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Bulimia clinical trials

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NCT ID: NCT01552759 Completed - Clinical trials for Binge Eating Disorder

Appetite Hormones in Binge Eating Disorder

Start date: May 2007
Phase: N/A
Study type: Interventional

This study investigates the hormones that the body produces in response to food intake and in response to stress, and the way that stress influences food intake. In particular, it compares the hormone levels and food intake of people with and without binge eating disorder. In order to find out how these appetite- and stress-related hormones are linked to brain activity, the study also includes an fMRI scan, a non-invasive procedure that looks at which regions of the brain are most active during a food-related scenario.

NCT ID: NCT01517906 Completed - Anorexia Nervosa Clinical Trials

Developing Identity: An Eating Disorder Randomized Clinical Trial

Start date: April 2002
Phase: N/A
Study type: Interventional

The purpose of this research study is to test a new type of counseling developed to decrease symptoms of anorexia nervosa and bulimia nervosa and improve health and well-being in women with these eating disorders. At this time, the most effective form of treatment for anorexia nervosa and bulimia nervosa is cognitive behavioral therapy. However, this form of treatment leads to a complete absence of symptoms in only about 50% of persons completing the treatment program. In this study we will test the effectiveness of a new form of counseling that focuses on identifying and building personal strengths and positive views of the self as the means to decrease eating disorder symptoms and improve health. This study will involve 150 women between the ages of 18 and 35 years who currently have symptoms of anorexia nervosa or bulimia nervosa. To participate in this study, women must also be: 1) not pregnant, 2) without any other diagnosable mental disorder, 3) not currently taking medications for their eating disorder or other mental disorder symptoms, 4) not ill enough to require inpatient treatment for their eating disorder and 5) willing to refrain from seeking other treatment for their eating disorder for the duration of this study. Each participant will participate in a 20-week treatment program that includes nutritional counseling and medical care. Both of these forms of treatment are considered by the American Psychiatric Association to be essential parts of treatment for eating disorders and have been found help to reduce symptoms. In addition, participants will receive one of two types of counseling: 1. Experimental counseling that focuses on building strengths and positive self-views 2. Standard counseling that helps the participant identify and solve problems that are believed to contribute to their eating disorder symptoms. The type of counseling that a participant receives will be determined randomly. To determine whether the experimental counseling is effective, eating disorder symptoms, psychological and functional health will be measured before the treatment begins and three times after the treatment ends (immediately after treatment ends, 6 and 12 months later). The findings of this research study are expected to contribute to the development of effective interventions to decrease eating disorder symptoms, and increase health and well-being in women with anorexia nervosa and bulimia nervosa.

NCT ID: NCT01493362 Completed - Eating Disorders Clinical Trials

Imaging the Dopamine Systems in Bulimia Nervosa

Start date: January 2008
Phase: N/A
Study type: Observational

This study will use positron emission tomography imaging to investigate the dopamine systems in people with bulimia nervosa.

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: NCT01291173 Completed - Clinical trials for Binge Eating Disorder

Forced-dose Titration of SPD489 in Adults With Binge Eating Disorder

BED
Start date: May 10, 2011
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy of SPD489 compared to placebo in the treatment of moderate to severe binge eating disorder as measured by the number of binge days per week

NCT ID: NCT01282736 Completed - Clinical trials for Binge Eating Disorder

Guided Self-Help for Binge Eating Disorder

Start date: June 2010
Phase: N/A
Study type: Interventional

The proposed study will employ a randomized design to evaluate the efficacy of two group-based guided self-help treatments: Integrative Response Therapy (IRT) and Cognitive Behavior Therapy Guided Self-Help, a treatment of known efficacy, in group-format (CBT-GSHg) in the treatment of Binge Eating Disorder (BED), and explore (1) moderators and mediators of treatment, (2) the relative cost-effectiveness of the two treatments, and (3) between group differences on secondary measures (e.g., eating disorder and general psychopathology).

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.