Transcranial direct current stimulation for laryngeal dystonia
Official title: Network Targeted Transcranial Direct Current Stimulation (tDCS) as a Treatment for Laryngeal Dystonia (LD)
Run by Yale University · NCT06830174 · Data updated 2026-11-12
This trial will try transcranial direct current stimulation (tDCS) in people with laryngeal dystonia to see if it improves voice control.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 10 (estimated) |
| Sponsor | Yale University Academic / other |
| Locations | 1 site (New Haven, Connecticut) |
| Status | Recruiting |
| Started | April 14, 2025 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | February 9, 2026 |
| Trial ID | NCT06830174 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with a confirmed diagnosis of laryngeal dystonia who have no other speech or voice disorders, are not pregnant, and can attend multiple sessions at the study site are appropriate candidates.
✕Probably not a fit
People with a history of epilepsy or significant depression, those who are claustrophobic or pregnant, or those with other active voice disorders would likely be ineligible or unlikely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Participants will undergo baseline MRI and EEG recordings and then attend multiple testing sessions across five days. People with laryngeal dystonia will receive 20 minutes of high-definition tDCS (HD-tDCS) via the Starstim system while watching videos or performing a word-production task. Stimulation will be applied to several brain regions thought to be involved in voice control to alter neural activity. Outcomes will compare voice measures and neuroimaging/EEG signals before and after the stimulation protocol.
Why it matters
Potential benefit: If successful, this approach could reduce voice spasms and improve speech quality using a noninvasive, clinic-based treatment.
How similar studies have gone: Noninvasive brain stimulation methods like tDCS have produced mixed but promising findings in small studies of movement and voice disorders, so this approach is experimental but plausible.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Participants must be clinically evaluated for the diagnosis of LD or have the proof of LD diagnosis. (Not applicable for control participants) * No other known or history of speech, voice disorder other than LD. * Provision of signed and dated informed consent form. * Stated willingness to comply with all study procedures and availability for the duration of the study * Must not be pregnant. Exclusion Criteria: * All individuals who do not meet the above mentioned criteria are excluded from the study. * Subjects with a history of epilepsy or depression or is claustrophobic.
Where it's running
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Yale University
New Haven, Connecticut, United States Recruiting
Study contacts
- Principal investigator: Nabin Koirala, PhD — Yale University
- Study coordinator: Nabin Koirala, PhD
- Email: nabin.koirala@yale.edu
- Phone: 203 7852527
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.