Neurofeedback During Eating for Bulimia Nervosa
Recruiting
N/A
Interventional Study
Bulimia Nervosa
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 45
- Sex
- Female
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 30 (estimated)
- Sponsor
- Icahn School of Medicine at Mount Sinai · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
Inclusion criteria:
* 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
Exclusion criteria:
* Ongoing medical treatment, major medical condition, or psychiatric disorder tha…
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