RECRUITING

Tinnitus Patient Preferences Survey

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this survey is to assess several aspects related to patient preferences regarding interventions for alleviating tinnitus through invasive electrical brain stimulation (neuromodulation). This survey covers the acceptance of a surgically-placed brain implant, of its associated risks related to the neurosurgical procedure, usability considerations, and the willingness/ability to pay for such a treatment. Neurosoft Bioelectronics will use the collected patients' feedback and usability preferences data for the development of a novel minimally invasive brain implant aimed at alleviating tinnitus.

Official Title

Tinnitus Patient Preferences Survey

Quick Facts

Study Start:2025-01-13
Study Completion:2025-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06782308

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Individuals aged 18 or older suffering from subjective tinnitus
  2. * Self-reported or healthcare professional-diagnosed chronic (lasting 3 months or longer), subjective, burdensome tinnitus
  1. * Individuals under 18 years of age
  2. * Healthy volunteers without tinnitus

Contacts and Locations

Study Contact

Nicolas Gninenko, PhD
CONTACT
000-000-0000
clinical@neurosoft-bio.com

Principal Investigator

Nicolas Gninenko, PhD
PRINCIPAL_INVESTIGATOR
Neurosoft Bioelectronics

Study Locations (Sites)

Neurosoft Bielectronics US Inc.
New York, New York, 10016
United States

Collaborators and Investigators

Sponsor: Nicolas Gninenko

  • Nicolas Gninenko, PhD, PRINCIPAL_INVESTIGATOR, Neurosoft Bioelectronics

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-01-13
Study Completion Date2025-12-30

Study Record Updates

Study Start Date2025-01-13
Study Completion Date2025-12-30

Terms related to this study

Keywords Provided by Researchers

  • tinnitus
  • iBCI
  • brain implant
  • survey
  • risks acceptance
  • user preferences
  • patient preferences
  • subjective tinnitus
  • chronic tinnitus
  • severe tinnitus
  • catastrophic tinnitus
  • invasive neuromodulation
  • surgical treatment

Additional Relevant MeSH Terms

  • Tinnitus, Subjective
  • Tinnitus, Bilateral
  • Tinnitus, Noise Induced
  • Tinnitus, Hearing Loss, Cochlear Implant Users