Status:
COMPLETED
Genetics Adviser: Evaluating a Digital Decision Support Tool for Genetic Results
Lead Sponsor:
Unity Health Toronto
Conditions:
Cancer
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Oncologists are increasingly using genomic sequencing to diagnose and optimize care for their patients. A consequence of this technology is its capacity to detect a patient's risk for thousands of cur...
Detailed Description
BACKGROUND: Genomic sequencing (GS) is a driver of precision oncology. Oncologists are increasingly using tumour GS for precision oncology care, which is often times accompanied by germline GS on norm...
Eligibility Criteria
Inclusion
- Previous control participants from the Incidental Genomics study who have given permission to be re-contacted for related research or a patient who has undergone germline genetic testing (single gene or panel) and received a negative or inconclusive result.
- 18 years old or older
- Speak and read English.
Exclusion
- For participants newly recruited (not part of parent trial CTO# 0819)
- Received positive panel testing or panel sequencing
- Have not had germline single gene testing related to their primary cancer condition (e.g., BRCA1/2 for breast/ovarian cancer, MLH, MSH, PMS colorectal cancer, etc.)
- Received a positive germline genetic test for a cancer gene mutation (e.g., BRCA1/2, MLH, MSH, PMS, APC, MUTYH, etc.)
- Currently under cancer treatment
- In stage 4, progressive metastatic cancer
- For all
- Do not speak or read English
- Under 18 years of age
Key Trial Info
Start Date :
June 22 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 6 2024
Estimated Enrollment :
133 Patients enrolled
Trial Details
Trial ID
NCT04725565
Start Date
June 22 2021
End Date
April 6 2024
Last Update
May 31 2024
Active Locations (3)
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1
Sunnybrook Hospital
Toronto, Ontario, Canada, M4N 3M5
2
Mount Sinai Hospital
Toronto, Ontario, Canada, M5G 1X5
3
Princess Margret Cancer Centre
Toronto, Ontario, Canada, M5G 2C1