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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...

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Autores principales: Cassarly, Christy, Doyle, Anna, Ly, Trinh, Horn, Janet, Aitchison, Mary, Elm, Jordan, Fridriksson, Julius, Bonilha, Leonardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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.
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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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