Does Caffeine Facilitate Human Reward Learning Behaviors?

NCT ID: NCT05325502

Last Updated: 2023-08-31

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-05-05

Study Completion Date

2024-12-31

Brief Summary

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"Learning from the rewards" is underlying the formulation of knowledge and habits in daily life. Caffeine is the most commonly used "psychoactive" substance that could change one's mind state by affecting the brain and nervous system. By such effects, caffeine enhances reward signals - dopamine - in human brains. In this research study, we will find out whether taking caffeine acutely or daily can enhance reward learning processes.

Detailed Description

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Reward learning is associated with the formulation of habits, memories, and beliefs. Positive (receiving an unexpected reward) and negative reinforcement (eliminating an unwanted state) learning are primarily modulated by striatal dopamine D1 and D2 receptors. While caffeine, a psychostimulant regularly consumed by 80% worldwide population, is known to facilitate striatal dopamine signaling, the potential of caffeine on enhancing reward learning in humans remains unknown.

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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Caffeine

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Placebo

7 days placebo intake.

Group Type PLACEBO_COMPARATOR

mannitol

Intervention Type DIETARY_SUPPLEMENT

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.

Group Type ACTIVE_COMPARATOR

caffeine

Intervention Type DIETARY_SUPPLEMENT

two doses per day: 200 mg caffeine in the morning; 100 mg caffeine in the afternoon

mannitol

Intervention Type DIETARY_SUPPLEMENT

two doses per day: 200 mg in the morning \& 100 mg in the afternoon

Daily caffeine

7 days caffeine intake

Group Type EXPERIMENTAL

caffeine

Intervention Type DIETARY_SUPPLEMENT

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

Intervention Type DIETARY_SUPPLEMENT

mannitol

two doses per day: 200 mg in the morning \& 100 mg in the afternoon

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Age ≥ 18 and ≤ 40
* Clinically healthy
* Non-smokers

Exclusion Criteria

* Habitual caffeine intake \< 100 mg or \> 450 mg
* 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
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Yu-Shiuan Lin

OTHER

Sponsor Role lead

Responsible Party

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Yu-Shiuan Lin

Postdoc researcher

Responsibility Role SPONSOR_INVESTIGATOR

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

Site Status RECRUITING

Countries

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Switzerland

Central Contacts

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Yu-Shiuan Lin, PhD

Role: CONTACT

+41613255474

Facility Contacts

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Béatrice Anderlohr-Streule

Role: primary

+ 41 61 325 54 74

Other Identifiers

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CChronobiology

Identifier Type: -

Identifier Source: org_study_id

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