ClinicalTrials.gg
Enrolling by invitationNCT07563387Updated May 4, 2026

taVNS for Speech and Language Recovery in Aphasia

An interventional study of taVNS and sham taVNS in Aphasia and Apraxia of Speech, sponsored by University of Florida. Enrolling by invitation at 1 site in United States. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-05-04.

Sponsored by University of Florida · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

The goal of this research study is to evaluate a novel approach to improving speech recovery in those with acquired apraxia of speech. We will enroll participants with apraxia of speech resulting from stroke or brain injury to complete several tasks and intervention. Testing will take place four times over the course of the study and intervention will take place 5 days a week for 16 weeks. Overall, you can expect to spend up to 17 weeks participating in this study.

02

Conditions studied

  • Aphasia
  • Apraxia of Speech

Keywords

  • taVNS
  • vagus nerve stimulation
  • stroke
  • traumatic brain injury
  • language
  • speech
03

In context

Aphasia

338 studies on the registry are indexed under Aphasia; 95 are open to participants now.

This study's planned enrollment of 12 is below the median of 30 across 298 interventional studies indexed under Aphasia.

Browse Aphasia studies →

Lead sponsor

University of Florida is the lead sponsor of 1,287 studies on the registry; 199 are open to participants now.

Of its 180 completed or terminated interventional studies of FDA-regulated products, 143 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults between 18-80
  • Native speakers of English or simultaneous bilinguals
  • At least 6 months post stroke or TBI
  • Diagnosed production type aphasia or apraxia of speech

Exclusion criteria

Exclusion Criteria:

  • Additional cognitive or neurological impairments (Autism, schizophrenia, seizures, etc)
  • Language comprehension deficits
  • Medications that influence key neurotransmitters
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
12 participants (estimated)

Study arms

  • Experimental
    Treatment A

    non-invasive vagus nerve stimulation is administered alongside standard intervention

    Device: taVNS

  • Placebo comparator
    Treatment B

    sham stimulation is administered alongside standard intervention

    Device: sham taVNS

Interventions

  • DevicetaVNS

    active vagus nerve stimulation

  • Devicesham taVNS

    sham vagus nerve stimulation

06

What researchers measure

Primary outcomes

  1. Adverse events

    Frequency and severity of adverse events will be monitored and evaluated for severity and impact on attrition.

    Time frame: 6 months

  2. Compliance

    Percentage of the population that remains engaged in the study and completes all stimulation sessions.

    Time frame: 6 months

Secondary outcomes

  1. Change in speech production scores

    Primary outcomes for this aim include the learning trajectory over 8 weeks of speech therapy as measured by weekly probes and the WAB when intervention is combined with taVNS versus control stimulation to determine the effect of taVNS on re-learning motor speech plans and the trajectory of motor speech recovery.

    Time frame: 6 months

07

Study locations

1 site
  • Brooks Rehabilitation Clinical Research Center
    Jacksonville, Florida 32216, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07563387
Collaborators
Eric Sorenson Motor Speech Program at Brooks Rehabilitation
Responsible party
Sponsor
First posted
May 4, 2026
Start date
Jan 1, 2026
Primary completion
Jan 1, 2027 (estimated)
Completion
Jan 1, 2028 (estimated)
Last update
May 4, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion