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临床试验/NCT02697799
NCT02697799已完成不适用

A Randomized Trial of Recruitment Strategies for Research Participation

University of Pennsylvania8 个研究点 分布在 1 个国家目标入组 1,296 人开始时间: 2016年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,296
试验地点
8
主要终点
The primary outcome is the proportion of people assigned to each recruitment strategy that consent to participate in the two parent RCTs.

研究概览

简要总结

In a multicenter, randomized clinical trial of attitudes towards research participation, we will evaluate the ethics, effectiveness, and cost- effectiveness of three recruitment strategies for research participation in a mobility trial among hospitalized patients and a smoking cessation trial among patients with depression.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Triple (Participant, Investigator, Outcomes Assessor)

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

  • Eligible for parent RCT
  • 18 years or older
  • No prior knowledge of recruitment strategies used for this trial
  • Speaks English

排除标准

  • Prior knowledge of recruitment strategies used for this trial

结局指标

主要结局

The primary outcome is the proportion of people assigned to each recruitment strategy that consent to participate in the two parent RCTs.

时间窗: Immediate- Several Days

Consent rates in each of the two parent RCTs

次要结局

  • Perceptions of influence or coercion(Immediate)
  • Retention through the end of treatment sessions(8 - 27 weeks)
  • Attitudes towards research(Immediate)
  • Attention to informed consent(Immediate)
  • Perceived risks of the research(Immediate)
  • Incidence of therapeutic misconceptions(Immediate)
  • Understanding of the trial(Immediate)

研究者

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

Scott Halpern

Associate Professor of Medicine

University of Pennsylvania

研究点 (8)

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