- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06123273
The Effect of Exercise-Oriented Training on Physical Activity Level and Exercise Awareness in Overweight and Obese Women
November 7, 2023 updated by: Yasemin Cayir, Ataturk University
The Effect of Exercise-Oriented Training on Physical Activity Level and Exercise Awareness in Overweight and Obese Women: A Randomized-Controlled Trial
This study aimed to investigate the effect of an exercise-oriented training on physical activity level and exercise awareness in overweight and obese women.
Participants will randomized into intervention group (IG) and control group (CG) and followed-up for three months.
The International Physical Activity Questionnaire Short Form (IPAQ) will be applied to both groups at the beginning and end of the study to determine the level of physical activity, and the Exercise Health Belief Model Scale (EHBM) will be applied to evaluate the exercise awareness level, and anthropometric measurements (weight, body mass index, waist circumference) will recorded.
The CG will receive no other interventions other than routine recommendations.
The IG will be given face-to-face training to increase exercise awareness along with routine recommendations after the first meeting, and they will be contacted by phone every two weeks for three months.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Obesity and insufficient physical activity are among the most important health problems of today.
Both obesity and physical inactivity are risk factors for many chronic diseases.
This study aimed to investigate the effect of an exercise-oriented training on physical activity level and exercise awareness in overweight and obese women.
Participants (n=112) were randomized into intervention group (IG) and control group (CG) and followed-up for three months.
The International Physical Activity Questionnaire Short Form (IPAQ) was applied to both groups at the beginning and end of the study to determine the level of physical activity, and the Exercise Health Belief Model Scale (EHBM) was applied to evaluate the exercise awareness level, and anthropometric measurements (weight, body mass index, waist circumference) were recorded.
The CG received no other interventions other than routine recommendations.
The IG was given face-to-face training to increase exercise awareness along with routine recommendations after the first meeting, and they were contacted by phone every two weeks for three months.
Study Type
Interventional
Enrollment (Actual)
112
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
-
-
-
Erzurum, Turkey, 25040
- Ataturk University Hospital
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- BMI 25-34.9 g/m2
- Female
- Turkish
Exclusion Criteria:
- Individuals with disabilities to exercise
- pregnant/breastfeeding women
- Individuals with Stage 2-3 obesity (BMI >35 kg/m2)
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention group
The intervention group was given an exercise-oriented training
|
IG received an exercise-oriented training with a 20-minute presentation including graphics, in line with clinical guidelines, in addition to routine recommendations.
The training included information about the benefits of exercise and the harms of a sedentary life, the relationship between exercise and chronic diseases, suggestions to have a more active lifestyle and on how to exercise, the duration and form of exercise necessary for a healthy life, and the things to be considered while exercising.
During the three-month follow-up, the subjects in the IG were called every two weeks to ask about their weight measurements, their level of exercise, and how much they walked.
The subjects' questions, if any, were answered, and the interview was completed by making exercise suggestions.
Other Names:
|
No Intervention: Control group
The control group was given only routine recommendations
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The International Physical Activity Questionnaire Short Form was used to determine the physical activity level at the beginning and end of the study
Time Frame: 3 months
|
The International Physical Activity Questionnaire Short Form was used to determine the physical activity level at the beginning and end of the study.
The minimum score is <600 Maximal Exercise Test (MET) -minute/week while the maximum score is >3000 MET-minute/week .
High score means high exercise belief.
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Exercise Health Belief Model Scale
Time Frame: 3 months
|
Exercise Health Belief Model Scale was used to evaluate the exercise awareness levels of all participants.
The minimum score is 25 while the maximum score is 125.
High score means high exercise belief.
|
3 months
|
Anthropometric measure
Time Frame: 3 months
|
Body Mass Index was used as an anthropometric measurement.
All of the participants were recorded .
It is measured as weight in kilograms divided by height in meters squared.
|
3 months
|
Body fat
Time Frame: 3 months
|
body fat percentage were recorded.
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Zehranur Kacar, Ataturk 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)
August 1, 2021
Primary Completion (Actual)
February 1, 2022
Study Completion (Actual)
March 1, 2022
Study Registration Dates
First Submitted
September 5, 2023
First Submitted That Met QC Criteria
November 7, 2023
First Posted (Estimated)
November 8, 2023
Study Record Updates
Last Update Posted (Estimated)
November 8, 2023
Last Update Submitted That Met QC Criteria
November 7, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TTU-2021-9585
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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