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NCT ID: NCT02179749 Completed - Alcoholism Clinical Trials

Mifepristone Treatment of Alcohol Use Disorder

Start date: September 2014
Phase: Phase 2
Study type: Interventional

This is an 8-week, randomized, double-blind, placebo-controlled, 2 arm, parallel groups, study of 1-week of treatment with mifepristone (0, 1200 mg/d) given in conjunction with 8 weeks of manual-guided counseling, and a follow-up visit at Week 12.

NCT ID: NCT02176317 Completed - Clinical trials for Autism Spectrum Disorder

Autologous Umbilical Cord Blood Infusion for Children With Autism Spectrum Disorder (ASD)

Start date: June 2014
Phase: Phase 1
Study type: Interventional

This study is a prospective phase 1 single-center trial designed to determine the safety of a single intravenous infusion of autologous umbilical cord blood in children with Autism Spectrum Disorder (ASD) and assess the feasibility of various outcome measures to determine which measure(s) can be used as primary and secondary endpoints for a future randomized phase 2 clinical trial. All subjects will receive infusion of cord blood cells at baseline with follow up assessments at 6 and 12 months.

NCT ID: NCT02176226 Completed - Clinical trials for Major Depressive Disorder

IntelliCare: Artificial Intelligence in a Mobile Intervention for Depression and Anxiety (AIM)

Start date: March 2015
Phase: N/A
Study type: Interventional

This study will evaluate a Smartphone intervention for depression and anxiety that uses machine learning to tailor treatment for patients. The intervention, referred to as IntelliCare, delivers patient-specific treatment material and motivational messaging via a mobile phone, to help individuals with depression and/or anxiety. Information and data received from the patient will inform the tailored treatment approach through machine learning. The purpose of this study is to obtain preliminary information on the feasibility and effectiveness of IntelliCare in improving symptoms of depression and anxiety.

NCT ID: NCT02166086 Recruiting - Clinical trials for Diagnosis of a Pancreaticobiliary Disorder

Advanced Imaging Registry for Diagnosing Pancreatico-biliary Disorders

Start date: September 2011
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this registry is to record information and evaluate the impact of advanced imaging techniques on the management of pancreatico-biliary disorders. The registry will evaluate diagnostic performance and overall clinical management impacted by advanced imaging techniques.

NCT ID: NCT02164487 Completed - Eating Disorders Clinical Trials

Thiamin (Vitamin B1) Levels in Eating Disorder Adolescent Patients

Start date: March 2013
Phase:
Study type: Observational

Vitamin B1 (Thiamine) is a water soluble essential nutrient; it is synthesized by a variety of plants and microorganisms. Since animals usually cannot synthesis it, humans must be supplied with exogenous vitamin B1 in the diet. The human storage of thiamine is small- about 30mg, an intake of 1-2 mg a day is needed to maintain this pool. Deficiency might occur when the vitamin is depleted from the diet in a short period. Vitamin B1 has a role in energy metabolism and main biosynthetic pathways. Low thiamine causes illnesses in the central and peripheral nervous systems as well as affecting the heart and gastrointestinal systems. Deficiency may occur from malnutrition of different mechanisms such as alcoholism, lack in diet and recently secondary to anti-obesity surgery and few case reports described eating disorders as the reason for developing deficiency causing neuropathy, (1,2) and encephalopathy (3,4,5). One of the presentations of thiamine deficiency is peripheral neuropathy mimicking Guillain-Barre syndrome, and administering the lacking vitamin improves the symptoms. One study examined the prevalence of vitamin B1 deficiency in adult anorexia nervosa patients (6) by measurement of the activation of the enzyme erythrocyte transketolase following addition of thiamin pyrophosphate and comparing them to control of blood donors. This study found significant lower levels of vitamin B1 in the anorectic patient compared to the controls. Rational of the study: The investigators assume that these few cases described of overt neurologic impairment due to vitamin B1 deficiency because of distorted eating are just the "tip of the iceberg" and more eating disorders patients lack thiamine, that may have neuropsychiatric effect on the illness and identifying and treating the shortage may improve the symptoms of the disorder and maybe even the distorted thoughts that are fundamental in eating disorders.

NCT ID: NCT02163941 Completed - Clinical trials for Prolonged Post-traumatic Stress Disorder

Meditation for Emotional Numbing in Post-Traumatic Stress Disorder

Start date: May 2014
Phase: Phase 1
Study type: Interventional

For individuals suffering from posttraumatic stress disorder (PTSD), the emotional numbing and isolation that are a core aspect of their suffering and consistently impedes remediation often remains after first-line treatments are administered. Few interventions have proven successful for enhancing the empathy and social connectedness that will ultimately allow patients to flourish, and the search for target therapies is made more difficult by the fact that very little is known about the underlying physiology of emotional numbing and social isolation. The proposed study is designed to (1) investigate the hormonal, neural and immunological biomarkers related to emotional numbing, and (2) test whether cognitively-based compassion training (CBCT), an intervention designed and proven to enhance empathy, will reduce emotional numbing and increase empathy and social connectedness in veterans. To this end, thirty medically healthy males diagnosed with PTSD who continue to report emotional numbing symptoms after prolonged exposure therapy will receive 8 weeks of training in CBCT. Prior to, and again after the training, the investigators will assess patients' levels of oxytocin, inflammation, and self-reported emotional numbing and social connectedness. The investigators will also assess their neural response during a video task that assesses their ability to accurately read others' emotions. The investigators hypothesize that oxytocin, neural activity, and inflammation will predict social numbing, isolation, and empathy, and also that CBCT will positively impact the social outcomes that will pave the way toward health and well-being.

NCT ID: NCT02162030 Completed - Clinical trials for Long-term Physical Health Conditions

A Component Analysis of Acceptance and Commitment Therapy

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

The purpose of this study is to determine whether a specific component of Acceptance and Commitment Therapy (ACT) called 'Self as Context' is an important and necessary part of this therapeutic approach.

NCT ID: NCT02161718 Completed - Schizophrenia Clinical Trials

A Study of ALKS 3831 in Subjects With Schizophrenia and Alcohol Use Disorder

Start date: May 2014
Phase: Phase 2
Study type: Interventional

This double-blind, randomized study will evaluate the efficacy, safety and tolerability of ALKS 3831 in subjects with schizophrenia and alcohol use disorder (AUD).

NCT ID: NCT02160886 Completed - Clinical trials for Autism Spectrum Disorder

Effects of a Task Oriented Intervention With Two Goal-setting Approaches

Start date: October 2011
Phase: N/A
Study type: Interventional

A randomized trial investigating if effects of a goal-directed task oriented intervention is influenced by who takes the decision and establishes the goal (the child or the parent) and whether establishing a goal per se influence performance and goal-achievement. The main hypothesis are that children's participation in the goal-setting process would positively influence goal achievement, children's self-identified goals would be achievable and that both groups would achieve goals that were the target of a goal-directed intervention.

NCT ID: NCT02160249 Completed - Schizophrenia Clinical Trials

RISE (Rehabilitation Intervention for People With Schizophrenia in Ethiopia)

RISE
Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether community-based rehabilitation plus facility-based care is superior to facility-based care alone in reducing disability related to schizophrenia in rural Ethiopia.