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Clinical Trials/NCT03319290
NCT03319290
Unknown
N/A

Medical Provider Experience Assessment Healthcare Decisions Post-Testing, Risk Reducing, and Preventative Strategies Using BRCA2 and BRCA2 Genetic Testing

Data Collection Analysis Business Management1 site in 1 country2,000 target enrollmentOctober 17, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Hereditary Cancer
Sponsor
Data Collection Analysis Business Management
Enrollment
2000
Locations
1
Primary Endpoint
Provider Structures and Processes
Last Updated
7 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 17, 2017
End Date
October 17, 2020
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Data Collection Analysis Business Management
Responsible Party
Sponsor

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Provider Structures and Processes

Time Frame: 36 months

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

Study Sites (1)

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