About this trial
The goal of this observational study is to understand the mechanisms underlying tinnitus, and improve the clinical assessment strategies needed to develop targeted therapeutic interventions by comparing endogenous attention capacities in healthy subjects and subjects with tinnitus
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age ≥ 18 years
Good written and oral comprehension of the French language
Normal or corrected vision
Disqualifiers
Presence of a known neurological disorder
Presence of a known degenerative pathology
Presence of a known hearing impairment
Presence of a motor disability of the upper limbs
Trial design
Parallel
Treatments tested in this trial
Quality of Life questionnaires
Other interventionSubjects will complete a number of self-questionnaires on subjects such as attention span, anxiety levels and sleep quality.
Hearing tests
Other interventionlistening to sounds on headphones and repeating words
Auditory prediction task
Behaviorallistening to sounds and assessing auditory perception
Attention task
Behavioralassessment of reaction time to visual or auditory cues
Treatment groups
Trial outcomes
Primary outcomes
Contingent negative variation (CNV) in EEG
Secondary outcomes
Response reaction time (in ms)
Comparison of reaction time (RT) variability following response button presses in behavioural tasks
Answer accuracy (% correct answers)
Comparison of the variability of the number of correct responses following button presses in behavioural tasks.
Cerebral oscillations (alpha bands) obtained by EEG during behavioural tasks
Skin conductance (μS)
during behavioral task
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Institut Pasteur
Lead sponsor
IHU reConnect
Collaborator
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