Status:
UNKNOWN
Refining Information Technology Support for Genetics in Medicine
Lead Sponsor:
Brigham and Women's Hospital
Collaborating Sponsors:
National Institutes of Health (NIH)
National Library of Medicine (NLM)
Conditions:
Hypertrophic Cardiomyopathy
Hearing Loss
Eligibility:
All Genders
Brief Summary
The clinical use of genetic testing is expanding and, as a result, the number of variants identified in patients is growing. Knowledge of the clinical impact of these variants improves over time. Howe...
Detailed Description
A. Specific Aims Aim 1: To assess the usability of successive versions of our EHR genetic display screens and variant-based patient search functionality. Formal usability studies will be conducted w...
Eligibility Criteria
Inclusion
- Study subjects selected from Partners HealthCare and non-Partners study sites include:
- treating clinicians
- geneticists
- genetic counselors
- pathologists
Exclusion
- N/A
Key Trial Info
Start Date :
September 1 2009
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 1 2014
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT01225978
Start Date
September 1 2009
End Date
December 1 2014
Last Update
January 24 2014
Active Locations (9)
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1
Brigham and Women's Hospital Cardiovascular Genetics Center
Boston, Massachusetts, United States, 02115
2
Children's Hospital Boston's Cardiovascular Genetics Clinic
Boston, Massachusetts, United States, 02115
3
Children's Hospital Boston's Ear, Nose, and Throat Clinic
Boston, Massachusetts, United States, 02115
4
Massachusetts General Hospital Division of Pulmonary Oncology
Boston, Massachusetts, United States, 02115