12 Participants Needed

Caffeine for Learning in Healthy Adults

(Caffeine-RAC Trial)

HW
Overseen ByHsiao-Ying Wey, PhD
Prior Safety DataThis treatment has passed at least one previous human trial

Trial Summary

What is the purpose of this trial?

This research study aims to determine whether and how caffeine intake affects learning process through reward feedback compared to placebo. The data acquired from this study would improve our understanding on the consequence and mechanism of caffeine intake in the aspect of learning process.Participants will perform a reinforcement learning task (i.e. Probabilistic Selection Task) and a motor inhibition task (i.e. Go/NoGo task) in a brain scan. The scan will be done with the Siemens Biograph mMR positron emission tomography (PET)/ magnetic resonance imaging (MRI) 3 Tesla scanner. The PET allows us to see the changes in the "reward signals" - dopamine - in the brain using a radioactive dye called \[11C\]Raclopride. The MRI, on the other hand, enables us to take detailed pictures of the brain activities during cognitive tasks using a high-powered magnet. Reviewing these pictures will help us understand the influence of caffeine on reward signals and brain activities during the learning process.

Eligibility Criteria

This trial is for healthy adults interested in how caffeine affects learning. Participants will do tasks during a brain scan to see changes in dopamine, which helps with reward signals. They must be eligible based on certain health criteria not specified here.

Inclusion Criteria

Non-smokers
Clinically healthy
Habitual caffeine intake ≥ 100 mg and ≤ 450 mg daily
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Exclusion Criteria

Recent exposure to radiation (i.e., PET from other research studies) that, when combined with this study, would be above the allowable limits
Pregnancy or breastfeeding: A negative serum or urine pregnancy test is required on the day of the PET procedure
I have diabetes or another metabolic disease.
See 14 more

Timeline

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Washout

Participants undergo a 6-day ambulatory washout period abstaining from caffeine, alcohol, and drugs

1 week
No visits

Treatment

Participants receive either caffeine or placebo and undergo PET/fMRI scans to assess neurochemical and hemodynamic changes

1 day
1 visit (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

1-2 weeks

Treatment Details

Interventions

  • Caffeine
Trial Overview The study tests the effects of a 200 mg caffeine dose versus a placebo on reinforcement learning and motor inhibition using advanced PET/MRI brain imaging to track dopamine levels and brain activity during cognitive tasks.
Participant Groups
2Treatment groups
Experimental Treatment
Placebo Group
Group I: CaffeineExperimental Treatment1 Intervention
Caffeine tablet, 200mg
Group II: PlaceboPlacebo Group1 Intervention
Lactose tablet

Find a Clinic Near You

Who Is Running the Clinical Trial?

Hsiao-Ying Wey

Lead Sponsor

Trials
1
Recruited
10+
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