subject comfort / acoustic noise burden Subject Comfort / Participant Well-being
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Healthy subject (defined as a volunteer free of any signs and symptoms of disease or disorders that could influence the MRI scan) - Concurrent participation in research scan of study MEC-2020-0308 - At least 18 years old and not older than 60 years old - Proficiency in Dutch or English (all relevant information is only available in these two languages) - Signed informed consent (IC) for participation in study MEC-2020-0308 and a separate signed IC for participation in this study
Exclusion criteria
Exclusion criteria: - Subjects with contra-indication to a MRI exam. - Subjects with metal implants. - Woman who are pregnant or lactating - Subjects who are claustrophobic - Subjects who have tinnitus or hyperacusis - Subjects having any physical or mental status that interferes with the informed consent - Subjects who use medication that could interfere with the protocol - Subjects who do not want to be informed in case of incidental finding
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Parameters of subject experience: perceived acoustic noise burden, perceived acoustic noise reduction; Parameters of auditory functional MRI: Background activity in auditory cortex, activation map quality. | — |
Countries
Netherlands