- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05027750
Theory-Based Obesity Intervention Program for Women
July 14, 2023 updated by: SEDA GOGER, Sakarya University
Application Of The Theory Of Planned Behavior For Weight Control In Women: A Randomized Controlled Study
The aim of this study is to examine the effect of education and counseling given to women according to the Theory of Planned Behavior on weight management.
This study will be conducted as a single-blind randomized controlled study consisting of intervention and control groups.
A total of 78 overweight and obese women included in the study.
The participants assigned to either of the groups by the block randomization method.
A training program consisting of a total of five sessions applied to the intervention group, and counseling will be provided for 6 months.
The data will be analyzed with Statistical Package for Social Sciences (SPSS) 22.0 package program.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
78
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
-
-
Adapazarı
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Sakarya, Adapazarı, Turkey, 54000
- Sakarya Provincial Directorate of Health
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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
14 years to 45 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Volunteering to participate in the study
- Being a woman in the age group of 18-49 years
- Having a body mass index (BMI) of 25.0-30.0 kg/m2 (overweight) or >30.0 kg/m2 (obese)
- Not going through menopause
- Not having diabetes
- Not having thyroid disease
- Not using hormonal contraceptive pills
- Not having polycystic ovarian disease
- Not having a metabolic disease
- Not having Cushing's syndrome
- Not having a disease that prevents physical activity
- Not having hypertension
- Not being pregnant or breastfeeding
- Owning and using a smart phone
- Having a mail account in Google and being able to use it
Exclusion Criteria:
- Women who do not meet the inclusion criteria
- Not volunteering to participate in the study
- Women with communication problems
- Women who did not give consent at any stage of the study and who quit the study
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
The selected womens were associated with obesity risk factors about obesity (overweight) or obese and between 18-49 years old) and randomly assigned to the experimental group.
Obesity training consisting of a total of five sessions structured according to Theory of Planned Behavior was scheduled for the intervention group.
Each session lasted for approximately 30 minutes.
|
The training to be imparted to the participants was applied online in groups of 5-6 people via the Google Meet program.
Obesity training consisting of a total of five sessions.
Each session lasted for approximately 30 minutes.
After the training given to intervention group, the women will be followed-up for 6 months.
The women in the intervention group will be given counseling service by the researchers, and their status will be evaluated every month.
|
|
No Intervention: Control
The control group of the Randomized Controlled Trial (RCT) was composed of 39 womens (between 18-49 years old) randomly assigned to the control group who are BMI was between 25.0-29.9
or BMI was between ≥30.0 according to the risk rating scales.
A standard obesity training consisting of a single session was scheduled for the control group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Healthy Lifestyle Behaviors-II Scale
Time Frame: 6 months
|
Healthy Lifestyle Behaviors-II Scale aims to measure the health promotion behaviors of individuals.
The scale consists of 52 items.
It is a four-point Likert-type scale (1: "never," 2: "sometimes," 3: "often," and 4: "regularly").
The lowest score that can be obtained is 52, and the highest score is 208.
High scores indicate that the individual practices the specified health behaviors at a high level.
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6 months
|
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International Physical Activity Questionnaire Short Form
Time Frame: 6 months
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International Physical Activity Questionnaire Short Form, the intensity (mild, moderate, and severe) of physical activity is taken into account to accommodate different types of physical activities.
The questionnaire provides information about sitting, walking, and the time spent in moderately intense and vigorous activities.
Vigorous physical activities have a value of 8.0 MET, moderate activities have a value of 4.0 MET, and walking has a value of 3.3 MET.
The minute and frequency (day) values of the relevant activities are multiplied by the MET values.
The total physical activity value is obtained by summing the multiplication values obtained at the last stage.
Accordingly, the physical activity levels of individuals are classified as physically inactive (<600 MET-min/week), low physical activity (600-3000 MET-min/week), and adequate physical activity (health benefits) (>3000 MET-min/week).
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6 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in body mass index
Time Frame: 6 months
|
Weight and height will be combined to report BMI in kg/m^2.
The change in body mass index will be evaluated.
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6 months
|
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Change in waist/hip ratio
Time Frame: 6 months
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Waist and hip will be combined to report Waist/Hip in cm.
The change in waist/hip ratio will be evaluated
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6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
April 5, 2021
Primary Completion (Actual)
June 18, 2021
Study Completion (Actual)
December 24, 2021
Study Registration Dates
First Submitted
August 11, 2021
First Submitted That Met QC Criteria
August 25, 2021
First Posted (Actual)
August 30, 2021
Study Record Updates
Last Update Posted (Actual)
July 17, 2023
Last Update Submitted That Met QC Criteria
July 14, 2023
Last Verified
August 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 162146620500104273
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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