ClinicalTrials.gg
RecruitingNCT06092814Updated Aug 24, 2026

tACS to Enhance Language Abilities

An interventional study of Active transcranial alternating current stimulation (tACS) in Stroke, Aphasia, Acquired and Aphasia, sponsored by University of Pennsylvania. Recruiting at 1 site in United States. Open to participants aged 18 Years to 85 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-24.

Sponsored by University of Pennsylvania · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2024; still recruiting 2 years 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

The goal of this study is to see if transcranial alternating current stimulation (tACS) can be used to enhance language abilities in people with post-stroke aphasia. Participants will receive real and sham tACS in conjunction with various language tests. Researchers will compare the post-stroke aphasia group with aged matched controls to see if brain response to tACS differs between groups.

Read the detailed description

This research will investigate whether transcranial alternating current stimulation (tACS), a form of noninvasive brain stimulation, can be used to enhance language abilities in people with aphasia (PWA) due to stroke and healthy older adults when compared to placebo (sham) tACS. The investigators hypothesize that alpha vs. sham tACS will improve language abilities. In addition, the investigators propose that alpha vs. sham tACS will increase local alpha power as well as alpha-induced functional connectivity, and the degree to which alpha tACS increases will be related to the degree of language performance improvement. Finally, the investigators hypothesize that PWA will exhibit abnormalities in alpha-related activity when compared to matched controls, and aphasia severity will be associated with the degree of PWA dysfunction in alpha power and alpha-driven functional connectivity.

02

Conditions studied

  • Stroke
  • Aphasia, Acquired
  • Aphasia

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Keywords

  • non-invasive brain stimulation
  • transcranial alternating current stimulation (tACS)
  • EEG
03

In context

Stroke

8,255 studies on the registry are indexed under Stroke; 2,056 are open to participants now.

This study's planned enrollment of 120 is above the median of 49 across 6,024 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

University of Pennsylvania is the lead sponsor of 1,668 studies on the registry; 235 are open to participants now.

Of its 158 completed or terminated interventional studies of FDA-regulated products, 109 (69%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria for Persons with Aphasia:

  1. Presence of aphasia
  2. Suffered a single, left hemisphere stroke
  3. Stroke ≥6 months old (chronic) at the time of enrollment

Inclusion Criteria for Healthy Controls:

  1. Right-handedness
  2. Must be able to understand the nature of the study, and give

Exclusion criteria for Persons with Aphasia:

  1. Inability to understand the nature of the study
  2. Marked naming impairment
  3. Impaired non-verbal, conceptual processing
  4. History of significant medical or neurological disorder (other than stroke)
  5. History of significant or poorly controlled psychiatric disorders
  6. Current abuse of alcohol or drugs, prescription or otherwise
  7. Nursing a child, pregnancy, or intent to become pregnant during the study
  8. hearing loss
  9. to tACS
  10. Contraindications to MRI

Exclusion Criteria for Healthy Controls

  1. Diagnosis of a neurodegenerative disease or clinically significant cognitive complaint
  2. Any unrelated neurologic or physical condition that impairs communication ability
  3. History of unrelated neurological conditions including but not limited to traumatic brain injury, stroke, or small vessel disease that has resulted in a neurologic deficit
  4. Any additional neurological condition that would likely reduce the safety of study participation, including central nervous system (CNS) vasculitis, intracranial tumor, intracranial aneurysm, multiple sclerosis or arteriovenous malformations
  5. A medically unstable cardiopulmonary or metabolic disorder
  6. Terminal illness associated with survival \<12 months
  7. Major active psychiatric illness that may interfere with required study procedures or treatments as determined by the enrolling physician
  8. Current abuse of alcohol or drugs, prescription or otherwise
  9. Contraindications to tACS
  10. Contraindications to MRI
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
120 participants (estimated)

Study arms

  • Active comparator
    real-tACS

    The active stimulation will consist of an alternating current delivered in the alpha frequency band with a peak-to-peak intensity of 4 milliamps (mA) for 20 minutes. Participants will complete sentence completion and verb generation task during stimulation.

    Device: Active transcranial alternating current stimulation (tACS)

  • Placebo comparator
    sham-tACS

    Sham stimulation involves the delivery of 60 seconds of the actual stimulation waveform ("ramp up") which is then gradually reduced to 0 milliamps (mA) ("ramp down"). Participants will complete sentence completion and verb generation task during stimulation.

    Device: Active transcranial alternating current stimulation (tACS)

Interventions

  • DeviceActive transcranial alternating current stimulation (tACS)

    Transcranial Alternating Current Stimulation (tACS) is a device that applies a low-intensity electrical current to the brain through electrodes on the scalp.

    Also known as: Sham transcranial alternating current stimulation [(ACS)

06

What researchers measure

Primary outcomes

  1. Performance on the Blocked-Cyclic Naming (BCN) Task

    The BCN tasks involves naming a set of pictures repeatedly. Sets of pictures come from either the same semantic category (high competition condition; e.g., categorically related: "dog", "cat", "panda") or different semantic categories (low competition condition; e.g., unrelated: dog, eye, crib).

    Time frame: 5-10 minutes after a single session of active (alpha tACS) and sham (fake tACS).

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2024 (actual). Primary completion is estimated for Aug 2028, 49 months after the start.

Of 3,108 non-industry interventional studies with no phase under Stroke, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 46. This study's planned 49 months is above that.

Counting every sponsor, half of 3,252 studies reached it within 23 months; a quarter within 10 and three quarters within 46.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 28, 2023
First posted
Oct 23, 2023
StartActual
Jul 12, 2024
Primary completionEst.
Aug 31, 2028
CompletionEst.
Aug 31, 2028
Last update
Aug 24, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06092814
Responsible party
Sponsor
First posted
Oct 23, 2023
Start date
Jul 12, 2024
Primary completion
Aug 31, 2028 (estimated)
Completion
Aug 31, 2028 (estimated)
Last update
Aug 24, 2026

Study contacts

Daniela Sacchetti, MS
Contact
danielas@pennmedicine.upenn.edu
215 573 4336
Denise Harvey, PhD
Contact
harveyde@pennmedicine.upenn.edu
215 573 4336

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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