- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06614075
Diet Quality and Diabetes Risk in Overweight and Obese Adults
The Relationship Between Sociodemographic Characteristics, Lifestyle, and Diet Quality With Diabetes Risk in Overweight and Obese Adults
The goal of this observational study is to learn about the relationship between diabetes risk with sociodemographic characteristics, lifestyle and diet quality in overweight and obese individuals. The main question it aims to answer is:
Is there a relationship between diabetes risk and diet quality in overweight and obese individuals?
Participants who are overweight and obese will answer survey questions about sociodemographic characteristics and lifestyle behaviors. 24 hour dietary recalls will be taken to evaluate diet quality. FINDRISC questionnaire will be applied to assess diabetes risk.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Çubuk
-
Ankara, Çubuk, Turkey, 06760
- Ankara Yıldırım Beyazıt University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Body mass index (BMI) ≥25 kg/m²
Exclusion Criteria:
- Diabetes mellitus
- Psychiatric disorders
- Pregnant and lactating
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Adults
Overweight and obese adults
|
Questionnaire including sociodemographic characteristics, lifestyle habits, body weight, height, dietary assessment and diabetes risk; Anthropometric measurement including waist circumference
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Finnish Diabetes Risk Score (FINDRISC)
Time Frame: Baseline
|
Scores can range from a minimum of 0 to a maximum of 26 points.
According to the FINDRISC scoring system, scores are classified as follows: a score of less than 7 indicates low risk, 7-11 indicates mild risk, 12-14 indicates moderate risk, 15-20 indicates high risk, and a score of less than 20 indicates very high risk.
|
Baseline
|
|
Healthy eating index-2015 (HEI-2015)
Time Frame: Baseline
|
A 24 hour dietary recall was used to assess dietary intake.
Nutrient intake obtained from dietary recalls were evaluated using Ebispro for Windows, Stuttgart, Germany; Turkish Version (BeBiS 9).
The HEI- 2015 and its sub-scores are calculated based on the quantity of food and nutrient intake per 1,000 kilocalories consumed by individuals.
HEI-2015 scores range from a minimum of 0 to a maximum of 100.
Based on the calculated scores, a score greater than 80 indicates good diet quality, a score between 51 and 80 is categorized as moderate diet quality, and a score of 50 or less is defined as poor diet quality.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body weight
Time Frame: Baseline
|
Body weight in kg
|
Baseline
|
|
Height
Time Frame: Baseline
|
Height in cm
|
Baseline
|
|
Sociodemographic characteristics
Time Frame: Baseline
|
number and percentage
|
Baseline
|
|
Lifestyle habits
Time Frame: Baseline
|
number and percentage
|
Baseline
|
|
Waist circumference
Time Frame: Baseline
|
waist circumference in cm
|
Baseline
|
Collaborators and Investigators
Investigators
- Principal Investigator: Rahime E Karakaya, PhD, Ankara Yildirim Beyazıt University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AnkaraYBU-KARAKAYA002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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