neurowetenschappelijk onderzoek dejection mood
Conditions
Interventions
The intervention includes a previously established off-line rTMS-protocol with
the intention to produce short-term inhibitory effects on the functioning of
the target region (mPFC). The intervention
Sponsors
Radboud Universiteit Nijmegen
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Only healthy, competent participants, 18*45 years old, with normal vision or corrected to normal vision by means of contact lenses.
Exclusion criteria
Exclusion criteria: Skin diseases at intended electrode sites (EMG, EEG, tCS) (History of) psychiatric disorder/ treatment (History of) neurological disorder/ treatment Disorders of vision (i.e., deviation from *normal or corrected-to-normal vision*) Any prescribed medication that can alter cortical excitability (e.g. antiepileptics, tricyclicanti-depressives or benzodiazepines) or can have an influence on the participant*s vigilance or cognitive performance within two weeks prior to participation Having minimal sleep, or excess consumption of alcohol/recreational drugs/caffeine in the 24 hours prior to the experimental TMS session. (History of) sleep disorder Shift work for the past 3 months Transmedial flights for the past month Extreme chronotype Regular nappers Extreme caffeine consumers Heavy smokers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameters are the amount of items remembered (hits), amount of critical lures remembered (FA) in all groups and subjective measures (e.g. mood induction check). | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary study parameters are the measured sleep parameters e.g. amount of REM sleep and amount of frontal theta and gamma power. | — |
Countries
Netherlands
Outcome results
None listed