Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
Healthy Volunteers
NCT06092814

tACS to Enhance Language Abilities

Led by University of Pennsylvania · Updated on 2025-08-08

120

Participants Needed

1

Research Sites

215 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

tACS to Enhance Language Abilities

Who Can Participate

Age: 18Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Presence of aphasia
  • Single, left hemisphere stroke
  • Stroke occurred 6 months or more before enrollment
  • Right-handedness (for healthy controls)
  • Ability to understand the study and give informed consent (for healthy controls)
Not Eligible

You will not qualify if you...

  • Inability to understand the study
  • Marked naming impairment
  • Impaired non-verbal, conceptual processing
  • History of significant medical or neurological disorders other than stroke
  • Significant or poorly controlled psychiatric disorders
  • Current abuse of alcohol or drugs
  • Nursing, pregnancy, or intent to become pregnant during the study
  • Clinically significant hearing loss
  • Contraindications to tACS
  • Contraindications to MRI
  • Diagnosis of neurodegenerative disease or significant cognitive complaints (healthy controls)
  • Neurologic or physical conditions impairing communication ability (healthy controls)
  • History of unrelated neurological conditions causing deficits (healthy controls)
  • Neurological conditions reducing safety of participation (e.g., CNS vasculitis, tumors, aneurysm, multiple sclerosis)
  • Medically unstable cardiopulmonary or metabolic disorder
  • Terminal illness with expected survival under 12 months
  • Major active psychiatric illness interfering with study participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

D

Daniela Sacchetti, MS

CONTACT

D

Denise Harvey, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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