Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 9:07 PM
Ignite Modification Date: 2025-12-24 @ 9:07 PM
NCT ID: NCT05660304
Eligibility Criteria: Inclusion Criteria: 1. Diagnosis of non-fluent aphasia due to a single, left-hemisphere stroke 2. ≧ six months post-stroke onset 3. WAB-R Fluency, Grammatical Competence, and Paraphasias Score between 2-6 4. 18+ years of age 5. Premorbidly right-handed 6. English-speaking 7. Ability to participate in fMRI / TMS protocol Exclusion Criteria: 1. Cardiac pacemaker or pacemaker wires; neurostimulators; implanted pumps 2. Metal in the body (rods, plates, screws, shrapnel, dentures, IUD) or metallic particles in the eye 3. Surgical clips in the head or previous neurosurgery 4. Any magnetic particles in the body 5. Cochlear implants 6. Prosthetic heart valves 7. Epilepsy or any other type of seizure history 8. History of significant head trauma (i.e., extended loss of consciousness, neurological sequelae) 9. Significant other disease (heart disease, malignant tumors, mental disorders) 10. Significant claustrophobia 11. Ménière's disease 12. Medications that increase risk of seizures, for instance antipsychotic and antidepressant medications acting primarily on the central nervous system, which lower the seizure threshold such as antipsychotic drugs (chlorpromazine, clozapine) or tricyclic antidepressants 13. Non-prescribed drug use, for instance recreational marijuana 14. Unable to refrain from using any alcohol and nicotine products for at least 24 hours before the study Visits.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT05660304
Study Brief:
Protocol Section: NCT05660304