The SMARTER-CM Study
Research type
Research Study
Full title
Genetics, Imaging And Artificial Intelligence for Precision Care in Cardiomyopathy
IRAS ID
313058
Contact name
Becky Ward
Contact email
Sponsor organisation
Imperial College London
Duration of Study in the UK
4 years, 10 months, 31 days
Research summary
Cardiomyopathies are diseases of the heart muscle. Known genetic factors may account for some cardiomyopathy cases but there is still much to understand about the genetic and environmental causes and how the disease progresses. Finding new ways to diagnose and treat cardiomyopathies could improve the health and well-being of patients with these conditions.
This study will collect data from individuals with cardiomyopathy or related heart muscle disease, or with a possible genetic predisposition to cardiomyopathy, and follow them over time to observe the progress of their heart and health.
We will collect DNA, blood samples, and detailed clinical & lifestyle information at the start of the study, and data collected during routine healthcare visits over time.
• learn what causes cardiomyopathy, and therefore how to treat it
• understand why cardiomyopathy progresses differently in different people, so that we can improve our ability to recognise who will benefit from different treatments at different timesWe will collaborate with other centres internationally (the SHaRe consortium) to collect a large of group of participants with similar cardiomyopathies, providing us with the power to identify new pathways that cause disease and ways of predicting which participants are at risk of having more severe disease.
REC name
East of Scotland Research Ethics Service REC 2
REC reference
22/ES/0044
Date of REC Opinion
23 Jan 2023
REC opinion
Further Information Favourable Opinion