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Enhancing Speech Fluency With Non-invasive Brain Stimulation in Developmental Stuttering

Enhancing Speech Fluency With Non-invasive Brain Stimulation in Developmental Stuttering

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02288598
Enrollment
30
Registered
2014-11-11
Start date
2014-10-31
Completion date
2016-03-14
Last updated
2017-01-31

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

Conditions

Fluency Disorders, Speech Disorders, Stuttering

Keywords

Stammering, Brain stimulation

Brief summary

This study aims to test whether the addition of transcranial direct current stimulation (TDCS) to speech fluency training results in improvements in speech fluency in adults with developmental stuttering. Half of the participants will receive anodal TDCS on five consecutive days, the other half will receive a sham stimulation for the same amount of time.

Detailed description

Studies using TDCS have shown improvements in motor performance, and in expressive language skills in clinical and healthy populations. The benefits of single sessions of TDCS are short-lived. However, stimulation over multiple sessions can increase and prolong learning effects that can persist for several weeks after the end of the stimulation period. We aim to target left hemisphere frontal regions involved in speech production with TDCS, and to pair this stimulation with speech fluency training.

Interventions

DEVICEAnodal TDCS

20 minutes 1mA anodal stimulation to left inferior frontal cortex. Cathode positioned on right supra-orbital ridge.

Speech tasks will be completed using fluency-enhancing techniques: metronome-timed speech and auditory choral speech.

Sponsors

University of Oxford
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Native speaker of English. * Right handed. * Participant has moderate to severe Developmental Stuttering (Stammering)

Exclusion criteria

* Speech, language or communication disorder other than Developmental Stuttering. * Sensory impairment (hearing loss or visual impairment) * History of drug abuse. * History of seizures * History of a neurological or psychiatric illness. * History of neurosurgical procedure. * Currently taking certain prescription medications such as anti-depressants and anti-malarial medication (as these may lower the seizure threshold)

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline proportion of stuttering in speech sample1 week post-treatmentQuantitative measurement of stuttering

Secondary

MeasureTime frameDescription
Change from baseline on the Stuttering Severity Instrument version 4 (SSI-4)1 week post-treatmentStandardised assessment of frequency and duration of stuttering and associated physical concomitants
Change from baseline on Overall Assessment of Speaker's Experience of Stuttering (OASES)6 weeks post-treatmentStandardised assessment of the functional impact of stuttering on a person's life

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026