- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04955769
Body Image, Self-stigma, Intuitive Eating and Exercise Behavior in Overweight and Obese
June 30, 2021 updated by: Nur Elcin Boyacıoglu, Istanbul University - Cerrahpasa (IUC)
Investigation of Body Image, Self-stigma, Intuitive Eating and Exercise Behavior in Overweight and Obese
This study, it was aimed to investigate the relationship between body image, self-stigma, intuitive eating and exercise attitude levels, which are thought to be effective on the mental well-being of overweight and obese individuals.
For this purpose, the Body Image Scale, Intuitive Eating Scale-2, Exercise Stages of Change Scale-Short Form and Decisional Balance Scale in Exercise will be used to assess overweight and obese individuals.
100 people will be included in the study.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nur Elçin Boyacıoğlu, Assist Prof
- Phone Number: +905054949960
- Email: nur.boyacioglu@istanbul.edu.tr
Study Contact Backup
- Name: Nilay Arman, Assist Prof
- Phone Number: +905534558707
- Email: saimenilayarman@istanbul.edu.tr
Study Locations
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Kadıköy
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Istanbul, Kadıköy, Turkey, 34714
- DiyeTat-Beslenme ve Danışmanlık
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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 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Overweight and obese individuals between the ages of 18-65 will be included in the study.
Description
Inclusion Criteria:
- Individuals aged between 18-65
- BMI ≥30 kg/m2,
- No surgical operation in the last 6 months
Exclusion Criteria:
- Musculoskeletal disorders or systemic diseases that may prevent exercise
- The presence of psychiatric or neurological disease affecting cooperation and cognitive functions
- Presence of acute pain
- Heart pain
- Presence of previous myocardial infarction, subjective heart failure, uncontrolled diabetes and hypertension
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body Image Scale
Time Frame: Baseline
|
It was developed by Secord and Jourand in 1953, and was adapted to Turkish society after being validated and reliable by Hovardaoğlu in 1989.
The scale includes 40 items and each item is related to an organ or a part of the body (such as arm, leg, face) or a function (such as sexual activity level).
|
Baseline
|
|
Intuitive Eating Scale-2
Time Frame: Baseline
|
The Intuitive Eating Scale-2 was developed by Tylka and Kroon Van Diest (2013) to measure intuitive eating behaviors.
The scale consists of 21 questions and four sub-titles.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exercise Stages of Change Scale-Short Form
Time Frame: Baseline
|
This 5-optioned scale evaluates the changes of exercise behavior of participants in five stages of pre contemplation, contemplation, preparation, action, and consistency.
Participants have to select one of the 5 options that evaluate the intention to participate in physical activity and sports now and in the future.
|
Baseline
|
|
Decisional Balance Scale in Exercise
Time Frame: Baseline
|
The scale is used to measure the individual decision to exercise with 10 questions designed to evaluate exercise beliefs (positive beliefs and obstacles).
Participants are asked to choose on a 5-point Likert scale, in what way important every statement was with respect to their intentions to exercise, or not.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Nur Elçin Boyacıoğlu, Assist Prof, Istanbul Universitesi-Cerrahpasa
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 (ANTICIPATED)
August 1, 2021
Primary Completion (ANTICIPATED)
September 15, 2021
Study Completion (ANTICIPATED)
October 1, 2021
Study Registration Dates
First Submitted
June 30, 2021
First Submitted That Met QC Criteria
June 30, 2021
First Posted (ACTUAL)
July 9, 2021
Study Record Updates
Last Update Posted (ACTUAL)
July 9, 2021
Last Update Submitted That Met QC Criteria
June 30, 2021
Last Verified
June 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IstanbulUC9325
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.