MedPath

Increase Surveillance for Breast and Ovarian Cancers, Also to Determine Targeted Risk-reducing and Preventative Strategies

Conditions
Hereditary Cancer
Registration Number
NCT03319290
Lead Sponsor
Data Collection Analysis Business Management
Brief Summary

Observational study is to increase surveillance for breast and ovarian cancers, also to determine targeted risk-reducing and preventative strategies.

Detailed Description

The general design of this study is collecting data and reviewing the Principal Investigators' (P.I.) Standard Operating Procedures (SOP) on BRCA testing and changes made to their specific SOP.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
2000
Inclusion Criteria
  • Must be a Medical Practitioner

    • Medical Doctor (MD)
    • Doctor of Osteopathic (DO)
    • Physician Assistant (PA)
    • Advanced Practice Registered Nurse (APRN)
    • Nurse Practitioner (NP)
  • Must have a current standard operating procedure that includes obtaining/reviewing medical history and family medical history

Exclusion Criteria
  • Government-funded insurance data cannot be included in the study.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Provider Structures and Processes36 months

Plan of Care Changes due to BRCA testing. Provider based observational survey system on the health and well-being of patients and populations

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

DCABM

🇺🇸

Land O' Lakes, Florida, United States

DCABM
🇺🇸Land O' Lakes, Florida, United States
© Copyright 2025. All Rights Reserved by MedPath