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Clinical Trials/NCT00669188
NCT00669188
Completed
Not Applicable

Patient-Provider Communication and Interaction in a Virtual Clinical Setting

National Human Genome Research Institute (NHGRI)1 site in 1 country326 target enrollmentApril 24, 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy Volunteer
Sponsor
National Human Genome Research Institute (NHGRI)
Enrollment
326
Locations
1
Primary Endpoint
treatment recommendations
Status
Completed
Last Updated
last year

Overview

Brief Summary

Summary:

A few studies have explored factors which influence patient-provider communication in a controlled setting. However, more information is needed about how different factors affect communication so that it can be improved.

Third- and fourth-year medical students may be eligible for this study. Participants are recruited from the Washington, D.C. area.

At the research center, participants will use a virtual reality headset to view a virtual clinic environment and interact with a virtual patient.

After interacting with the virtual patient, participants will complete a questionnaire about their experience within the virtual clinic and other research-related information.

The total time for the study visit is 60 minutes.

Eligibility:

Third- and fourth-year medical students at least 18 years of age. You may not take part in the study if you have a history of seizures and/or are pregnant.

Detailed Description

This study will investigate research questions regarding factors influencing patient-provider communication. Participants will interact with a virtual patient in a virtual clinical setting. Third- or fourth-year medical students may be eligible for this study. Participants are recruited from the Washington, D.C. area. Study participants will perform one task and complete one set of questions at the study appointment. The task involves viewing a virtual patient s health information and interacting with the virtual patient in a virtual environment clinical scenario. While in the virtual environment, the subject wears a head-mounted video unit that allows him or her to see elements of the environment. The activities in the virtual environment take about 15 minutes. The total time for the study is about 60 minutes.

Registry
clinicaltrials.gov
Start Date
April 24, 2008
End Date
July 8, 2020
Last Updated
last year
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

treatment recommendations

Time Frame: at time of study

recommendations made for the virtual patient's treatment

Study Sites (1)

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