- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04177784
Web Based Intervention to Reduce Weight Bias Among Dietitians
January 7, 2020 updated by: Emily Dhurandhar, Texas Tech University
Weight bias in dietitians is prevalent and may affect patient care.
The investigators conducted a randomized controlled trial to test if explicit and implicit bias could be influenced by a short, 20 minute educational video.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
This randomized controlled trial studied the effect of three different videos on weight bias in a nationally representative sample of dietitians.
The "intervention" group (I) watched a video about the etiology of obesity, reasons for weight regain, and how to talk to patients about weight.
The first "control" group (C1) received information about the role of the environment and individual behavior in weight gain, and tools to help patients control their weight.
The second control group (C2) received a weight neutral video about the role of dieticians in society.
Bias measures were taken before and just after watching the video, and again one month later.
Study Type
Interventional
Enrollment (Actual)
166
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
-
-
Texas
-
Lubbock, Texas, United States, 79409
- Texas Tech 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
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Any dietitian in the Clinical Dietitian Registry Database.
Exclusion Criteria:
- None
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention (I)
This arm was randomized to a 20 min video that emphasized information about factors other than individual behaviors that influence weight, weight loss and ability to maintain weight.
It also indirectly addressed weight bias by explaining how to have conversation about weight and health with a patient with obesity that is free of biases.
|
The videos were developed by the researchers based on a prior study to test if specific information about obesity and weight control influence weight bias.
|
Active Comparator: Weight Control (C1)
This arm was randomized to a 20 min video that emphasized the controllable aspects of weight and gave dietitians an overview of a tool to help plan and monitor weight loss.
|
The videos were developed by the researchers based on a prior study to test if specific information about obesity and weight control influence weight bias.
|
Placebo Comparator: Weight Neutral Control (C2)
The arm was randomized to a 20 min video about the role dietitians play in society, that made no mention of weight or obesity.
|
The videos were developed by the researchers based on a prior study to test if specific information about obesity and weight control influence weight bias.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in "Blame" explicit bias
Time Frame: Change from pre to immediately post intervention (1 hour)
|
"Blame" subscore of Anti-fat Attitudes Test, higher score means more bias
|
Change from pre to immediately post intervention (1 hour)
|
Change in "Blame" explicit bias
Time Frame: Change from pre to 1 month post intervention
|
"Blame" subscore of Anti-fat Attitudes Test, higher score means more bias
|
Change from pre to 1 month post intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in "Social" explicit bias
Time Frame: Change from pre to immediately post intervention (1 hour)
|
"Social" subscore of Anti-fat Attitudes Test, higher score means more bias
|
Change from pre to immediately post intervention (1 hour)
|
Change in "Social" explicit bias
Time Frame: Change from pre to 1 month post intervention
|
"Social" subscore of Anti-fat Attitudes Test, higher score means more bias
|
Change from pre to 1 month post intervention
|
Change in "Physical" explicit bias
Time Frame: Change from pre to immediately post intervention (1 hour)
|
"Physical" subscore of Anti-fat Attitudes Test, higher score means more bias
|
Change from pre to immediately post intervention (1 hour)
|
Change in "Physical" explicit bias
Time Frame: Change from pre to 1 month post intervention
|
"Physical" subscore of Anti-fat Attitudes Test, higher score means more bias
|
Change from pre to 1 month post intervention
|
Change in Implicit Bias
Time Frame: Change from pre to immediately post intervention (1 hour)
|
Category of bias from Weight Implicit Association Test; Categories 1-4, higher category means more bias
|
Change from pre to immediately post intervention (1 hour)
|
Change in Implicit Bias
Time Frame: Change from pre to 1 month post intervention
|
Category of bias from Weight Implicit Association Test; Categories 1-4, higher category means more bias
|
Change from pre to 1 month post intervention
|
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)
May 1, 2019
Primary Completion (Actual)
August 8, 2019
Study Completion (Actual)
August 8, 2019
Study Registration Dates
First Submitted
November 22, 2019
First Submitted That Met QC Criteria
November 25, 2019
First Posted (Actual)
November 26, 2019
Study Record Updates
Last Update Posted (Actual)
January 10, 2020
Last Update Submitted That Met QC Criteria
January 7, 2020
Last Verified
January 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB2019-321
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
We have a primary and secondary analysis planned for these data, once they are both published we will share the data within 6 months time via ICSPR database.
IPD Sharing Time Frame
Within 6 months of publication, data will be available.
IPD Sharing Access Criteria
Public Access Database.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
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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