- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06282276
Anti-fat Attitudes and Weight Stigma Among Orthopedic Surgeons
February 20, 2024 updated by: Hillel Yaffe Medical Center
Anti-fat Attitudes and Weight Stigma Among Orthopedic Surgeons and Their Correlation to the Therapeutic Approach to Patients With Obesity
Evidence shows that anti-fat attitudes and weight stigma are prevalent among healthcare professionals and may affect treatment decisions regarding patients with obesity.
The present study aimed to examine the presence of anti-fat attitudes and weight stigma among orthopedic surgeons and their correlation to the therapeutic approach to patients with obesity.
In this cross-sectional survey, 150 orthopedic surgeons will complete a web-based questionnaire. the questionnaire is based on Antifat Attitudes Questionnaire (AFA), developed by Crandall in 1994.
In addition, the questionnaire will include a questionnaire developed by Bocquier in 200521 to explore weight stigma among physicians.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Data will be collected through an online questionnaire consisting of four parts.
Part 1 will gather socio-demographic data using nine items.
Part 2 will utilize the Antifat Attitudes Questionnaire (AFA), developed by Crandall in 1994.
The questionnaire, comprising 13 items, will assess three subscales:1.
"Dislike" measuring explicit antipathy toward fat individuals.2.
"Fear of Fat" measuring personal concerns about weight or becoming overweight.3.
"Willpower" measuring beliefs about personal control over being overweight.
Participants will rate items on a 10-point Likert scale, with higher scores indicating greater anti-fat bias.
Part 3 will include a questionnaire developed by Bocquier in 2005 to explore weight stigma among physicians, consisting of 12 items.
Participants will rate items on a 6-point Likert scale, with higher scores indicating stronger weight stigma.
Part 4 will investigate the therapeutic approach of orthopedic surgeons to patients with obesity using five items.
Participants will items on a 6-point Likert scale, with higher scores indicating a stronger preference for a conservative approach.
Study Type
Observational
Enrollment (Actual)
150
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
-
-
-
Hadera, Israel, 38000
- Hillel Yaffe Medical Center
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
150 orthopedic surgeon's
Description
Inclusion Criteria: orthopedic surgeon age 18 till 80 -
Exclusion Criteria:
-
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 |
|---|---|---|
|
anti fat attitudes
Time Frame: 3 months
|
Orthopedic surgeons' personal beliefs about weight
|
3 months
|
|
Weight stigma
Time Frame: 3 months
|
Orthopedic surgeons' personal beliefs about weight
|
3 months
|
|
Therapeutic approach
Time Frame: 3 months
|
Orthopedic surgeons' magnitude of preference for a conservative approach when treating patients with obesity
|
3 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)
October 1, 2022
Primary Completion (Actual)
January 1, 2023
Study Completion (Actual)
January 1, 2023
Study Registration Dates
First Submitted
February 5, 2024
First Submitted That Met QC Criteria
February 20, 2024
First Posted (Actual)
February 28, 2024
Study Record Updates
Last Update Posted (Actual)
February 28, 2024
Last Update Submitted That Met QC Criteria
February 20, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 012922HYMC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
Research data may be available on a reasonable request
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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