10 days between each visit. At the first visit, after initial screening and provision of informed consent, each participant will undergo a performance screening and familiarization session to confirm eligibility and become accustomed to the study procedures. This familiarization session will include initial assessments of bench press, barbell back squat, and conventional deadlift maximal strength in order to determine final eligibility. Additionally, body composition will be assessed via dual-energy X-ray absorptiometry and digital anthropometry at this session for descriptive purposes. Following the familiarization session, each participant will complete two laboratory visits consisting of completion of the resistance training workout described below after consuming the provided meals either divided between breakfast and lunch (~3-4 hours after breakfast), or solely at lunch. This will ensure each participant consumes identical quantities and types of foods prior to both exercise sessions. Thus, the only difference will be the food distribution as two meals (breakfast and lunch) or one meal (lunch). Throughout the study, participants will be asked to maintain their normal lifestyle practices. In addition, participants will report their dietary intake during the 24-hour period prior to the first testing session and will be asked to replicate this intake during the 24-hour period prior to the subsequent testing sessions. A background questionnaire will also be completed to assess general supplement use.

PURPOSE

The purpose of this investigation is to examine the effect of breakfast consumption or omission on afternoon resistance training performance in habitual breakfast consumers and non-consumers.

GENERAL HYPOTHESIS

It is hypothesized that afternoon resistance training performance will be impaired in habitual breakfast consumers when breakfast is omitted, but similar decrements will not be observed in habitual non-consumers.

HYPOTHESES TO BE TESTED/SPECIFIC AIMS

Specific Aim 1. To determine the effect of breakfast consumption on afternoon resistance training performance.

Hypothesis. It is hypothesized that afternoon resistance training performance will not be impacted by breakfast consumption or omission when the cohort is examined as a whole.

Specific Aim 2. To determine whether habitual breakfast consumption patterns impact afternoon resistance training performance following consumption or omission of breakfast.

Hypothesis. It is hypothesized that habitual breakfast consumption patterns will impact the effect of breakfast consumption on resistance training performance. More specifically, performance will be negatively affected by the omission of breakfast in those who habitually consume breakfast. Yet the omission of breakfast will not negatively impact resistance training performance in those that regularly do not consume breakfast.

Specific Aim 3. To determine the impact of breakfast consumption on subjective responses throughout an afternoon resistance training session.

Hypothesis. It is hypothesized that subjective responses during afternoon resistance training will not be impacted by breakfast consumption or omission when the cohort is examined as a whole.

Specific Aim 4. To determine whether habitual breakfast consumption patterns influence subjective responses throughout an afternoon resistance training session, following consumption or omission of breakfast.

Hypothesis. It is hypothesized that worsened subjective responses will be observed after breakfast omission only in those who habitually consume breakfast.

Study Type

Interventional

Enrollment (Actual)

39

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Lubbock, Texas, United States, 79409
        • Department of Kinesiology & Sport Management

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Between the ages of 18 and 40
  • Body mass between 50 - 110 kg (110-242 lb)
  • Generally healthy (defined as an absence of any disease or medical condition which could potentially be negatively affected by consumption of the commercially available dietary supplements or performance of exercise, including but not limited to musculoskeletal or cardiovascular diseases).
  • Resistance-trained, defined as completing 2+ resistance training sessions per week for at least three months prior to screening.
  • Participants must self-report either consuming or skipping breakfast ≥ 5 times per week for three months prior to screening.
  • Participants must have reported regular training of the lower body through a multi-joint exercise such as the squat or leg press at least once weekly during the three-month period prior to screening.
  • Participants must have reported regular training of the bench press or chest press variation at least once weekly during the three-month period prior to screening.
  • Participants must have reported regular training of the deadlift or deadlift variation at least once weekly during the three-month period prior to screening.
  • Female participants will be required to bench press ≥ 0.5 x body mass, barbell back squat ≥ 0.75 x body mass, and deadlift ≥ 1.0 x body mass to be eligible or this study.
  • Male participants will be required to bench press ≥ 1.0 x body mass, barbell back squat ≥ 1.375 x body mass, and deadlift ≥ 1.75 x body mass to be eligible or this study.

Exclusion Criteria:

  • Failing to meet any of the aforementioned inclusion criteria.
  • Pregnant or breastfeeding (for female participants)
  • Taking prescription medication which could reasonably make participation unsafe for the participant or influence study outcomes
  • An inability to complete resistance exercise due to injury or medical condition
  • Inability to complete a 16 hour fast.
  • Allergy to any of the ingredients in the provided breakfast and lunch.
  • Current use of anabolic steroids
  • Presence of a pacemaker or other implanted electrical device.
  • Inability to perform the exercises with safe and proper form as determined by members of the research team.

Study Plan

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

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Breakfast Omission
This arm will consist of omission of breakfast and consumption of standardized food items solely at lunch preceding afternoon resistance exercise.
Breakfast omission will consist of not eating breakfast on the morning of afternoon resistance training performance assessment.
Active Comparator: Breakfast Consumption
This arm will consist of consumption of standardized food items at breakfast and lunch preceding afternoon resistance exercise.
Breakfast consumption will consist of eating a standardized breakfast on the morning of afternoon resistance training performance assessment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total Repetition Volume
Time Frame: 1 hour
The total number of repetitions completed across four sets of the barbell back squat exercise, four sets of the barbell bench press exercise, and four sets of the conventional barbell deadlift exercise.
1 hour
Squat Repetition Volume
Time Frame: 20 minutes
The total number of repetitions completed across four sets of the barbell back squat exercise.
20 minutes
Bench Press Repetition Volume
Time Frame: 20 minutes
The total number of repetitions completed across four sets of the barbell bench press exercise.
20 minutes
Deadlift Repetition Volume
Time Frame: 20 minutes
The total number of repetitions completed across four sets of the conventional barbell deadlift exercise.
20 minutes
Average Concentric Barbell Velocity for Squat
Time Frame: 20 minutes
The average barbell velocity during the concentric portion of the squat exercise across all repetitions.
20 minutes
Average Concentric Barbell Velocity for Bench Press
Time Frame: 20 minutes
The average barbell velocity during the concentric portion of the bench press exercise across all repetitions.
20 minutes
Average Concentric Barbell Velocity for Deadlift
Time Frame: 20 minutes
The average barbell velocity during the concentric portion of the deadlift exercise across all repetitions.
20 minutes
Peak Concentric Barbell Velocity for Squat
Time Frame: 20 minutes
The peak barbell velocity during the concentric portion of the squat exercise across all repetitions.
20 minutes
Peak Concentric Barbell Velocity for Bench Press
Time Frame: 20 minutes
The peak barbell velocity during the concentric portion of the bench press exercise across all repetitions.
20 minutes
Peak Concentric Barbell Velocity for Deadlift
Time Frame: 20 minutes
The peak barbell velocity during the concentric portion of the deadlift exercise across all repetitions.
20 minutes
Average Power for Squat
Time Frame: 20 minutes
The average power during the squat exercise across all repetitions.
20 minutes
Average Power for Bench Press
Time Frame: 20 minutes
The average power during the bench press exercise across all repetitions.
20 minutes
Average Power for Deadlift
Time Frame: 20 minutes
The average power during the deadlift exercise across all repetitions.
20 minutes
Peak Power for Squat
Time Frame: 20 minutes
The peak power during the squat exercise across all repetitions.
20 minutes
Peak Power for Bench Press
Time Frame: 20 minutes
The peak power during the bench press exercise across all repetitions.
20 minutes
Peak Power for Deadlift
Time Frame: 20 minutes
The peak power during the deadlift exercise across all repetitions.
20 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hunger
Time Frame: 1 hour
Subjective rating of hunger as assessed by visual analog scale.
1 hour
Desire to Eat
Time Frame: 1 hour
Subjective rating of desire to eat as assessed by visual analog scale.
1 hour
Fullness
Time Frame: 1 hour
Subjective rating of fullness as assessed by visual analog scale.
1 hour
Energy
Time Frame: 1 hour
Subjective rating of energy as assessed by visual analog scale.
1 hour
Focus
Time Frame: 1 hour
Subjective rating of focus as assessed by visual analog scale.
1 hour
Fatigue
Time Frame: 1 hour
Subjective rating of fatigue as assessed by visual analog scale.
1 hour

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 17, 2021

Primary Completion (Actual)

May 16, 2022

Study Completion (Actual)

May 16, 2022

Study Registration Dates

First Submitted

November 2, 2021

First Submitted That Met QC Criteria

November 2, 2021

First Posted (Actual)

November 15, 2021

Study Record Updates

Last Update Posted (Actual)

August 9, 2022

Last Update Submitted That Met QC Criteria

August 8, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • IRB2021-649

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

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