Tinnitus
Conditions
Keywords
Tinnitus, Transcranial direct current stimulation, Transcranial magnetic stimulation
Brief summary
The purpose of this study is to determine if repeated sessions of transcranial direct current stimulation (tDCS) are effective for treating chronic subjective tinnitus. Previous studies have reported brief improvements in tinnitus after safe and noninvasive stimulation of the auditory cortex or limbic system. The investigators hypothesize that a greater improvement in tinnitus will be achieved following repeated sessions of tDCS that target both auditory and limbic systems.
Detailed description
Subjective tinnitus is a distressing condition characterized by the sensation of sound or noise in the absence of internal or external stimuli. Research indicates that tinnitus may develop due to maladaptive plastic changes in the auditory cortex and limbic system. These changes can be targeted using safe and noninvasive brain stimulation techniques like transcranial direct current stimulation (tDCS). TDCS alters the excitability of the cortex using a weak direct current and may lead to long-term plastic changes, making it a potential therapeutic tool for the treatment of tinnitus. Transient improvements in tinnitus have been reported after inhibitory stimulation of the auditory cortex and after excitatory stimulation of the prefrontal cortex, however the effects of a combined stimulation paradigm remain unknown. The investigators hypothesize that a cumulative effect will be observed following repeated sessions of tDCS by modulating both the excitability of the auditory cortex and prefrontal cortex.
Interventions
DEVICEBrainSTIM Transcranial Stimulator
Cathodal stimulation of the auditory cortex with an anode (reference electrode) over the prefrontal cortex. Stimulation will be applied for 20 minutes at 2 mA.
Sponsors
Centre Hospitalier Universitaire Vaudois
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age of at least 18 years * Chronic tinnitus for at least 1 year * Diagnosis of chronic subjective non-pulsatile tinnitus * Age-adjusted normal (sensorineural) hearing * Score of 25 or above on the Mini-mental state examination (MMSE) * Must comply with use of contraceptives during interventions
Exclusion criteria
* Objective tinnitus * Concurrent treatment for tinnitus * Prior exposure to transcranial direct current stimulation (tDCS) * Electronic implants or metallic objects in body, including cardiac pacemakers, cochlear implants, implanted medical pump, metal plate in skull, metal implant in the skull or eyes (other than dental appliances or fillings) * Skin conditions where electrodes will be applied * Major neurological co-morbidities * History of epilepsy and/or seizures * Pregnancy and/or lactation
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Tinnitus Handicap Inventory (THI; Newman, Jacobson, & Spitzer, 1996; French version: Ghulyan-Bédikian et al., 2010) | Baseline, 1 month after last intervention | Assesses the change in tinnitus from baseline to 1 month after intervention. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Tinnitus Handicap Inventory (THI) | Baseline, session 5 (day 5), 1 and 3 months after the last intervention | Assesses change in tinnitus from baseline to follow-up periods post interventions. |
| Visual Analogue Scales (VAS) of perceived tinnitus loudness and distress | Baseline, before and after each intervention, 1 and 3 months after the last intervention | Self assessment of tinnitus loudness and tinnitus distress. |
| Hospital Anxiety and Depression Scale (HAD) | Baseline, 1 month after intervention | Assesses anxiety and depression. |
| Subjective Tinnitus Severity Scale (STSS) | Baseline, session 5 (day 5), 1 and 3 months after the last intervention | Assesses tinnitus severity. |
| Clinical Global Impression Scale (CGI) | Session 5 (day 5), 1 and 3 months after the last intervention | Patient rating of worsening/improvement in condition following interventions. |
Countries
Switzerland
Outcome results
None listed