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临床试验/NCT00669188
NCT00669188已完成不适用

Patient-Provider Communication and Interaction in a Virtual Clinical Setting

National Human Genome Research Institute (NHGRI)1 个研究点 分布在 1 个国家目标入组 326 人开始时间: 2008年4月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
326
试验地点
1
主要终点
treatment recommendations

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •INCLUSION CRITERIA:
  • •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).

排除标准

  • •persons with seizure or vestibular disorders; 2) women with known pregnancy; 3) persons who are highly prone to motion sickness; 4) those with low, uncorrected vision or hearing; 5) all current and past employees and contractors of
  • •NHGRI; and 6) persons who have received information about the study purpose or procedure from a past participant.

研究组 & 干预措施

Information Type 1

Experimental

genetic risk information

干预措施: Information (Other)

Information Type 2

Sham Comparator

information absent

干预措施: Information absent (Other)

结局指标

主要结局

treatment recommendations

时间窗: at time of study

recommendations made for the virtual patient's treatment

次要结局

未报告次要终点

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (1)

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