Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

Transcranial magnetic stimulation for adult stuttering

Official title: Modulating Bilateral Cortical Activation In Adults Who Stutter: A Pilot Study

Run by Kansas State University · NCT07389694 · Data updated 2026-11-12

We will test whether repeated transcranial magnetic stimulation (rTMS) to a language-related brain area can reduce stuttering in adults who stutter.

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment10 (estimated)
SponsorKansas State University
Academic / other
Locations1 site (Manhattan, Kansas)
StatusRecruiting
StartedFebruary 15, 2026
Main results expectedDecember 15, 2027
Study endsDecember 15, 2028
Registry record updatedAugust 5, 2026
Trial IDNCT07389694 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–65 who self-identify as currently stuttering, are monolingual English speakers with normal or corrected hearing and vision, and who have no contraindications to MRI or TMS are ideal candidates.

Probably not a fit

People with epilepsy or seizure history, prior neurosurgery or structural brain lesions, metallic implants or other MRI/TMS contraindications, significant medical or psychiatric disorders, non-English speakers, or those outside the 18–65 age range are unlikely to benefit or will be excluded.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Participants will receive structural MRI and resting-state fMRI for neuronavigation, then complete 10 rTMS sessions targeting the left inferior frontal gyrus guided by each participant's MRI. rTMS will be delivered at 10 Hz for 10 minutes per session at 120% of resting motor threshold. Three pre-treatment visits and two post-treatment visits will collect resting-state EEG, eye-tracking during phonological tasks, and spontaneous speech samples to measure percent syllables stuttered. The protocol compares brain and behavioral measures before and after the rTMS course to see if neural changes accompany reduced stuttering.

Why it matters

Potential benefit: If successful, the treatment could reduce the frequency of stuttered syllables and improve everyday speaking fluency for adults who stutter.

How similar studies have gone: This approach is relatively novel for stuttering: small pilot studies and case reports show mixed but sometimes promising results, while larger controlled trials remain limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age from 18 to 65 years
* Self-identifies as a person who currently stutters
* Right-handed or left-handed
* Normal hearing and (corrected) vision
* Able to understand and give informed consent
* Monolingual English speaker

Exclusion Criteria:

* Cardiac pacemaker or pacemaker wires; neurostimulators; implanted pumps
* Metal in the body (rods, plates, screws, shrapnel, dentures, IUD) or metallic particles in the eye
* Facial tattoos
* Not having medical insurance
* Surgical clips in the head or previous neurosurgery
* Any magnetic particles in the body
* Cochlear implants
* Prosthetic heart valves
* Epilepsy or any other type of seizure history
* History of significant head trauma (i.e., extended loss of consciousness, neurological sequelae)
* Known structural brain lesions
* Pre-existing speech, language, or neurological disorder (except for stuttering)
* Significant other disease (heart disease, malignant tumors, mental disorders)
* Significant claustrophobia; Ménière's disease
* Women who are trying to get pregnant and sexually active women (of reproductive age) not on a reliable contraceptive
* Pregnancy, breastfeeding
* Medications increasing the risk for seizures
* Non-prescribed drug use
* Use of recreational drugs such as medical marijuana
* Failure to perform the behavioral tasks or neuropsychological evaluation tests
* Prisoners

Where it's running

  • Bluemont Hall, Department of Psychological Sciences, Kansas State University
    Manhattan, Kansas, United States
    Recruiting

Study contacts

  • Principal investigator: Kristin Pelczarski, Ph.D. — Kansas State University
  • Study coordinator: Kristin Pelczarski, Ph.D.
  • Email: kpelczar@ksu.edu
  • Phone: 785-532-6879

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.