Evaluating In Home Cancer Therapy Versus In Clinic Cancer Therapy in Black Men With Locally Advanced, Biochemically Recurrent and Metastatic Prostate Cancer
NCT07073794 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 38
Last updated 2026-03-25
Summary
This phase II trial evaluates the impact of cancer therapy in the patients' home compared to in the clinic on safety, side effects, patient preference, and satisfaction in Black men with prostate cancer that has spread to nearby tissue or lymph nodes (locally advanced), that has increasing prostate-specific antigen after treatment (biochemically recurrent) or that has spread from where it first started (primary site) to other places in the body (metastatic). Typically drug-related cancer care is conducted at a medical center which causes patients to have to spend considerable time away from family, friends, and familiar surroundings. This separation may add to the physical, emotional, social, and financial burden for patients and their families during this difficult time in their lives. Therapy administered to a patient in the patients' residence in the comfort of familiar surrounding using Cancer Connected Access and Remote Expertise (CARE) Beyond Walls (CCBW) may help reduce psychological and financial distress, increase access to care and improve treatment compliance. Giving cancer therapy in the home compared in the clinic may be safe, tolerable and improve patient satisfaction with overall cancer care in Black men with locally advanced, biochemically recurrent or metastatic prostate cancer.
Conditions
- Biochemically Recurrent Prostate Carcinoma
- Locally Advanced Prostate Carcinoma
- Metastatic Prostate Carcinoma
- Stage III Prostate Cancer AJCC v8
- Stage IV Prostate Cancer AJCC v8
Interventions
- DRUG
-
Cancer Therapeutic Procedure
Given standard of care cancer treatment in clinic
- DRUG
-
Cancer Therapeutic Procedure
Given standard of care cancer treatment in home
- OTHER
-
Health Care Delivery
Receive in home cancer treatment with CCBW
- OTHER
-
Questionnaire Administration
Ancillary studies
Sponsors & Collaborators
-
Congressionally Directed Medical Research Programs
collaborator FED - lead OTHER
Principal Investigators
-
Roxana S. Dronca, MD · Mayo Clinic
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- MALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-08-27
- Primary Completion
- 2028-08-27
- Completion
- 2028-08-27
Countries
- United States
Study Locations
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