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Sexual and Urinary Function Improvement for Cancer Survivors

NYU Langone Health logo

NYU Langone Health

Status

Begins enrollment in a year or more

Conditions

Urinary Dysfunction
Sexual Dysfunction

Treatments

Behavioral: SUFICS-PACT

Study type

Interventional

Funder types

Other

Identifiers

NCT06637852
23-00945

Details and patient eligibility

About

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.

Enrollment

200 estimated patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

SUFICS-PACT
Experimental group
Description:
The Sexual and Urinary Function Improvement for Cancer Survivors- Promoting Access to Collaborative Treatment (SUFICS-PACT) intervention integrates a collaborative care model in primary care to facilitate problem identification, comprehensive treatment, and close follow-up for sexual and urinary dysfunction.
Treatment:
Behavioral: SUFICS-PACT
Usual care
No Intervention group
Description:
Participants assigned to this group will continue with usual care.

Trial contacts and locations

1

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Central trial contact

Favour Nnah; Nnenaya Mmonu, MD, MS

Data sourced from clinicaltrials.gov

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