Healthy participants
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: 1. Age between 18 and 30 2. Sufficient understanding of Dutch Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 72 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range
Exclusion criteria
Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: 1. Cardiac, hepatic, renal, neurological or psychiatric disorders 2. Personal or family history of depression 3. Migraine 4. Drug use and medication use
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: The main goal of the present study is to examine whether acetaminophen decreases the cardiac response to unexpected social rejection in a social evaluation task. ;Secondary Objective: Secondary goals are how acetaminophen affects the subjective evaluation of social rejection, the brain response to social evaluation and the expectation bias in the social judgment task. Finally we are interested in how acetaminophen affects crying behaviour as subjectively indicated by the participants. ;Primary end point(s): Cardiac deceleration following unexpected social rejection;Timepoint(s) of evaluation of this end point: 1 hour after ingestion of paracetamol | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary end point(s): Expectancy bias in terms of expected rejection events, P3 amplitude following unexpected rejection and theta power following unexpected social rejection. Subjectively reported crying behavior ;Timepoint(s) of evaluation of this end point: 1 hour after ingestion of paracetamol | — |
Countries
Netherlands
Contacts
Erasmus University Rotterdam