Transcranial Magnetic Stimulation in Laryngeal Dystonia
Starting soon · Not applicable · Has a placebo group
Conditions studied: Laryngeal Dystonia, Spasmodic Dysphonia
In brief
This randomized clinical trial with a crossover design aims to investigate the effects of neuromodulation through repetitive transcranial magnetic stimulation (rTMS) applied to patients diagnosed with laryngeal dystonia. Participants will undergo three experimental conditions: (1) rTMS alone, (2) rTMS combined with speech-language therapy, and (3) sham rTMS combined with speech-language therapy. The order of the conditions will be randomized. Each phase of the protocol will consist of five consecutive sessions. Outcomes will include acoustic vocal quality parameters, perceptual-auditory voice assessment, self-ratings of vocal effort, smoothed cepstral peak prominence measures, and global perceived change following the intervention. It is expected that the study will contribute to a better understanding of the effects of the intervention on vocal outcomes, supporting the optimization and standardization of therapeutic protocols for laryngeal dystonia.
Key facts
- Study ID
- NCT07683767
- Run by
- Universidade Federal de Pernambuco
- People needed
- 20
- Starts
- 2026-06-01
- Expected to finish
- 2027-02-01
- Last updated by the study team
- 2026-07-06
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults (≥18 years) of any sex with a confirmed diagnosis of laryngeal dystonia
- Participants not undergoing botulinum toxin treatment at the time of the intervention
- Ability to provide informed consent
- Ability to complete all study assessments and intervention procedures
You may not qualify if…
- Other forms of dystonia
- Vocal fold lesions
- Vocal fold paralysis
- Contraindications to repetitive transcranial magnetic stimulation (rTMS)
- Inability to complete study assessments or intervention procedures
Full record on ClinicalTrials.gov
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