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Anxiety Disorders clinical trials

View clinical trials related to Anxiety Disorders.

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NCT ID: NCT02615483 Completed - Depression Clinical Trials

Lumbar Spinal Fusion - Web-based Platform Targeting Anxiety and Depression

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

The purpose of the present study is to investigate the effect of a Web- based Platform (WP) on anxiety and depression and health economics among patients undergoing lumbar spine fusion (LSF).

NCT ID: NCT02615119 Completed - Clinical trials for Major Depressive Disorder

Neural Basis of Meal Related Interoceptive Dysfunction in Anorexia Nervosa

Start date: October 1, 2015
Phase: N/A
Study type: Interventional

This study aims to identify the brain regions responsible for encoding cardiorespiratory 'interoceptive' sensations and determine whether they are dysfunctional in individuals affected by eating disorders, anxiety, depression, or brain injury. By evaluating the same interoceptive sensations across different human illnesses, the investigators hope to provide convergent evidence resulting in identification of core underlying neural processes, and to discern relative contributions in each condition.

NCT ID: NCT02614443 Completed - Depression Clinical Trials

Effectiveness and Acceptability of Internet-delivered Treatment for Depression, Anxiety and Stress

EAITDAS
Start date: October 2015
Phase: N/A
Study type: Interventional

The aims of this study are to test the effectiveness and acceptability of internet-delivered treatment for depression, anxiety and stress in university students. These data will inform the methods for a future randomized controlled trial. The trial will establish an initial estimate of the effectiveness of these online interventions for students in terms of within-group effect sizes associated with changes in depression, anxiety and stress from pre to post-intervention and follow-up. These data will be used to estimate the sample size for a future trial to ensure that the study is sufficiently powered. A conservative estimate using the 90% upper confidence limit will be used to inform the sample size calculation of the definitive RCT. Acceptability of the intervention to participants will be assessed using data on usage and engagement with the intervention (e.g. percentage of participants completing each module, average number of log ins, average time spent per session and total time spent on the program). These data are acquired through the online SilverCloud system. Satisfaction with will be assessed through the use of a post-intervention questionnaire on satisfaction with accessing and using an online delivery format for treatment.

NCT ID: NCT02605668 Completed - Panic Disorder Clinical Trials

Providing Tools for Effective Care and Treatment of Anxiety Disorders

PROTECT-AD
Start date: December 12, 2015
Phase: N/A
Study type: Interventional

PROTECT-AD is a cognitive behavioral treatment study involving highly qualified psychotherapeutic centers at seven German universities. It is our goal to further investigate and optimize existing effective treatments of anxiety disorders. In order to achieve this, the investigators want to investigate the effect of extinction learning in an "intensified" psychological intervention on treatment outcome in adults and children with anxiety disorders. The intensified psychological intervention is characterized by a higher number of exposure trials over a short time period. In the control condition the exposure trials take place in a weekly interval, analog to standard care.

NCT ID: NCT02604706 Completed - Anxiety Clinical Trials

Auricular Acupuncture in Substance Abuse: Effects on Anxiety, Sleep, Drug Use.

Start date: October 2010
Phase: Phase 2
Study type: Interventional

Background. A common alternative treatment for substance abuse is ear acupuncture. The aim of the study was to evaluate the short and long-term effect of auricular acupuncture on anxiety, sleep, drug use and addiction treatment utilization in adults with substance abuse. Method. Adults with substance abuse and psychiatric comorbidity were randomly assigned to either of two variants of auricular acupuncture - The National Acupuncture Detoxification Association protocol (NADA) or a local protocol (LP) - or relaxation training (controls). Primary outcomes were measured using the Beck Anxiety Inventory (BAI) and Insomnia Severity Index (ISI) with assessment before treatment and follow-ups after five weeks and three months. Secondary outcomes were drug use and addiction service utilization.

NCT ID: NCT02593734 Completed - Schizophrenia Clinical Trials

Integrating Psychotropic Medication Into the Care of People With Mental Disorders in a Prayer Camp in Ghana

JFR
Start date: July 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate a bundled intervention of psychotropic drugs and daily contact with a nurse for people with mental health disorders in a prayer camp and secondly to assess whether the attitudes of the prayer camp staff toward mental health disorders and conventional medicines remain the same after the intervention.

NCT ID: NCT02591797 Completed - Pain Clinical Trials

Effectiveness of Hand/Eyes/Mouth Behavior Management Technique During Local Anesthesia in Preschool Children

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

This will be a randomized, controlled, parallel-group clinical trial. The aim of this studio will be to evaluate the effectiveness of "Hands/Eyes/mouth" behavior management technique versus a conventional technique (covering the patient´s vision) during an inferior alveolar and lingual nerve block in preschool children referred for treatment at the School of Dentistry, Cardenal Herrera CEU University (Valencia, Spain). The sample will consist of 52 children from 3 years old to 5 years 11 months old who need dental pulp treatment and/or tooth extraction of primary molars. Preschool children with no history of allergies to Lidocaine or systemic/neurological diseases and who did not take local anesthesia before the study will be include in this research.

NCT ID: NCT02588079 Completed - Dental Anxiety Clinical Trials

Internet-Based Cognitive Behavioral Therapy for Children With Dental Anxiety

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

The purpose of this study is to determine whether internet-based cognitive behavioral therapy (ICBT) is effective in the treatment of children and adolescents with dental anxiety. The investigators hypothesis is that children and adolescents who have been offered ICBT show significant better performance on outcome measures compared with patients in control group.

NCT ID: NCT02580656 Completed - Depression Clinical Trials

An Open Trial of Metacognitive Therapy for Anxiety and Depression in Cancer

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

Survival rates in cancer continue to improve, with over 2 million adult cancer survivors in the United Kingdom, projected to increase to 4 million by 2030. Around 25% of these survivors require treatment for clinical levels of emotional distress. The investigators will conduct a phase I open trial to test the potential efficacy of MCT in cancer survivors.

NCT ID: NCT02579928 Completed - Clinical trials for Major Depressive Disorder

Ketamine Infusion for Adolescent Depression and Anxiety

Start date: October 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the tolerability and short-term efficacy of a single ketamine infusion for the treatment of adolescents with 1) medication-refractory major depressive disorder (MDD) and/or 2) medication-refractory anxiety disorders (social anxiety disorder, panic disorder, generalized anxiety disorder and/or separation anxiety disorder).