MedPath

se of an aid to improve communication of genetic risk information amongst families with hypertrophic cardiomyopathy.

Not Applicable
Recruiting
Conditions
Hypertrophic cardiomyopathy
Human Genetics and Inherited Disorders - Other human genetics and inherited disorders
Cardiovascular - Other cardiovascular diseases
Registration Number
ACTRN12617000706370
Lead Sponsor
The University of Sydney
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
45
Inclusion Criteria

Consecutive hypertrophic cardiomyopathy (HCM) probands (first individual to present to the clinic) attending the genetic heart disease and/or HCM clinic at RPA hospital and Charles Perkins Clinical Research Facility with a diagnosis of HCM and a genetic test result ready for return. Inclusion criteria are sufficient English, over 18 years and having a genetic result for HCM available.

Exclusion Criteria

Under 18 years, genetic result unavailable, low level English.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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