Measuring the Impact of Real Time fMRI Neurofeedback in Borderline Personality Disorder

Completed · Not applicable

Conditions studied: Borderline Personality Disorder

In brief

This study will test the impacts of real time fMRI neurofeedback in patients with Borderline Personality Disorder. This is a pilot study in a small number of people enrolled in clinical programs at Yale New Haven Hospital.

Key facts

Study ID

NCT04306341

Run by

Yale University

People needed

3

Starts

2020-11-15

Expected to finish

2022-10-07

Last updated by the study team

2023-05-22

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• enrolled in YNHH DBT-IOP
• must meet specific clinical criteria
• Inclusion in Experimental group requires participants meet standard safety and quality control requirements for MR scanning
• For female participants, not pregnant and willing to use a reliable method of contraception during the study

You may not qualify if…

• IQ<70
• vision problem not able to be corrected to normal range
• medication changes w/in one month
• Lifetime hx of schizophrenia, schizoaffective d/o, bipolar I disorder.
• illicit substance use within 7 days of MRI scans
• taking scheduled opiates
• taking scheduled benzodiazepines
• taking scheduled anti-histamines
• history of seizures
• significant current or past neurologic illness
• BMI < 16.5

Where it is running

• Connecticut Mental Health Center — New Haven, Connecticut, United States

Full record on ClinicalTrials.gov

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