跳至主要内容
临床试验/NCT06637852
NCT06637852尚未招募不适用

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

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2026年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
200
试验地点
1
主要终点
Number of patients identified and treated for sexual dysfunction

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •At least 18 years old
  • •Have a diagnosis of prostate cancer
  • •Have sought care/treatment for prostate cancer

排除标准

  • •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.

研究组 & 干预措施

SUFICS-PACT

Experimental

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.

干预措施: SUFICS-PACT (Behavioral)

Usual care

No Intervention

Participants assigned to this group will continue with usual care.

结局指标

主要结局

Number of patients identified and treated for sexual dysfunction

时间窗: Year 5

Number of patients identified and treated for urinary dysfunction

时间窗: Year 5

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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