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Speech Entrainment for Aphasia Recovery (SpARc) phase II trial design
BACKGROUND: and purpose: Speech entrainment therapy (SET) is a computerized therapeutic approach that involves mimicking an audiovisual speech model to improve speech production. In a pilot study using SET for treatment of post-stroke non-fluent aphasia, significant gains were achieved in verbs per...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606333/ https://www.ncbi.nlm.nih.gov/pubmed/34841125 http://dx.doi.org/10.1016/j.conctc.2021.100876 |
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author | Cassarly, Christy Doyle, Anna Ly, Trinh Horn, Janet Aitchison, Mary Elm, Jordan Fridriksson, Julius Bonilha, Leonardo |
author_facet | Cassarly, Christy Doyle, Anna Ly, Trinh Horn, Janet Aitchison, Mary Elm, Jordan Fridriksson, Julius Bonilha, Leonardo |
author_sort | Cassarly, Christy |
collection | PubMed |
description | BACKGROUND: and purpose: Speech entrainment therapy (SET) is a computerized therapeutic approach that involves mimicking an audiovisual speech model to improve speech production. In a pilot study using SET for treatment of post-stroke non-fluent aphasia, significant gains were achieved in verbs per minute (VPM) during discourse using untrained items 1 and 6 weeks after treatment, suggesting that SET may yield meaningful improvements in fluent spontaneous speech for individuals with non-fluent aphasia. METHODS: The Speech Entrainment for Aphasia Recovery (SpARc) trial is a prospective, randomized, assessor-blinded, multicenter phase II clinical trial studying persons with chronic post-stroke non-fluent aphasia. Participants will be randomized to 3 weeks, 4.5 weeks, or 6 weeks of SET delivered via telehealth or a no SET control condition for 6 weeks. 80 adults (ages 21–81) with history of left hemisphere ischemic or hemorrhagic stroke with residual chronic (>6 months post stroke) non-fluent aphasia diagnosed by the Western Aphasia Battery-Revised (WAB-R) will be randomized (1:1:1:1) over 4 years. The trial will be conducted at the clinical research facilities at three sites: the Medical University of South Carolina, the University of South Carolina, and the University of Utah. CONCLUSIONS: This paper details the trial design of the SpARc trial, which aims to determine the dose of SET that will generate the highest effect size on speech fluency, VPM, sustained at 3 months post-treatment compared to a no SET control arm, for individuals with chronic post-stroke non-fluent aphasia to permit a future definitive trial to test the clinical utility of SET. |
format | Online Article Text |
id | pubmed-8606333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-86063332021-11-26 Speech Entrainment for Aphasia Recovery (SpARc) phase II trial design Cassarly, Christy Doyle, Anna Ly, Trinh Horn, Janet Aitchison, Mary Elm, Jordan Fridriksson, Julius Bonilha, Leonardo Contemp Clin Trials Commun Article BACKGROUND: and purpose: Speech entrainment therapy (SET) is a computerized therapeutic approach that involves mimicking an audiovisual speech model to improve speech production. In a pilot study using SET for treatment of post-stroke non-fluent aphasia, significant gains were achieved in verbs per minute (VPM) during discourse using untrained items 1 and 6 weeks after treatment, suggesting that SET may yield meaningful improvements in fluent spontaneous speech for individuals with non-fluent aphasia. METHODS: The Speech Entrainment for Aphasia Recovery (SpARc) trial is a prospective, randomized, assessor-blinded, multicenter phase II clinical trial studying persons with chronic post-stroke non-fluent aphasia. Participants will be randomized to 3 weeks, 4.5 weeks, or 6 weeks of SET delivered via telehealth or a no SET control condition for 6 weeks. 80 adults (ages 21–81) with history of left hemisphere ischemic or hemorrhagic stroke with residual chronic (>6 months post stroke) non-fluent aphasia diagnosed by the Western Aphasia Battery-Revised (WAB-R) will be randomized (1:1:1:1) over 4 years. The trial will be conducted at the clinical research facilities at three sites: the Medical University of South Carolina, the University of South Carolina, and the University of Utah. CONCLUSIONS: This paper details the trial design of the SpARc trial, which aims to determine the dose of SET that will generate the highest effect size on speech fluency, VPM, sustained at 3 months post-treatment compared to a no SET control arm, for individuals with chronic post-stroke non-fluent aphasia to permit a future definitive trial to test the clinical utility of SET. Elsevier 2021-11-16 /pmc/articles/PMC8606333/ /pubmed/34841125 http://dx.doi.org/10.1016/j.conctc.2021.100876 Text en © 2021 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/3.0/igo/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/igo/). |
spellingShingle | Article Cassarly, Christy Doyle, Anna Ly, Trinh Horn, Janet Aitchison, Mary Elm, Jordan Fridriksson, Julius Bonilha, Leonardo Speech Entrainment for Aphasia Recovery (SpARc) phase II trial design |
title | Speech Entrainment for Aphasia Recovery (SpARc) phase II trial design |
title_full | Speech Entrainment for Aphasia Recovery (SpARc) phase II trial design |
title_fullStr | Speech Entrainment for Aphasia Recovery (SpARc) phase II trial design |
title_full_unstemmed | Speech Entrainment for Aphasia Recovery (SpARc) phase II trial design |
title_short | Speech Entrainment for Aphasia Recovery (SpARc) phase II trial design |
title_sort | speech entrainment for aphasia recovery (sparc) phase ii trial design |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606333/ https://www.ncbi.nlm.nih.gov/pubmed/34841125 http://dx.doi.org/10.1016/j.conctc.2021.100876 |
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