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临床试验/NCT04701450
NCT04701450已完成不适用

Questionnaire Study to Evaluate Patient Satisfaction Between Digital, Telephonic and Conventional Obtaining of Consent for Anaesthesia

Medical University of Vienna1 个研究点 分布在 1 个国家目标入组 750 人开始时间: 2020年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
750
试验地点
1
主要终点
Patient satisfaction after informed consent

研究概览

简要总结

In this study, the investigators aim to evaluate patient satisfaction between three methods of obtaining informed consent for anaesthesia. Patients are asked to partake in a short survey after being informed about the anaesthetic procedure either conventionally in the anesthesia department, telephonically or digitally.

详细描述

Patient satisfaction plays an important role to improve the process of medical procedures as well as patient outcome. Evaluating the subjectively experienced satisfaction is challenging. The investigators will use a questionnaire and assess waiting times in the process to determine patient satisfaction between digital, telephonic and conventional obtaining of informed consent for anaesthesia.

In this questionnaire study, patients are asked to partake in a survey after the process of obtaining consent for anaesthesia is completed. The questionnaire covers aspects of patient satisfaction with the process, such as subjective assessment of comprehensibility, waiting time and privacy.

Patients are divided into three groups. In one group, consent is obtained conventionally, in form of a visit to our anaesthesia department. In the other two groups, consent is obtained telephonically and digitally, respectively. Patients are not randomised into these groups, but included into the study after the process of obtaining consent by one of the three methods mentioned above is completed.

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

  • Patients for whom consent for anaesthesia is obtained

排除标准

  • Age < 18 years
  • Language barrier
  • Patients with appointed legal guardians
  • Patients unable to provide informed consent

结局指标

主要结局

Patient satisfaction after informed consent

时间窗: Immediately after obtaining informed consent

Assessment of subjectively experienced satisfaction with the process of obtaining informed consent for anesthesia

次要结局

  • Time expense of informed consent(Up to 60 minutes; from start until end of informed consent)
  • Intraoperative complications(Up to 12 hours; From start until end of the planned surgical procedure)
  • Overall waiting time of patients(Up to three hours; from administration for informed consent until completion of informed consent)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

David M Baron, MD, PhD

Assoc. Prof. PD Dr. David Baron, EDIC

Medical University of Vienna

研究点 (1)

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