H93.1
Conditions
Interventions
Group 1: It is an experimental, single-arm pilot study. The duration of the study should be 6 weeks for the individual participants
a total period of around 12 months is planned for recruitment and implementation.
Upon inclusion, the participants will be informed about the study and patient/disease data (age, sex, onset of symptom
Sponsors
Medizinische Fakultät der RWTH Aachen
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Patient age = 18 years - chronic (> 3 months), unilateral, subjective tinnitus (ICD-10 code: H93.1) - Routine ENT diagnostics (complete ENT findings, audiological examinations, cMRI to rule out a retrocochlear lesion) are carried out - Exclusion of treatable causes (otosclerosis, chronic otitis media, etc.) is carried out
Exclusion criteria
Exclusion criteria: - Patient age < 18 years - pregnancy - dementia - Epilepsy - Acute psychiatric diseases (according to self-declaration, no corresponding diagnosis) - visual disturbances - Wounds in the area of ??the facial skin
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is the drop-out rate and the usability of the system. | — |
Secondary
| Measure | Time frame |
|---|---|
| As a secondary goal, the changes in tinnitus-associated symptoms are determined in a 6x2 design using a variance analysis. If necessary, covariates are integrated into the model, which are also recorded via course measurements. | — |
Countries
Germany
Contacts
Public ContactJohannes Taeger
Uniklinikum Aachen
Outcome results
None listed