Effects of Resistance Exercise on Metabolic Responses

March 14, 2022 updated by: National Taiwan Normal University

Effects of Volume-matched Resistance Exercise With Different Loads on Metabolic Responses

Healthy young adults will complete three trials in a randomized crossover counter-balanced order, including two different loads of resistance exercise and sedentary control. During each trial, blood samples will be collected.

The investigators hypothesized that high-load and low-load resistance exercise exert similar metabolic responses.

Study Overview

Study Type

Interventional

Enrollment (Actual)

11

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, 162
        • 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

20 years to 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Age: 20-30
  • Healthy male
  • Without experience of resistance training

Exclusion Criteria:

  • No acute or chronic musculoskeletal symptoms
  • Smoking
  • Alcohol or drug abuse
  • Fail 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: High-load resistance exercise
4 high-load resistance exercises that target all major muscle groups.
Subjects in high-load trial performed 4 sets per exercise, 8 repetitions with load of 85%-8RM with 90 sec of rest between sets.
Experimental: Low-load resistance exercise
4 low-load resistance exercises that target all major muscle groups.
Subjects in low-load trial performed 4 sets per exercise, 15 repetitions with load of 45%-8RM with 90 sec of rest between sets.
No Intervention: Sedentary control
Subjects in control trial stayed sedentary during the period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in glucose
Time Frame: 4-hour during each study intervention
glucose in mg/dL
4-hour during each study intervention
Changes in insulin
Time Frame: 4-hour during each study intervention
insulin in mU/L
4-hour during each study intervention
Changes in TG
Time Frame: 4-hour during each study intervention
TG mg/dL
4-hour during each study intervention
Changes in uric acid
Time Frame: 4-hour during each study intervention
uric acid mg/dL.
4-hour during each study intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in biomarkers of inflammation
Time Frame: 4-hour during each study intervention
Biomarkers of inflammation will be measured such as IL-10 in pg/mL and IL-6 in pg/mL.
4-hour during each study intervention
Changes in cortisol
Time Frame: 4-hour during each study intervention
cortisol in ng/mL
4-hour during each study intervention
Changes in lactate
Time Frame: 4-hour during each study intervention
lactate in mmol/L
4-hour during each study intervention
Changes in complete blood count
Time Frame: 4-hour during each study intervention
blood cell count in count per µL
4-hour during each study intervention
Borgs Ratings of Perceived Exertion (RPE)
Time Frame: 1-hour during each exercise intervention
Borgs RPE is a method of estimating exertion rating, based on a 6 to 20 rating scale (6 being the no exertion at all, 20 being maximal exertion).
1-hour during each exercise intervention
Changes in ET-1
Time Frame: 4-hour during each study intervention
ET-1 in pg/mL
4-hour during each study intervention
Changes in NO
Time Frame: 4-hour during each study intervention
NO in µmol/L
4-hour during each study intervention
Changes in biomarkers of muscle damage
Time Frame: 4-hour during each study intervention
Biomarkers of muscle damage will be measured such as CK in U/L and LDH in U/L.
4-hour during each study intervention
Heart rate (HR)
Time Frame: 6-hour during each study intervention
HR will be measured during each study intervention.
6-hour during each study intervention
Visual Analogue Scale (VAS) of appetite
Time Frame: 6-hour during each study intervention
Hunger, fullness, desire to eat, and prospective food consumption will be measured via VAS ratings, based on a 100 mm long scale (0 being "not at all", 100 being "extremely").
6-hour during each study intervention
Changes in biomarkers of appetite
Time Frame: 4-hour during each study intervention
Biomarkers of appetite will be measured such as ghrelin in pg/mL and PYY in pg/mL.
4-hour 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)

February 18, 2021

Primary Completion (Actual)

March 7, 2021

Study Completion (Actual)

December 31, 2021

Study Registration Dates

First Submitted

August 30, 2021

First Submitted That Met QC Criteria

September 10, 2021

First Posted (Actual)

September 21, 2021

Study Record Updates

Last Update Posted (Actual)

March 16, 2022

Last Update Submitted That Met QC Criteria

March 14, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 202011HM005

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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