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Anxiety and Fear clinical trials

View clinical trials related to Anxiety and Fear.

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NCT ID: NCT06339047 Not yet recruiting - Pain Clinical Trials

The Effect of Projector Kaleidoscope and Cartoons on Anxiety, Fear, and Pain in Children

Start date: June 1, 2024
Phase: N/A
Study type: Interventional

The research will be conducted with children hospitalized in Tarsus State Hospital Children's Clinics and who meet the sampling criteria. The population of the study, which is planned as a randomized controlled experimental study, will consist of children aged 4-10 years old who are admitted to the pediatric surgery service of Tarsus State Hospital and will undergo outpatient surgical intervention. In collecting research data; the Introductory Information Form, Child Anxiety Scale, Child Fear Scale, Wong-Baker Pain Scale and Vital Signs Follow-up Form will be used.

NCT ID: NCT06174051 Not yet recruiting - Anxiety and Fear Clinical Trials

Flashforward EMDR Treatment for Patients With an ICD

eFFective
Start date: February 2024
Phase: N/A
Study type: Interventional

The goal of this randomized controlled trial is to test whether flashforward (FF) EMDR alone is effective in reducing anxiety symptoms in patients with an implantable cardioverter defibrillator (ICD). Participants will fill out several questionnaires to asses their level of anxiety, depression symptoms and quality of life before, during and after treatment.

NCT ID: NCT05614687 Not yet recruiting - Depression Clinical Trials

Art as Healing: A Community-informed Art-based Programme (CiAbP) for Reintegrating Ex-offenders Into Society in Nigeria

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

The goal of this pilot experimental study is to test a community-informed art-based programme in improving community members trauma from crime and to aid the reintegration of ex-offenders into society. The main question it aims to answer are: • What is the feasibility in terms of recruitment, retention, adherence to the intervention and communities/victims' satisfaction with CiAbP to promote healing and improve the successful reintegration of ex-offenders into society? Participants will be randomly allocated into two groups. The first group, the intervention group, will receive the Community-informed Art-based programme (CiAbP). The second group will receive government intervention involving media messages from the National Orientation Agency devoid of CiAbP. The CiAbP. sessions will cover relevant aspects of art, such as photo story, story telling, poetry, and drawing in tackling trauma and negative attitudes towards ex-offenders reintegration. Researchers will compare CiAbP group with the media orientation group to see if there are differences between a change in attitude towards ex-offenders' reintegration at base line, end of intervention and three months follow up.

NCT ID: NCT05378581 Not yet recruiting - Virtual Reality Clinical Trials

Use of Virtual Reality Mask During Blood and Skin Allergic Tests in 7 to 13 Children

REVAPRICK
Start date: June 2022
Phase: N/A
Study type: Interventional

Main objective : Evaluate the effect of using a virtual reality mask during the blood test and pricks tests in allergic children aged from 7 to 13 years. Hypothesis : Using virtual reality mask during blood test and pricks tests for allergic kids from 7 to 13 would reduce anxiety and pain

NCT ID: NCT05283382 Not yet recruiting - Anxiety and Fear Clinical Trials

Cannabidiol Effects on Learning and Anxiety

Start date: February 1, 2024
Phase: Early Phase 1
Study type: Interventional

To examine the extent to which Cannabidiol (CBD) enhances fear conditioning extinction in college undergraduates who show elevated social anxiety. Undergraduates who display elevated social anxiety on standard assessments will be recruited at the University of Connecticut. All participants will be put in a standard fear conditioning paradigm where they are conditioned to fear a face that occasionally is followed by a shock to their wrist. The other face never is paired with a shock. After everybody learns this, half of the participants will receive 600 mg CBD Isolate Gel Capsules one time, and the other half will receive a placebo dose. Participants will then be presented with the faces with no shocks, and the rate and duration of extinction as measured by electrodermal response as well as subjective fear ratings via a visual analogue scale will be examined. It is hypothesized that participants that receive CBD will display enhanced extinction compared to the placebo group, as evidenced by reduced electrodermal response and reduced visual analogue fear ratings.