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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05051306
Other study ID # 202011HM005
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 18, 2021
Est. completion date December 31, 2021

Study information

Verified date March 2022
Source National Taiwan Normal University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 11
Est. completion date December 31, 2021
Est. primary completion date March 7, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 30 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
High-load resistance exercise
Subjects in high-load trial performed 4 sets per exercise, 8 repetitions with load of 85%-8RM with 90 sec of rest between sets.
Low-load resistance exercise
Subjects in low-load trial performed 4 sets per exercise, 15 repetitions with load of 45%-8RM with 90 sec of rest between sets.

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 glucose glucose in mg/dL 4-hour during each study intervention
Primary Changes in insulin insulin in mU/L 4-hour during each study intervention
Primary Changes in TG TG mg/dL 4-hour during each study intervention
Primary Changes in uric acid uric acid mg/dL. 4-hour during each study intervention
Secondary Changes in biomarkers of inflammation 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
Secondary Changes in cortisol cortisol in ng/mL 4-hour during each study intervention
Secondary Changes in lactate lactate in mmol/L 4-hour during each study intervention
Secondary Changes in complete blood count blood cell count in count per µL 4-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
Secondary Changes in ET-1 ET-1 in pg/mL 4-hour during each study intervention
Secondary Changes in NO NO in µmol/L 4-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. 4-hour during each study intervention
Secondary Heart rate (HR) HR will be measured during each study intervention. 6-hour during each study intervention
Secondary Visual Analogue Scale (VAS) of appetite 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
Secondary Changes in biomarkers of appetite Biomarkers of appetite will be measured such as ghrelin in pg/mL and PYY in pg/mL. 4-hour during each study intervention
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