- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06624111
Assessing Weight Bias Among Turkish Dietitians
October 1, 2024 updated by: Ezgi Bellikci Koyu
Assessing Weight Bias Among Turkish Dietitians: Determinants and Impact on Professional Practice
The objective of this study was to examine weight bias among Turkish dietitians.
and to investigate the effect of the patient's weight status on the dietitian's assessment and dietetic practice.
Study Overview
Status
Completed
Conditions
Detailed Description
The dietitians were randomly assigned to an online case study with lactose intolerance, with all patient information identical except for the patient's weight and photograph.
In one case there was a photograph of a woman with obesity and in the other a woman of normal weight.
The objective of the case study was to evaluate how the body weight of a patient who consulted a dietitian for a reason unrelated to the body weight affected professional practices.
Study Type
Observational
Enrollment (Actual)
411
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
-
-
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Izmir, Turkey, 35620
- Izmir Katip Çelebi University
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
The study sample consisted of dietitians working Türkiye
Description
Inclusion Criteria:
- Dietitians working in Turkiye
Exclusion Criteria:
- Pregnancy
- breastfeeding
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
Cohorts and Interventions
Group / Cohort |
|---|
|
Picture belong to a patient with obesity
Dietitians were randomly assigned to a case study via SurveyMonkey.
All the information (demographics, biochemical parameters and diet history physical activity level) about the cases was the same, only their weight and, therefore, their photographs were different.
In this case there was a photograph of a woman with obesity
|
|
Picture belong to a patient with normal-weight
Dietitians were randomly assigned to a case study via SurveyMonkey.
All the information (demographics, biochemical parameters and diet history physical activity level) about the cases was the same, only their weight and, therefore, their photographs were different.
In this case there was a photograph of a woman with normal weight.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Differences between dietitians' lifestyle recommendations among groups.
Time Frame: Baseline
|
Dietitians' recommendations lifestyle recommendations (such as dietary intake of energy and macronutrients) were assessed using a 5-point Likert-type scale (1; should be greatly reduced, 5; should be greatly increased).
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Differences between the biochemical status rated by dietitians between groups
Time Frame: Baseline
|
Dietitians rated the biochemical status of the case with a 5-point Likert type scale (1; very good, 5; very poor).
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Baseline
|
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Differences between the diet quality rated by dietitians between groups
Time Frame: Baseline
|
Dietitians rated the diet quality of the case with a 5-point Likert type scale (1; very good, 5; very poor).
|
Baseline
|
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Differences between dietatians' expectations regarding the patient's adherence to the diet between groups
Time Frame: Baseline
|
Dietatians' expectations regarding the patient's adherence to the diet were assessed using the statements "the patient is willing to be treated", "the patient is expected to comply with the treatment recommendations", "the patient will be successful in making dietary changes", "the patient will be able to sustain recommendations", "the patient understood treatment recommendations".
A 5-point Likert type scale (1; strongly disagree, 5; strongly agree) was used to rate these statements.
|
Baseline
|
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)
August 10, 2021
Primary Completion (Actual)
November 30, 2021
Study Completion (Actual)
November 30, 2021
Study Registration Dates
First Submitted
September 30, 2024
First Submitted That Met QC Criteria
October 1, 2024
First Posted (Actual)
October 2, 2024
Study Record Updates
Last Update Posted (Actual)
October 2, 2024
Last Update Submitted That Met QC Criteria
October 1, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1919B012005303
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
All IPD that underlie results in a publication
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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