Sexual and Urinary Function Improvement for Cancer Survivors

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.

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Key information

Conditions

Urinary Dysfunction Genital Diseases Sexual Dysfunction Sexual Dysfunction, Physiological Urogenital Diseases

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

NYU Langone Health

New York, 10016, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

SUFICS-PACT

Behavioral

SUFICS-PACT includes sexual and urinary dysfunction screening, collaborative treatment of sexual and urinary dysfunction, and care managers who are mental health professionals with training in psychosexual counseling. Mental health professionals will facilitate a comprehensive approach to sexual dysfunction, as emphasized by the biopsychosocial model of sexual health. SUFICS-PACT also emphasizes close follow up, which is important for sexual function recovery after prostate cancer treatment.

Primary outcomes

Number of patients identified and treated for sexual dysfunction

Time frame: Year 5
Number of patients identified and treated for urinary dysfunction

Time frame: Year 5

Study contacts

Contact information is provided by the study sponsor or research team.

Favour Nnah

CONTACT

[email protected]

917-854-5895

Nnenaya Mmonu, MD, MS

CONTACT

[email protected]

646-825-6300

Sponsors and collaborators

Lead sponsor

NYU Langone Health

Other

Registry information

Official study title

Sexual and Urinary Function Improvement for Cancer Survivors- Promoting Access to Collaborative Treatment (SUFICS-PACT)

Important dates

Study start: 2026
Primary completion: 2029
Study completion: 2030
First posted: Oct 15, 2024
Registry last updated: Jul 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

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