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Bulimia Nervosa clinical trials

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NCT ID: NCT01832792 Completed - Bulimia Nervosa Clinical Trials

Guided Self-help for Binge Eating

Start date: August 2013
Phase: N/A
Study type: Interventional

Guided self-help (GSH) is a recommended first-step treatment for bulimia nervosa, binge eating disorder, and atypical variants of these disorders. The current study proposes to investigate the effectiveness of providing GSH either face-to-face or via e-mail, also using a delayed treatment control condition. Symptom outcomes will be assessed, and an estimate of cost-effectiveness made. Results are proposed to be disseminated locally and internationally (through submission to conferences and peer-reviewed journals), and will hopefully inform local service provision. Please note that we are only able to offer the intervention to individuals who are currently registered with a General Practitioner that is covered by Oxford Health NHS Foundation Trust - this is typically restricted to practices in Oxfordshire, Buckinghamshire, and parts of Wiltshire.

NCT ID: NCT01830374 Completed - Bulimia Nervosa Clinical Trials

Bulimia Nervosa: A Biobehavioral Study (The Eating Disorder Study)

TEDS
Start date: August 2012
Phase:
Study type: Observational

The purpose of this study is to examine biological (e.g., energy expenditure, neuroendocrine and appetitive hormones)and behavioral (e.g., binge eating and purging) correlates of weight suppression and current dieting status in women with bulimia nervosa. The investigators have differentiated between a diet-induced long-term energy imbalance (weight suppression, or the difference between one's highest-ever body weight and current weight) and a short-term energy imbalance (current dieting to either lose weight or avoid weight gain). This study will elucidate how two common yet largely unexplored types of dieting influence biological and behavioral variables in patients with bulimia nervosa, which could lead to modifications of prevailing models of bulimia nervosa and new strategies for improving treatment outcome.

NCT ID: NCT01757847 Completed - Clinical trials for Binge-Eating Disorder

Stress and Eating Study

Start date: January 2013
Phase: N/A
Study type: Interventional

This study proposes to compare a brief Acceptance and Commitment Therapy (ACT) group intervention to an active control group in a sample of 154 overweight or obese binge eating Veterans who have completed the VA's national behavioral weight management program (MOVE!). This study anticipates that the ACT intervention will reduce binge eating and distress while improving functioning and maintenance of weight loss.

NCT ID: NCT01693237 Active, not recruiting - Clinical trials for Bulimia Nervosa (BN)

Improving Patient Outcome in Group Therapy for Eating Disorders

F-EAT
Start date: August 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The current trial aims to investigate the impact of continuous feedback on dropout and outcome in group therapy. The hypothesis is that continuous feedback to patient and therapist on treatment progress and alliance will 1) increase adherence and 2) increase treatment outcome.

NCT ID: NCT01567670 Active, not recruiting - Clinical trials for Binge Eating Disorder

Clinical Trial on Binge Eating Disorder, Treatment With Naloxone Spray

BED
Start date: August 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The investigators are studying a new treatment for one subtype of obesity. Obesity is not a disease. It is a symptom of several different diseases. These diseases have distinct etiologies, being caused by aberrations in different mechanisms. Forms of obesity caused by such non-critical mechanisms might be corrected fairly easily and safely. The investigators are interested in overeating and obesity that is caused by the opioidergic system. The opioidergic system appears to be responsible for a subtype of obesity associated with binge eating disorder (BED). People, especially with the right genetic predisposition, can become addicted to foods that release endorphins, in the way that people become addicted to exogenous opiates and other drugs that release endorphins. The particular application in our proposed clinical trial is for intranasal (IN) naloxone. The peak levels of naloxone were similar and the bioavailability of naloxone intranasally was 100% (the same) of that available IV." IN administration of naloxone has since been broadly tested in humans, as well, where it has been shown to be safe, with pharmacokinetics similar to those of naloxone given by injection .

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: NCT01544400 Terminated - Anorexia Nervosa Clinical Trials

Description and Evaluation of Eating Disorders in Elite Athletes (TCA SHN)

TCA SHN
Start date: June 2010
Phase: N/A
Study type: Observational

Athletes in particular elite athletes have obsessional food and body concerns, in bond with a worship of the performance more and more invading, which lead to clinical and subclinical eating disorders. These eating disorders differ according to the disciplines and are difficult to diagnose in athletes because there are insufficiently described. Our aim at estimating the frequency of eating disorders in athletes and describing eating disorders by means of somatic, dietetic and psychological evaluations.

NCT ID: NCT01530906 Recruiting - Bulimia Nervosa Clinical Trials

Efficiency of Repetitive Transcranial Magnetic Stimulation (rTMS) in Bulimia

rTMS&bulimia
Start date: January 2012
Phase: N/A
Study type: Interventional

Bulimia nervosa is defined by recurrent episodes of binge eating followed by compensatory behaviors (such as induced vomiting) to prevent weight gain. It is a common and serious disease for which current treatment strategies have to be improved. The aim of this study is to assess whether a transcranial magnetic stimulation reduces bulimic symptoms in a short term.

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.