human cognition physical discomfort visual processing
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: The recruitment of participants takes place as follows. Practitioners at the department of Psychiatry will inform healthy participants via hand-outs and online flyers about our study. If someone is willing to participate in the study, we will email them to inform them of the entire procedure. This email will ensure that they have the opportunity to fully understand the procedure. If they are still interested in participating, they will sign an informed consent and we will perform screening for inclusion and exclusion criteria. Demographics and a clinician-related questionnaire (M.I.N.I) will be assessed to make sure that the individual can participate. If a participant meets any of the exclusion criteria, then they are excluded from participating in this study.;Inclusion criteria: - Men and women. - Age between 25-65. - No previous diagnosis of a mental disorder - No previous diagnosis of chronic pain
Exclusion criteria
Exclusion criteria: - A DSM-V diagnosis for any mental disorder - Diagnosed with having chronic pain
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - Augmented reality task, the main study parameters consist of self-reports measured by a VAS and physiological recordings of heart rate and Skin Conductance level (SCL) measured by the VU-AMS. - Non-augmented reality task, the main study parameters consist of self-reports measured by a VAS and physiological recordings of heart rate and Skin Conductance level (SCL) measured by the VU-AMS. | — |
Countries
Netherlands