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Not Yet Recruiting NCT06637852

Sexual and Urinary Function Improvement for Cancer Survivors

Conditions: Urinary Dysfunction, Sexual Dysfunction

Sex: Male
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 200
Sponsor: NYU Langone Health

Location: NYU Langone Health New York New York

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.

Eligibility Criteria

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.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06637852). StuddyBuddy aggregates publicly available trial information.