Actively Recruiting
LPFC Organization in Emotion-Duration Difference Estimation
Led by University of California, Santa Barbara · Updated on 2026-05-04
50
Participants Needed
1
Research Sites
217 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To support optimal behavior in daily life, goals and responses following emotional events should ideally incorporate not only the valence and intensity of prior emotional episodes but also their temporal features, such as the relative duration of positive vs. negative attributes. However, how specific brain regions contribute to the integration of temporal and emotional information and promote goal-directed response remains unknown. The goal of this study is to examine how specific brain regions track both emotional and temporal information of dynamic emotional events to inform other related brain regions to guide goal-oriented and context-appropriate actions. The investigators will scan healthy human participants using functional MRI (fMRI) while they view emotional image sequences and track the associated emotional and temporal (duration) information, and act accordingly. The investigators will employ multivariate patterns analysis and pattern similarity analysis to identify brain regions that represent (can decode) emotion, time, and their combined signals, as well as brain regions that represent the associated action goal. In addition, to infer the causal contributions of these brain regions in forming task-relevant representations (emotion, time, and action goal), the same participants will be recruited to receive transcranial magnetic stimulation (TMS) in these regions.
CONDITIONS
Official Title
LPFC Organization in Emotion-Duration Difference Estimation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Right-handed
- Between the ages of 18 and 45
- Fluent English speaker
- Normal to corrected-to-normal vision
You will not qualify if you...
- Current or past psychiatric disorder requiring hospitalization or current psychiatric medication use
- History of neurological disease such as stroke, concussion, epilepsy, major head trauma, or complicated migraine
- History of seizures
- Family history of epilepsy or seizure disorders
- History of fainting
- Sleep deprivation (for TMS sessions)
- History of surgery with metal clips, implants, devices, prosthetics, cardiac or neural implants, or cochlear implants
- Inability to safely complete MRI due to metal in body, recent surgery, implanted devices not cleared for MRI, extreme claustrophobia, tattoos on head or neck, or non-removable metal piercings
- Pregnancy or possibility of pregnancy
- History of hearing issues including loss, sensitivity to loud noises, tinnitus, high noise exposure jobs, or chronic migraines
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of California, Santa Barbara
Santa Barbara, California, United States, 93106
Actively Recruiting
Research Team
M
Mengsi Li, M.S.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
BASIC_SCIENCE
Number of Arms
1
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