220 Participants Needed

Visual Tools for Prostate Cancer

DU
TG
Overseen ByTaylor Greene
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: UNC Lineberger Comprehensive Cancer Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

Trial Summary

What is the purpose of this trial?

This prospective study will compare pre-post pilot test of surgeon-facing, visual decision support among urologists seeing patients with newly diagnosed localized prostate and kidney cancer. Up to 20 urologists (10 academic and 10 community) will be enrolled. The goal will be to capture up to 10 pre- and 10 post-intervention patient encounters for each urologist with an accrual target of 200 unique patient visits (100 pre and 100 post-intervention) over a half-year period. Patient encounters pre- and post-intervention will be audio recorded, transcribed, and coded for discussion of risks/benefits of surgery and strength of recommendation. Patients and urologists will complete additional surveys on their perceptions of patient-provider communication. Urologists will further describe their experience and rate their satisfaction with visual decision support. Communication (content and perceived) will be compared pre- and post-intervention with secondary comparisons by race and care setting.It was hypothesized that the discussion of risks and benefits of cancer surgery will increase post-intervention and that the strength of recommendation and perceptions of patient-provider communication will change. The secondary hypothesis is that these changes will differ by patient race and care setting.

Research Team

HT

Hung-Jui Tan, MD

Principal Investigator

UNC Lineberger Comprehensive Cancer Center

Eligibility Criteria

This trial is for urologists treating patients with newly diagnosed localized prostate and kidney cancer. It aims to include up to 20 surgeons from both academic and community settings, targeting a total of 200 unique patient visits.

Inclusion Criteria

Verbal informed consent was obtained to participate in the study
For physician subjects, practicing urologist in North Carolina at UNC Health, Novant Health, or an affiliated site and sees patients with suspected or confirmed prostate or kidney cancer
I am willing and able to follow the study's requirements.
See 1 more

Exclusion Criteria

Non-English speaking
I am willing and able to give informed consent.
My cancer is advanced or has spread, and I was diagnosed over 6 months ago.

Timeline

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Pre-Intervention

Patient encounters are audio recorded, transcribed, and coded for discussion of risks/benefits of surgery and strength of recommendation before the intervention

3 months
10 visits per urologist

Intervention

Implementation of visual decision support tools for urologists

1 month

Post-Intervention

Patient encounters are audio recorded, transcribed, and coded for discussion of risks/benefits of surgery and strength of recommendation after the intervention

3 months
10 visits per urologist

Follow-up

Participants are monitored for changes in patient-physician communication and decision-making

6 months

Treatment Details

Interventions

  • Visual
Trial Overview The study tests visual decision support tools designed for cancer surgeons. Surgeons' discussions about surgery risks/benefits and their recommendations will be compared before and after the intervention using recorded patient encounters.
Participant Groups
2Treatment groups
Experimental Treatment
Group I: Physician participantsExperimental Treatment1 Intervention
Physician participants seeing patients with newly diagnosed localized prostate cancer and clinical T1 renal masses suspicious for kidney cancer.
Group II: Patient participantsExperimental Treatment1 Intervention
Patient participants will complete a 10-minute baseline survey, 15-minute after-visit survey and 5-minute 6-month survey.

Find a Clinic Near You

Who Is Running the Clinical Trial?

UNC Lineberger Comprehensive Cancer Center

Lead Sponsor

Trials
377
Recruited
95,900+
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