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Risk taking during stress

Conditions
GASICAStressDecision-makingFeedbackBesluitvormingFeedback
Registration Number
NL-OMON29232
Lead Sponsor
niversity Medical Center Utrecht
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
42
Inclusion Criteria

Age 18-65
Normal or corrected-to-normal vision

Exclusion Criteria

Drug or alcohol abuse over a period of six months prior to the experiment
Unwillingness to view or hear aversive stimuli from the IAPS or IADS
Previously diagnosed with, or under treatment for, psychological or psychiatric disorders (e.g. depression, schizophrenia, neuroticism, etc.).
Previously diagnosed with, or under treatment for, medical indications (e.g. closed- or open-head injury, neurological illness, epilepsy, PTSD, cardiovascular indications, endocrinological dysfunction, etc.).
Use of medication (chronic/recently)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The measured physiological stress responses (heart rate, systolic and diastolic blood pressure and electrodermal response) during all tasks. <br>The amplitude of the P300 and Feedback Related Negativity (FRN) component in response to both positive and negative feedback in the BART task during different stressor intensities.
Secondary Outcome Measures
NameTimeMethod
ot applicable.
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