Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
Healthy Volunteers
NCT06276400

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

Age: 18Years - 45Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Right-handed
  • Between the ages of 18 and 45
  • Fluent English speaker
  • Normal to corrected-to-normal vision
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

University of California, Santa Barbara

Santa Barbara, California, United States, 93106

Actively Recruiting

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here