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Anxiety Disorders clinical trials

View clinical trials related to Anxiety Disorders.

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NCT ID: NCT02303691 Completed - Anxiety Clinical Trials

Attention Bias Modification for Transdiagnostic Anxiety

Start date: April 2013
Phase: N/A
Study type: Interventional

This project seeks to identify neural mechanisms underlying the tendency for anxious individuals to pay more attention to threatening information than to other types of information. A computerized treatment designed to train individuals to reduce their attention towards threat will be tested, with a focus on understanding the aspects of brain function that predict response to the treatment. This work could ultimately lead to the ability to treat anxiety more effectively by directly targeting the aspects of brain function that are altered in a given patient.

NCT ID: NCT02286674 Completed - Clinical trials for Pediatric Preoperative Anxiety

Use of Handheld Audiovisual Devices to Treat Pediatric Preoperative Anxiety

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

Anxiety in children undergoing surgery is a central concern to both parents and healthcare workers, including nurses, surgeons, and anesthesiologists. It has been ranked by anesthesiologists as one of the top five important low-morbidity anesthesia outcomes (1). This study would determine whether such devices would decrease anxiety in children prior to induction of anesthesia for outpatient surgery. Two hundred children ages 2-12 will be enrolled.

NCT ID: NCT02286466 Completed - Cancer Clinical Trials

Mobile App of CBT for Anxiety and Cancer

Start date: February 18, 2015
Phase: N/A
Study type: Interventional

The proposed study seeks to implement a randomized controlled trial to evaluate the effectiveness and generalizability of an efficacious cognitive-behavioral therapy (CBT) intervention for use as a self-administered mobile application (mobile app) to treat anxiety in patients with metastatic cancer.

NCT ID: NCT02270073 Completed - Major Depression Clinical Trials

The Process Outcome Mindfulness Effects in Trainees (PrOMET)-Study

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

Background: Mindfulness has its origins in an Eastern Buddhist tradition that is over 2500 years old and can be defined as a specific form of attention that is non-judgemental, purposeful, and focused on the present moment. It has been well established in cognitive behavior therapy in the last decades, while it has been investigated in manualized group settings. Consequently, the demand to investigate mindfulness under effectiveness conditions in trainee therapists has been highlighted. Methods/Design: To fill in this research gap, the investigators designed the PrOMET-Study. In this study, the investigators will analyze the effects of brief, audio-tape presented, in-session mindfulness interventions conducted by both trainee therapists and their patients at the beginning of individual therapy sessions in a randomized, controlled longitudinal design under effectiveness conditions in a total of 30 trainee therapists and 150 patients in a large outpatient training center. The investigators hypothesize the mindfulness intervention will have positive effects on therapeutic processes and outcome in contrast to a progressive muscle relaxation and a treatment as usual group. The investigators will conduct multilevel modeling to address the nested data structure. Discussion: The study results could provide important practical implications, as they could inform ideas on how to improve clinical training of psychotherapists that could be implemented very, as there is no need for complex infrastructures or additional time concerning these brief, in-session mindfulness interventions that are directly implemented in treatment sessions.

NCT ID: NCT02266693 Completed - Clinical trials for Major Depressive Disorder

Transdiagnostic iCBT for Depression and Anxiety

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

This 8-week, pilot randomized, controlled trial to evaluate the benefits of transdiagnostic Internet-based CBT (iCBT) in young adults with MDD, SAD, PD or GAD. The investigators hypothesize that patients who receive iCBT will show significant improvement in anxiety symptoms and functioning, compared to a wait-list group. This pilot randomized controlled study will assess the efficacy of transdiagnostic iCBT in 60 young adults.

NCT ID: NCT02266680 Completed - Clinical trials for Social Anxiety Disorder

Breathing Focused Yoga in Social Anxiety Disorder

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

The goal of this study is to determine the safety and effectiveness of Breathing Focused Yoga (BFY) in improving symptoms of social anxiety disorder (SAD). Patients with SAD will be randomized to 8 weeks of yoga or 8 weeks of wait-list. Symptom severity and quality of life will be compared between the two groups before and after the 8 weeks.

NCT ID: NCT02266446 Completed - Anxiety Disorders Clinical Trials

Developing a Low-Intensity Primary Care Intervention for Anxiety Disorders

AIM-PC
Start date: June 2014
Phase: N/A
Study type: Interventional

The purpose of the study is to develop a personalized, user-friendly computerized treatment for anxiety disorders linked to primary care. The computerized treatment is a type of Cognitive Bias Modification, which targets attention and interpretation biases known to maintain anxiety disorders.

NCT ID: NCT02265588 Completed - Depression Clinical Trials

Healthy Approach to Physical and Psychological Problems in Youngsters With IBD (HAPPY-IBD).

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

The presented study aims to reduce symptoms of depression and anxiety in adolescents with inflammatory bowel disease and increased symptoms of anxiety and depression by using the disease specific CBT program (PASCET-PI)in order to improve quality of life and to improve the clinical course of disease.

NCT ID: NCT02265211 Completed - Anxiety Clinical Trials

Mindfulness and Acceptance-Based Treatments for Social Anxiety: Defusion App

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

This study evaluates a self-help app in the treatment of shyness and social anxiety in adults. All participants will be assigned to the treatment group. It is expected that using this app will result in a reduction in social anxiety.

NCT ID: NCT02263768 Completed - Anxiety Clinical Trials

Impact of Two Recall Intervals on Dental Caries Incidence, Anxiety and Quality of Life of Preschool Children

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

Objectives: To assess the effectiveness of two recall intervals on dental caries incidence (primary outcome) in preschool children with low and moderate caries risk. The level of anxiety, oral health related quality of life (OHRQoL), time and cost (secondary outcomes) according to each interval will also be assessed. Methods: The sample will consist of 224 children between 3-5 years of age, of both genders, with low and moderate caries risk according to the clinical criteria adapted from the Secretary of Health of São Paulo. Children will be randomly allocated into two study groups: Group 1 (G1) - oral clinical examination + orientation for oral health and diet on the recall of 12 months; and Group 2 (G2) - oral clinical examination + orientation for oral health and diet on the recall of 18 months.