Actively Recruiting
Developing Transcranial Neuromodulation Protocols for Learning and Decision-Making
Led by National Institute on Drug Abuse (NIDA) · Updated on 2026-06-08
600
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are exploring how changes in brain activity may affect learning and decision-making, particularly in people with substance use disorder. This study aims to develop and test non-invasive brain stimulation methods called neuromodulation protocols that target specific cognitive functions and brain networks involved in these processes. The research focuses on healthy volunteers aged 18 to 45 years who are right-handed to reduce variability in brain function measurements. Participants may join up to five different experiments, each involving 2 to 8 clinic visits lasting 3 to 7 hours. Some visits include transcranial magnetic stimulation (TMS) using different devices: continuous theta burst stimulation (cTBS), intermittent theta burst stimulation (iTBS), or sham TBS as a placebo. During TMS, a magnetic coil is placed on the head to deliver brief magnetic pulses, sometimes while participants tense muscles. Other visits involve functional MRI (fMRI) scans where participants perform tasks while brain activity is recorded. Throughout the study, participants will complete computer-based tasks involving images, sounds, smells, or tastes to assess cognitive functions related to learning and decision-making. Vital signs and eye movements may be monitored during activities. Researchers will measure task performance after each intervention to determine if the neuromodulation protocols effectively influence cognitive functions and brain networks. The total participation time depends on the number of experiments joined and visits required.
CONDITIONS
Brief Title
Developing Transcranial Neuromodulation Protocols for Learning and Decision-Making
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18-45 years
- In good general health based on the assessment of the MAI
- Right-handed
You will not qualify if you...
- Any neurological disorder increasing seizure risk, such as stroke, brain lesions, epilepsy, or history of seizures or fainting
- Predisposition to seizures, including family history of epilepsy
- Recent use of investigational or psychotropic drugs within past two weeks or daily use for more than one week within past three months
- Unable to undergo MRI or TMS due to implants, claustrophobia, or other reasons
- History of noise-induced hearing loss or tinnitus
- Recent major psychiatric disorders or learning disabilities within past 12 months
- Pattern of harmful alcohol or drug use in past 12 months
- Daily nicotine, alcohol, or drug use for at least 4 continuous weeks within past 12 months
- Participation in neuromodulation sessions (other than current) in past two weeks
- History of severe allergies or anaphylaxis related to tasks involving taste or smell
- Uncorrected severe visual impairments
- Non-English speaking
- Pregnancy
- Any other condition judged incompatible by investigators
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single session per experiment
Participants receive non-invasive neuromodulation using different Theta Burst Stimulation protocols to target specific cognitive functions involved in learning and decision making.
1 visit (in-person) per experiment
Trial Site Locations
Total: 1 location
1
National Institute on Drug Abuse
Baltimore, Maryland, United States, 21224
Actively Recruiting
Research Team
N
NIDA IRP Screening Team
T
Thorsten Kahnt, Ph.D.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
5
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