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临床试验/NCT01514786
NCT01514786已完成不适用

Decision Aid to Technologically Enhance Shared Decision Making

University of Michigan14 个研究点 分布在 1 个国家目标入组 570 人开始时间: 2012年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
570
试验地点
14
主要终点
Number of Participants Reporting Preferred Screening Type as Reported by Chart Audits

研究概览

简要总结

Physicians face a challenge in promoting colorectal cancer screening (CRCS) in the face of multiple competing demands. A decision aid (DA) that clarifies patient preferences and improves decision quality could aid shared decision making (SDM) and be effective at increasing CRCS rates. However, exactly how such DA improves SDM is not clear. This 4-year R01 study funded by the National Cancer Institute seeks to provide detailed understanding of how an interactive DA affects patient-physician communication and SDM, and ultimately CRCS adherence.

详细描述

This two-armed randomized controlled trial (300 patients/arm) will compare Colorectal Web (CW), the interactive DA, to a non-interactive control website in ten practices in Metro Detroit. Patients will be adults aged 50 years and over, not current on CRCS. In the clinic before the patient-physician encounter, participants will complete a Patient Baseline Survey. They will be randomized to CW or the control website. Data will be collected after the patient reviews the respective website (Post-Intervention Survey), during the patient-physician encounter (digital audio recording), and after it (Post-Encounter Survey). Chart audit will be performed six months after the encounter to determine whether the patient underwent CRCS.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

年龄范围
50 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •50-75 years of age
  • •not current with colorectal cancer screening
  • •scheduled for HME, Health Maintenance Exam, or chronic care visit with participating physician
  • •able to read English
  • •current contact information

排除标准

  • •history of colon cancer or adenomatous polyps
  • •history of dementia or psychosis
  • •contraindication to CRCS

研究组 & 干预措施

Control

No Intervention

Same information is presented in the control website as is found in the intervention website, but no interactive component: preferences and risk assessment.

Intervention with Colorectal Website

Active Comparator

Intervention website includes an interactive component including preferences and risk assessment.

干预措施: Colorectal Web (Behavioral)

结局指标

主要结局

Number of Participants Reporting Preferred Screening Type as Reported by Chart Audits

时间窗: 6 months following intervention a chart audit will be conducted to determine if CRCS was completed.

Chart audits were conducted 6 months after the participant's study visit to determine if screening had occurred and if the type of screen was the same as the participant's preferred type of screening.

次要结局

未报告次要终点

研究者

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

Masahito Jimbo, MD

Clinical Associate Professor, Family Medicine

University of Michigan

研究点 (14)

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