somato-sensore informatie verwerking cognitive functioning nociception
Conditions
Interventions
None listed
Sponsors
Katholieke Universiteit Nijmegen
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Between 18-60 years of age.
Exclusion criteria
Exclusion criteria: Neurologic / psychiatric history Use of psychoactive substances Visual/auditory impairment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main parameters will be ERP component amplitudes (in µV) and VAS values (on a continuous scale between 0-10). ERP component amplitudes from both visual warning stimuli (N1, P2, N2 and P3, as well as CNV) and noxious stimuli (N140, P260) will be determined. In a previous pilot experiment with healthy volunteers (CMO-nr.: 2005/288) we found marked effects on noxious stimulus predictability on both the CNV preceding the noxious stimuli and the P260 following the noxious stimuli. | — |
Secondary
| Measure | Time frame |
|---|---|
| Behavioral responses to the attentional task 1. Omissions and Error rates 2. Reaction Times Test scores to the Thayer scales ECG: heart rate and heart rate variability demographic data | — |
Countries
Netherlands
Outcome results
None listed