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Bulimia Nervosa clinical trials

View clinical trials related to Bulimia Nervosa.

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NCT ID: NCT01470508 Completed - Bulimia Nervosa Clinical Trials

Engaging Latino Families in Eating Disorders Treatment

PAS
Start date: August 2010
Phase: N/A
Study type: Interventional

Promoviendo Alimentacion Saludable (PAS)"Promoting Healthy Eating" is a research project funded by the National Institute of Mental Health. The purpose of this study is to develop and test a treatment for eating disorders in Latina adults that is appropriate for their age and includes culturally appropriate family intervention.

NCT ID: NCT01395355 Completed - Clinical trials for Binge Eating/Loss of Control Eating

An Integrative Intervention for Loss of Control Eating Among Adolescent Girls

Start date: August 2011
Phase: N/A
Study type: Interventional

This study aims to develop a manualized and culturally sensitive intervention for adolescent girls targeting binge and loss of control (LOC) eating. The investigators will evaluate the feasibility and acceptability of the intervention in a controlled pilot trial. The investigators hypothesize that this intervention will serve to reduce binge and LOC eating, as well as improve psychosocial functioning as evidenced by decreased depression, anxiety, eating disorder cognitions, and impulsivity, and improved quality of life.

NCT ID: NCT01208272 Completed - Clinical trials for Binge Eating Disorder

Psychological Treatment of Overweight Binge Eaters

Start date: April 1994
Phase: Phase 1/Phase 2
Study type: Interventional

Cognitive-behavioral therapy (CBT) has documented efficacy for the treatment of binge eating disorder (BED). Interpersonal psychotherapy (IPT) has been shown to reduce binge eating but its long-term impact and time course on other BED-related symptoms remain largely unknown. This study compares the effects of group CBT and group IPT across BED-related symptoms among overweight individuals with BED.

NCT ID: NCT01208259 Completed - Clinical trials for Binge Eating Disorder

The Psychological Treatment of Overweight Binge Eaters Minority Supplement

Start date: April 1997
Phase: Phase 1/Phase 2
Study type: Interventional

Cognitive-behavioral therapy (CBT) has documented efficacy for the treatment of binge eating disorder (BED). Interpersonal psychotherapy (IPT) has been shown to reduce binge eating but its long-term impact and time course on other BED-related symptoms remain largely unknown. This study compares the effects of group CBT and group IPT across BED-related symptoms among overweight individuals with BED.

NCT ID: NCT01172210 Completed - Bulimia Nervosa Clinical Trials

Examining Common Substrates of Eating and Alcohol Use Disorders

Start date: July 2009
Phase: N/A
Study type: Observational

A substantial percentage of individuals with bulimia nervosa (BN) also meet criteria for a co-occurring substance use disorder, such as alcohol abuse or dependence; however, research examining this sub-group of patients with BN is limited. Understanding characteristics common to both eating and alcohol use disorders may enhance understanding of the mechanisms that could contribute to the co-occurrence and perpetuation of these disorders. Individuals with BN and alcohol use disorders appear to share some behavioral traits, and therefore, the primary aim of the current study is to compare patients with BN with and without an alcohol use disorder and normal controls on measures assessing an individual's mood and ability to perform certain tasks. Participants will be asked to complete computer-administered and paper-and-pencil assessments and two laboratory test meals on separate days. By probing the underpinnings of BN and alcohol use disorders, the investigators can determine whether these disorders have a shared diathesis, which will lay an essential foundation for future research to examine biological and genetic correlates of these disorders. Finally, as little is known about the treatment of patients with BN and a co-occurring alcohol use disorder, an exploratory aim of the current study is evaluate the suitability and efficacy of a 20-session cognitive-behavioral treatment (CBT) addressing both bulimic symptoms and alcohol use.

NCT ID: NCT01106053 Withdrawn - Clinical trials for Binge Eating Disorder

Pramipexole for Binge Eating Disorder

Start date: April 2010
Phase: Phase 3
Study type: Interventional

This study is being conducted to evaluate the effects that the drug pramipexole has on mood, food craving, and other behaviors that may be related to binge eating disorder.

NCT ID: NCT01098435 Completed - Clinical trials for Binge Eating Disorder

ALK33-101: A Study of RDC-0313 (ALKS 33) in Adults With Binge Eating Disorder

Start date: May 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety of daily doses of RDC-0313 (ALKS 33) compared with placebo in adults with binge-eating disorder (BED). An additional objective is to explore the efficacy of RDC-0313 treatment in comparison with placebo in adults with binge-eating disorder.

NCT ID: NCT01038128 Completed - Bulimia Nervosa Clinical Trials

An Open Label Trial of Memantine in the Treatment of Bulimia Nervosa and Body Dysmorphic Disorder

Start date: December 2009
Phase: N/A
Study type: Interventional

The primary objective of this 13-week clinical trial is to test the hypothesis that treatment with Memantine will significantly improve the symptoms of those suffering from either bulimia nervosa, purging type or suffering from body dysmorphic disorder.

NCT ID: NCT01033149 Terminated - Bulimia Nervosa Clinical Trials

N-acetylcysteine in the Treatment of Bulimia Nervosa

Start date: December 2009
Phase: Phase 3
Study type: Interventional

The specific aim of this study is to evaluate the efficacy, tolerability, and safety of N-acetylcysteine (NAC) in the treatment on bulimia nervosa.

NCT ID: NCT00988481 Withdrawn - Bulimia Nervosa Clinical Trials

Topiramate Augmentation in Bulimia Nervosa Partial Responders

Start date: September 2009
Phase: Phase 4
Study type: Interventional

The goal of this study is to generate pilot data exploring the addition of an augmentation (additional) medication to patients suffering from bulimia nervosa who have responded but not had complete symptom resolution with a course of standard medication treatment.