MedPath

Learning and Decision-making

Not Applicable
Completed
Conditions
Motivation
Interventions
Registration Number
NCT06014606
Lead Sponsor
Maastricht University
Brief Summary

A fundamental aspect of daily life decision-making involves the evaluation of costs and benefits. Neural systems underlying cost-benefit evaluation have been extensively examined, but the specific role of different neurotransmitters remains unclear. Numerous studies suggest that both dopamine (DA) and norepinephrine (NE) are closely related to reinforcement learning, guided exploration/exploitation, and behavioural energisation, although no studies to date have investigated the distinct role of DA and NE on cost-benefit decision-making and learning in human subjects.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Willingness to sign an informed consent
  • Age between 18 and 35
  • Body-Mass Index (BMI) between 17.5-30
  • Availability for participation through the duration of the study
Exclusion Criteria
  • Diagnosis of a psychiatric or neurological disorder, including substance abuse or dependence (yes/no self-report - lifetime)
  • Use of any psychopharmacological treatment 3 weeks before the test day (yes/no self-report)
  • Use of any blood pressure medication (yes/no self-report - lifetime)
  • Pregnancy (confirmed via urine pregnancy test) or nursing (yes/no self-report) or have plans to get pregnant in the near future (yes/no self-report) (females only)
  • Diagnosis of a cardiac disease (medical questionnaire), obstructive respiratory disease (medical questionnaire), abnormal blood pressure (diastolic< 60mmHg; systolic< 90mmHg) (medical screening)
  • Chronic renal failure (medical questionnaire)
  • Hypothyroidism (medical questionnaire)
  • Diabetes (medical questionnaire)
  • Hypersensitivity to phenothiazines (medical questionnaire)
  • Diagnosis of a cardiac disease (medical questionnaire)
  • Alcohol consumption in the 24 hours before the test session starts (yes/no self-report)
  • Food intake less than 3 hours before the test day (yes/no self-report)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
HV/Haloperidolhaloperidol 2mg2mg (oral)
HV/Propranololpropranolol 40mg40mg (oral)
HV/PlaceboplaceboOral placebo (tablet)
Primary Outcome Measures
NameTimeMethod
Cost-benefit reinforcement learning performance~ 2.5 hours post-drug administration

2-choice reinforcement learning task (based on Voulgaropoulou et al., 2021 PNEC)

Secondary Outcome Measures
NameTimeMethod
Effort-based decision-making~ 2 hours post-drug administration

motivation to acquire rewards (e.g., Reddy et al. 2015)

Trial Locations

Locations (1)

Maastricht University

🇳🇱

Maastricht, Netherlands

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