Intensive speech and language therapy in patients with chronic aphasia after stroke: a randomised, open-label, blinded-endpoint, controlled trial in a health-care setting
- PMID: 28256356
- DOI: 10.1016/S0140-6736(17)30067-3
Intensive speech and language therapy in patients with chronic aphasia after stroke: a randomised, open-label, blinded-endpoint, controlled trial in a health-care setting
Erratum in
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Department of Error.Lancet. 2017 Apr 15;389(10078):1518. doi: 10.1016/S0140-6736(17)30955-8. Lancet. 2017. PMID: 28422028 No abstract available.
Abstract
Background: Treatment guidelines for aphasia recommend intensive speech and language therapy for chronic (≥6 months) aphasia after stroke, but large-scale, class 1 randomised controlled trials on treatment effectiveness are scarce. We aimed to examine whether 3 weeks of intensive speech and language therapy under routine clinical conditions improved verbal communication in daily-life situations in people with chronic aphasia after stroke.
Methods: In this multicentre, parallel group, superiority, open-label, blinded-endpoint, randomised controlled trial, patients aged 70 years or younger with aphasia after stroke lasting for 6 months or more were recruited from 19 inpatient or outpatient rehabilitation centres in Germany. An external biostatistician used a computer-generated permuted block randomisation method, stratified by treatment centre, to randomly assign participants to either 3 weeks or more of intensive speech and language therapy (≥10 h per week) or 3 weeks deferral of intensive speech and language therapy. The primary endpoint was between-group difference in the change in verbal communication effectiveness in everyday life scenarios (Amsterdam-Nijmegen Everyday Language Test A-scale) from baseline to immediately after 3 weeks of treatment or treatment deferral. All analyses were done using the modified intention-to-treat population (those who received 1 day or more of intensive treatment or treatment deferral). This study is registered with ClinicalTrials.gov, number NCT01540383.
Findings: We randomly assigned 158 patients between April 1, 2012, and May 31, 2014. The modified intention-to-treat population comprised 156 patients (78 per group). Verbal communication was significantly improved from baseline to after intensive speech and language treatment (mean difference 2·61 points [SD 4·94]; 95% CI 1·49 to 3·72), but not from baseline to after treatment deferral (-0·03 points [4·04]; -0·94 to 0·88; between-group difference Cohen's d 0·58; p=0·0004). Eight patients had adverse events during therapy or treatment deferral (one car accident [in the control group], two common cold [one patient per group], three gastrointestinal or cardiac symptoms [all intervention group], two recurrent stroke [one in intervention group before initiation of treatment, and one before group assignment had occurred]); all were unrelated to study participation.
Interpretation: 3 weeks of intensive speech and language therapy significantly enhanced verbal communication in people aged 70 years or younger with chronic aphasia after stroke, providing an effective evidence-based treatment approach in this population. Future studies should examine the minimum treatment intensity required for meaningful treatment effects, and determine whether treatment effects cumulate over repeated intervention periods.
Funding: German Federal Ministry of Education and Research and the German Society for Aphasia Research and Treatment.
Copyright © 2017 Elsevier Ltd. All rights reserved.
Comment in
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Does intensity matter in aphasia rehabilitation?Lancet. 2017 Apr 15;389(10078):1494-1495. doi: 10.1016/S0140-6736(17)30546-9. Epub 2017 Feb 28. Lancet. 2017. PMID: 28256354 No abstract available.
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Intensive speech and language therapy after stroke - Authors' reply.Lancet. 2017 Jul 15;390(10091):228-229. doi: 10.1016/S0140-6736(17)31801-9. Lancet. 2017. PMID: 28721875 No abstract available.
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Intensive speech and language therapy after stroke.Lancet. 2017 Jul 15;390(10091):228. doi: 10.1016/S0140-6736(17)31800-7. Lancet. 2017. PMID: 28721876 No abstract available.
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