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临床试验/NCT03284359
NCT03284359已完成不适用

A Randomized Trial of Nudges To Enhance Enrollment in Critical Care Research

University of Pennsylvania2 个研究点 分布在 1 个国家目标入组 182 人开始时间: 2018年2月19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
182
试验地点
2
主要终点
Consent Rate

研究概览

简要总结

Difficulties enrolling patients in randomized clinical trials (RCTs) have long been recognized as a major barrier to successful evaluation of medical interventions. This is particularly problematic among intensive care unit (ICU) trials, of which more than one-third do not reach target enrollment. Under-enrollment and selective enrollment reduce RCTs' abilities to answer the research questions, thereby degrading the trials' scientific value and ethics.

Current evidence suggests that financial incentives can ethically increase study enrollment, but this approach can pose large up-front costs to researchers. However, several nonmonetary behavioral interventions, or nudges, may offer novel and easily scalable approaches to increase enrollment in RCTs.

The investigation team propose a 2-arm RCT in 10 ICUs at Penn to test the relative effectiveness of nudges on enrollment rates. Investigators hypothesize that a bundle of nudges during recruitment will increase enrollment rates compared to usual recruitment procedures will increase enrollment.

Investigators will enroll 182 critically ill patients' surrogate decision makers(participants) to engage in recruitment procedures for a simulated RCT comparing two mechanical ventilation weaning protocols among mechanically ventilated patients. Investigators will also measure participants' assessment of risk of the simulated trial after the informed consent process. This work will provide the first empirical evidence regarding the efficacy of inexpensive, scalable nudges to potentially augment enrollment and reduce costs of future clinical trials.

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
Single (Participant)

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

  • Surrogate decision-makers of patients who are:
  • Patient and surrogate is 18 years of age or older
  • Surrogate is English-proficient
  • Patient is mechanically ventilated
  • Patient is admitted to participating ICU

排除标准

  • Surrogate decision-makers of patients who are:
  • Patient is receiving comfort care only
  • Patient has anticipated extubation in the next 24 hours.
  • Patient with tracheostomy.
  • Bedside clinician declines patient participation.
  • Surrogate decision maker not available to approach prior to patient being extubated.

结局指标

主要结局

Consent Rate

时间窗: Up to 96 hours

The primary outcome is consent rate for a simulated RCT. This is an easily measurable binary outcome that has the potential for significant impact on future trial recruitment.

次要结局

  • Risk Assessment(Up to 96 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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