Actively Recruiting
Neurofeedback During Eating for Bulimia Nervosa
Led by Icahn School of Medicine at Mount Sinai · Updated on 2026-01-30
30
Participants Needed
1
Research Sites
185 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to examine the effects of noninvasive prefrontal cortex (PFC) neurofeedback during eating in women with bulimia nervosa (BN) using a wearable brain imaging device, functional near-infrared spectroscopy (fNIRS). The investigators will examine how this training may influence inhibitory control and BN symptoms.
CONDITIONS
Official Title
Neurofeedback During Eating for Bulimia Nervosa
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female
- Aged 18 to 45 years
- Meet diagnostic criteria for bulimia nervosa
- Current body mass index greater than or equal to 18.5kg/m2 but under 30kg/m2
- English-speaking
You will not qualify if you...
- Ongoing medical treatment, major medical condition, or psychiatric disorder that may interfere with study variables or participation
- Current psychotherapy focused primarily on eating disorder symptoms
- Pregnancy or planned pregnancy, or lactation during the study period
- Allergy to ingredients in the standardized meal or in the shake
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Center for Computational Psychiatry at the Icahn School of Medicine at Mount Sinai
New York, New York, United States, 10027
Actively Recruiting
Research Team
S
Sila Sozeri, B.A.
CONTACT
L
Laura A Berner, Ph.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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