跳至主要内容
临床试验/NCT03098303
NCT03098303已完成不适用

Criteria Associated With Patient Willingness to Participate in Biomedical Research: a Prospective, Observational Study

University Hospital, Montpellier4 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2014年12月23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
1,000
试验地点
4
主要终点
Acceptation or refusal to participate in a biomedical research study

研究概览

简要总结

The primary objective of this study is to determine the variables associated with patient acceptation or refusal to participate in a clinical research protocol when seen in during a pneumology consultation (excluding oncology and tobaccology).

详细描述

The secondary objectives of this study are:

  • To compare patient acceptance rates for participation in a clinical research protocol before and after January 15, 2016.
  • To determine the variables associated with accepting or refusing to participate in a clinical research protocol for patients seen during a pneumology consultation (excluding oncology and tobaccology) before January 15, 2016.
  • To determine the variables associated with accepting or refusing to participate in a clinical research protocol for patients seen during a pneumology consultation (excluding oncology and tobaccology) after January 15, 2016.
  • To describe the patient population seen during pneumology consultations.
  • To determine the variables associated with accepting or refusing to participate in a clinical research protocol sponsored by a pharmaceutical laboratory.
  • To determine the variables associated with accepting or refusing to participate in a clinical research protocol sponsored by an academic institution.
  • Construct clusters (homogeneous groups) of patients seen during the pneumology consultations.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Cross Sectional

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

  • The patient was informed about the study.
  • The patient is scheduled for a consult in the pneumology department

排除标准

  • The patient is under judicial protection or is an adult under any kind of guardianship
  • The patient expresses opposition to the study
  • It is impossible to correctly inform the patient about the study
  • The patient cannot fluently read French
  • The patient is pregnant
  • The patient is breastfeeding
  • The patient has cancer
  • The patient is consulting in tabaccology

结局指标

主要结局

Acceptation or refusal to participate in a biomedical research study

时间窗: Day 0 (cross-sectional study)

Positive or negative response to the question "If a biomedical research protocole were proposed to you, would you accept to participate?"

次要结局

  • The PROTOACCEPT questionnaire(Day 0 (cross-sectional study))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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