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