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Post-Stroke Aphasia TMS

Precision Neuromodulation in Post-Stroke Aphasia Using TMS

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06974279
Acronym
TaMS
Enrollment
50
Registered
2025-05-15
Start date
2025-09-01
Completion date
2036-12-31
Last updated
2026-07-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aphasia, Language, Stroke

Keywords

Aphasia, Stroke, Language, TMS

Brief summary

The investigator proposes to examine the effects of excitatory transcranial magnetic stimulation (TMS) combined with semantic feature analysis (SFA) language therapy to improve word-finding abilities in stroke survivors with aphasia (SWA).

Detailed description

In this project, the investigator will use functional neuroimaging and inhibitory TMS to determine precise therapy-responsive targets for excitatory TMS therapy with SFA. One group of stroke survivors will receive SFA + TMS targeting the precision site, and another group will receive SFA + TMS targeting a control site. The primary outcome will be changes in picture naming accuracy. We expect that excitatory TMS targeting a precision site would result in larger improvements in naming accuracy than TMS targeting a control site. Results will provide the efficacy of precision TMS in post-stroke aphasia.

Interventions

DEVICEPrecision TMS with SFA

Excitatory TMS delivered using a precision site finding approach and intermittent theta burst stimulation protocol

DEVICEControl TMS with SFA

Excitatory TMS using intermittent theta burst stimulation delivered to a control vertex site.

Sponsors

Medical College of Wisconsin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosed with left hemisphere stroke * 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 (e.g. schizophrenia, bipolar disease) * A chronic medical condition that is not treated or is unstable * The presence of cardiac stimulators or pacemakers or intracardiac lines, neurostimulators, medication infusion device, any other implants near the scalp (e.g., cochlear implants) or in the eye, metal in the body (e.g., splinters, fragments, clips) * Pregnancy * History of skull fractures, or skin diseases * History of ongoing or unmanaged seizures * Presence of factors that potentially decrease seizure thresholds: on pro-convulsant medications, untreated sleep deprivation or insomnia, ongoing alcoholism or illegal drug abuse (e.g., cocaine or MDMA users) * History of dyslexia or other developmental learning disabilities

Design outcomes

Primary

MeasureTime frameDescription
Accuracy on a picture naming testimmediately after and 8-12 weeks after last SFA+TMS treatmentChanges in accuracy on untrained stimuli after SFA+TMS compared between groups (precision, control).

Countries

United States

Contacts

CONTACTSidney Schoenrock, MA
sschoenrock@mcw.edu414-955-7579
CONTACTAri Hjelmeseth
ahjelmeseth@mcw.edu414-955-7578

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 11, 2026