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Anxiety Disorders clinical trials

View clinical trials related to Anxiety Disorders.

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NCT ID: NCT02723188 Completed - Clinical trials for The Study Assessed the Potential Utility of tES for Enhancing Treatment of Anxiety Disorders. This Preliminary Study Was Conducted Healthy Participants

Modulation of Fear Extinction Processes Using Transcranial Electrical Stimulation

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

The aim of this study is to examine the effects of transcranial electrical stimulation on processes associated with fear extinction in healthy humans.

NCT ID: NCT02713516 Completed - Anxiety Clinical Trials

Virtual Reality System to Increase Access to Exposure Therapy for Anxiety and OCD

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

Cognitive Behavioral Therapy with fear provoking exposures is the most effective therapy for anxiety disorders. Investigators aim to enhance this therapy with the use of virtual reality exposures and to make therapy more available and accessible for patients with anxiety disorders. The societal benefit of increased access to therapy is that, if successful, it will increase the number of patients who receive appropriate treatment for an anxiety disorder.

NCT ID: NCT02713425 Completed - Anxiety Clinical Trials

Pediatric Anxiety Intervention With an Entertaining Video Game: Feasibility Study

Start date: October 1, 2016
Phase: N/A
Study type: Interventional

This research study aims to test the feasibility and effectiveness of using an entertaining video game as an addition to traditional therapy for the treatment of anxiety disorders in youth, particularly those youth who may have limited access to mental health treatment in the traditional clinical setting.

NCT ID: NCT02713360 Completed - Anxiety Clinical Trials

Screening and Intervention Reducing Anxiety in Patients With Implanted Cardioverter Defibrillator (ICD)

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

The hypothesis is that there is a significant difference in anxiety scores between intervention and usual care group after intervention. The aim of this randomised trial is (I) to determine the type of anxiety in ICD patients and (ii) to investigate the effect of screening followed by randomisation to intervention with consultations based on cognitive therapeutic principals to reduce anxiety in patients with ICD or usual care.

NCT ID: NCT02690597 Completed - Pain Clinical Trials

Validation and Pertinence of Anxiety Analogic Visual Scale in Pain Management

ANXYDOL
Start date: February 2015
Phase: N/A
Study type: Interventional

Screening of anxiogenic part of pain is an imperative during a medical pain consultation. The actual tools for evaluation of this specific part are complex and time consuming. To date, it lacked a reliable and reproductive tool to quickly evaluate anxiety of patient in pain. The purpose of this study is to demonstrate the pertinence and validity of anxiety analogic visual scale by comparison with the actual reference the self-assessment questionnaire State Trait Inventory Anxiety Y-A form.

NCT ID: NCT02686333 Completed - Depression Clinical Trials

Meditation for Depression and Anxiety Symptoms in Dialysis Patients

Start date: March 2016
Phase: Phase 3
Study type: Interventional

This study examines the use of brief meditation interventions for patients with symptoms of anxiety and depression who are undergoing dialysis. Half of the participants will receive meditation interventions 3 times a week, while the other half will receive treatment as usual. This study will examine whether meditation is feasible and whether it has any effect on reducing symptoms of anxiety or depression.

NCT ID: NCT02685488 Completed - Depression Clinical Trials

Investigating Transcranial Ultrasound as a Potential Intervention for Depression

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

Depression is the leading cause of disability worldwide. Because a significant number of people with depression do not respond to medication or therapy, alternative treatment options are greatly needed. Recent research has focused on brain stimulation methods due to their therapeutic utility for treating depression. Yet, current brain stimulation methods have drawbacks, including invasive surgery and limited precision in targeting specific areas. A novel brain stimulation method, transcranial ultrasound (TUS), is noninvasive, has greater spatial precision than most existing methods, and is proven safe for humans. TUS has been found to increase positive mood in chronic pain patients. In a double blind study, TUS increased positive mood in over 140 healthy undergraduates at the University of Arizona. Despite evidence that TUS can increase positive mood in humans, it has yet to be investigated whether TUS can increase positive mood in humans who are experiencing chronic low mood or depression. The present study will, for the first time, examine whether TUS can improve depressive symptoms. Twenty to thirty participants with mild to moderate depressive symptoms (Beck Depression Inventory Score between 10 and 25) will be randomly assigned to a TUS sham or TUS activation condition. In the TUS activation condition, TUS will be used to stimulate the right fronto-temporal area, which has previously been shown to increase positive mood. Participants in the TUS sham condition will not receive any brain stimulation. Participants will attend five sessions within seven days or ten sessions within fourteen days. At each session, in addition to brain stimulation, self-reported mood and depressive symptoms will be recorded. Furthermore, the investigators will use electroencephalogram (EEG) to record changes in brain electrical signals during TUS stimulation. Based on prior research, the investigators predict that mood will increase and depressive symptoms will decrease with TUS stimulation.

NCT ID: NCT02678624 Completed - Panic Disorder Clinical Trials

Project Collabri for Treatment of Anxiety

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

The purpose of this study is to determine whether treatment of patients with anxiety according to the Collabri Model is more effective in reducing symptoms compared to treatment as usual (TAU)

NCT ID: NCT02667847 Completed - Clinical trials for Anxiety, Preoperative

Preoperative Anxiety Evaluation: a New Visual Smileys Scale

Start date: December 2012
Phase: N/A
Study type: Observational

Preoperative anxiety is a complex clinical concept with both physiological and psychological consequences.

NCT ID: NCT02665403 Completed - Anxiety Clinical Trials

Play Interventions to Reduce Anxiety and Negative Emotions in Hospitalized Children

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

Hospitalization is a stressful and threatening experience, which can be emotionally devastating to children. Hospital play interventions have been widely used to prepare children for invasive medical procedures and hospitalization. Nevertheless, there is an imperative need for rigorous empirical scrutiny of the effectiveness of hospital play interventions, in particular, using play activities to ease the psychological burden of hospitalized children. This study tested the effectiveness of play interventions to reduce anxiety and negative emotions in hospitalized children. A non-equivalent control group pre-test and post-test, between subjects design was conducted in the two largest acute-care public hospitals in Hong Kong. A total of 304 Chinese children (ages 3-12) admitted for treatments in these two hospitals were invited to participate in the study. Of the 304 paediatric patients, 154 received hospital play interventions and 150 received usual care.