Actively Recruiting

Age: 65Years +
MALE
NCT05497024

Older Men's Decision Making About Active Surveillance for Prostate Cancer - Aim 3: Decision Aid Cognitive and Usability Testing

Led by M.D. Anderson Cancer Center · Updated on 2026-04-16

45

Participants Needed

1

Research Sites

233 weeks

Total Duration

On this page

Sponsors

M

M.D. Anderson Cancer Center

Lead Sponsor

A

American Cancer Society, Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

This protocol describes development and user testing of an educational shared decision making intervention to help men with prostate cancer who are on active surveillance make decisions with their health care providers about if and when to de-escalate surveillance testing. The project is important because for many patients their cancer does not progress to the point of needed curative treatment or their health status changes such that they are no longer good candidates for treatment. For these men, de-escalating ongoing surveillance (e.g., fewer biopsies or imaging studies) is a reasonable option.

CONDITIONS

Official Title

Older Men's Decision Making About Active Surveillance for Prostate Cancer - Aim 3: Decision Aid Cognitive and Usability Testing

Who Can Participate

Age: 65Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Male aged 65 or older
  • Diagnosis of localized prostate cancer
  • On active surveillance for 12 or more months
  • Fluent in English
  • Caregivers aged 18 or older involved in care of eligible patient
  • Caregivers fluent in English
  • Clinicians aged 18 or older providing care for prostate cancer patients
  • Clinicians fluent in English
Not Eligible

You will not qualify if you...

  • Receiving treatment for another cancer (primary or recurrence)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

M D Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

L

Lisa Lowenstein, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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