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Modafinil Effects on EEG Biomarkers of Reward and Motivation

Neurophysiological Biomarkers of Behavioral Dimensions From Cross-species Paradigms

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03616717
Enrollment
23
Registered
2018-08-06
Start date
2018-10-16
Completion date
2021-09-30
Last updated
2022-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Adults

Brief summary

The effects of modafinil on measures of brain electrical activity will be tested.

Interventions

DRUGModafinil

Drug: modafinil Each participant receives a single pill of placebo or active drug (modafinil 100 mg or 200 mg) 30 minutes after arriving at the lab. The participant then completes approximately 6 hours of testing in the laboratory. The participant stays at the lab for 7.5 hours in order to monitor physical condition in case the participant received the active pill. One week later, that participant receives a single pill of an alternate comparator and is again tested in the laboratory. Thus, in total, each participant receives one placebo pill and two active pills, each time separated by one week. Other Names: Provigil Alertec Modavigil

DRUGplacebo

Drug: Placebo Each participant receives a single pill of placebo or active drug (modafinil 100 mg or 200 mg) 30 minutes after arriving at the lab. The participant then completes approximately 6 hours of testing in the laboratory. The participant stays at the lab for 7.5 hours in order to monitor physical condition in case the participant received the active pill. One week later, that participant receives a single pill of an alternate comparator and is again tested in the laboratory. Thus, in total, each participant receives one placebo pill and two active pills, each time separated by one week.

Sponsors

University of California, San Diego
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

University of California, San Diego Experimental Pharmacy randomizes dose order and provides masked pills

Intervention model description

Experimental medicine model; not an intervention. Within-subject double-blind placebo-controlled dose-response study.

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Exclusion criteria

* history of substance abuse * mental illness in a first degree relative * significant medical illness (e.g. cancer, diabetes, heart disease, HIV) * history of seizure * open head injury or closed head injury with loss of consciousness \> 1 min * pregnancy * current psychotropic drug use * R-hand injury * hearing or visual impairment * urine toxicology positive for recreational drug use

Design outcomes

Primary

MeasureTime frameDescription
Reward Positivity1 yearFrontal alpha power by block in the probabilistic learning task
Motivation Signal1 yearParietal EEG alpha power peak in first - final step toward breakpoint

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026