NCT07528378

Brief Summary

This study will investigate the use of real-time fMRI to change how participants perceive social information.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for all trials

Timeline
8mo left

Started Sep 2026

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 2, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

April 14, 2026

Completed
5 months until next milestone

Study Start

First participant enrolled

September 1, 2026

Expected
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2027

Last Updated

April 14, 2026

Status Verified

April 1, 2026

Enrollment Period

8 months

First QC Date

April 2, 2026

Last Update Submit

April 9, 2026

Conditions

Keywords

individual differencessocial perceptionfMRI

Outcome Measures

Primary Outcomes (1)

  • Likelihood of certain social percepts (behavioral)

    Likelihood of participants to report perceiving certain types of interactions in social animations. Percepts are characterized according to if a social interaction was perceived, and if so, how it was perceived (on a valence axis from positive to neutral to negative).

    during fMRI session

Secondary Outcomes (1)

  • Control over brain activity (fMRI-based)

    during fMRI session

Interventions

During each fMRI session, we will monitor subjects' brain activity in real time and use univariate and/or multivariate activity patterns to trigger trial presentation. For each individual, we will select three regions: one key region early in the cortical hierarchy (e.g., MT), one key region late in the cortical hierarchy (e.g., anterior temporal), and one control region that does not show strong tuning to social information (e.g., primary auditory). These regions will be functionally defined for each individual using data from their characterization sessions. Subjects will report percepts behaviorally after each trial. For each region for each individual, we will then test the correlation between pre-stimulus activity and the likelihood of reporting certain percepts across trials.

Neurofeedback is a type of biofeedback that uses real-time displays of brain activity in an attempt to teach subjects to self-regulate their brain function. Here we will use implicit neurofeedback, meaning that subjects will see a feedback signal, but will not be told what that feedback signal represents (i.e., which brain region) or what the expected effects of learning to control that brain region might be. This type of neurofeedback is less prone to suggestibility and other confounding effects. Each of the two scan sessions dedicated to this intervention will be split into four equal blocks in a 2x2 design with region (early or late) and direction of modulation (up or down). Subjects will see a continuous feedback signal representing the region and direction, and will be asked to try to modulate the signal using any strategy that occurs to them.

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Healthy individuals between 18 and 35 years of age

You may qualify if:

  • willingness and availability to come for a total of 6 MRI scan sessions
  • good fMRI data quality in previous, non-clinical trial study, including low head motion, high vigilance during the task as measured via simultaneous eye tracking, consistent behavioral responses

You may not qualify if:

  • metallic objects in body contraindicated for the MRI scanner
  • history of severe psychiatric or neurological disease
  • currently on medication for a psychiatric condition
  • illicit drug use
  • claustrophobia
  • heavy nicotine or alcohol use
  • prior head injury
  • pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

April 2, 2026

First Posted

April 14, 2026

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

May 1, 2027

Study Completion (Estimated)

May 1, 2027

Last Updated

April 14, 2026

Record last verified: 2026-04