Performance of the Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS) in multicenter clinical trials
- PMID: 9419047
- DOI: 10.1016/s0022-510x(97)00237-2
Performance of the Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS) in multicenter clinical trials
Abstract
The Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS) is a 10-item functional inventory which was devised for use in therapeutic trials in ALS. Each item is rated on a 0-4 scale by the patient and/or caregiver, yielding a maximum score of 40 points. The ALSFRS assesses patients' levels of self-sufficiency in areas of feeding, grooming, ambulation and communication. Rotated factor analysis of the ALSFRS found that the rating items group logically and consistently into four categories. The ALSFRS has been validated both cross-sectionally and longitudinally against muscle strength testing, the Schwab and England ADL rating scale, the Clinical Global Impression of Change (CGIC) scale, and independent assessments of patient's functional status. In this report, we use the data provided by the placebo patients who participated in the ALS CNTF Treatment Study (ACTS) to demonstrate the robustness, test-retest reliability and consistency of the ALSFRS as employed in a large, multicenter clinical trial.
Similar articles
-
The Amyotrophic Lateral Sclerosis Functional Rating Scale. Assessment of activities of daily living in patients with amyotrophic lateral sclerosis. The ALS CNTF treatment study (ACTS) phase I-II Study Group.Arch Neurol. 1996 Feb;53(2):141-7. Arch Neurol. 1996. PMID: 8639063 Clinical Trial.
-
[Study of functional rating scale for amyotrophic lateral sclerosis: revised ALSFRS(ALSFRS-R) Japanese version].No To Shinkei. 2001 Apr;53(4):346-55. No To Shinkei. 2001. PMID: 11360474 Japanese.
-
Exploratory double-blind, parallel-group, placebo-controlled study of edaravone (MCI-186) in amyotrophic lateral sclerosis (Japan ALS severity classification: Grade 3, requiring assistance for eating, excretion or ambulation).Amyotroph Lateral Scler Frontotemporal Degener. 2017 Oct;18(sup1):40-48. doi: 10.1080/21678421.2017.1361441. Amyotroph Lateral Scler Frontotemporal Degener. 2017. PMID: 28872915 Clinical Trial.
-
Remote-Use Applications of the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised Clinical Outcome Assessment Tool: A Scoping Review.Value Health. 2024 Oct;27(10):1454-1465. doi: 10.1016/j.jval.2024.05.005. Epub 2024 May 23. Value Health. 2024. PMID: 38795957
-
Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND).Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):191-206. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129806 Review.
Cited by
-
Validation of the German version of the extended ALS functional rating scale as a patient-reported outcome measure.J Neurol. 2013 Sep;260(9):2242-55. doi: 10.1007/s00415-013-6955-6. Epub 2013 Jun 5. J Neurol. 2013. PMID: 23736973
-
Predicting Early Bulbar Decline in Amyotrophic Lateral Sclerosis: A Speech Subsystem Approach.Behav Neurol. 2015;2015:183027. doi: 10.1155/2015/183027. Epub 2015 Jun 2. Behav Neurol. 2015. PMID: 26136624 Free PMC article.
-
Advances in clinical trials for amyotrophic lateral sclerosis.Curr Neurol Neurosci Rep. 2005 Feb;5(1):48-54. doi: 10.1007/s11910-005-0023-2. Curr Neurol Neurosci Rep. 2005. PMID: 15676108 Review.
-
How common are ALS plateaus and reversals?Neurology. 2016 Mar 1;86(9):808-12. doi: 10.1212/WNL.0000000000002251. Epub 2015 Dec 9. Neurology. 2016. PMID: 26658909 Free PMC article. Clinical Trial.
-
Discriminant Ability of the Eating Assessment Tool-10 to Detect Swallowing Safety and Efficiency Impairments.Laryngoscope. 2022 Dec;132(12):2319-2326. doi: 10.1002/lary.30043. Epub 2022 Feb 9. Laryngoscope. 2022. PMID: 35137963 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous
