fundamenteel onderzoek bij gezonde proefpersonen NA
Conditions
Interventions
None listed
Sponsors
Radboud Universiteit Nijmegen
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: - aged between 18 and 35 - normal or corrected to normal vision - not color blind - normal hearing - right- handedness - non-smoking - females taking contraceptives
Exclusion criteria
Exclusion criteria: Exclusion criteria for participation include metal in cranium, use of psychotropic drugs, including cannabis, XTC,amphetamines and cocaine, epilepsy or family history of epilepsy, history of closed-head injury, history of neurological or psychiatric disorders, medication use (i.e., benzodiazepines, antidepressants and neuroleptica), cardiac pacemaker, pregnancy and electronic hearing devices.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| A repeated measures ANOVA with TMS (sham TMS, left rTMS, right rTMS) and distractor (CS+, CS-) as factors will be carried out on difference RT score and error rates. If appropriate, planned comparisons between the conditions will be performed. The alpha level of significance will be set at 0.05 (two-tailed) throughout. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pearson*s correlation coefficient will determine the correlation between the level of state anxiety as measured by the VAS and attentional capture by threatening distractors as indexed by the difference RT score. | — |
Countries
Netherlands
Outcome results
None listed