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临床试验/NCT03477591
NCT03477591已完成不适用

McMaster Choices Study: Evaluating the Impact of Evidence-based Information About PSA Testing on Prostate Cancer Screening Decisions

McMaster University2 个研究点 分布在 1 个国家目标入组 308 人开始时间: 2018年10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
308
试验地点
2
主要终点
Decisional conflict

研究概览

简要总结

Patient decision aids are tools that help guide individuals through a healthcare-related decision making process. They help users combine evidence-based information and recommendations by a health care provider with their personal needs, values and preferences. Through this project, Dr. Dobbins and her research team will explore whether the use of patient decision aids with high-quality and user-friendly summaries of research evidence, or summaries of research evidence alone, help to improve the quality of decision making by men facing prostate cancer screening decisions.

详细描述

Guidelines for prostate screening in Canada are based on low-moderate quality evidence of effectiveness and screening is associated with potential harms. Patient Decision Aids (PDAs) are tools that assist users to understand treatment options, risks and benefits to align decisions with values and preferences. The investigators would now like to know whether use of a PDA alongside evidence-based information provided through the McMaster Optimal Aging Portal, or simply access to evidence-based information alone, can help users to make informed decisions about prostate cancer screening in men.

研究设计

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

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • English speaking men, > 50 years old

排除标准

  • History of prostate cancer or PSA test in the last 12 months

结局指标

主要结局

Decisional conflict

时间窗: Change from baseline to 6-mo

Decisional Conflict Scale

次要结局

  • Decision quality(Change from baseline to 6-mo)
  • Preparation for decision making(Change from baseline to 6-mo)
  • Screening behaviour(Change from baseline to 6-mo)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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