Weight Management Interactions in a Virtual Clinical Environment

Sponsor
National Human Genome Research Institute (NHGRI) (NIH)
Overall Status
Completed
CT.gov ID
NCT01443910
Collaborator
(none)
318
1

Study Details

Study Description

Brief Summary

This study is part of an effort to learn about interactions between doctors and patients. We aim to understand how women feel about techniques that doctors use to talk with patients about their weight. We are studying women s reactions to these techniques using a virtual reality version of a doctor s office to create as realistic a model of a doctor s visit as possible. This can help us better understand what happens during real doctor s visits.

Women between the ages of 20 and 50 who are currently overweight may be eligible for this study. Participants will be recruited from the Washington D.C. area. This is not a weight treatment study.

Participants undergo the following procedures:
  • Complete an online questionnaire about themselves, their experiences, and their thoughts about their weight

  • Participate in activities in a virtual reality environment in which they interact with a virtual doctor in a virtual clinical scenario. For this experiment, participants wear a head-mounted display that allows them to see the virtual world images.

  • Fill out a questionnaire after completing the virtual reality activities. This questionnaire includes information on the participants' virtual reality experience, the information provided in the experience, and additional questions about themselves and their thoughts.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The primary goal of this research project is to build an evidence base related to primary care encounters that include discussions about a patient s body weight. We are particularly interested in how encounters impact patients health-related and weight-related attitudes and beliefs. Furthermore, this project aims to determine how a physician s approach to the health care encounter impacts its outcome.

    The current study is a controlled experiment in which participants will be participate in a weight counseling encounter with a virtual reality-based doctor. The virtual doctor will present weight etiology information. Participants will fill out a self-report questionnaire online, prior to this encounter. They will then come in to the Immersive Virtual Environment Testing Area in the NIH Clinical Center for a visit. During this visit, they will engage in the interaction with the virtual doctor and then fill out a post-test questionnaire. Participants in the main trial will include approximately 222 healthy adult females between 20-50 years of age who have a BMI of greater than or equal to 25 and are dissatisfied with their current weight.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    318 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Weight Management Interactions in a Virtual Clinical Environment
    Actual Study Start Date :
    Feb 29, 2012

    Arms and Interventions

    Arm Intervention/Treatment
    behavior, supportive

    receiving information about behavior with supportive provider communication

    behaviors, directive

    receiving information about behavior with directive provider communication

    genetics, directive

    receiving information about genetics with directive provider communication

    genetics, supportive

    receiving information about genetics with supportive provider communication

    Outcome Measures

    Primary Outcome Measures

    1. attitudes, beliefs, and behavior [cross-sectional]

      self-report outcomes

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 50 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    • INCLUSION CRITERIA:
    1. being between 20 and 50 years old

    2. having a self-reported body mass index of greater than or equal to 25

    3. having the ability to read, write, and converse in English

    4. being able to come to the NIH Clinical Center for one visit

    EXCLUSION CRITERIA:
    1. having a vestibular or seizure disorder

    2. having a high propensity for motion sickness

    3. known pregnancy

    4. uncorrected low vision or hearing

    5. inability to complete tasks in the virtual environment

    6. being an NHGRI employee

    7. being or training to become a health care provider

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda Maryland United States 20892

    Sponsors and Collaborators

    • National Human Genome Research Institute (NHGRI)

    Investigators

    • Principal Investigator: Susan Persky, Ph.D., National Human Genome Research Institute (NHGRI)

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    National Human Genome Research Institute (NHGRI)
    ClinicalTrials.gov Identifier:
    NCT01443910
    Other Study ID Numbers:
    • 110238
    • 11-HG-0238
    First Posted:
    Sep 30, 2011
    Last Update Posted:
    Aug 25, 2022
    Last Verified:
    Feb 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by National Human Genome Research Institute (NHGRI)
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 25, 2022