Tinnitus
Conditions
Keywords
tinnitus, transcranial magnetic stimulation
Brief summary
In the first visit a magnetic resonance imaging measurement will be done for the use of a neuronavigation System with the aim to control for stable coil position over the course of the trial. EEG positions CP5/CP6 will be used for positioning the coil. Two test sessions will examine the temporary reductions in tinnitus loudness after 1Hz, 10Hz, 20Hz and 0.1Hz rTMS as control condition over left and right temporo-parietal junction accompanied by electroencephalography. For the two-week treatment three arms will be evaluated: standard treatment (1Hz left-sided) in the groups with and without temporary reductions in test sessions and the best protocol as elicited in test sessions.
Detailed description
Efficacy of repetitive transcranial magnetic stimulation (rTMS) in chronic tinnitus is moderate. So far single sessions and daily treatment of rTMS were rarely combined. Thus it is not clear if temporary reductions in tinnitus loudness as elicited by short single rTMS sessions can be transferred to daily rTMS treatment. Thus, the aim of the study is to investigate the efficacy and reliability of single sessions of rTMS in chronic tinnitus with respect to temporary reductions in tinnitus loudness accompanied with resting state electroencephalography measurements to investigate the neurophysiological correlates of tinnitus reductions. Two test sessions within one week will be done on the left and right temporoparietal junction using 1Hz, 10Hz, 20Hz and 0.1Hz as active control condition. In the next step patients are divided into three arms with the aim to investigate the efficacy of individualized rTMS. The three arms are 1) patients with temporary tinnitus reductions in test sessions: treatment with the best, most reliable, controlled and most tolerable protocol, 2) patients with temporary tinnitus reductions in test sessions: treatment with 1Hz left-sided rTMS, 3) patients with no temporary tinnitus reductions in test sessions: treatment with 1Hz left-sided rTMS. Treatment will be done for 10 days (Monday - Friday) using 2000 pulses with 110% resting motor threshold. Coil position will be tracked with neuronavigation to ensure stable coil Position over the course of the trial.
Interventions
DEVICErepetitive transcranial magnetic stimulation
Stimulation of the temporoparietal junction with repetitive transcranial magnetic stimulation * 2000 pulses * intensity of 110% resting motor threshold * 10 sessions (daily from Monday to Friday) * positioning of coil according to EEG position CP5/CP6
Sponsors
University of Regensburg
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* chronic tinnitus (\> 6 months) * at least moderate tinnitus distress * no or consistent medication * no or consistent Treatments * residence in Germany and German speaking
Exclusion criteria
* objective tinnitus * serious and not stable illness (e.g. acute psychosis, severe depression or substance dependence, epilepsy, brain tumor) * meeting the contraindications for transcranial magnetic stimulation or magnetic resonance imaging (electric devices or metal implants in the body, e.g. cardiac pace maker, insulin pump) * neurological disorders (e.g. cerebrovascular events, neurodegenerative disorder, epilepsy, brain malformation, severe head trauma) * addictive disorder with consumption in the last two years * regular intake of benzodiazepines * participation in another study parallel to the trial * pregnancy or breastfeeding period * psychiatric confinement
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| TFI | 2 weeks | Tinnitus Functional Index |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mini-TQ | 12 weeks | Tinnitus Questionnaire short version |
| THI | 12 weeks | Tinnitus Handicap inventory |
| Tinnitus Severity | 12 weeks | Tinnitus numeric Rating scales \[0(best) - 10(worst)\] |
| TFI | 12 weeks | Tinnitus Functional Index |
| WHO-QOL BREF | 12 weeks | Quality of life \[4(worst) - 20(best)\] |
| CGI | 12 weeks | clinical global Impression Change \[1(best) - 7(worst)\] |
| MDI | 12 weeks | Major Depression Inventory |
Countries
Germany
Outcome results
None listed