Tinnitus Patient Preferences Survey

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNicolas Gninenko

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Individuals aged 18 or older suffering from subjective tinnitus

Self-reported or healthcare professional-diagnosed chronic (lasting 3 months or longer), subjective, burdensome tinnitus

Disqualifiers

Individuals under 18 years of age

Healthy volunteers without tinnitus

Trial population

Adult patients (over 18 years old) with chronic, subjective severe tinnitus

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Survey using a questionnaire.

    Other intervention

    patients preferences survey

Treatment groups

500 Participants
are divided into 1 treatment group
Group A: patients with tinnitus1 intervention

Trial outcomes

Primary outcomes

1

Acceptance of invasive neuromodulation treatments for chronic tinnitus

Risks acceptance and user preferences will be assessed through responses to the survey. The outcome will be summarized in the form of a percentage or similar statistics on acceptances rates for surgical interventions in patients with chronic tinnitus. Acceptance rates will also be evaluated in accordance to several clinical characteristics of tinnitus, such as its perceived annoyance or loudness.

Time frame
1 year

Secondary outcomes

1

Usability preferences for implantable neuromodulation systems for chronic tinnitus

Usability preferences will be assessed through responses to the survey. This secondary outcome will be summarized in the form of a percentage or similar statistics on usability preferences between different solutions involving surgical interventions in patients with chronic tinnitus. Usability preferences will also be evaluated with respect to different reported tinnitus characteristics, such as perceived annoyance or loudness.

Time frame
1 year
2

Willingness and ability to pay for novel invasive neuromodulation solutions for chronic tinnitus

Willingness to pay (WTP) will be assessed through responses to the survey. This secondary outcome will be summarized in the form of a range ($ US) or similar statistics on willingness and ability to pay with respect to different solutions involving surgical interventions in patients with chronic tinnitus. WTP will also be evaluated with respect to different reported tinnitus characteristics, such as perceived annoyance or loudness.

Time frame
1 year

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Nicolas Gninenko

Lead sponsor

Neurosoft Bioelectronics SA

Sponsor institution