Augmenting Cognitive Behavioral Therapy With Inhibitory Control Training
Status unconfirmed · Not applicable · Has a placebo group
Conditions studied: Binge-Eating Disorder, Bulimia Nervosa
In brief
The primary aim of this study is to determine whether a computerized inhibitory control training (ICT) will improve CBT treatment outcomes for Bulimia Nervosa and Binge Eating Disorder.
Key facts
- Study ID
- NCT04076553
- Run by
- Drexel University
- People needed
- 60
- Starts
- 2019-10-15
- Expected to finish
- 2022-07-01
- Last updated by the study team
- 2021-08-09
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- age 18-55
- meet DSM-5 criteria for Bulimia Nervosa (i.e., at least one episode of binge eating and compensatory behavior per week on average for the past 3 months) or Binge Eating Disorder (i.e., at least one episode of binge eating per week on average for the past 3 months).
- be stable on psychiatric medications for at least 3 months
You may not qualify if…
- have a diagnosis of anorexia nervosa or a BMI < 18.5
- have extreme malnutrition or other medical complications that require acute hospitalization
- are at acute suicide risk
- are currently experiencing other severe psychopathology that would require a more intensive or specialized treatment program than the current study provides (e.g. severe depression, active psychotic disorder)
- have previously completed a trial of CBT for Bulimia Nervosa or Binge Eating Disorder
- have a diagnosis of an intellectual disability or autism spectrum disorder
- currently taking stimulant medications
- score of 95% or higher on 550ms block of Go/No-Go assessment task, indicating high inhibitory control at Baseline
Where it is running
- Drexel University — Philadelphia, Pennsylvania, United States (enrolling)
Full record on ClinicalTrials.gov
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