Actively Recruiting

Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT05977439

RECOVERS - Realigning Emotion and COgnition Via prEcision Regulation networkS

Led by Medical University of South Carolina · Updated on 2025-09-02

30

Participants Needed

1

Research Sites

243 weeks

Total Duration

On this page

Sponsors

M

Medical University of South Carolina

Lead Sponsor

C

Columbia University

Collaborating Sponsor

AI-Summary

What this Trial Is About

In this research study, the investigators are examining how brain activity (electrical and blood flow) changes during tests of emotional processing, attention and memory in the magnetic resonance imaging (MRI) scanner and outside the MRI using functional near-infrared spectroscopy (fNIRS). Investigators are also using non-invasive brain stimulation to probe different parts of the brain and measuring brain activity (electrical and blood flow). Study 1 This study includes healthy participants and researchers hope this will help us develop improved brain-based treatments for emotional difficulties like depression. Study 2 This study includes participants with depression and researchers hope this will help us develop improved brain-based treatments for emotional difficulties like depression.

CONDITIONS

Official Title

RECOVERS - Realigning Emotion and COgnition Via prEcision Regulation networkS

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female
  • Age 18-65
  • For healthy participants: good health with no history of mental or physical illness or implanted metal
  • For participants with depression: current depression with HAM-D scores 65 17 and no history of psychosis or mania
  • English as a primary language
  • Capacity to consent
  • Negative urine pregnancy test if female of childbearing potential
  • Willingness to adhere to the study schedule and assessments
Not Eligible

You will not qualify if you...

  • Any current psychiatric diagnosis or Clinical Global Impression rating of psychiatric illness > 1 (for healthy participants)
  • Neurodevelopmental disorders, history of CNS disease, concussion, overnight hospitalization, or other neurological conditions such as tumors, seizures, meningitis, encephalitis, or abnormal brain imaging
  • Any head trauma resulting in loss of consciousness
  • Visual impairment (except the use of glasses)
  • Inability to complete cognitive testing
  • Active participation or plans for enrollment in clinical trials affecting psychosocial function
  • Repeated abuse or dependence on drugs (excluding nicotine and caffeine) or use of stimulants, modafinil, thyroid medication, or steroids
  • Implanted devices or ferrous metal of any kind
  • History of seizure or epilepsy or currently taking medications that lower seizure thresholds
  • Claustrophobia or conditions preventing MRI assessment
  • Pregnancy or plans to become pregnant in the short term
  • Inability to adhere to the treatment schedule

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medical Univeristy of South Carolina

Charleston, South Carolina, United States, 29425

Actively Recruiting

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Research Team

L

Lisa McTeague, PhD

CONTACT

J

Jacob Eade, MS

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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