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Clinical Trials/NCT02419846
NCT02419846TerminatedNot Applicable

The Effectiveness of a Proposed Prostate Cancer Outreach Program in a Predominantly African American Community That Promotes Informed Decision-making for Prostate Cancer Screening and Utilizes Community Navigation

Case Comprehensive Cancer Center1 site in 1 country319 target enrollmentStarted: June 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
319
Locations
1
Primary Endpoint
Proportion of participants over age 18 that demonstrate improved knowledge about prostate cancer screening

Study Overview

Brief Summary

This clinical trial studies an informed decision making intervention of screening for prostate cancer in predominantly African American participants. It also evaluates participants' knowledge about prostate cancer screening and to improve understanding. Using decision aids such as culturally sensitive written material, verbal information, and videos to educate patients about screening may increase patient participation and knowledge. This may increase confidence in participants' decisions. Raising awareness about prostate cancer in the communities may increase the participants' willingness to be screened for prostate cancer once they have learned about it.

Detailed Description

PRIMARY OBJECTIVES:

(A) To assess the effectiveness of a proposed educational model for informed decision about Prostate Cancer in high risk men over age 40 which compares informed decision making and shared decision making (B) to improve knowledge about prostate cancer in men over age 18

OUTLINE:

Participants complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences. Some participants then undergo a screening exam comprising a prostate specific antigen level and digital rectal exam.

After completion of study, participants are followed up periodically.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Screening
Masking
None

Eligibility Criteria

Ages
19 Years to — (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Men over the age of 18 will be asked to participate in the educational component of the program; men over the age of 40 will be offered the screening component after the educational portion of the event; participants over age of 40 will have the opportunity to make an informed decision in regards to prostate cancer screening based on this information and the educational material; American Cancer Society (ACS) guidelines recommend having a discussion about screening in men who have an expected mortality of greater than 10 years; data on comorbidities and 10-year mortalities will be collected on every participant using the University of California at San Francisco (UCSF) mortality index
  • •Educational component: men over the age of 18
  • •Screening component: men over age 40

Exclusion Criteria

  • •Known personal history of prostate cancer
  • •Active malignancy, metastatic disease, or anyone undergoing treatment for malignancy

Arms & Interventions

Men over 40: Screening with intervention

Experimental

Participants over the age of 40 complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences. Participants may undergo a screening exam comprising a prostate specific antigen level and digital rectal exam.

Intervention: Educational Intervention (Other)

Men over 40: Screening with intervention

Experimental

Participants over the age of 40 complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences. Participants may undergo a screening exam comprising a prostate specific antigen level and digital rectal exam.

Intervention: digital rectal examination (Procedure)

Men over 40: Screening with intervention

Experimental

Participants over the age of 40 complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences. Participants may undergo a screening exam comprising a prostate specific antigen level and digital rectal exam.

Intervention: Pre-test administration (Other)

Men over 40: Screening with intervention

Experimental

Participants over the age of 40 complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences. Participants may undergo a screening exam comprising a prostate specific antigen level and digital rectal exam.

Intervention: Survey Administration (Other)

Men over 40: Screening with intervention

Experimental

Participants over the age of 40 complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences. Participants may undergo a screening exam comprising a prostate specific antigen level and digital rectal exam.

Intervention: Prostate-specific antigen measurement (Other)

Men 18-39: Educational intervention

Experimental

Participants between 18 and 39 complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences.

Intervention: Post test administration (Other)

Men over 40: Screening with intervention

Experimental

Participants over the age of 40 complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences. Participants may undergo a screening exam comprising a prostate specific antigen level and digital rectal exam.

Intervention: Post test administration (Other)

Men 18-39: Educational intervention

Experimental

Participants between 18 and 39 complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences.

Intervention: Educational Intervention (Other)

Men 18-39: Educational intervention

Experimental

Participants between 18 and 39 complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences.

Intervention: Pre-test administration (Other)

Men 18-39: Educational intervention

Experimental

Participants between 18 and 39 complete an educational intervention comprising a 10-20 minute PowerPoint presentation given by an experienced healthcare professional that discusses prostate cancer facts, screening guidelines, risks, benefits, and consequences.

Intervention: Survey Administration (Other)

Outcomes

Primary Outcomes

Proportion of participants over age 18 that demonstrate improved knowledge about prostate cancer screening

Time Frame: Up to 1 year

Improved understanding will be defined as an increase in the number of correct answers seen on the post Prostate Screening Education Questionnaire. The underlying likelihood of a positive response, or improved understanding of prostate cancer screening, can be estimated using a 95% confidence interval that has a maximum half-width of 6%.

Proportion of participants over age 40 who find this education and screening model helpful in making an informed decision about prostate cancer screening as measured by the satisfaction survey questions

Time Frame: Up to 1 year

Helpfulness of the program will be measured on a 5-point Likert scale where the two uppermost categories are considered a positive response.

Secondary Outcomes

  • Proportion of participants who choose screening after educational intervention(Up to 1 year)
  • Proportion of participants referred to a primary care physician who did not previously have a primary care physician(Up to 1 year)
  • Proportion of participants who asked the physician to make a decision for them in spite of educational intervention(Up to 1 year)
  • Proportion of abnormal results found with screening and referred to follow-up assessed as per National Comprehensive Cancer Network guidelines(Up to 1 year)
  • Proportion of participants with family history of prostate cancer(Up to 1 year)
  • Proportion of participants who choose to enter the clinical trial(Up to 1 year)
  • Proportion of participants with a high 10-year mortality based on UCSF index who choose to be screened for prostate cancer after educational intervention(Up to 1 year)
  • Proportion of participants diagnosed with malignancy based on follow up biopsies and work-up during the course of the study(Up to 1 year)
  • Proportion of participants who expressed satisfied with this proposed informed consent and education model(Up to 1 year)
  • 10-year expected mortality based on USCF 10-year Mortality Index for all participants(Up to 1 year)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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