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Anxiety Disorders clinical trials

View clinical trials related to Anxiety Disorders.

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NCT ID: NCT03232502 Not yet recruiting - Depression Clinical Trials

Pharmacogenetics in Primary Care Psychotropics

Start date: August 15, 2017
Phase: Phase 3
Study type: Interventional

Pragmatic trial of pharmacogenetic testing at the time of prescription for a selective serotonin reuptake inhibitor, tricyclic antidepressant or atypical antipsychotic. Does real time intervention improve patient outcomes?

NCT ID: NCT03229720 Not yet recruiting - Anxiety, Dental Clinical Trials

Evaluation of Audio-Visual Distraction Technique on Child's Anxiety

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

Audio-Visual (AV) Distraction is a recent modality introduced to the entertaining market technology for adults and children. Some practitioners started using this modality of distraction in the dental practice to aid in psychological management of patients. This study is designed to compare between conventional dental visits (No Distraction) and dental visits aided with audio-visual distraction. Providing a safe, comfortable and entertaining dental environment will give pediatric children a better perception regarding the dental environment and motivate them for repetitive dental visits for better dental health care.

NCT ID: NCT03228628 Not yet recruiting - Pain Clinical Trials

Nitrous Oxide for Lumbar Puncture

NO for LP
Start date: October 1, 2017
Phase: Phase 4
Study type: Interventional

Lumbar puncture (LP) is a frequent exam that can cause pain and anxiety. In a pilot single-center study, it has been shown that nitrous oxide use during the procedure was able to reduce both pain and anxiety (Moisset et al., Eur J Neurol 2017). The goal of this multi-center trial is to confirm these results in a larger and more heterogeneous group of patients having a LP.

NCT ID: NCT03224845 Not yet recruiting - Anxiety Disorder Clinical Trials

Courageous Parents, Courageous Children

COACH
Start date: September 2017
Phase: N/A
Study type: Interventional

Anxiety disorders usually start in childhood and adolescence and are associated with social and occupational difficulties in adulthood. Children who have a parent with an anxiety disorder and who find new situations distressing and avoid them are at an increased risk for developing an anxiety disorder. Research suggests that anti-anxiety parenting can help children grow up courageous and calm. It is, however, difficult to parent in an anti-anxiety way when the parent has an anxiety disorder himself or herself. This research study will test the efficacy of a new program designed to prevent the onset or persistence of anxiety disorders in children at risk for anxiety disorders. The investigators will first help parents learn skills to cope with their own anxiety and then coach them to share these skills with their children and parent in an anti-anxiety way. The goal is to intervene early enough in the children's lives so that they can be free of anxiety disorders and lead happy, healthy and productive lives in adulthood.

NCT ID: NCT03019705 Not yet recruiting - Health Anxiety Clinical Trials

An Examination of the Effects of Health-related Internet Use in Individuals With Pathological Health Anxiety Using Ambulatory Assessment

Start date: n/a
Phase: N/A
Study type: Observational

The purpose of the current explorative study is to examine the effects of health-related internet use in individuals with pathological health anxiety using ambulatory assessment. In a naturalistic setting participants answer over a seven-day period questionnaires about their health-related internet use and its effects on affect, health anxiety and symptom severity in their usual daily lives.

NCT ID: NCT03015285 Not yet recruiting - Major Depression Clinical Trials

CBT for Anxiety Sensitivity vs. Disorder-specific CBT: An RCT

Start date: January 2017
Phase: N/A
Study type: Interventional

Adults with high anxiety sensitivity (AS) and a mental health diagnosis of anxiety, depression, or posttraumatic stress will be recruited and will be randomly assigned to either transdiagnostic cognitive behavioural therapy (CBT) for AS or disorder-specific CBT for their primary mental health problem. The study outcomes - AS, anxiety, mood, and substance use symptoms, and functional impairment - will be assessed at pre-and post-treatment and 6 and 12 months post-treatment via standardized self-report measures completed by participants and a standardized diagnostic interview.

NCT ID: NCT02924610 Not yet recruiting - Clinical trials for Social Anxiety Disorder

Brief Intervention to Reduce Fear

Start date: October 2016
Phase: Phase 4
Study type: Interventional

The study will test the efficacy of propranolol or placebo, administered after retrieval of a previously acquired public speaking fear, in reducing fear and avoidance of public speaking.

NCT ID: NCT02800733 Not yet recruiting - Clinical trials for Patients With Mild to Moderate GAD

Effects of Saffron on Mild to Moderate Generalized Anxiety Disorder (GAD)

Start date: June 2016
Phase: Phase 2/Phase 3
Study type: Interventional

anxiety disorder is one of the major public health problems worldwide. 25% of people experience anxiety disorders throughout life. Generalized anxiety disorder (GAD) is known as the most prevalent anxiety disorder. Saffron has previously approved as an effective adjuvant therapy in depression and might alleviate GAD symptoms.Since up to the best of our knowledge no human studies have assessed the therapeutic effect of saffron as an adjuvant therapy in GAD patients, Therefore, this study is planned to evaluateThe effect of saffron (Crocus satious L.) in the treatment of mild to moderate generalized anxiety disorder:

NCT ID: NCT02784301 Not yet recruiting - Pain Clinical Trials

Evaluation of a Biofeedback Tool to Minimize Procedural Pain and Anxiety in Children

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

Belly breathing is a popular relaxation technique used to reduce anxiety and pain in children during medical procedures. The investigators have developed a biofeedback game that will help teach children how to belly breathe in an interactive way. Existing studies have shown that biofeedback tools are effective ways to teach relaxation techniques to children. The purpose of this study is to evaluate 1) whether this new biofeedback tool is a more a effective and engaging way to teach belly breathing to children and 2) whether the application is more effective in reducing procedural pain and anxiety compared to standard of care, self-directed belly breathing alone or self-directed belly-breathing combined with visual distraction. The investigators hypothesize that: 1. The smartphone-based biofeedback game for belly breathing will reduce self-reported procedural anxiety and pain in children during a blood collection procedure compared to: 1. standard of care 2. belly breathing + standard care procedures 3. belly breathing with visual components of the application with no coaching or biofeedback distraction. 2. The smartphone-based biofeedback game will increase compliance with belly breathing compared to self-directed breathing. 3. Belly breathing with smartphone-based biofeedback game will be more engaging compared to self-directed belly breathing.

NCT ID: NCT02631785 Not yet recruiting - Clinical trials for Pediatric Anxiety Disorders

Fear Conditioning, Extinction and Its Recall in Anxious Youth

FCPA
Start date: February 2016
Phase: N/A
Study type: Interventional

The proposed research aims to isolate brain-based information-processing mechanisms implicated in perturbed fear learning and extinction characteristic of pediatric anxiety. The study will focus on the therapeutic relevance of dysfunction in fear learning and extinction for treatment by examining the associations between brain functioning and response to exposure intervention in anxious children.