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)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 3 (9 locations)

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