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

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

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.

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.

Clinical Trials on Intervention Video (I)

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