earned oxytocin responses
Completed
- Conditions
- Conditioning in healthy subjects
- Registration Number
- NL-OMON20692
- Lead Sponsor
- eiden University
- Brief Summary
n/a
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 99
Inclusion Criteria
1.Between 18 and 35 years old;
2.Good understanding of written and spoken Dutch;
Exclusion Criteria
1.Current psychiatric (DSM-IV) conditions;
2.All conditions that might interfere with the participant's safety and/or the study protocol: claustrophobia, metal parts in or on the body that are not removable, Raynaud’s phenomenon, severe neurological or neurosurgical conditions;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The main study parameter is the difference in salivary oxytocin levels during evocation between the experimental group and the placebo group.
- Secondary Outcome Measures
Name Time Method Secondary study parameters assessed at baseline are: salivary cortisol and pain sensitivity levels in response to the cold pressor test. During the evocation phase (1st and 2nd evocation days), psychophysiological state and task-related assessments will be measured. During the third evocation day, resting state and task-related brain activity will be measured.