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Anxiety Disorders clinical trials

View clinical trials related to Anxiety Disorders.

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NCT ID: NCT03744845 Recruiting - Perioperative Pain Clinical Trials

The Use of Virtual Reality to Reduce Anxiety and Pain in Perioperative Settings

Start date: December 10, 2018
Phase: N/A
Study type: Interventional

We will investigate whether the use of Virtual Reality (VR) preoperatively and intraoperatively can help treat pain and anxiety, as measured by patient feedback, vital signs trends, and the amounts of anesthetics, pain medications and anxiolytics used during surgical procedures. The VR intervention will be studied during short hand surgeries normally performed using local anesthesia and sedation.

NCT ID: NCT03743571 Suspended - Social Anxiety Clinical Trials

Augmenting Exposure Therapy for Social Anxiety With Transcranial Direct Current Stimulation

Start date: April 2, 2019
Phase: N/A
Study type: Interventional

This study will examine whether transcranial direct current stimulation (tDCS) can be used to improve outcomes from exposure therapy for social anxiety disorder, and facilitate extinction of fear responding toward individuals outside one's own ethnic group (i.e., ethnic out-group members).

NCT ID: NCT03741361 Completed - Depression Clinical Trials

The Impact of Anxiety or Depression on the Sedative Concentration of Propofol

Start date: November 27, 2018
Phase:
Study type: Observational

120 consecutive female patients, 18-65 years old, American Society of Anesthesiologists (ASA) physical status I to II, scheduled for hysteroscopic surgery under propofol-based intravenous anesthesia will be recruited in this cohort study. The day before surgery, participants will be assessed the state of preoperative anxiety and depression. On the day of surgery, propofol will be administered by target controlled infusion (TCI) pump. During induction of anesthesia, the level of sedation will be evaluated. The induction dose of propofol, target effect-site concentration(Cet), plasma concentration(Cp) and effect-site concentration (Ce) of propofol will be recorded.

NCT ID: NCT03739346 Not yet recruiting - Pain Clinical Trials

Efficacy of Hypnosis in Anxiety/Pain Reduction in Children During Pulpotomies

Start date: November 20, 2018
Phase: N/A
Study type: Interventional

Anxiety and pain are emotions that the child often experiences in the dental office, generating the appearance of negative, uncooperative and even disruptive behaviors during the treatment; these make it difficult for dental care and the possibility of establishing a relationship of trust between the pediatric dentist and the patient. The pediatric dentist must promote a positive attitude of the child throughout the dental treatment, keep the child calm and avoid feeling pain is essential at each appointment. When carrying out dental treatments that are more invasive or painful for the patient, such as pulpotomies, it is difficult to distinguish and separate anxiety from pain. In this project, anxiety/pain will be managed as a whole, to assess it with the same scale, and to correlate the scores obtained with the variations in skin conductance and heart rate, before, during and after perform pulpotomies in children.

NCT ID: NCT03730532 Recruiting - Anxiety Clinical Trials

Guided Self-help for Anxiety - a Patient Preference Trial

Start date: January 29, 2019
Phase: N/A
Study type: Interventional

Supporting patients in exerting choice over their treatment is a central aspect of modern healthcare. In Improving Access to Psychological Therapies (IAPT) services, then patients treated at step 2 are only and always offered cognitive-behaviourally informed guided self-help (GSH), when they are deemed suitable for treatment at step 2 of IAPT services (termed CBT-GSH). Step 2 interventions are guided self-help (GSH) delivered by Psychological Wellbeing Practitioners (PWPs). Recently, a new type of GSH has been developed and found to be feasible and effective in IAPT services - this is called cognitive-analytic guided self-help (CAT-GSH). This research aims to test the efficacy of CAT-GSH by comparing outcomes over time achieved in both types of GSH and interviewing participants about their experience of the GSH. The methodology to support patient choice is a patient preference trial. In this method, then patients that meet inclusion criteria for the trial are offered and choose between either CAT-GSH and CBT-GSH. Those patients that are unconcerned with the type of treatment are randomised to either CAT-GSH or CBT-GSH. The primary outcome measure is the Beck Anxiety Inventory. No changes to the standard practice of the PWPs will occur during the trial, the trial will be situated in a standard IAPT service and be a therefore conducted in a routine practice setting.

NCT ID: NCT03722771 Completed - Dental Anxiety Clinical Trials

Influence of Lavender Oil on Vital Signs in Oral Surgery Patients

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

The aim of this study is to investigate the impact of lavender oil (Lavandula angustifolia) on anxiety, mood, vital signs (blood pressure, respiratory rate, heart rate and saturation) for oral surgery patients.

NCT ID: NCT03720795 Completed - Clinical trials for Autism Spectrum Disorder

Stepped-Care Cognitive-Behavioral Treatment for Youth With ASD and Anxiety

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

This study implements a parent-led, flexible, individually-tailored cognitive-behavioral intervention for children with ASD and anxiety.

NCT ID: NCT03712267 Recruiting - Depression Clinical Trials

Electronic Media and Its Application in Psychotherapy

Start date: December 13, 2018
Phase: N/A
Study type: Interventional

This randomized control trial aims to establish whether viewing and discussing patients' electronic communication (texts, emails, Facebook direct messaging, etc) impacts clinical care and decision making across the lifespan.

NCT ID: NCT03711201 Completed - Hypertension Clinical Trials

Effects of Preoperative Operating Room Environment Presentation in Hypertensive Patients

Start date: October 30, 2018
Phase: N/A
Study type: Interventional

The aim of this study was to investigate the effects of preoperative operating room environment introduction on preoperative hypertension and blood pressure in hypertensive patients.

NCT ID: NCT03709615 Completed - Clinical trials for Social Anxiety Disorder

Therapeutic Processes in iCBT for SAD

Start date: December 20, 2017
Phase: N/A
Study type: Interventional

The current study examines therapeutic processes during internet-based cognitive-behavioral therapy for social anxiety disorder. Participants will be randomized to either treatment or wait-list conditions. Participants in the wait-list condition will receive active treatment following the wait-list period.