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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05042167
Other study ID # 202012HM020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2021
Est. completion date December 31, 2022

Study information

Verified date January 2023
Source National Taiwan Normal University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 80 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Resistance exercise
4 total resistance exercises that target all major muscle groups.

Locations

Country Name City State
Taiwan National Taiwan Normal University Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan Normal University

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in biomarkers of inflammation Biomarkers of inflammation will be measured such as IL-10 in pg/mL, IL-6 in pg/mL, TNF-a in pg/mL. 24-hour during each study intervention
Secondary Changes in glucose glucose in mg/dL 24-hour during each study intervention
Secondary Changes in metabolic parameters Metabolic parameters will be measured such as TC in mg/dL, TG in mg/dL, and HDL in mg/dL. 24-hour during each study intervention
Secondary Changes in biomarkers of muscle damage Biomarkers of muscle damage will be measured such as CK in U/L and LDH in U/L. 24-hour during each study intervention
Secondary Changes in molecular markers in peripheral blood mononuclear cells (PBMC) 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. 24-hour during each study intervention
Secondary Changes in complete blood count (CBC) The white blood cell count and the count of each white blood cell type will be measured. 24-hour during each study intervention
Secondary Borgs Ratings of Perceived Exertion (RPE) 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
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