Neurofeedback Enhanced Cognitive Reappraisal Training - Phase 4
- Conditions
- AnxietySocial Anxiety DisorderPanic DisorderGeneralized Anxiety Disorder
- Registration Number
- NCT06563310
- Lead Sponsor
- University of Michigan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not yet recruiting
- Sex
- All
- Target Recruitment
- 110
Inclusion Criteria:<br><br> - Primary diagnosis (primary source of distress and/or interference) of generalized<br> anxiety disorder, social anxiety disorder, panic disorder or illness anxiety<br> disorder based on structured interview. Comorbid phobic disorders allowed, but these<br> cannot be the primary source of interference or distress due to the lowered chances<br> of encountering anxiety-provoking stimuli during the study period<br><br> - Medically and physically able to consent<br><br> - Not taking any medication, prescription or non-prescription with psychotropic<br> effects other than birth control or antidepressant (i.e., selective serotonin<br> reuptake inhibitor (SSRI) or serotonin-norepinephrine reuptake inhibitor (SNRI) with<br> stable dosage for past 4 week<br><br> - For females, not currently pregnant or actively trying to become pregnant<br><br> - Ability to tolerate small, enclosed spaces without anxiety<br><br> - No metals, implants or metallic substances within or on the body that might cause<br> adverse effects to the subject in a strong magnetic field, or interfere with image<br> acquisition (per protocol)<br><br> - Size compatible with scanner gantry (per protocol)<br><br>Exclusion Criteria:<br><br> - Current diagnosis of Obsessive Compulsive Disorder or Posttraumatic Stress Disorder<br><br> - Current course of individual or group psychotherapy<br><br> - Current substance abuse or dependence (past 6 months)<br><br> - Active suicidality with plan or intent<br><br> - Current psychosis<br><br> - History of serious neurological illness or current medical condition that could<br> compromise brain function, such as liver failure<br><br> - History of closed head injury, e.g., loss of consciousness greater (>) approximately<br> (~) 5 minutes, hospitalization, neurological sequela
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in ventrolateral prefrontal cortex (vlPFC) activity (baseline to transfer run) from the reappraise > look contrast.;Change in negative affect ratings of images from the International Affective Picture System (IAPS).
- Secondary Outcome Measures
Name Time Method Change in amygdala-vlPFC functional connectivity (baseline to transfer) from reappraise > look contrast.