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临床试验/NCT05102487
NCT05102487撤回不适用

Patient Comprehension, Retention and Satisfaction With Anesthesia Consent Process

University of Chicago1 个研究点 分布在 1 个国家开始时间: 2021年10月15日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Patient satisfaction

研究概览

简要总结

Currently at University of Chicago Medical Center (UCMC) consent for anesthesia is obtained verbally by qualified anesthesia providers. Later this year, the investigators will be moving to a written informed consent form for anesthesia that must be signed by patients before proceeding with elective surgery. The department's aim is to study patient satisfaction and retention of information presented before and after this change is made.

After consent for anesthesia is obtained, study personnel will approach patients >= 18 years of age scheduled for elective surgery and, after seeking verbal consent for this study, will administer a questionnaire which will assess patient satisfaction and retention of the risks that were presented.

详细描述

Currently at UCMC consent for anesthesia is obtained verbally by qualified anesthesia providers. Later this year, the investigators will be moving to a written informed consent form for anesthesia that must be signed by patients before proceeded with elective surgery. The aim is to study patient satisfaction and retention of information presented before and after this change is made.

Study Procedures After consent for anesthesia is obtained, study personnel will approach patients >= 18 years of age scheduled for elective surgery and, after seeking verbal consent for this study, will administer a questionnaire which will assess patient satisfaction and retention of the risks that were presented.

Demographic data will be recorded, including age, sex, classification of surgery (by service), urgency of case, as well as role of person obtaining anesthesia consent (resident vs. CRNA/APN vs. attending anesthesiologist). Method of obtaining anesthesia consent will also be recorded. Patient identifiers, including name, MRN and date of birth will NOT be recorded as part of this study.

Patients will be approached for participation in this study preoperatively, in the pre-op holding area, immediately after anesthesia consent is obtained by the appropriate anesthesia provider. The patient's electronic medical record will NOT be accessed in order to pre-screen for participation no PHI will be collected in this study.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • English speaking Age> 18 years old

排除标准

  • Emergency cases Pt unable to consent for themselves Age <18 yo Pregnant women for delivery

结局指标

主要结局

Patient satisfaction

时间窗: Upon receiving consent for anesthesia, pre-operatively

How well patients are satisfied with the anesthesia consent process by using a 6 question questionnaire developed for this study.

次要结局

  • Patient Retention(Upon receiving consent for anesthesia, pre-operatively)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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