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Anxiety State clinical trials

View clinical trials related to Anxiety State.

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NCT ID: NCT04568551 Completed - Anxiety State Clinical Trials

COVID-19-associated Anxiety of Pregnant Women for Anomalies, Stillbirth and Preterm Labor

CAASP
Start date: October 30, 2020
Phase:
Study type: Observational

Capture of anxiety for anomalies, stillbirth and preterm Labor of pregnant women during COVID-19 pandemia

NCT ID: NCT04544618 Completed - Anxiety State Clinical Trials

Evaluation of a Pre-surgical Virtual Reality Simulation for Cancer Surgery Patients

Start date: December 1, 2021
Phase: N/A
Study type: Interventional

This study will pilot test and explore the feasibility of a virtual reality simulation of the operating room environment to reduce anxiety/distress in cancer surgery patients. Study objectives are to evaluate recruitment and data collection procedures, outcome measures, participant feedback on the virtual reality operating room intervention, and the inclusion of a treatment as usual group, and effects of the intervention on symptoms of anxiety/distress. Results of this study will inform the design of an upcoming larger-scale RCT to assess the efficacy of this intervention

NCT ID: NCT04357418 Completed - COVID-19 Clinical Trials

Psychological Outcome of COVID-19 Lockdown on Psychiatric Hospital Staff and Close Relatives

ICOS
Start date: April 1, 2020
Phase:
Study type: Observational

The purpose of the investigators is to study the psychological impact of the COVID-19 lockdown on the members of the Ville Evrard Hospital staff and their close relatives, and to identify potential lockdown conditions that could increase anxiety, anger and depressive symptoms in this population.

NCT ID: NCT04287595 Completed - Nausea Clinical Trials

Effect of Orange Aroma on Nausea, Vomiting and Anxiety During Autologous Stem Cell Transplantation

Start date: March 28, 2015
Phase: N/A
Study type: Interventional

Patients undergoing stem cell transplantation for the first time will be entered. Participants will be randomized to one of two study arms: Arm 1: intervention (routine care+ inhalation aromatherapy); Arm 2: Control (Routine care) Hypotheses: (1) Patients receiving inhalation aromatherapy will experience less severe nausea and less frequent vomiting episodes than those receiving only routine care; and (2) patients receiving inhalation aromatherapy will demonstrate lower anxiety levels just after AHSCT than those receiving only routine care.

NCT ID: NCT04276506 Completed - Anxiety State Clinical Trials

Effect of Information Given and Music on the Care of Patient Who Will Undergo Coronary Angiography

Start date: November 10, 2019
Phase: N/A
Study type: Interventional

Today, due to the increasing frequency of cardiovascular diseases the number of coronary angiography performed has also risen. This invasive procedure has an effect on patients which causes anxiety. Its important to determine of the level of anxiety so experienced nurses carried out various interventions to reduce anxiety. This study aims to determine the effect of listening music and getting information on the level of anxiety and vital signs of the patients who are planned to undergo coronary angiography. For this purpose, calming music which is suitable for the heart rhythm and booklets which is prepared with various visuals will be used. In the study, apart from a control group that routine clinical procedures will be applied, there will be two more groups which are called as music and information groups. Patients' participation in these groups will be distributed randomly by computer.

NCT ID: NCT04260399 Completed - Anxiety Clinical Trials

Anxiety Reduction During Office Procedural Medicine Using Aromatherapy

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

This goal of this study is to assess whether lavender aromatherapy during gynecologic and urogynecologic outpatient procedures is associated with a decrease in patient anxiety levels. Based on similar interventions in other specialties of medicine, the investigators hypothesize that patients exposed to lavender aromatherapy during their procedure will have less anxiety than those who are not exposed to lavender aromatherapy.

NCT ID: NCT04192097 Completed - Anesthesia Clinical Trials

Impact of a Curriculum About Professionalism on Stress Response During a Critical Situation

Start date: December 15, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact of a curriculum about professionalism on stress response during a critical situation in anesthesiology residents. Residents in anesthesiology will complete a training program on professionalism during their first postgraduate year. They will go through a standardized simulated scenario where they have to manage an intra-hospital cardiorespiratory arrest and then meet the patient's family. Stress response will be assessed and compared to a control group that did not receive the training program.

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: 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.

NCT ID: NCT04045977 Completed - Clinical trials for Coronary Artery Disease

Virtual Therapy as a Method Supporting the Cardiac Rehabilitation

Start date: June 6, 2019
Phase: N/A
Study type: Interventional

This study evaluates the effectiveness of virtual reality (VR) therapy in the treatment of depression and anxiety symptoms in patients undergoing second stage of cardiac rehabilitation. Half of the study group will receive VR therapy (VR group) as an addition to cardiologically monitored physical training. The other half of the group (control group) will receive Schultz Autogenic Training as a standard supplement to cardiological training.