How distressing is it to participate in medical research? A calibration study using an everyday events questionnaire.

JRSM short reports Pub Date : 2013-09-13 eCollection Date: 2013-01-01 DOI:10.1177/2042533313493271
Keith J Petrie, Kate Faasse, Tracey Anne Notman, Ronan O'Carroll
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引用次数: 10

Abstract

Objectives: To investigate how distressing participating in medical research is perceived to be, compared to everyday events.

Design: Anonymous questionnaire.

Setting: Scotland and New Zealand.

Participants: One hundred members of the Scottish general public, 94 University of Auckland students, 22 New Zealand Ministry of Health ethics committee members.

Main outcome measures: Distress ratings made on a 0-10 scale for everyday events and common medical research procedures.

Results: Both general population and student samples generally rated the distress caused by participating in various medical research procedures as low or very low. Most research procedures were rated less than the distress caused by not being able to find a car park at a supermarket. In contrast, the ethics committee members rated the distress caused by most of the medical research procedures at a significantly higher level than the ratings of the student and general population samples. Ethics committee members overestimated the distress caused by interview or questionnaire assessments (M = 203.31%, SE = 11.42, 95% CI [179.79, 226.83]) more than medical testing for research (M = 158.06%, SE = 12.33, 95% CI [132.66, 183.46], p = 0.04) and everyday events (M = 133.10%, SE = 7.80, 95% CI [117.03, 149.16], p < 0.001).

Conclusions: Common medical research procedures are not rated as particularly distressing by the general public, and ethics committees may be adopting an over-protective role when evaluating research applications that involve the use of questionnaire or survey methodology.

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参与医学研究有多痛苦?一项使用日常事件问卷的校准研究。
目的:调查与日常事件相比,参与医学研究的痛苦程度。设计:匿名问卷。背景:苏格兰和新西兰。参与者:100名苏格兰公众,94名奥克兰大学学生,22名新西兰卫生部伦理委员会成员。主要结果测量:对日常事件和常见医学研究程序进行0-10级的痛苦评分。结果:一般人群和学生样本普遍认为参与各种医学研究程序所造成的痛苦为低或非常低。大多数研究过程的评分都低于因在超市找不到停车位而造成的痛苦。相比之下,伦理委员会成员对大多数医学研究程序造成的痛苦的评分明显高于学生和一般人群样本的评分。伦理委员会成员对访谈或问卷评估造成的痛苦的高估(M = 203.31%, SE = 11.42, 95% CI[179.79, 226.83])高于对研究(M = 158.06%, SE = 12.33, 95% CI [132.66, 183.46], p = 0.04)和日常事件(M = 133.10%, SE = 7.80, 95% CI [117.03, 149.16], p。一般公众并不认为普通医学研究程序特别令人痛苦,伦理委员会在评估涉及使用问卷调查或调查方法的研究申请时可能采取了过度保护的作用。
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