NCT04789018

Brief Summary

This study assesses perceived usefulness of a web-based virtual prostate cancer genetics board for providers across academic, community, and veteran affairs settings to discuss prostate cancer genetics cases, precision treatment, and screening recommendation. Information gained from interviews and surveys of participants taking part in the virtual genetics board may lend insights into perceived usefulness, perceived ease of use, acceptability, self-efficacy, genetics knowledge, and barriers/facilitators to implementation to refine the process.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
118

participants targeted

Target at P50-P75 for all trials

Timeline
0mo left

Started Jan 2020

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 21, 2020

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

February 19, 2021

Completed
18 days until next milestone

First Posted

Study publicly available on registry

March 9, 2021

Completed
5.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 24, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 24, 2026

Last Updated

October 10, 2025

Status Verified

October 1, 2025

Enrollment Period

6.4 years

First QC Date

February 19, 2021

Last Update Submit

October 8, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Mean Likert scaled perceived usefulness scores of the virtual genetics board

    Perceived usefulness will be judged against a benchmark mean score of 5/7.

    After virtual genetics board

Secondary Outcomes (4)

  • Means or changes in means of Likert scaled acceptability/feasibility

    Before and after virtual genetics board

  • Perceived ease of use

    After virtual genetics board

  • Self-efficacy for recommendations

    Before and after virtual genetics board

  • Change in mean scores on 17 genetics knowledge test questions

    Baseline up to post-virtual genetics board

Study Arms (1)

Observational (survey, virtual genetic board, interview)

Participants complete a survey about genetic knowledge and self efficacy and then attend virtual genetics board. After virtual genetics board meeting, participants complete a second survey about perceived usefulness, ease of use, acceptability, feasibility, self-efficacy and genetic knowledge. Participants may also complete a semi-structured interview after virtual genetics board.

Other: Educational InterventionOther: Survey AdministrationOther: Interview

Interventions

Attend virtual genetics board

Also known as: Education for Intervention, Intervention by Education, Intervention through Education, Intervention, Educational
Observational (survey, virtual genetic board, interview)

Complete survey

Observational (survey, virtual genetic board, interview)

Complete interview

Observational (survey, virtual genetic board, interview)

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Non-genetic providers who perform prostate cancer (PCA) genetic testing for men in their practices (medical oncologists, radiation oncologists, urologists, primary care providers, mid-level providers)

You may qualify if:

  • Healthcare providers (medical oncologists, radiation oncologists, urologists, primary care providers, mid-level providers) who evaluate, manage, or treat men with prostate cancer or screen men for prostate cancer.
  • Providers who perform prostate cancer genetic testing for men (genetic counselors or healthcare providers)
  • Scientists and researchers
  • Advocacy or patient stakeholder organization members

You may not qualify if:

  • Non-medical providers

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University

Philadelphia, Pennsylvania, 19107, United States

Location

MeSH Terms

Conditions

Prostatic Neoplasms

Interventions

Early Intervention, EducationalEducational StatusMethodsInterviews as Topic

Condition Hierarchy (Ancestors)

Genital Neoplasms, MaleUrogenital NeoplasmsNeoplasms by SiteNeoplasmsGenital Diseases, MaleGenital DiseasesUrogenital DiseasesProstatic DiseasesMale Urogenital Diseases

Intervention Hierarchy (Ancestors)

Child Health ServicesCommunity Health ServicesHealth ServicesHealth Care Facilities Workforce and ServicesPreventive Health ServicesSocioeconomic FactorsPopulation CharacteristicsInvestigative TechniquesData CollectionEpidemiologic MethodsHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Amy Leader, DrPH, MPH

    Thomas Jefferson University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 19, 2021

First Posted

March 9, 2021

Study Start

January 21, 2020

Primary Completion (Estimated)

June 24, 2026

Study Completion (Estimated)

June 24, 2026

Last Updated

October 10, 2025

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Locations