跳至主要内容
临床试验/NCT07089953
NCT07089953招募中不适用

Patient Perception of Physician's Compassion, Communication Skills, and Professionalism During Clinic Visits: a Randomized Controlled Trial (EHR Study #3)

M.D. Anderson Cancer Center2 个研究点 分布在 1 个国家目标入组 88 人开始时间: 2026年8月3日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
88
试验地点
2
主要终点
Questionnaires/Videos

研究概览

简要总结

To learn about how patients view a doctor's compassion, communication skills, and professionalism based on whether the doctor uses the Electronic Health Record (EHR) during a visit with a patient.

详细描述

Primary Objectives 1. To compare participants' perception of physicians' compassion after they watch two scripted-video vignettes of physicians: one portraying a traditional face to face clinical visit without the use of examination room computer, and the other one portraying a physician using an integrated model of EHR use for communication during the visit.

Secondary Objectives

1. Study To compare participants' perception of physicians' communication skills after they watch two scripted-video vignettes of physicians: one portraying a traditional face to face clinical visit without examination room computer use, and the other one portraying a physician using an integrated model of EHR use during communication.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
Double (Participant, Care Provider)

盲法说明

The research coordinator will be blinded to the allocation sequence throughout the study. Actors and patients will be blinded to the specific hypothesis of the study.

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

  • •Eligibility Criteria
  • •Participants with a diagnosis of cancer either early disease or advanced cancer defined as locally advanced, recurrent, or metastatic disease.
  • •Outparticipants (either new referrals or follow-ups) seen in the Supportive Care Clinic.
  • •Age >/= 18 years old.
  • •Able to read, write, and speak English.
  • •Participants with normal cognitive status (Memorial Delirium Assessment Scale (MDAS) </= 6/30) who can understand the nature and purpose of the study and have the ability to complete the consent process.

排除标准

  • •Participants who are experiencing severe symptom distress, including severe emotional distress, which may interfere with study participation. This will be measured by the Edmonton Symptom Assessment Scale (ESAS). Eligibility of participants with ESAS score >/= 7 on any item will be determined by the principal investigator and/or attending physician who is caring for the patient during that visit.
  • •Participants with cognitive dysfunction (Memorial Delirium Assessment Scale (MDAS) >/= 7/30 will be excluded from the study.

研究组 & 干预措施

Arm 4

Other

Physician B - Prime EHR

干预措施: Video (Other)

Arm 3

Other

Physician A - Prime EHR

干预措施: Questionnaire (Other)

Arm 3

Other

Physician A - Prime EHR

干预措施: Video (Other)

Arm 1

Other

Physician A - No EHR

干预措施: Questionnaire (Other)

Arm 1

Other

Physician A - No EHR

干预措施: Video (Other)

Arm 2

Other

Physician B - No EHR

干预措施: Questionnaire (Other)

Arm 4

Other

Physician B - Prime EHR

干预措施: Questionnaire (Other)

Arm 2

Other

Physician B - No EHR

干预措施: Video (Other)

结局指标

主要结局

Questionnaires/Videos

时间窗: Through study completion; an average of 1 year

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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