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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05097196
Other study ID # 2021/439
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 30, 2021
Est. completion date September 20, 2022

Study information

Verified date May 2023
Source Afyonkarahisar Health Sciences University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine the effects of commercially produced new generation smart step board and step-aerobic exercises for 6 weeks on the functional capacity and physical performance of young sedentary individuals.


Description:

The aim of this study is to determine the effects of commercially produced new generation smart step board and step-aerobic exercises for 6 weeks on the functional capacity and physical performance of young sedentary individuals. The primary outcomes to be evaluated are the functional improvements in individuals' balance, functional capacity, muscle strength, and resting heart rate after 6 weeks of step-aerobic exercises. Secondary results are the evaluation of the effects of individuals on jumping performance and exercise motivation. It is thought that the results obtained in the study will reveal new information for studies investigating home-based exercise and rehabilitation practices and may provide evidence for larger studies involving a diagnosis of a disease in the future.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date September 20, 2022
Est. primary completion date May 10, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria: - Not participating in an exercise program that is followed regularly for at least 6 months - Able to use a wearable device and willing to regularly step aerobic exercise - In possession of a smart phone, tablet or computer - BMI 25 to 40 kg/m2 Exclusion Criteria: - Severe concomitant diseases: chronic heart failure, liver cirrhosis, kidney failure, active cancer, and cardiovascular, orthopedic, neurological psychological other diseases - Not continuing the exercise program for more than three - Loss of balance due to loss of consciousness or dizziness in the last 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Moderate-intensity aerobic activities
The exercise intensity of the individual is planned at 50-60% heart rate reserve using the Karvonen method.

Locations

Country Name City State
Turkey Afyonkarahisar Health Science University Afyonkarahisar

Sponsors (1)

Lead Sponsor Collaborator
Afyonkarahisar Health Sciences University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Functional capacity Six minute walk test (6MWT) distance of the participants will be evaluated using the G-Walk sensor system 10 weeks
Primary Resting heart rate Resting heart rate measurements are beats per minute taken in the morning 10 weeks
Secondary Flamingo Balance Test Static balances of the subjects will be determined with the Flamingo Balance Test. 10 weeks
Secondary Quadriceps Strength Testing will be done at 90 degrees of knee flexion using Mechanical Push/Pull Dynamometer (MPPD) 22 lb (Fabrication Enterprises Inc., USA). 10 weeks
Secondary Counter movement jump The jump parameters of the participants will be evaluated using the G-Walk sensor system (BTS G-Walk BTS Bioengineering Company, Italy). 10 weeks
Secondary Exercise motivation Motivation will be measured after exercise using a visual analog scale consisting of a 100 mm line. Individuals will mark on the line how motivated they are during exercise. Motivation points will be obtained by measuring the distance from zero to point o 10 weeks
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