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Speech Entrainment for Aphasia Recovery (SpARc) phase II trial design. | LitMetric

AI Article Synopsis

  • Speech Entrainment Therapy (SET) is being tested in a pilot study for improving speech production in individuals with non-fluent aphasia post-stroke, showing significant increases in verbs per minute after treatment.
  • The ongoing SpARc trial aims to investigate the effectiveness of different durations of SET (3, 4.5, or 6 weeks) using a randomized control design, enrolling 80 adults with chronic non-fluent aphasia across three clinical research sites.
  • The trial seeks to determine the optimal dose of SET for improving speech fluency and sustained gains within three months post-treatment, setting the stage for future studies to validate SET's clinical benefits.

Article Abstract

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606333PMC
http://dx.doi.org/10.1016/j.conctc.2021.100876DOI Listing

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