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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06031675
Other study ID # K0001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 12, 2023
Est. completion date September 1, 2023

Study information

Verified date September 2023
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this clinicaltrial is to assess and compare isokinetic performance, surface electromyography, laboratory parameters, and cardiorespiratory function both before and after engaging in vigorous intermittent lifestyle physical activity(VILPA) within a healthy population. The main question it aims to answer is: [1] Does VILPA yield effective outcomes? Throughout the course of the trial, participants will engage in a simulated regimen of vigorous intermittent lifestyle physical activity for a duration of 8 weeks. The efficacy of the exercise protocol will be quantified and evaluated through the utilization of a wearable device.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date September 1, 2023
Est. primary completion date July 10, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Healthy Adults 2. No exercise habits (more than 3 months) Exclusion Criteria: 1. Exercising = 3 times per week; 2. the presence of chronic diseases, such as hypertension, hyperglycemic states, etc; 3. have conducted an exercise program in the past three months.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Vigorous intermittent lifestyle physical activity
The specific exercise regimen involves performing rope jumping activities three times a day, with each session aimed at surpassing the exercise threshold (not conducted in a continuous manner), where the heart rate should exceed 160 beats per minute. This routine will be undertaken five times a week, continuously for a span of 8 weeks.

Locations

Country Name City State
China Guangdong Pharmaceutical University Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Xiao-dong Zhuang

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Isometric Strength Test Isokinetic muscle strength testing with the Isomed 2000 15 minutes
Primary Surface electromyography 30 minutes
Primary Exercise Flat Test cardiopulmonary function 30 minutes
Secondary Fasting glucose 5 minutes
Secondary Blood lipid 5 minutes
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