- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04209647
A Comparison of Continuous Moderate Training and Reduced High Intensity Interval Training in Obese Young Adults
July 28, 2020 updated by: Yasemin Çırak, Istinye University
A Comparison of Reduced HIIT and Moderate Intensity Continuous Exercise in Obese Young Adults
Exercise is a key component of obesity management.
Obese subjects cannot attend or sustain exercise program because of increased general fatigue, dyspnea and muscle fatigue.
And they feel more exertion when comparing with normal weight subjects.
Reduced-exertion high-intensity interval training (REHIT) is a alternative method to continuous exercise programs.
The investigators aimed comparing metabolic effects of REHIT and continuous exercise in young adults, in this study.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
24
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
-
-
-
Istanbul, Turkey
- Istınye 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
16 years to 20 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Between the ages of 18-22,
- BMI ≥ 30,
- Female gender,
Exclusion Criteria:
- Smoking history,
- Having any metabolic disease except obesity,
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Continuous Exercise
At %60 of maximal heart rate, 30-60 minutes exercise
|
At %50 of maximum heart rate, 30-60 minutes aerobic exercise
|
Experimental: REHIT Exercise
At %100 of heart rate 15 seconds, after this period 15 sec recovery period for all step
|
-Start with warm-up period --> %50 of maximum work rate, 3 minutes One Exercise Cycle consists of:
Total Duration: 10 minutes |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Aerobic Capacity
Time Frame: 1 year
|
Maximum Oxygen Uptake
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Total Exercise Duration
Time Frame: 1 year
|
Exercise Test Duration
|
1 year
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Body Fat Percentage
Time Frame: 1 year
|
Total Body Fat Percentage
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Nurgul Durustkan Elbasi, PhD, Istinye University
- Study Chair: Yunus Emre Tutuneken, PT, Istinye University
- Principal Investigator: Yasemin Cirak, Ass Prof, Istınye U
- Study Chair: Duygu Korkem, PhD, University of Health science
- Study Chair: Beyza Karaduz, MsC, Hacettepe University
- Study Chair: Ebru Calik Kutukcu, PhD, Hacettepe 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)
May 1, 2018
Primary Completion (Actual)
April 1, 2019
Study Completion (Actual)
August 1, 2019
Study Registration Dates
First Submitted
December 20, 2019
First Submitted That Met QC Criteria
December 23, 2019
First Posted (Actual)
December 24, 2019
Study Record Updates
Last Update Posted (Actual)
July 30, 2020
Last Update Submitted That Met QC Criteria
July 28, 2020
Last Verified
July 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- 0004
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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