Literature DB >> 10631656

Development and validation of a short measure of health status for individuals with amyotrophic lateral sclerosis/motor neurone disease: the ALSAQ-40.

C Jenkinson1, R Fitzpatrick, C Brennan, M Bromberg, M Swash.   

Abstract

In recent years there has been an increased appreciation of the importance of measuring health status from the patient's point of view, but until now no attempt has been made to develop an amyotrophic lateral sclerosis (ALS)-specific health status measure. The development of such an instrument is especially relevant now with the introduction of drugs that prolong life in ALS but limited data is available on the impact such treatments have on quality of life. This paper reports on the development of an ALS-specific measure, the forty item ALS assessment questionnaire (ALSAQ-40). The development of the ALSAQ-40 followed three main stages. Stage 1 consisted of in-depth, semi-structured exploratory interviews conducted on a sample of 18 patients to identify areas of salience and concern to patients with ALS. These interviews generated 78 candidate questions. In stage 2, the 78-item questionnaire was used in a postal survey to identify appropriate rephrasing/shortening and to determine the acceptability of the measure. In addition, this exercise helped identify sub-scales of the instrument addressing different dimensions of ALS. Finally in stage 3 the data collected in stage 2 was analysed to areas measured by the instrument and to remove redundant questions. The resulting measure contains forty questions measuring five areas of health status: Eating and Drinking, Communication, ADL/independence, Physical mobility, Emotional Functioning. The measure has high face, internal and construct validity and is likely to prove a useful measure in the evaluation of treatment regimes for ALS/MND.

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Year:  1999        PMID: 10631656     DOI: 10.1007/bf03161085

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  9 in total

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Review 2.  Health outcome and quality-of-life measurements in amyotrophic lateral sclerosis.

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Journal:  Med Care       Date:  1999-01       Impact factor: 2.983

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Authors:  G Bensimon; L Lacomblez; V Meininger
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9.  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.

Authors: 
Journal:  Arch Neurol       Date:  1996-02
  9 in total
  25 in total

Review 1.  Measurement of quality of life in neurodegenerative disorders.

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2.  Difference in chronological changes of outcome measures between untreated and placebo-treated patients of spinal and bulbar muscular atrophy.

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4.  Efficacy and safety of leuprorelin acetate for subjects with spinal and bulbar muscular atrophy: pooled analyses of two randomized-controlled trials.

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Journal:  J Neurol       Date:  2019-03-07       Impact factor: 4.849

5.  Safety and Efficacy of Nanocurcumin as Add-On Therapy to Riluzole in Patients With Amyotrophic Lateral Sclerosis: A Pilot Randomized Clinical Trial.

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Journal:  Neurotherapeutics       Date:  2018-04       Impact factor: 7.620

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Authors:  Josephine M Norquist; Ray Fitzpatrick; Crispin Jenkinson
Journal:  Qual Life Res       Date:  2004-10       Impact factor: 4.147

Review 7.  Evaluation of quality of life in individuals with severe chronic motor disability: A major challenge.

Authors:  Marie-Christine Rousseau; Karine Baumstarck; Thierry Billette de Villemeur; Pascal Auquier
Journal:  Intractable Rare Dis Res       Date:  2016-05

8.  Patients' health-related quality-of-life and health state values for motor neurone disease/amyotrophic lateral sclerosis.

Authors:  C Green; G Kiebert; C Murphy; J D Mitchell; M O'Brien; A Burrell; P N Leigh
Journal:  Qual Life Res       Date:  2003-08       Impact factor: 4.147

9.  Validation of the German version of the extended ALS functional rating scale as a patient-reported outcome measure.

Authors:  Susanne Abdulla; Stefan Vielhaber; Sonja Körner; Judith Machts; Hans-Jochen Heinze; Reinhard Dengler; Susanne Petri
Journal:  J Neurol       Date:  2013-06-05       Impact factor: 4.849

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Authors:  Vanina Dal Bello-Haas; Julaine M Florence
Journal:  Cochrane Database Syst Rev       Date:  2013-05-31
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