cognitive impairment, working memory problems
Conditions
Interventions
This is not a clinical trial, thus there is no investigational product. Participants will receive either 400mg sulpiride or placebo in the pharmaco-fMRI session, in separate sessions in a counterbalan
Sponsors
Radboud Universitair Medisch Centrum
Eligibility
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: Healthy volunteers between 18 and 45 years of agePredominant right-handedness18.5 < BMI < 30
Exclusion criteria
Exclusion criteria: Neuropsychiatric disorders; Relevant medical disorders; History of drug abuse; Pregnancy; Metal objects in or around the body (see section 4.3 of the Research Protocol C1 for full list of exclusion criteria)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| BOLD signal measured with laminar fMRI; behavioural performance on cognitive tasks. | — |
Secondary
| Measure | Time frame |
|---|---|
| Behavioural performance on cognitive tasks/questionnaires. | — |
Countries
Netherlands
Contacts
Public ContactH.S. Olraun
Radboud Universitair Medisch Centrum
Outcome results
None listed