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Anorexia Nervosa clinical trials

View clinical trials related to Anorexia Nervosa.

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NCT ID: NCT03100656 Recruiting - Anorexia Nervosa Clinical Trials

Study of Food Aversion in Patients With Anorexia Nervosa

Start date: November 10, 2016
Phase: N/A
Study type: Interventional

This study uses a meal-challenge protocol to assess if patients with anorexia nervosa show a differential metabolism in response to food in comparison to healthy controls. This study determines how heritable and biochemical factors influence food metabolism in anorexia nervosa in order to develop more effective treatment strategies.

NCT ID: NCT03097874 Completed - Anorexia Nervosa Clinical Trials

Adaptive Treatment for Adolescent Anorexia Nervosa

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

The investigators are conducting a randomized controlled trial using an adaptive design for adolescents (ages 12-18) with anorexia nervosa to compare standard Family Based Treatment (FBT) to adaptive FBT with an Intensive Parental Coaching (IPC) component. If participants do not reach expected milestones by session 4 of treatment, participants may be randomized to receive additional IPC or continue treatment as usual with regular FBT.

NCT ID: NCT03075371 Completed - Healthy Clinical Trials

Homeostatic and Non-homeostatic Processing of Food Cues in Anorexia Nervosa

Start date: September 2014
Phase: N/A
Study type: Interventional

The goal of the present study is to investigate metabolic gut-brain signaling and the neural correlates of distraction from visual food cues in patients with Anorexia nervosa and healthy controls.

NCT ID: NCT03019081 Active, not recruiting - Anorexia Nervosa Clinical Trials

Augmented Interoceptive Exposure Training in Anorexia Nervosa

Start date: January 2017
Phase: N/A
Study type: Interventional

The researchers propose to utilize a pharmacological approach involving infusions of the sympathomimetic agent isoproterenol to repeatedly trigger cardiorespiratory sensations and anxiety during meal anticipation, to facilitate the development of tolerance or a reduction of the anxiety/fear response in individuals with anorexia nervosa. The investigators aim to conduct a proof of principle study to assess for evidence of initial efficacy of this new treatment approach. As a comparator condition, the researchers propose using repeated administration of saline infusions.

NCT ID: NCT03003429 Completed - Anorexia Nervosa Clinical Trials

Correlation Study Between Heart Rate Variability and Anxiety in Anorexia Nervosa

VARIASTRESS
Start date: March 1, 2017
Phase: N/A
Study type: Interventional

The heart rate variability (HRV) is a measure of the autonomic nervous system (ANS). In the model of anorexia nervosa, ANS is disturbed with mostly a predominance of activation of the parasympathetic nervous system and a decrease of the sympathetic system. Various explanations of this these dysfunctions are proposed in literature, mainly malnutrition, physical hyperactivity, anxiety, that are known characteristics of anorexia nervosa. The primary aim of this study is to evaluate correlation between ANS dysfunction and anxiety in anorexia nervosa. Other objectives of this study are firstly to evaluate correlation between ANS dysfunction and others parameters (weight, body mass index, depression, physical activity, purgative ou restrictive type, duration of disease, smoking) in anorexia nervosa and secondly to see if HRV is a predictive parameter of the evolution of anorexia nervosa.

NCT ID: NCT02995226 Recruiting - Anorexia Nervosa Clinical Trials

Abnormal Regulation, Estimation and Cognitive Impacts of Physical Efforts as an Endophenotype of Anorexia Nervosa

CAPANOX
Start date: February 27, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to check if patients, but also relatives (as they share familial and genetic risk factors), are having more difficulties in regulating a spontaneous, pleasant physical effort (doing "too much") compared to healthy controls, and if physical efforts are participating to core symptoms of anorexia nervosa, such as more appetite (instead of less), less pain, more abnormal body image, and less cognitive flexibility. Such a result could help to further understand the role of difficulties with physical exercise as part of the phenotype of anorexia nervosa.

NCT ID: NCT02962726 Completed - Anorexia Nervosa Clinical Trials

Microbiome Shifts in Adolescent Anorexia Nervosa

MaAN
Start date: September 1, 2016
Phase:
Study type: Observational

The aim of this study is to evaluate the effect of starvation and recovery in adolescent anorexia nervosa patients in regard to microbiome activity and composition and to elucidate potential connections between weight gain, depression and other comorbidities, further to capture hormone levels and inflammation parameters in a longitudinal design.

NCT ID: NCT02960152 Recruiting - Clinical trials for Periodontal Diseases

Periodontal Impact of Eating Disorders (the PERIOED Study)

PERIOED
Start date: October 2014
Phase: N/A
Study type: Observational

This study evaluated the periodontal status of patients suffering from eating disorders (anorexia nervosa and bulimia nervosa). The work hypothesis is that eating disorder patients have a higher risk for periodontal diseases than non-eating disorder subjects.

NCT ID: NCT02948452 Completed - Anxiety Clinical Trials

Anxiety and Reward Interaction and Prediction of Outcomes in Anorexia Nervosa

Start date: November 2015
Phase:
Study type: Observational

This study is designed to understand responsiveness to reward in adolescents with restricting-type anorexia nervosa compared with non-clinical controls, and how it is affected by potential-threat perception.

NCT ID: NCT02937259 Completed - Anorexia Nervosa Clinical Trials

Self-admission: A New Treatment Approach for Patients With Severe Eating Disorders

Start date: August 2014
Phase: N/A
Study type: Interventional

Self-admission is a novel treatment tool whereby patients who are well-known to a service who have high previous utilization of health care are offered the possibility of self-admission to the inpatient ward for up to seven days without having their motive for admission questioned. Patients are free to admit themselves because of deteriorating mental health, acute stress, lack of structure in their everyday life, loneliness, boredom, or any other reason. The patients decide when they want to admit themselves and can discharge themselves at any time. The purpose behind the self-admission model is to increase the availability of inpatient care for severely ill patients, to avoid stressful and possibly destructive visits to the emergency service, and to decrease total inpatient care utilization. Patients offered a contract for self-admission usually have a history of repeated and prolonged hospitalizations. By encouraging them to monitor their own mental health status and allowing them to seek help swiftly when they are feeling poorly, the delay from first signs of deterioration to admission can be minimized and full-blown relapse can be avoided, ultimately reducing the total time spent in hospital. Until now, projects of self-admission have mainly targeted patients with long-standing psychotic disorders, such as schizophrenia, or bipolar disorder. Starting in August 2014, a four-year clinical project at the Stockholm Centre for Eating Disorders began offering self-admission to patients with severe and enduring eating disorders. The purpose of this study is to determine whether this model is viable in a specialized eating disorders treatment setting, if it does lead to increased patient participation and agency and a reduction of the total time spent hospitalized for this particular patient group, and if it is cost-effective.