Effects of Exercise on Energy Intake-Prescription of Resistance Exercise

January 15, 2024 updated by: National Taiwan Normal University

Effects of Acute Resistance Exercise With Varying Training Volume and Rest Intervals Under Equal Load on Appetite Control, Food Reward, and Energy Intake: a Five-arm Crossover Randomized Controlled Trial

Healthy young males will complete five trials in a randomized crossover counter-balanced order, including three different inter-set rest of resistance exercise in equal training volume, one repeated until failure and sedentary control. During each trial, blood samples will be collected.

The investigators hypothesized that different inter-set rest and training volume would affect subjective appetite and energy intake.

Study Overview

Study Type

Interventional

Enrollment (Actual)

18

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

      • Taipei, Taiwan, 106
        • National Taiwan Normal University

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age: 20-30
  • Healthy male

Exclusion Criteria:

  • No acute or chronic musculoskeletal symptoms
  • Smoking
  • Alcohol or drug abuse
  • Failure to conduct resistance exercise

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: short inter-set rest
3 multi-joints resistance exercise with short (60s) inter-set rest
Subjects in short inter-set rest trial performed 3 sets per exercise, 7 repetitions with load of 70%-1RM with 60 sec of rest between sets.
Experimental: medium inter-set rest
3 multi-joints resistance exercise with medium(120s) inter-set rest
Subjects in medium inter-set rest trial performed 3 sets per exercise, 7 repetitions with load of 70%-1RM with 120 sec of rest between sets.
Experimental: long inter-set rest
3 multi-joints resistance exercise with long (180s) inter-set rest
Subjects in long inter-set rest trial performed 3 sets per exercise, 7 repetitions with load of 70%-1RM with 180 sec of rest between sets.
Experimental: medium inter-set rest with failure
3 multi-joints resistance exercise with medium (120s) inter-set rest repeated to failure each set
Subjects in long inter-set rest trial performed 3 sets per exercise, repeated to failure with load of 70%-1RM with 120 sec of rest between sets.
No Intervention: control
stayed sedentary during the period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Subjective appetite
Time Frame: 4-hour during each study intervention
The appetite perceptions were obtained through a 0-100 mm visual analog scale. The variables assessed included perceptions of hunger (i.e., "How hungry do you feel?"), satisfaction (i.e., "How satisfied do you feel?"), fullness (i.e., "How full do you feel?"), prospective food consumption (i.e., "How much do you think you can eat?"), and nausea (i.e., "How nauseous do you feel?"), with 0 indicating "not at all" and 100 signifying "extremely.".
4-hour during each study intervention
Change in acyl-Ghrelin
Time Frame: 4-hour during each study intervention
acyl-Ghrelin in pg/mL
4-hour during each study intervention
Change in total-Ghrelin
Time Frame: 4-hour during each study intervention
total-Ghrelin in pg/mL
4-hour during each study intervention
Change in PYY
Time Frame: 4-hour during each study intervention
PYY in pg/mL
4-hour during each study intervention
Change in active-GLP-1
Time Frame: 4-hour during each study intervention
active-GLP-1 in pg/mL
4-hour during each study intervention
Change in total-GLP-1
Time Frame: 4-hour during each study intervention
total-GLP-1 in pg/mL
4-hour during each study intervention
Change in lactate
Time Frame: 4-hour during each study intervention
insulin in mmol/L
4-hour during each study intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in TG
Time Frame: 4 hours during each study intervention
TG in mg/dL
4 hours during each study intervention
Change in glucose
Time Frame: 4 hours during each study intervention
glucose in mg/dL
4 hours during each study intervention
Change in insulin
Time Frame: 4 hours during each study intervention
insulin in mU/L
4 hours during each study intervention
Explicit liking
Time Frame: 4 hours during each study intervention
A visual analog scale ranging from 0 to 100 mm was utilized to evaluate the question, "How pleasant would it be to taste some of this food now?" with 0 indicating "not at all" and 100 signifying "extremely."
4 hours during each study intervention
Explicit wanting
Time Frame: 4 hours during each study intervention
A visual analog scale ranging from 0 to 100 mm was utilized to evaluate the question, "How much do you want some of this food now?" with 0 indicating "not at all" and 100 signifying "extremely."
4 hours during each study intervention
Implicit wanting
Time Frame: 4 hours during each study intervention
Participants were given a set of food image pairs and were asked to select their preference by answering the question, "Which food do you desire the most at the moment?". The implicit wanting calculation involved further consideration of response time data based on preference choices using a standardized equation.
4 hours during each study intervention
Relative preference
Time Frame: 4 hours during each study intervention
Participants were given a set of food image pairs and were asked to select their preference by answering the question, "Which food do you desire the most at the moment?". The relative preference was the sum of the times each type of food was chosen, with a maximum value of 48 and a minimum value of 0.
4 hours during each study intervention
Fat appeal bias
Time Frame: 4 hours during each study intervention
Fat preference (high or low) was calculated by subtracting the mean low-fat scores from the mean high-fat scores. Positive values suggest a preference for high-fat foods, while negative scores indicate a preference for low-fat or savory foods, and a score of 0 signifies an equal preference between fat content.
4 hours during each study intervention
Taste appeal bias
Time Frame: 4 hours during each study intervention
Taste preference (savoury or sweet) was calculated by subtracting the mean savory scores from the mean sweet scores. Positive values suggest a preference for sweet foods, while negative scores indicate a preference for savory foods, and a score of 0 signifies an equal preference between taste categories.
4 hours during each study intervention
Energy intake
Time Frame: 3 days during each study intervention
Participants are required to record their diet for the day before, the current day, and the day following the experiment.
3 days during each study intervention

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Hung-Wen Liu, Ph.D., National Taiwan Normal University

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)

October 28, 2022

Primary Completion (Actual)

March 31, 2023

Study Completion (Actual)

March 31, 2023

Study Registration Dates

First Submitted

January 4, 2024

First Submitted That Met QC Criteria

January 15, 2024

First Posted (Estimated)

January 25, 2024

Study Record Updates

Last Update Posted (Estimated)

January 25, 2024

Last Update Submitted That Met QC Criteria

January 15, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 202112HM039

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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