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Anorexia Nervosa clinical trials

View clinical trials related to Anorexia Nervosa.

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NCT ID: NCT03273205 Completed - Anorexia Nervosa Clinical Trials

Transcranial Direct Current Stimulation (tDCS) in the Treatment of Anorexia Nervosa

SANO
Start date: May 22, 2017
Phase: N/A
Study type: Interventional

Anorexia Nervosa (AN) is a serious and often chronical eating disorder characterized by an extreme effort for weight loss and intense fear of becoming fat despite the obvious thinness. The treatment is very difficult and not always effective. That´s the reason why we are looking for new ways of the therapeutic approach. Transcranial direct current stimulation (tDCS) is a neuromodulation technique, which modulates the neuronal excitability. According to previous research it has a potential to help people with Anorexia Nervosa. The device for the tDCS has two electrodes, an anode (the excitatory one) and a cathode (the inhibitory one). We put them on the skull into the different positions, in dependence on the fact, if we want to excite or on to inhibit the parts of the brain under the electrodes. There are several hypothesis how could the tDCS help in patients with AN. One of them speaks about the hyperactivity of the right hemisphere in Anorexia Nervosa. Therefore could the anodal (excitatory) tDCS over the left hemisphere and the cathodal (inhibitory one) help in resetting the inter-hemispheric balance.

NCT ID: NCT03230435 Active, not recruiting - Anorexia Nervosa Clinical Trials

Health Related Quality of Life for Patients With Anorexia Nervosa in Denmark.

QOLAN-DK
Start date: March 1, 2017
Phase:
Study type: Observational

Eating disorders (ED) comprise a multitude of symptoms involving a disturbed body image and a preoccupation with food or bodyweight. EDs are often difficult to treat, in part due to the lack of motivation for improvement. Anorexia nervosa (AN) has the highest mortality rate of any psychiatric disease, and less than half of patients will recover from the disease. Studies have found that patients suffering from AN have impaired health-related quality of life (HRQoL) compared to the general population. It has also been suggested that despite improvement in clinical parameters, patients report deterioration in HRQoL, which is in line with a study finding low agreement between patient perceived outcome and clinician assessed characteristics. To evaluate the patients' perception of their disease, it is important to develop reliable and valid assessment tools. Previously generic questionnaires have been used to assess HRQoL in Danish ED patients, as no disease-specific questionnaires have been developed. Translating and validating a disease-specific questionnaire would provide a useful tool in assessing current treatment and in developing new treatment options. This study aimed to develop a Danish version of an internationally disease-specific HRQoL questionnaire. Furthermore, HRQoL is assessed in patients who have gone through shorter or longer treatment.

NCT ID: NCT03224091 Recruiting - Anorexia Nervosa Clinical Trials

PROspective Longitudinal All-comer Inclusion Study in Eating Disorders

PROLED
Start date: January 25, 2016
Phase:
Study type: Observational

The PROLED study is a prospective and longitudinal study of patients with Eating Disorders. Annual interviews and collection of biological samples are done, as well as during changes in disease course e.g. during hospitalization. Included are qualitative interviews, psychometric tests, questionnaires which are used to collect data on psychopathology. There is also collection of blood, urine and faeces.

NCT ID: NCT03172533 Terminated - Anorexia Nervosa Clinical Trials

Estrogen Replacement in Anorexia Nervosa

HOSAN
Start date: March 15, 2016
Phase: Phase 2
Study type: Interventional

The present study is a placebo-controlled randomised study on the effects of estrogen replacement upon AN-associated psychopathology, several neurocognitive domains and appetite-regulating circuits in female patients with AN. The investigators aim at assessing peripheral concentrations of neuroendocrinological components of the Hypothalamus-Pituitary-Gonadal (HPG) and Hypothalamus-Pituitary-Adrenal (HPA) axis, as well as appetite-regulating hormones in AN and to examine associations with AN-associated psychopathology and neurocognitive performances before (baseline), during and after inpatient psychotherapy of female patients receiving concomitant treatment with estrogens (vs. placebo).

NCT ID: NCT03168893 Recruiting - Anorexia Nervosa Clinical Trials

Deep Brain Stimulation for Patients With Chronic, Severe and Resistant Anorexia Nervosa

Start date: May 23, 2017
Phase: N/A
Study type: Interventional

Deep brain stimulacion (DBS) clinical study in the subcallosal cingulate (CSG) and accumbens nucleus (NAc) for 8 patients with treatment-refractory, cronic and severe anorexia nervosa (AN) patients. The main objective is to show efficacy and safety. Studies show that SSG and NAc are strategical targets in the pathophysiology and the hypothetical surgical treatment in AN patients. The patients distribution (4 patients in each target) it will made by the AN type and the comorbidity associated, the reasons are: 1- It is well known the comorbidity treatment imoportance in the AN evolution, 2- The two differentes types of AN have differents clinical behaviour and prognosis, 3- Studies show efficacy in TOC and DM patients with NAc DBS and in DM patients with CSG DBS. The main variable is BMI. After a 6 months stabilization evaluation phase will be followed (only in patients that have increase 10% BMI) by a double-bind, crossover phase, where patients will receive 3 months with stimulation turned on and 3 month with turned off. All patients will have a 12 months follow up. The study secondary objectives are to know the relation btween the stimulacion answer (increase 10% BMI) and the differents variables, specially AN type, associated cormobidity, selected target and preoperative MRI tractography study.

NCT ID: NCT03151135 Terminated - Anorexia Nervosa Clinical Trials

Energy Turnover in Patients With Anorexia Nervosa

Start date: March 1, 2017
Phase:
Study type: Observational

Pilot study to assess energy turnover at end of inpatient treatment in 10 patients with Anorexia nervosa.

NCT ID: NCT03144986 Completed - Anorexia Nervosa Clinical Trials

Insula-coil Deep TMS for Treatment Resistant Anorexia Nervosa

Start date: September 2012
Phase: N/A
Study type: Interventional

OBJECTIVE: Anorexia Nervosa (AN) is a complex disorder of unknown etiology that is characterized by disordered eating behaviors and specific psychopathology. In the course of anorexia around 50% will recover in the first 10 years, 25% will continue to experience symptoms but will be able to function, and 25% will go to develop chronic course, and by definition become severe treatment resistant(Tr). There is little if anything to offer to this population where the range of treatment options is limited to weight restoration interventions. Transcranial magnetic stimulation (rTMS) is a non-invasive intervention, which presents a particular interest in people with severe TrAN, specifically because of its ability to target deeper areas of the brain, such as insula, which has been argued to be a possible trait marker for AN. METHODS: This pilot study will test the efficacy and safety of deep-rTMS delivered with the H-coil in subjects with long standing treatment resistant severe anorexia nervosa (TrAN).

NCT ID: NCT03119272 Completed - Anorexia Nervosa Clinical Trials

Microbiome-mediated Weight, Anxiety, and Stress Dysregulation in Anorexia Nervosa

Microbiome
Start date: April 2016
Phase:
Study type: Observational

The purpose of this research study is to analyze the microorganisms residing in the gut of patients with anorexia nervosa. Research has begun to link changes in the intestinal microbiota with diseases such as inflammatory bowel disease (IBS), asthma, and obesity, but although some studies have investigated the intestinal microbiota in overweight/obese individuals, very little is known about the intestinal microbiota in underweight individuals. The investigators aim to identify the enteric bacterial groups associated with adiposity, BMI, anxiety, and stress in patients with anorexia nervosa.

NCT ID: NCT03118921 Terminated - Anorexia Clinical Trials

Body Image Disorder in Anorexia Nervosa and Virtual Reality

REVAM
Start date: April 20, 2017
Phase: N/A
Study type: Interventional

Evaluation of the tolerance and acceptability of the virtual representation of its body image.

NCT ID: NCT03107221 Completed - Anorexia Nervosa Clinical Trials

Eating Disorders: Online Self-help & Usual Treatment (TAU) vs TAU Only

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

A pilot study exploring whether individuals receiving usual treatment (CBT) from the specialist NHS Tayside Eating Disorders Service and accessing the online self-help "Smart Eating" programme have improved treatment outcomes compared to those receiving usual treatment only. The study will also explore acceptability of the "Smart Eating" self-help programme via a feedback questionnaire.