Skip to content

Transcranial Stimulation Combined With Auditory Training

Transcranial Stimulation Combined With Auditory Training

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06738030
Enrollment
94
Registered
2024-12-17
Start date
2025-11-07
Completion date
2027-03-01
Last updated
2026-07-29

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

Conditions

Difficulties Understanding Speech in Noise

Brief summary

The goal of this clinical trial is to learn if non-invasive brain stimulation (called transcranial stimulation) can enhance the benefits from auditory training in people who struggle to understand one talker when many people are talking at the same time. The main questions it aims to answer are: * Does transcranial stimulation improve speech-on-speech understanding in people who struggle with this task? * Does transcranial stimulation enhance the benefits of a commercially available auditory training program? Researchers will compare transcranial stimulation to sham stimulation (no stimulation is applied during the listening task). Participants will: * Receive login information to an online auditory training program to complete at home over 2 weeks * Visit the laboratory 4 times to receive transcranial stimulation while listening to speech-on-speech: once before at-home training, two times during the at-home training period, and once after at-home training has ended

Interventions

The transcranial alternating current stimulation is delivered during the speech stimulus and the current matches the envelope of the target speech

An at-home auditory training program that adaptively and interactively trains the listener in degraded speech, cognitive skills, and communication strategies

Sponsors

Boston University Charles River Campus
Lead SponsorOTHER
National Institute on Deafness and Other Communication Disorders (NIDCD)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Intervention model description

Participants are randomly assigned to active transcranial stimulation or sham stimulation groups.

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 50 years of age or older * Audiometric thresholds that do not exceed 90 dB HL at any frequency from 250-6000 Hz * Able to provide informed consent and understand experimental instructions * Able to read print on a computer screen * Difficulty with speech-on-speech understanding * Access to computer or mobile phone with access to internet that can play sound (for the at-home training)

Exclusion criteria

* Non-native speakers of English * History of skull fracture, scalp tissue damage, metallic implants around the head, seizures, neurological disorders, or traumatic brain injury, current or suspected pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Speech-on-speech intelligibility percent correctFrom enrollment to the end of participation at 6 weeksPercent correct score on the speech-on-speech task assessed in the lab
Pupillometry measured listening effortFrom enrollment to the end of participation at 6 weeksThe peak pupil dilation subtracted from pre-trial baseline pupil dilation, averaged across trials in a block, assessed in the lab
QuickSIN SNR LossDays 1, 6, and 14 of the two-week auditory trainingA speech-in-noise test assessed as part of the at-home auditory training program
Hearing Handicap InventoryDays 1 and 14 of the two-week auditory training programA listening effort questionnaire given as part of the at-home auditory training program

Countries

United States

Contacts

CONTACTElin Roverud, AuD, PhD
erover@bu.edu617-358-7440
PRINCIPAL_INVESTIGATORElin Roverud, AuD, PhD

Boston University Charles River Campus

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 30, 2026