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NCT03322176 Clinical Trial

Healthcare Decisions Post-Testing, Risk-reducing and Preventative Strategies Using LYNCH Genetic Testing Reducing, and Preventative Strategies Using LYNCH Genetic Testing

Colon Cancer Clinical Trial

Official title:
Medical Provider Experience Assessment Healthcare Decisions Post-Testing, Risk-Reducing, and Preventative Strategies Using LYNCH Genetic Testing

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT03322176
Other study ID # PAS1461
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date October 17, 2017
Est. completion date November 1, 2020

Study information
Verified date January 2019
Source Data Collection Analysis Business Management
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Increase surveillance for LYNCH Syndrome

Description:

The purpose of this minimal risk, observational survey is to increase surveillance for Lynch Syndrome (hereditary non-polyposis colon cancer), Colorectal, and Endometrial cancer, also to determine targeted risk-reducing and preventative strategies.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 200
Est. completion date November 1, 2020
Est. primary completion date October 17, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 64 Years
Eligibility 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

Related Conditions & MeSH terms

Intervention

Other:
• Genetic testing
LYNCH genetic testing

Locations
Country Name City State
United States DCABM Land O' Lakes Florida

Sponsors (2)
Lead Sponsor Collaborator
Data Collection Analysis Business Management PAS Research Services

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Provider Structures and Processes Plan of Care Changes due to LYNCH genetic testing. Provider based observational survey system on the health and well-being of patients and populations 36 months
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