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临床试验/NCT03135444
NCT03135444已完成不适用

Testing of a Brief Tool (PSA TOOL) for Prostate Cancer Screening Discussions in Primary Care Settings

Case Comprehensive Cancer Center2 个研究点 分布在 1 个国家目标入组 95 人开始时间: 2017年5月2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
95
试验地点
2
主要终点
Score from Perceived Usefulness scale

研究概览

简要总结

The study team created a tool to help identify patients who may benefit from shared decision making in the primary care setting. This tool is a guide to aid in decision making for prostate cancer screening. The team proposes the topics to be discussed in the screening conversation include the risk for developing prostate cancer based upon age, race/ethnicity, family history of prostate cancer, history of previous digital rectal exam, and history of previous prostate specific antigen (PSA) as well as self-reported health status and preferences for treatment. The team now proposes 1) testing this tool first for ease of use in primary care clinics 2) revising this tool based upon feedback from patients and providers, then 3) testing this tool for effectiveness in improving patient knowledge that they have an option to be screened for prostate cancer and of specific factors to be considered in the screening decision.

详细描述

Objectives:

  1. To pilot test a decision making tool, the PSA TOOL, for prostate cancer screening for usefulness and ease of use in primary care practices.
  2. To revise the PSA TOOL based upon provider and patient feedback.
  3. To assess patient knowledge about the option to be screened for prostate cancer and factors to consider in the prostate cancer screening decision before and after use of the tool.

Study Design:

This protocol is for field testing of a brief tool to improve prostate cancer screening discussions that occur at previously scheduled primary care outpatient visits.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
40 Years 至 69 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Provider at selected primary care practices in the Cleveland Clinic Health System
  • Willing to utilize a guide to aid in decision making for prostate cancer screening
  • Patient of participating Cleveland Clinic primary care provider who is scheduled for a routine appointment with the provider

排除标准

  • Not a patient or provider of the Cleveland Clinic Health System

研究组 & 干预措施

Provider Field Test

Experimental

15 providers will be given an initial version of the PSA TOOL, over a 4 week period, they will be able to provide feedback on the tool. This will be used to revise the screening decision aid. Informal interviews with providers will also be conducted by a member of the study team to obtain feedback about ease of use and usefulness of the tool.

干预措施: PSA TOOL (Behavioral)

Provider Field Test

Experimental

15 providers will be given an initial version of the PSA TOOL, over a 4 week period, they will be able to provide feedback on the tool. This will be used to revise the screening decision aid. Informal interviews with providers will also be conducted by a member of the study team to obtain feedback about ease of use and usefulness of the tool.

干预措施: Informal Interview (Behavioral)

Patient test of revised PSA TOOL

Experimental

150 patients will be asked to use the revised PSA TOOL. Pre- and Post-tests will be given to see if the tool changed the knowledge that patients have an option to be screened for prostate cancer and of specific factors to be considered in the screening decision. Informal interviews with patients who are exposed to the tool will also be conducted by a member of the study team to obtain feedback on issues addressed by the survey questions.

干预措施: Revised PSA TOOL (Behavioral)

Patient test of revised PSA TOOL

Experimental

150 patients will be asked to use the revised PSA TOOL. Pre- and Post-tests will be given to see if the tool changed the knowledge that patients have an option to be screened for prostate cancer and of specific factors to be considered in the screening decision. Informal interviews with patients who are exposed to the tool will also be conducted by a member of the study team to obtain feedback on issues addressed by the survey questions.

干预措施: Informal Interview (Behavioral)

结局指标

主要结局

Score from Perceived Usefulness scale

时间窗: Up to 4 weeks after getting PSA TOOL

scale will be summarized as means and standard deviations

Score from Perceived Ease of Use scale

时间窗: Up to 4 weeks after getting PSA TOOL

scale will be summarized as means and standard deviations

Change in Score from Pre-Test to Post-Test

时间窗: Up to 30 minutes after Pre-Test

The paired t-test will be used to compare the pre- and post- patient survey scores

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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