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Anxiety Disorders clinical trials

View clinical trials related to Anxiety Disorders.

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NCT ID: NCT04116944 Completed - Clinical trials for Analogue Generalized Anxiety Disorder

The Resistance Exercise Training for Worry Trial

Start date: January 18, 2018
Phase: N/A
Study type: Interventional

This protocol details the full methods of two parallel, randomized controlled trials of an eight-week resistance exercise training intervention compared to a wait-list control condition among young adults with and without analogue-Generalized Anxiety Disorder.

NCT ID: NCT04115891 Completed - Anxiety Disorder Clinical Trials

Lavender Oil Inhalation Help to Overcome Dental Anxiety Among Children

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the impact of lavender oil (Lavandula angustifolia) on anxiety, pain and vital signs (blood pressure, heart rate and saturation) among children planned to undergone surgical intervention.

NCT ID: NCT04111874 Completed - Clinical trials for Autism Spectrum Disorder

Parent-Led Cognitive-Behavioral Teletherapy for Anxiety in Youth With ASD

Start date: July 30, 2019
Phase: N/A
Study type: Interventional

This study implements an anxiety-focused, parent-led, therapist-assisted cognitive behavioral teletherapy for parents of youth with ASD and anxiety.

NCT ID: NCT04110379 Completed - Dental Anxiety Clinical Trials

Effect of Virtual Reality Glasses as a Distraction Method on Child's Anxiety During Dental Treatment

Start date: July 20, 2019
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate and compare the effect of virtual reality glasses (VR) to conventional behavior management techniques as a distraction method on child's dental anxiety during dental treatment

NCT ID: NCT04097782 Completed - Stress Clinical Trials

Effects of Antenatal Education on Fear of Birth, Depression, Anxiety, Childbirth Self-efficacy, and Mode of Delivery in Primiparous Pregnant Women

Antenatal
Start date: April 1, 2019
Phase: N/A
Study type: Interventional

Background: Caesarean delivery rates are quite high, especially in primipara, in Turkey. Fear of birth, low childbirth self-efficacy, and psychological factors may be among the primary causes. Since antenatal educations are not universal and there are differences in educational contents, there is not sufficient evidence on this topic in international studies. Objective: To investigate the effects of antenatal education on birth fear, depression, anxiety, stress, childbirth self-efficacy, and mode of delivery in primiparous pregnant women.

NCT ID: NCT04093154 Completed - Pain Clinical Trials

Effect of VR on Pain, Fear and Anxiety During Accessing a Port With Huber Needle in Pediatric Cancer Patients

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

Virtual Reality (VR) can be used during needle-related procedures in children with cancer. The aim of this study was to investigate the effect of VR during access the venous port with Huber needle-related pain, fear and anxiety of children and adolescents with cancer.

NCT ID: NCT04091139 Completed - Anxiety Disorders Clinical Trials

Research of Unified Protocol for the Treatment of Common Mental Disorders in Adolescents in Hong Kong

Start date: September 24, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

The Unified Protocol (UP) is an emotion-focused, cognitive-behavioural intervention that is developed to target core temperamental characteristics underlying anxiety and depressive disorders. Ehrenreich and colleagues developed UP for adolescents (UP-A). The current study aims at evaluating efficacy of UP-A for the treatment of emotional disorders in Chinese adolescents in Hong Kong. The current study would recruit 27 Chinese-speaking patients, age 13 to 18, with a primary diagnosis of any Diagnostic and Statistical Manual (Fifth edition) anxiety disorders and/or depressive disorder. They would be randomized into one of the two treatment arms, namely UP-A treatment condition (UP-A), and treatment-as-usual (TAU) condition. Following randomization, participants in the UP-A condition would attend individual treatment based on UP-A, which last for 10 to 12 weeks. Participants in the TAU condition would be provided with usual clinical psychological service (i.e. treatment as usual) in the first 12 weeks before they start attending the same individual treatment program. Primary outcomes would be patient's self-rated measures on clinical symptoms, and secondary outcomes would be their clinical diagnoses, parent-rated and other self-rated measures. It is hypothesized that, comparing to those in TAU, participants in the UP-A condition would show improvements in depressive symptoms, anxiety symptoms and functional impairment at the end of treatment. When the outcomes of all participants are combined, it is hypothesized that participants will show demonstrate improvement in depressive symptoms, anxiety symptoms, and functional impairment after completing the UP-A and at the 3-month follow-up.

NCT ID: NCT04087564 Completed - Healthy Clinical Trials

The Impact of Music on Nociceptive Processing

Start date: June 13, 2019
Phase: N/A
Study type: Interventional

The investigators are studying the ways that different music may change pain perception

NCT ID: NCT04082871 Completed - Depression, Anxiety Clinical Trials

Medication Review in Women With Depression and Anxiety

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

This study sought to assess the impact of the MMR service on identifying and resolving TRPs, improving adherence, depression and anxiety scores in females diagnosed with depression and anxiety in Jordan

NCT ID: NCT04079309 Completed - Anesthesia Clinical Trials

Anxiolytic Effects of Lavender and Orange Oil

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to determine the possible anxiety reducing effects of lavender oil and orange oil on parents with children receiving dental care under sedation during perioperative wait.