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Reliability of the triple-timed up-and-go test
Donald B Sanders1, Jeffrey T Guptill1, Kathy L Aleš2
1Neuromuscular Section, Department of Neurology, Duke University Medical Center, Box 3403, Durham, North Carolina, 27710, USA.
The triple-timed up-and-go (3TUG) test reliably assesses clinical function in Lambert-Eaton myasthenia (LEM) patients. This quick, noninvasive test demonstrates excellent reproducibility and agreement for measuring weakness in LEM.
Area of Science:
- Neurology
- Clinical Assessment
- Reproducibility Studies
Background:
- Lambert-Eaton myasthenia (LEM) is a rare autoimmune disorder affecting neuromuscular transmission.
- Assessing clinical function in LEM patients is crucial for monitoring disease progression and treatment efficacy.
- A reliable and objective measure is needed to quantify functional deficits in LEM.
Purpose of the Study:
- To evaluate the reliability of the novel triple-timed up-and-go (3TUG) test.
- To assess the intrarater reproducibility and interrater agreement of the 3TUG test in various participant groups.
- To determine if the 3TUG test is a suitable measure for clinical function in LEM patients.
Main Methods:
- The 3TUG test was administered to 25 control participants, 24 patients with non-LEM neuromuscular disease, and 12 LEM patients.
- Intrarater reproducibility and interrater agreement were assessed using the coverage probability (CP) method.
- Acceptable agreement was defined as a CP value ≥0.90 and <20% difference in test times.
Main Results:
- The 3TUG test demonstrated acceptable intrarater reproducibility across all participant groups (CP > 0.90).
- Interrater agreement for the 3TUG test was also confirmed to be acceptable in all groups (CP > 0.90).
- These findings indicate high reliability for the 3TUG test in measuring functional performance.
Conclusions:
- The 3TUG test is a reliable, noninvasive, and easily performable measure for assessing clinical weakness in LEM patients.
- The test requires minimal training and provides clinically relevant functional data.
- Further validation in a larger LEM cohort is ongoing to solidify its role as a clinical tool.
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