Currently, there are no standardised fall risk scores or guidelines on when to use appropriate assistive gait devices (AGDs) for people with neuromuscular disorders (NMDs). There is a clear medical unmet need to provide a battery of appropriate locomotor gait assessments to determine the risk of falling for patients with NMDs and give clear guidelines to prescribe an appropriate AGD. The primary goal is to confirm whether the clinical battery assessments (Heel-Rise Test (HRT), Chair-Rise Test (CRT), Semi-tandem Stand (STS), Trunk-Rise Test (TRT), Foot-Tapping Test (FTT), Timed Up and Go (TUG), 10-Meter-Walk Test (10MWT) and 6-Minute-Walk Test (6MWT) can be validated and generalized to other NMD target populations that meet broader eligibility criteria based on used clinical assessments. The second objective of this project is to provide intra- and inter-observer reliability and test-retest reliability of included clinical assessments used to determine the risk of falling for patients with NMDs. Finally, all data will be compared with norm data from the healthy population (n=15) collected retrospectively.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Chair-Rise Test (CRT)
Timeframe: Immediately after the ICF is signed
Trunk Rise Test (TRT)
Timeframe: Immediately after the ICF is signed
Heel-Rise Test (HRT)
Timeframe: Immediately after the ICF is signed
Semi-Tandem stand, eyes open (STSeo) and eyes closed (STSeo)
Timeframe: Immediately after the ICF is signed
Foot-Tapping Test (FTT) (sitting)
Timeframe: Immediately after the ICF is signed
10-Meter Walk Test
Timeframe: Immediately after the ICF is signed
Six-Minute Walk test
Timeframe: Immediately after the ICF is signed
Time Up and Go (TUG)
Timeframe: Immediately after the ICF is signed