- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05097196
Effects of Home Based Step Aerobic Exercises
January 29, 2024 updated by: Yunus Emre Kundakçı, Afyonkarahisar Health Sciences University
Effects of Home Based Step Aerobic Exercises on the Functional Capacity and Physical Performance of Sedentary Young Adults: A Pilot Study
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed 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.
Study Type
Interventional
Enrollment (Actual)
25
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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Afyonkarahisar, Turkey
- Afyonkarahisar Health Science University
-
-
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
18 years to 25 years (Adult)
Accepts Healthy Volunteers
Yes
Description
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 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: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Step Aerobic Group
Step aerobic exercise
|
The exercise intensity of the individual is planned at 50-60% heart rate reserve using the Karvonen method.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional capacity
Time Frame: 10 weeks
|
Six minute walk test (6MWT) distance of the participants will be evaluated using the G-Walk sensor system
|
10 weeks
|
|
Resting heart rate
Time Frame: 10 weeks
|
Resting heart rate measurements are beats per minute taken in the morning
|
10 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Flamingo Balance Test
Time Frame: 10 weeks
|
Static balances of the subjects will be determined with the Flamingo Balance Test.
|
10 weeks
|
|
Quadriceps Strength
Time Frame: 10 weeks
|
Testing will be done at 90 degrees of knee flexion using Mechanical Push/Pull Dynamometer (MPPD) 22 lb (Fabrication Enterprises Inc., USA).
|
10 weeks
|
|
Counter movement jump
Time Frame: 10 weeks
|
The jump parameters of the participants will be evaluated using the G-Walk sensor system (BTS G-Walk BTS Bioengineering Company, Italy).
|
10 weeks
|
|
Exercise motivation
Time Frame: 10 weeks
|
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
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Yunus Emre Kundakci, PhD, Afyonkarahisar Health Sciences 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)
December 30, 2021
Primary Completion (Actual)
May 10, 2022
Study Completion (Actual)
September 20, 2022
Study Registration Dates
First Submitted
September 26, 2021
First Submitted That Met QC Criteria
October 15, 2021
First Posted (Actual)
October 28, 2021
Study Record Updates
Last Update Posted (Actual)
January 30, 2024
Last Update Submitted That Met QC Criteria
January 29, 2024
Last Verified
May 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 2021/439
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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