Does Caffeine Facilitate Human Reward Learning Behaviors?
NCT ID: NCT05325502
Last Updated: 2023-08-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
36 participants
INTERVENTIONAL
2022-05-05
2024-12-31
Brief Summary
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Detailed Description
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In this double-blind, randomized, crossover study, 36 young healthy non-smoking habitual caffeine consumers (daily dose 100 - 450 mg) who are aged between 18 and 40 will be examined. Each of the 36 participants (18 F, 18 M) will undergo an acute caffeine condition, a daily caffeine condition, and a daily placebo condition. Each condition consists of 7 days - 6 ambulatory days followed by 1 laboratory visit.
In the ambulatory part, participants will abstain from caffeine, nicotine, medications, and recreational drugs. Compliance to the interventions and abstinence of caffeine will be monitored by salivary caffeine concentration every day. Bedtime and sleep quality will be recorded in sleep diary. On the laboratory visit, participants will perform cognitive tasks on a 2.5h task battery, which includes a probabilistic selection task, a motor inhibition task, and a salience attribution test. We also measure their arousal and anxiety levels 1h after the second intake on the laboratory visit.
We will use Bayes factor analyses to test our confirmatory hypotheses (on the primary outcomes): 1) Caffeine enhances the accuracy of reward learning; 2) Daily intake of caffeine facilitates the negative reinforcement compared to acute its intake. On the secondary outcomes, we examine the exploratory hypotheses that caffeine enhances motor inhibition and motivational salience. Arousal and anxiety levels will be examined as a covariate which potentially contribute to the caffeine-induced changes in reward learning performance.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
TRIPLE
Study Groups
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Placebo
7 days placebo intake.
mannitol
two doses per day: 200 mg in the morning \& 100 mg in the afternoon
Acute caffeine
6 days placebo followed by 1 day caffeine intake.
caffeine
two doses per day: 200 mg caffeine in the morning; 100 mg caffeine in the afternoon
mannitol
two doses per day: 200 mg in the morning \& 100 mg in the afternoon
Daily caffeine
7 days caffeine intake
caffeine
two doses per day: 200 mg caffeine in the morning; 100 mg caffeine in the afternoon
Interventions
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caffeine
two doses per day: 200 mg caffeine in the morning; 100 mg caffeine in the afternoon
mannitol
two doses per day: 200 mg in the morning \& 100 mg in the afternoon
Eligibility Criteria
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Inclusion Criteria
* Clinically healthy
* Non-smokers
Exclusion Criteria
* Pregnant or lactating women
* Women using hormonal contraceptives
* BMI \< 18.5 or \> 29.9
* Sleep disturbance or extreme chronotypes
* Nicotine or recreational drug users
* Depression, anxiety, psychosis, or neurologic disorders
* Severe heart or cardiovascular diseases
* Diabetes or metabolic diseases
* Under chronic medications
* Incapable to operate the tasks or comprehend the study information in German or English
* Users of the Bopomo alphates utilized as stimuli in the reward learning tasks
* Current enrolment in other clinical trials
18 Years
40 Years
ALL
Yes
Sponsors
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Yu-Shiuan Lin
OTHER
Responsible Party
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Yu-Shiuan Lin
Postdoc researcher
Principal Investigators
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Yu-Shiuan Lin, PhD
Role: PRINCIPAL_INVESTIGATOR
Centre for Chronobiology, University Psychiatric Clinics Basel
Locations
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Centre for Chronobiology, University Psychiatric Clinics Basel
Basel, Canton of Basel-City, Switzerland
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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CChronobiology
Identifier Type: -
Identifier Source: org_study_id
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