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Bulimia Nervosa clinical trials

View clinical trials related to Bulimia Nervosa.

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NCT ID: NCT04815044 Enrolling by invitation - Pregnancy Related Clinical Trials

Experiences From Pregnancy and Post-partum Period in Women With a History of Eating Disorders.

PREG_PED-t
Start date: December 1, 2020
Phase:
Study type: Observational

Women with the eating disorder bulimia nervosa (BN) have been found to have a higher risk of unplanned pregnancies than healthy women, and experience greater miscarriage, premature birth, birth complications, and postpartum depression. Other studies have found that women with eating disorders seem to find motivation to refrain from the eating disordered behavior for the sake of the fetus, but that it is highly different whether this gives sustained or only a temporary remission. Eating disorders are rarely detected in the primary health care service, nor during pregnancy or during follow-up in fertility clinics. Meeting a health care provider in the pregnancy care service who does not know about the eating disorder or who does not understand the disease well enough, can also make the management and experience of pregnancy and weight gain extra difficult. The aim of this study is to increase the knowledge on how women with a history of eating disorder experience their bodily changes, and how they experience the health service in pregnancy care and post-partum period.

NCT ID: NCT04174703 Enrolling by invitation - Anorexia Nervosa Clinical Trials

Preparing for Eating Disorders Treatment Through Compassionate Letter-Writing

Start date: September 29, 2020
Phase: N/A
Study type: Interventional

Compassion-focused therapy (CFT) seeks to lower shame and help people develop compassion for personal distress and shortcomings. There is increasing evidence to support the benefits of incorporating CFT-based interventions into the treatment of eating disorders (EDs). Building on the investigators' prior research, this study will examine the effects of a two-week CFT-based self-compassion letter-writing intervention on patients with eating disorders. Participants will be recruited from the wait-list of patients scheduled to begin treatment at the outpatient St. Joseph's Healthcare Hamilton Eating Disorders Program, and will be randomly assigned to the two-week letter-writing intervention or to a control group. Results will inform the integration of new empirically-derived interventions into ED treatments to improve the currently dismal rates of ED recovery.

NCT ID: NCT03471806 Enrolling by invitation - Bulimia Nervosa Clinical Trials

Dopamine Release to Food Reward in Bulimia Nervosa

Start date: February 16, 2018
Phase: N/A
Study type: Interventional

This study will assess the role of dopamine responses to food reward in Bulimia Nervosa patients, by performing simultaneous Positron Emission Tomography (PET) and Magnetic Resonance (MR) scanning. The dopamine response will be measured before and after treatment, and will be compared to healthy controls.

NCT ID: NCT03338387 Enrolling by invitation - Bulimia Nervosa Clinical Trials

Co-Feedback Action of Growth Hormone, PP and PYY on Ghrelin in Bulimia

Start date: May 6, 2003
Phase: Phase 2
Study type: Interventional

This study evaluates the addition of Acipimox or placebo to exercise on growth hormone release and ghrelin secretion in bulimic patients and in healthy women. Two groups of participants will receive Acipimox together with exercise versus identical placebo with exercise.