PSA TOOL for Prostate Cancer Screening Discussions
- Conditions
- Prostate Cancer
- Interventions
- Behavioral: Revised PSA TOOLBehavioral: PSA TOOLBehavioral: Informal Interview
- Registration Number
- NCT03135444
- Lead Sponsor
- Case Comprehensive Cancer Center
- Brief Summary
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.
- Detailed Description
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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 95
Provider:
- 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:
- Patient of participating Cleveland Clinic primary care provider who is scheduled for a routine appointment with the provider
- Not a patient or provider of the Cleveland Clinic Health System
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Arm && Interventions
Group Intervention Description Provider Field Test Informal Interview 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. Patient test of revised PSA TOOL Revised PSA TOOL 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. Provider Field Test PSA TOOL 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. Patient test of revised PSA TOOL Informal Interview 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.
- Primary Outcome Measures
Name Time Method Score from Perceived Usefulness scale Up to 4 weeks after getting PSA TOOL scale will be summarized as means and standard deviations
Score from Perceived Ease of Use scale 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 Up to 30 minutes after Pre-Test The paired t-test will be used to compare the pre- and post- patient survey scores
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Cleveland Clinic, Case Comprehensive Cancer Center
🇺🇸Cleveland, Ohio, United States