Neurofeedback for Borderline Personality Disorder

Kymberly Young

Status: Enrolling

Conditions: Borderline Personality Disorder

Treatments: Device: Amygdala Neurofeedback

Study type: Interventional

Funder types: Other

Identifiers

NCT05398627

STUDY22040107

Details and patient eligibility

About

The goal of this study is to evaluate whether rtfMRI-nf training to increase the amygdala response to positive memories may serve as an intervention for borderline personality disorder.

Full description

We will assess the treatment effects of real-time fMRI neurofeedback in adults with borderline personality disorder. This is an experimental longitudinal design where participants will be followed every two weeks after receiving 2 sessions of neurofeedback from the amygdala . Procedures involve a battery of self-report measures, fMRI and psychophysiological indices (heart rate, respiration).

Enrollment: 100 estimated patients

Sex: All

Ages: 18 to 55 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• right-handed adults (ages 18 - 55) with a primary diagnosis of Borderline Personality Disorder according to diagnostic criteria in the Structured Interview for DSM Personality Disorders
• must be able to give written informed consent prior to participation
• unmedicated or stable on an SSRI antidepressant regime (at least 3 weeks to ensure symptoms are stable)
• English speaking

Exclusion criteria

• have a clinically significant or unstable cardiovascular, pulmonary, endocrine, neurological, gastrointestinal illness or unstable medical disorder
• Current moderate or severe DSM-V alcohol or substance use disorder, with the exception of nicotine or caffeine. Clinician will access subjects' alcohol and substance use on a case-by-case to determine whether specific cases of mild alcohol or substance use would also interfere with the effects of the intervention.
• have a history of traumatic brain injury
• are unable to complete MRI scan due to claustrophobia or general MRI exclusions (e.g., shrapnel inside body)
• are currently pregnant or breast feeding
• are unable to complete questionnaires written in English
• current (within 3 weeks of testing) use of any antipsychotics, benzodiazepines, beta-blockers, or other medications (except SSRI antidepressants) likely to influence cerebral blood flow. Effective medications will not be discontinued for the purposes of the study. Inclusion of patients on stable antidepressant medications was decided in order to allow generalization towards a real world population
• have a DSM-5 diagnosis of psychotic or organic mental disorder
• have any eye problems or difficulties in corrected vision.
• Serious suidicial ideation

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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100 participants in 1 patient group

Amygdala Neurofeedback

Experimental group

Description:

Participants will undergo real-time fMRI neurofeedback training to increase their amygdala response while recalling positive autobiographical memories. 2 sessions will occur within a one week period.

Treatment:

Device: Amygdala Neurofeedback