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Anorexia clinical trials

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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.

NCT ID: NCT02932046 Completed - Anorexia Nervosa Clinical Trials

Hunger and Satiety in Anorexia Nervosa

HUSAAN
Start date: February 2014
Phase: N/A
Study type: Observational

Anorexia means loss of appetite. But there is disagreement about whether the appetite is changed by the disease anorexia nervosa (AN). Appetite is a subjective essential sense, which is regulated in a complex ensemble between brain, stomach - intestinal system and hormones. As a direct result of malnutrition, there are many somatic complications caused by the disease AN. Several of these complications may in itself affect hunger- and satiety perception. An example of this is delayed gastric emptying. Furthermore, changes in the hormone systems affects the biological "reward system" in the brain, which plays an important role in appetite regulation. There is clearly need for research that could lead to better treatments for AN. Hunger- and satiety perception has only been studied in a few small cross-sectional studies with no clear conclusion. The purpose of the study is to determine whether a visual analog scale measurement can detect changes in hunger- and satiety perception in a least 30 patients admitted to nutrition for life-threatening severe anorexia nervosa. It may lead to the first step in the development of a simple and inexpensive instrument which may prove to be useful in measuring the impact of new and ongoing treatments of the disease.

NCT ID: NCT02920073 Recruiting - Anorexia Nervosa Clinical Trials

Intestinal Metagenome of Undernourished in Patients

INT-METAVOSA
Start date: October 2016
Phase: N/A
Study type: Observational

The objective of this trial is to evaluate gut microbiota changes in undernourished patients with anorexia nervosa under enteral nutrition.

NCT ID: NCT02891356 Recruiting - Osteoporosis Clinical Trials

Bone Mass Changes in Anorexia Nervosa Patient Followed During 4 Years

AMOS
Start date: July 2013
Phase:
Study type: Observational

The mechanism of bone loss in anorexia nervosa is complex. Marrow adipose tissue seems to play a role in the regulation of bone metabolism. Adipocytes secrete cytokines and adipokines that either stimulate or inhibit adjacent osteoblasts. This study consist to explore the relationship in anorexia nervosa patients with change in bone mineral density and adipokines like leptin, adiponectin and Préf-1 Bone mineral densities will be measure in 180 anorexia nervosa patients at inclusion and every two years during 6 years.It is assessed blood and urinary calcium and phosphate levels, bone remodelling markers and adipokines (leptin, adiponectin and Préf-1)

NCT ID: NCT02887586 Completed - Cancer Clinical Trials

The Effectiveness and Mechanism Study of Auricular Needling in Treating Cancer Induced Anorexia

Start date: August 2016
Phase: N/A
Study type: Interventional

Controlling of cancer induced anorexia is highly demanded by advanced cancer patients. It plays an important role in improving the quality of life among advanced cancer patients. Through a randomized controlled single blinded clinical research, we will observe the differences of appetite, food intake amount, weight and KPS between the auricular needling treating group and control group before and after the treatment. Based on the results of the research, we can prove the clinical effectiveness of auricular needling in treating cancer induced anorexia and possible mechanism of the method.

NCT ID: NCT02883413 Completed - Anorexia Nervosa Clinical Trials

Cognitive Remediation Therapy for Adolescents With Anorexia Nervosa

Start date: August 2016
Phase: N/A
Study type: Interventional

The purpose of the current study is to investigate the role of Cognitive Remediation Therapy (CRT) as a pre-treatment intervention for adolescents who are hospitalized for Anorexia Nervosa (AN). The primary aims are to determine if CRT can result in greater treatment engagement post-discharge, increased rate of weight gain post-discharge, reduction in symptom accommodation, and increased behavioral flexibility in adolescents and parents.