RecruitingNCT06470750

Feasibility of Patient-Centered Home Care (PCHC) to Reduce Disparities in High-Risk Black Men (BM) With Prostate Cancer (CaP)

Feasibility of Patient-Centered Home Care (PCHC) to Reduce Disparities in High-Risk Black Men (BM) With Advanced Prostate Cancer (CaP)


Sponsor

Mayo Clinic

Enrollment

77 participants

Start Date

Jul 25, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

This study evaluates the possibility of patient-centered home care as a new model of cancer care to reduce disparities and improve health related quality of life and patient-reported outcomes in Black patients with prostate cancer.


Eligibility

Sex: MALEMin Age: 18 Years

Inclusion Criteria19

  • GROUP 1 FOCUS GROUPS:
  • Individuals identifying as Black and male who are familiar with the landscape of medical care and cancer
  • GROUP 1 SURVEYS:
  • Are 18 years of age or older
  • Have histologic evidence of prostate adenocarcinoma
  • Are requiring, have required, or will require prostate cancer treatment
  • Have an understanding of the protocol and its requirements
  • Are willing to fill in a questionnaire and participate in a focused interview
  • Are able and willing to sign an informed consent
  • GROUP 1 INTERVIEWS:
  • Enrollment in the survey phase of the protocol
  • GROUP 2:
  • Are 18 years of age or older
  • Are Black men or other discounted patients (older adults, individuals residing in rural or remote areas, and those facing transportation challenges)
  • Have histologic evidence of prostate adenocarcinoma
  • Are requiring active standard hormone-based therapies (degarelix or leuprolide), antibone resorptive agents (zoledronic acid or denosumab), oral anticancer treatments (abiraterone or second-generation androgen receptor blockers) or intravenous chemotherapy (docetaxel)
  • Are receiving part of supportive care/symptom management and/or anti-cancer therapy in the home as part of Cancer Care Beyond Walls (CCBW)
  • Have an understanding of the protocol and its requirements
  • Are able and willing to sign informed consent

Exclusion Criteria11

  • GROUP 1 FOCUS GROUPS:
  • Individuals who do not identify as Black or male or who have had no extensive interaction with the healthcare system
  • GROUP 1 SURVEYS:
  • Do not identify as Black men
  • Have not been diagnosed with prostate cancer
  • GROUP 1 INTERVIEWS:
  • Not enrolled in the survey phase of the protocol
  • GROUP 2:
  • Do not identify as Black men or other discounted patients (older adults, individuals residing in rural or remote areas, and those facing transportation challenges)
  • Have not been diagnosed with histologic evidence of prostate adenocarcinoma
  • Are not requiring active standard anti-cancer therapy

Interventions

OTHERNon-Interventional Study

Non-interventional study


Locations(1)

Mayo Clinic in Florida

Jacksonville, Florida, United States

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NCT06470750


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