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Anxiety Disorders clinical trials

View clinical trials related to Anxiety Disorders.

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NCT ID: NCT04729010 Not yet recruiting - Anxiety Clinical Trials

Acupuncture for Anxiety in Parkinson's Disease

Start date: October 2021
Phase: N/A
Study type: Interventional

This is a single-center, double-blind, placebo-controlled trial to see if acupuncture can safely and effectively manage anxiety in Parkinson's Disease. Eligible subjects will receive either real or sham acupuncture THREE times weekly for a total of SIX weeks.

NCT ID: NCT04726917 Completed - COPD Clinical Trials

Assessment of Stress Levels and Depressive and Anxiety Symptoms in Patients With COPD

Start date: October 1, 2020
Phase:
Study type: Observational

The aim of the study was to assess the levels of depression, anxiety and stress in patients with COPD qualified for In-hospital pulmonary rehabilitation program

NCT ID: NCT04722731 Active, not recruiting - Anxiety Disorders Clinical Trials

Prevention of Childhood Anxiety Disorders in Offspring of Anxious Parents

Start date: February 15, 2021
Phase: N/A
Study type: Interventional

This study aims to expand the evidence of prevention of anxiety disorders in children. Children of anxious parents are at increased risk of developing anxiety disorders. Twin studies support a direct environmental transmission of anxiety between parent and child, and a main mechanism is suggested to be the parenting style of anxious parents, characterised by criticism and rejection, overprotection and modelling of anxiety. This study will take a novel approach to prevent childhood anxiety disorders by evaluating the Confident Parents - Brave Children (CPBC) program, a parent program targeting anxious parents, in a randomised controlled trial (RCT).

NCT ID: NCT04721587 Completed - Anxiety Clinical Trials

Virtual Reality for Pain and Anxiety Distraction Strategy on Office Hysteroscopy

VRPAD
Start date: February 18, 2020
Phase: N/A
Study type: Interventional

Hysteroscopy is a minimally invasive endoscopic technique that allows direct visualization of the uterine cavity and constitutes the gold standard for the diagnosis and treatment of most intrauterine pathology, such as heavy menstrual bleeding, fibroids, endometrial polyps, uterine malformations, etc. The "see and treat" strategy allows diagnosis and treatment in the same surgical act, and gives the technique a high resolution capacity, reducing the number of procedures the patient must undergo. The technological development of instruments has made it possible to have small-caliber endoscopic systems that have made this technique possible in an outpatient setting. Outpatient management allows patients to avoid the possible risks and inconveniences associated with the surgical environment, such as the waiting list and the need for anesthesia, as well as an earlier return to their activities of daily life. Despite the high resolution rates, a not inconsiderable percentage of women experience anxiety or pain during outpatient hysteroscopy, and this is the leading cause of treatment failure. In order to improve the tolerance and comfort of the patient, the usefulness of various strategies, both pharmacological and non-pharmacological, has been evaluated for pain reduction, with different results. Virtual Reality (VR) has been used successfully to reduce perceived pain in various procedures such as chronic pain, burns, dental processes, chronic pruritus or venipuncture. There is no published study to our knowledge that evaluates the usefulness of VR in reducing the levels of anxiety and pain perceived during a hysteroscopic procedure. The working hypothesis to be evaluated with this study is that the use of a VR device with reproduction of relaxing and distraction environments reduces the perception of pain and anxiety of the patient during an outpatient hysteroscopy.

NCT ID: NCT04720963 Completed - Clinical trials for Sedative; Anxiety Disorder

Intranasal Remimazolam for Premedication in Pediatric Patient

Start date: February 7, 2021
Phase: Phase 4
Study type: Interventional

Anesthetic inhalation induction could be one of the most stressful experiences for children during the perioperative period, with almost 50% of them showing anxiety. It is an essential challenge for pediatric anesthesiologists on how to decrease anxiety for children in the operating room (OR) environment and to facilitate a smooth induction of anesthesia. Various factors like parental separation, unfamiliar surroundings, fear of physicians and needle injections can increase their preoperative anxiety. The researchers conducted the current study to investigate whether intranasal remimazolam can reduce anxiety in children before surgery.

NCT ID: NCT04719780 Completed - Depression, Anxiety Clinical Trials

An Attachment Based Approach for Anxiety and Depression

Start date: December 9, 2019
Phase: N/A
Study type: Interventional

The purpose of the current study is to examine the efficacy of Emotionally Focused Therapy for Individuals (EFIT) as a treatment for depression and anxiety. It is formulated as a trans-diagnostic treatment in line with the call for more transdiagnostic approaches to treat depression and anxiety given the many similarities in the underlying psychological and emotional factors of these disorders, the high levels of co-morbidity, and the preliminary success of transdiagnostic treatment approaches. EFIT has been formulated as an attachment-based alternative to current cognitive transdiagnostic approaches. The strong evidence for insecure attachment as an underlying factor in psychopathology, especially depression and anxiety, positions this theory well as a foundational principle to support psychotherapy for these conditions. EFIT has been formulated for the first time this year in the book that will serve as the therapy manual for this study. The current study aims to examine EFIT outcomes as compared to a control group (a wait-list control followed by online CBT intervention after the wait period). In particular, this research project aims to distinguish differences in initial and follow-up outcomes between EFIT versus control, and demonstrate significant changes in attachment/emotions and mechanisms of change across EFIT sessions. The primary hypotheses are outlined below.

NCT ID: NCT04719299 Completed - Dental Anxiety Clinical Trials

Smartphone Application in Reducing Dental Anxiety

Start date: April 20, 2020
Phase: N/A
Study type: Interventional

evaluating the effectiveness of smartphone applications (Tell-Play-Do) (TPD) in reduction of preoperative anxiety in children undergoing restorative treatment, as measured by heart rate and Venham's Picture Test.

NCT ID: NCT04716777 Recruiting - Depression Clinical Trials

Brief Transdiagnostic Group CBT for Adolescents With Internalizing Problems: A Randomized Waitlist Controlled Trial

Start date: October 15, 2020
Phase: N/A
Study type: Interventional

The investigators will evaluate a brief group-based cognitive-behavioral treatment program for adolescents aged 13-17 years with internalizing problems.

NCT ID: NCT04715906 Completed - Depression Clinical Trials

Project COPE (Coping Options for Parent Empowerment)

Start date: February 22, 2021
Phase: N/A
Study type: Interventional

The purpose of this research study is to collect information to better understand caregiver responses to COVID-19 stress and to help caregivers of children with Autism Spectrum Disorder (ASD) cope with these stressors.

NCT ID: NCT04715477 Recruiting - Anxiety Clinical Trials

Intensive Care Anxiety in SARS-CoV-2 Patients

Start date: January 17, 2021
Phase:
Study type: Observational

It should be known by the clinician that COVID-19 patients are prone to anxiety, and these disorders need to be properly diagnosed and addressed to improve prognosis, shorten hospital stay and avoid long-term mental health problems.