Patient Provider Communication and Interaction in a Virtual Clinical Setting
Patient-Provider Communication and Interaction in a Virtual Clinical Setting
2 other identifiers
interventional
326
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2008
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 24, 2008
CompletedFirst Submitted
Initial submission to the registry
April 29, 2008
CompletedFirst Posted
Study publicly available on registry
April 30, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 8, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
July 8, 2020
CompletedAugust 12, 2024
January 9, 2024
12.2 years
April 29, 2008
August 9, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
treatment recommendations
recommendations made for the virtual patient's treatment
at time of study
Study Arms (2)
Information Type 1
EXPERIMENTALgenetic risk information
Information Type 2
SHAM COMPARATORinformation absent
Interventions
Eligibility Criteria
You may qualify if:
- Healthy adult volunteers who are third or fourth-year medical students. Both men and women over age 18 will be eligible for this study (though in practice the age range is likely to naturally be constrained by the typical age of medical students).
You may not qualify if:
- NHGRI; and 6) persons who have received information about the study purpose or procedure from a past participant.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Related Links
Study Officials
- PRINCIPAL INVESTIGATOR
Susan Persky, Ph.D.
National Human Genome Research Institute (NHGRI)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- BASIC SCIENCE
- Intervention Model
- FACTORIAL
- Sponsor Type
- NIH
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 29, 2008
First Posted
April 30, 2008
Study Start
April 24, 2008
Primary Completion
July 8, 2020
Study Completion
July 8, 2020
Last Updated
August 12, 2024
Record last verified: 2024-01-09