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tDCS + Auditory Rehabilitation for Hearing Loss
Study Summary
This trial will test if a combination of electrical stimulation to the brain and at-home sound training can improve hearing for people with cochlear implants.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- I can use the internet for training and video calls with the study team.I do not have any mental health or neurological conditions that could affect the study.Your ability to understand sentences is less than 65% and your ability to recognize words is less than 75% one year after getting a cochlear implant.You have had a cochlear implant in one ear for at least 1 year.I am 18 years old or older.I am older than 18 years.You have implants near your collarbone that could interfere with the device used for tDCS.Your ability to understand sentences using a cochlear implant in one ear has been less than 65% for over a year.
- Group 1: tDCS during auditory training
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are individuals still being enrolled in this research effort?
"Clinicaltrials.gov states that this clinical trial is not enrolling patients right now, despite being initially posted on October 1st 2022 and most recently updated on September 29th 2022. However, there are 156 other medical studies actively recruiting participants as of today."
What are the key aims of this clinical exploration?
"This 6 month long clinical trial is assessing the proficiency of participants with tdcs training as its primary outcome. Secondary objectives include determining participant satisfaction with stimulation device utilisation, likelihood to recommend the programme and compensation for study participation - all assessed by means of a patient-completed questionnaire where 1 corresponds to 'strongly disagree' and 5 stands for 'strongly agree'."
Who else is applying?
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What portion of applicants met pre-screening criteria?
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