Aerobic Exercise Therapy in Ambulatory Patients With ALS: A Randomized Controlled Trial

Author:

van Groenestijn Annerieke C.123,Schröder Carin D.12,van Eijk Ruben P. A.1,Veldink Jan H.1,Kruitwagen-van Reenen Esther T.1,Groothuis Jan T.4,Grupstra Hepke F.3,Tepper Marga5,van Vliet Reinout O.6,Visser-Meily Johanna M. A.1,van den Berg Leonard H.1

Affiliation:

1. University Medical Center Utrecht, Netherlands

2. De Hoogstraat Rehabilitation, Utrecht, Netherlands

3. University of Amsterdam, Netherlands

4. Radboud University Medical Center, Nijmegen, Netherlands

5. University of Groningen, Netherlands

6. Roessingh, Center for Rehabilitation, Enschede, Netherlands

Abstract

Background: Weakness caused by motor neuron degeneration in amyotrophic lateral sclerosis (ALS) may result in avoidance of physical activity, resulting in deconditioning and reduced health-related quality of life (HRQoL). Objective: To study the effectiveness of aerobic exercise therapy (AET) on disease-specific and generic HRQoL in ambulatory patients with ALS. Methods: We conducted a multicenter, assessor-blinded, randomized controlled trial. Using a biphasic randomization model, ambulatory ALS patients were assigned (1:1) to AET+usual care (UC), or UC. AET consisted of a 16-week aerobic cycling exercise program. Primary outcome measures were the 40-item ALS assessment questionnaire (ALSAQ-40), and the mental component summary (MCS) and physical component summary (PCS) scores of the short-form survey (SF-36), using linear mixed effects models. Per-protocol (PP) analysis was performed for those patients who attended ≥75% of the training sessions; controls were matched (1:1) by propensity score matching. Results: Of 325 screened patients, 57 were randomized: 27 to AET+UC and 30 to UC. No significant mean slope differences between groups were observed for ALSAQ-40 (-1.07; 95% confidence interval [CI] -2.6 to 0.5, P=0.172) nor for SF-36 MCS (0.24; -0.7 to 1.1, P=0.576) or PCS (-0.51; -1.4 to 0.38, P=0.263). There were no adverse events related to the AET. PP-analyses showed significantly less deterioration in ALSAQ-40 (-1.88, -3.8 to 0.0, P=0.046) in AET+UC compared to UC. Conclusions: AET+UC was not superior to UC alone in preserving HRQoL in ambulatory ALS patient. However, the study was unfortunately underpowered, because only 10 patients completed the protocol. AET+UC may preserve disease-specific HRQoL in slow progressors. Clinical trial registration number: Netherlands National Trial Register (NTR): 1616.

Funder

This study was supported by the Netherlands Organization for Health Research and Development (ZonMw) and the Prinses Beatrix Spierfonds (PBS).

Publisher

SAGE Publications

Subject

General Medicine

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