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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05931211
Other study ID # 202305039RINB
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 30, 2023
Est. completion date December 31, 2024

Study information

Verified date May 2023
Source National Taiwan University Hospital
Contact Hsi-Wen Huang, MSc
Phone 886-2-23123456
Email lovelyeva39@gmail.com
Is FDA regulated No
Health authority
Study type Observational

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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date December 31, 2024
Est. primary completion date June 30, 2024
Accepts healthy volunteers No
Gender All
Age group 3 Years and older
Eligibility Inclusion Criteria: - Having a diagnosis of SMA with genetics confirmed as 5q SMA. - Above 3 years of age (capable of performing motor assessments). Exclusion Criteria: - Having severe respiratory and other medical conditions precluding safe participation in standardized motor function tests. - Having any orthopedic surgery during the past 6 months. - Women who are pregnant.

Study Design


Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Revised Upper Limb Module The physiotherapist will perform a serious of motor test to evaluate the patient's upper limb motor function. This test is to observe the manual ability on different tasks in sitting position, including drawing along the path, opening Ziploc container, or lifting weight. And the therapist will score for each item. The Revised Upper Limb Module (RULM) are consist of 19 items. It takes about 15-20 minutes for testing. 15-20 minutes
See also
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