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Clinical Trial Summary

This study will incorporate patients/ caregivers' perspectives to investigate the performance in daily activities of individuals with SMA and how it relates to their motor function abilities.


Clinical Trial Description

Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease that causes progressive muscle weakness and atrophy and eventually leads to loss of function. Despite recent advances in disease-modifying treatments, SMA can still significantly impact an individual's functioning in daily living and quality of life. This study will incorporate patients/ caregivers' perspectives to investigate the performance in daily activities of individuals with SMA and how it relates to their motor function abilities. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05931211
Study type Observational
Source National Taiwan University Hospital
Contact Hsi-Wen Huang, MSc
Phone 886-2-23123456
Email lovelyeva39@gmail.com
Status Not yet recruiting
Phase
Start date June 30, 2023
Completion date December 31, 2024

See also
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