fundamenteel onderzoek bij gezonde proefpersonen NA
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy, right-handed participants, between 18*35 years old, with normal or corrected-to-normal vision, normal hearing.
Exclusion criteria
Exclusion criteria: Exclusion criteria for participation include metal in cranium, epilepsy or family history of epilepsy, history of neurological or psychiatric disorders, medication use (i.e., benzodiazepines, antidepressants andneuroleptica), cardiac pacemaker, pregnancy and electronic hearing devices.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary study parameters/outcome: A repeated measures ANOVA with Target TMS SOA ( 30ms , 60ms , 90ms , 120ms , 150ms , 180ms , 210ms , 240ms , 270ms , 300ms ) and Target Type ( threatening ( CS + ) , non -threatening ( CS ) and Cuevalidity (valid, invalid ) as factors will be performed on percentage correct and reaction times. If appropriate, planned comparisons between the conditions will be carried out. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary study parameters/outcome: In addition to our primary objective , we will investigate a possible correlation between the degree of anxiety as measured by the VAS and the STAI -T with re - orienting, as indexed by the difference in performance on the CS + target and CS- target. | — |
Countries
Netherlands