- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05042167
The Effect of Resistance Exercise on Inflammation in Young and Older Adults
January 12, 2023 updated by: National Taiwan Normal University
The Acute Effect of High-load Resistance Exercise on Inflammation in Young and Older Adults
Healthy young and older adults will complete two trials in a randomized crossover counter-balanced order, including resistance exercise and sedentary control. During each trial, blood samples will be collected.
The investigators hypothesized that an acute bout of resistance exercise exert different inflammation responses in young and older adults.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
16
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
-
-
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Taipei, Taiwan, 162
- National Taiwan Normal University
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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 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Age: 20-80
- 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 |
|---|---|
|
No Intervention: Sedentary control
Subjects in control trial stayed sedentary during the period.
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Experimental: High-load resistance exercise
Subjects in high-load trial performed 3 sets per exercise, 8 repetitions with load of 70%-1RM with 90 sec of rest between sets, followed by a fourth set to voluntary failure.
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4 total resistance exercises that target all major muscle groups.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in biomarkers of inflammation
Time Frame: 24-hour during each study intervention
|
Biomarkers of inflammation will be measured such as IL-10 in pg/mL, IL-6 in pg/mL, TNF-α in pg/mL.
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24-hour during each study intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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).
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1-hour during each exercise intervention
|
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Changes in glucose
Time Frame: 24-hour during each study intervention
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glucose in mg/dL
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24-hour during each study intervention
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Changes in metabolic parameters
Time Frame: 24-hour during each study intervention
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Metabolic parameters will be measured such as TC in mg/dL, TG in mg/dL, and HDL in mg/dL.
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24-hour during each study intervention
|
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Changes in biomarkers of muscle damage
Time Frame: 24-hour during each study intervention
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Biomarkers of muscle damage will be measured such as CK in U/L and LDH in U/L.
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24-hour during each study intervention
|
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Changes in molecular markers in peripheral blood mononuclear cells (PBMC)
Time Frame: 24-hour during each study intervention
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Molecular markers in PBMC will be measured such as STAT3 in arbitrary units, IKK in arbitrary units, IkB in arbitrary units, p65 in arbitrary units, SOCS3 in arbitrary units, AMPK in arbitrary units, and SIRT1 in arbitrary units.
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24-hour during each study intervention
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Changes in complete blood count (CBC)
Time Frame: 24-hour during each study intervention
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The white blood cell count and the count of each white blood cell type will be measured.
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24-hour during each study intervention
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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 1, 2021
Primary Completion (Actual)
December 31, 2022
Study Completion (Actual)
December 31, 2022
Study Registration Dates
First Submitted
September 2, 2021
First Submitted That Met QC Criteria
September 10, 2021
First Posted (Actual)
September 13, 2021
Study Record Updates
Last Update Posted (Estimate)
January 13, 2023
Last Update Submitted That Met QC Criteria
January 12, 2023
Last Verified
January 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202012HM020
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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