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Neurofeedback to Reduce Spontaneous Recovery of Threat Expectancy

Description

This study tests the efficacy of a new behavioral intervention with the goal of reducing spontaneous recovery of threat expectancy in healthy adults. This real-time functional magnetic resonance imaging (fMRI) neurofeedback intervention delivers feedback based on a functional connection between the prefrontal cortex and the hippocampus.

Conditions

Healthy
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Related Conditions:

Healthy

Study Overview

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Study Details

Study overview

This study tests the efficacy of a new behavioral intervention with the goal of reducing spontaneous recovery of threat expectancy in healthy adults. This real-time functional magnetic resonance imaging (fMRI) neurofeedback intervention delivers feedback based on a functional connection between the prefrontal cortex and the hippocampus.

Reducing Spontaneous Recovery Using Functional Connectivity Based Real-time Functional Magnetic Resonance Imaging Neurofeedback Targeting the Memory Control Network

Neurofeedback to Reduce Spontaneous Recovery of Threat Expectancy

Condition
Healthy
Intervention / Treatment

-

Contacts and Locations

Princeton

Princeton Neuroscience Institute, Princeton, New Jersey, United States, 08540

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Adults aged 18-50
  • * No history of psychiatric disorders or neurological disorders affecting the central nervous system.
  • * Are not currently taking psychoactive medication or drugs of abuse.
  • * Must be eligible to enter an MRI (i.e., no permanent metal or medical implants)
  • * Normal color vision
  • * Right-handed
  • * Full reading and writing English comprehension
  • * Must exhibit spontaneous recovery behavior as determined by an experimenter in a prescreening experimental session
  • * Must be able to provide informed consent
  • * Pregnancy (female participants)
  • * Outside of age range
  • * History of psychiatric or neurological disease
  • * Currently taking psychoactive medication or drugs of abuse
  • * Color blindness
  • * Primary left-handedness
  • * Less than full reading and writing English comprehension
  • * Do not exhibit spontaneous recovery behavior as determined by an experimenter in a prescreening experimental session
  • * Refusing to provide informed consent

Ages Eligible for Study

18 Years to 50 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Trustees of Princeton University,

Kenneth A. Norman, Ph.D., PRINCIPAL_INVESTIGATOR, Princeton University

Study Record Dates

2028-06