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Not yet recruiting NCT06637852

Sexual and Urinary Function Improvement for Cancer Survivors

No phase Interventional Urinary Dysfunction Sexual Dysfunction

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: SUFICS-PACT.
Who it may be relevant to
Registry conditions: Urinary Dysfunction, Sexual Dysfunction. Basic parameters: from 18 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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.

Interventions

  • Behavioral SUFICS-PACT
    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 outcome measures

  • 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]

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

United States · 1 center
  • NYU Langone Health — New York

Identifiers

NCT: NCT06637852 · 23-00945

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗