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CompletedNCT06764992Updated Feb 4, 2026

Exploring Men s Prostate Cancer Genetic Risk Perceptions

An observational study in Prostate Cancer, sponsored by H. Lee Moffitt Cancer Center and Research Institute. Completed at 1 site in United States. Open to male participants aged 40 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-04.

Sponsored by H. Lee Moffitt Cancer Center and Research Institute · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
100
Ages
40 Years and older
Sex
Male
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Study summary

The exploring men's prostate cancer genetic risk perceptions and willingness to give a biospecimen for genetic risk testing study aims to assess prostate cancer genetic risk and susceptibility beliefs among unaffected men of diverse races/ethnicities who are considering undergoing prostate cancer screening and their willingness of men to provide a biospecimen (saliva sample) and test the samples for prostate cancer aggressiveness and determine risk category based on SNP genetic profile.

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Conditions studied

  • Prostate Cancer

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Keywords

  • Genetic Risk Perception and Beliefs
  • Biospecimen Donation for Genetic Risk Testing
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In context

Prostatic Neoplasms

6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,400 are open to participants now.

This study's enrollment of 100 is below the median of 200 across 1,181 observational studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

H. Lee Moffitt Cancer Center and Research Institute is the lead sponsor of 533 studies on the registry; 74 are open to participants now.

Of its 99 completed or terminated interventional studies of FDA-regulated products, 57 (58%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
40 Years and older
Sexes eligible
Male
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Racially and ethnically diverse Adult Men with no personal Prostate Cancer history/diagnosis.

Inclusion criteria

  • Racially/ethnically diverse men with emphasis on Men of African Ancestry.
  • Age 40 and older .
  • No personal prostate cancer history/diagnosis.
  • With or without family history of prostate cancer.

Exclusion criteria

Exclusion Criteria:

  • Previous personal Prostate Cancer history/diagnosis
  • Under 40 years of age
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Study design

Observational model
Other
Time perspective
Prospective
Enrollment
100 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Prostate Cancer Risk Group

    Participants will be asked to provide saliva samples and complete a questionnaire about their Prostate Cancer Genetic Risk beliefs.

    Other: Questionnaire · Other: Saliva Sample

Interventions

  • OtherQuestionnaire

    Participants will be asked to complete a questionnaire on demographics, risk beliefs and perception and prostate cancer screening behaviors, intentions and awareness of informed decision making.

  • OtherSaliva Sample

    Participants will be asked to provide a saliva sample for genetic risk testing to generate a SNP risk profile using a saliva sample collection kit with collection, storage and mailing instructions. We will assess the proportion of consented men who will provide a saliva sample.

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What researchers measure

Primary outcomes

  1. Prostate Cancer Genetic Risk and Susceptibility Beliefs

    Prostate Cancer Genetic Risk and Susceptibility beliefs will be summarized based on single items on the Prostate Cancer Risk Perception Questionnaire.

    Time frame: Up to 6 Months

Secondary outcomes

  1. Polygenic Risk Score (PRS) of Saliva Samples

    Polygenic Risk Score (PRS) of Saliva Samples will be based on genetic profiles from Single Nucleotide Polymorphisms (SNPs). Identified as prostate cancer susceptibility loci, genetic risk of developing prostate cancer will be categorized into 5 groups: Very Low Risk (\< 10%), Low Risk (10-25%) Moderate Risk (25-75%), High Risk (75-90%) or Very High Risk (\>90%).

    Time frame: Up to 6 Months

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Study locations

1 site
  • Moffitt Cancer Center
    Tampa, Florida 33612, United States
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References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06764992
Lead sponsor
H. Lee Moffitt Cancer Center and Research Institute
Responsible party
Sponsor
First posted
Jan 9, 2025
Start date
Aug 25, 2022
Primary completion
Apr 20, 2024
Completion
Jun 7, 2024
Last update
Feb 4, 2026

Study contacts

Jong Park, PhD
principal investigator · Moffitt Cancer Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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