MedPath

Sexual and Urinary Function Improvement for Cancer Survivors

Not Applicable
Not yet recruiting
Conditions
Urinary Dysfunction
Sexual Dysfunction
Registration Number
NCT06637852
Lead Sponsor
NYU Langone Health
Brief Summary

The purpose of this study is to test the efficacy of SUFICS-PACT to identify and treat sexual and urinary dysfunction in prostate cancer survivors at NYC H+ H/Bellevue, the oldest public hospital in the US. This study will evaluate the implementation of an adapted sexual and urinary function collaborative care model at NYC Health+Hospitals/Bellevue. The study will test the efficacy of this collaborative care model through a randomized controlled trial in the adult primary care clinic; the intervention arm will receive collaborative treatment consisting of a care manager who has specialty training in mental health and psychosexual counseling, a primary care nurse practitioner who leads symptom management, primary care physicians who supervise the team, and a team specialty consult liaison.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Male
Target Recruitment
200
Inclusion Criteria
  • At least 18 years old
  • Have a diagnosis of prostate cancer
  • Have sought care/treatment for prostate cancer
Exclusion Criteria
  • Patients under 18 years old
  • Patients who have not sought care/treatment for prostate cancer
  • Patients who are categorized as "vulnerable subjects," such as minors or incarcerated individuals.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Number of patients identified and treated for sexual dysfunctionYear 5
Number of patients identified and treated for urinary dysfunctionYear 5
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

NYU Langone Health

🇺🇸

New York, New York, United States

© Copyright 2025. All Rights Reserved by MedPath