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

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

      • Izmir, Turkey, 35620
        • Izmir Katip Çelebi University

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).
Baseline
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
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.

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

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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