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NCT Number: NCT06048159

Transcranial Alternating Current Stimulation (tACS) for the Recovery of Phonological Short-Term Memory in Patients With Aphasia After Stroke

This study will assess the effects of transcranial alternating current stimulation (tACS) on language recovery after stroke.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Aphasia is a debilitating disorder, typically resulting from damage to the left hemisphere, that can impair a range of communication abilities, including language production and comprehension, reading, and writing. Approximately 180,000 new cases of aphasia are identified per year, and approximately 1 million or 1 in 250 are living with aphasia in the United States. Treatments are limited and provide modest benefits at best. The current emphasis in aphasia rehabilitation is to formulate intensive speech and language therapies and augment therapeutic benefits, potentially with brain stimulation concurrent with therapies.

The current study will investigate the efficacy of high-definition tACS (HD-tACS) to help restore neural oscillatory activity in stroke survivors with aphasia. TACS differs from trancranial direct current stimulation (tDCS), a widely used brain stimulation paradigm, in that sinusoidal or alternating currents are delivered rather than direct currents. TACS is shown to manipulate ongoing oscillatory brain activity and also to modulate synchronization (or connectivity) between targeted brain areas. This feature of tACS is quite attractive, given the new body of evidence suggesting that language impairments stem from diminished brain connectivity and ensuing disruptions in the language network due to stroke.

The study will employ high-definition tACS (HD-tACS) in a parallel, double-blinded, sham-controlled design combined with language therapy targeting phonological short-term memory (STM) function in stroke survivors with aphasia. Magnetoencephalography (MEG) and fMRI BOLD data collection will occur to determine tACS parameters and to evaluate stimulation-induced neural changes, respectively. The investigators plan to recruit 120 stroke survivors with aphasia in a 2-group tACS study design.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed with left hemisphere stroke/aphasia
  • Consent date >= 1 month after stroke onset
  • Fluent in English
  • 18 years of age or older

Exclusion criteria

  • Severe cognitive, auditory or visual impairments that would preclude cognitive and language testing
  • Presence of major untreated or unstable psychiatric disease
  • A chronic medical condition that is not treated or is unstable
  • The presence of cardiac stimulators or pacemakers
  • Contraindications to MRI or tACS, e.g. patients with metallic implants, and/or history of skull fractures, pregnancy, skin diseases
  • History of ongoing or unmanaged seizures
  • History of dyslexia or other developmental learning disabilities

Treatment and study plan

HD-tACS

Device

High definition tACS will be applied during speech therapy.

Sham HD-tACS

Device

Sham high definition tACS will be applied during speech therapy.

Primary outcomes

  1. Accuracy on a phonological STM task

    Time frame: Upon the completion of therapy cycle (a cycle consists of 10 intervention days) and 10 weeks post

    Accuracy changes in a delayed sample-to-match task assessing phonological STM after tACS.

  2. fMRI measures of language network activation after tACS

    Time frame: Upon the completion of therapy cycle (a cycle consists of 10 intervention days) and 10 weeks post

    Activation in the language network regions involved in phonological STM will be assessed before and after tACS

Secondary outcomes

  1. Functional Communication Outcome

    Time frame: Upon the completion of therapy cycle (a cycle consists of 10 intervention days) and 10 weeks post

    Improvements in using language in daily life or functional communication as assessed by patient reported measure of Communication Effectiveness Index (CETI)

Study contacts

Contact information is provided by the study sponsor or research team.

Priyanka Shah-Basak, PhD

CONTACT

[email protected]

414-955-5752

Sidney E Schoenrock, MA

CONTACT

[email protected]

414-955-7579

Sponsors and collaborators

Lead sponsor

Medical College of Wisconsin

Other

Registry information

Official study title

TACS for the Recovery of Phonological STM After Stroke

Important dates

Study start
2023
Primary completion
2033
Study completion
2033
First posted
Sep 21, 2023
Registry last updated
Jul 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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