Neurofeedback to Reduce Spontaneous Recovery of Threat Expectancy (NCT07122739)
Reducing Spontaneous Recovery Using Functional Connectivity Based Real-time Functional Magnetic Resonance Imaging Neurofeedback Targeting the Memory Control Network
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: Princeton Neuroscience Institute — Princeton, New Jersey
Age range: 18 Years to 50 Years
🧪 Interventions in This Study
- Active Real-time fMRI Neurofeedback (BEHAVIORAL)
- Sham Real-time fMRI neurofeedback (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Princeton Neuroscience Institute — Princeton, New Jersey
📞 Contact the Study Coordinator
Phone: (609) 258-5032
Email: gus.hennings@princeton.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.