跳至主要内容
临床试验/NCT00806559
NCT00806559已完成不适用

SIT Trial: The Effect of Clinical Room Design on the Quality of the Clinical Encounter

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2007年7月1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
发起方
Mayo Clinic
入组人数
60
试验地点
1
主要终点
Patient and Clinician Interaction variables (duration of the encounter, patient sense of control in encounter, patient's ability to access information from the computer monitor and the quality of the verbal and non-verbal interaction).

研究概览

简要总结

The purpose of this study is to improve the clinical encounter through the design of the clinical environment. We will conduct a randomized controlled trial to measure the extent to which a newly designed clinical room, compared to a traditional room, affects the patient-physician interaction. We will judge this outcome by (a) videotaping encounters; and (b) conducting post-visit surveys with patients and an interview with physicians. We will use both qualitative and quantitative tools, including a validated and widely used interaction coding system on the videotapes, to draw inferences from these data.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Double (Participant, Outcomes Assessor)

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

  • •Eligible Clinicians:
  • •In the Department of GIM or Preventive Medicine
  • •Able and Willing to participate in research study.
  • •Eligible patients:
  • •Patient of a clinician participating in the study
  • •18 years or older
  • •Seeing clinician for return/summary visit.

排除标准

  • •1.) Not able to give informed consent.

研究组 & 干预措施

Usual room

Active Comparator

Patients in this arm will see their clinician in the usual clinical exam room

干预措施: Control room (Other)

Re-designed room

Experimental

Patients assigned to this arm will see the physician in a redesigned clinical exam room

干预措施: Re-designed room (Other)

结局指标

主要结局

Patient and Clinician Interaction variables (duration of the encounter, patient sense of control in encounter, patient's ability to access information from the computer monitor and the quality of the verbal and non-verbal interaction).

时间窗: Immediately post clinical visit (survey)

Patient experience of the clinical encounter. The following variables will be measured: patient satisfaction with the room, patient satisfaction with the encounter and the quality of the relationship.

时间窗: Immediately post visit

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other

研究点 (1)

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