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Anxiety clinical trials

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NCT ID: NCT03064061 Recruiting - Anxiety Clinical Trials

Impact of Virtual Reality Before Oocytes Retrieval on Anxiety and Pregnancy Rate

Start date: February 17, 2017
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate the impact of a session of virtual reality (VR) with the objective of lowering the anxiety level on the clinical pregnancy rate following an In-vitro fertilisation (IVF) procedure. Indeed, anxiety in relation to infertility happens frequently and over time, can become stressful for our patients. This level of stress influences the effect of the infertility treatment. Reducing anxiety levels could promote the ability of the patients to face this stress and promote a greater chance of pregnancy in that context.

NCT ID: NCT03061864 Recruiting - Anxiety Clinical Trials

The Periviable Birth Plan

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

Pregnant women who are at risk of delivering their infants in the periviable period can suffer a large amount of stress and anxiety. Moreover, many women feel a loss of control over their own pregnancy. There is some evidence that more counseling and planning can help reduce maternal stress and anxiety. Patients at risk of delivering in the periviable period will be randomized to either receive standard counselling or to complete the periviable birth plan.

NCT ID: NCT03057691 Recruiting - Depression Clinical Trials

The Impact of Depression and/or Anxiety on PCI Patients

Start date: March 11, 2017
Phase:
Study type: Observational

The purpose of this study is to evaluate how depression and/or anxiety could effect the prognosis of the patients post-ACS after PCI.

NCT ID: NCT03031990 Recruiting - Anxiety Clinical Trials

Stress and Fertility: How to Lower Stress When Trying to Conceive

Start date: January 2017
Phase: N/A
Study type: Interventional

Psychological stress and its sources differ among the population and can be reduced in various ways. The practice of yoga has been shown to be an effective stress reducing agent. IVF processes have also been shown to increase stress levels, particularly in patients with multiple failed IVF cycles. Less is known about stress levels in patients undergoing elective egg freezing for fertility preservation. The investigators demonstrated in a pilot project that yoga postures with a yoga focused discussion session decreases stress in infertility patients compared to controls. The goal of this study is to further explore the capability of yoga practice to reduce stress in a specific subset of infertility patients, those with a history of at least one failed IVF cycle and those undergoing elective oocyte cryopreservation. Additionally, the investigators are aiming to understand which aspect of the intervention (discussion vs. yoga) had the most impact and whether route of administration of the intervention (in person vs online) effects results.

NCT ID: NCT02970825 Recruiting - Depression Clinical Trials

Move and Feel Good : Effects of Intensive Physical Training on Brain Plasticity, Cognition and Psychological Well-being.

Move&FG
Start date: September 2016
Phase: N/A
Study type: Interventional

The investigators perform a prospective, randomized, clinical study involving students in education with mood disorders and randomized to an intensive exercise program or a control relaxation activity.

NCT ID: NCT02955784 Recruiting - Depression Clinical Trials

Sinasprite: A Pilot Feasibility Study for Patients With Anxiety or Stress

Start date: January 22, 2015
Phase: N/A
Study type: Interventional

The investigators are proposing a prospective one-arm cohort study testing the feasibility of a game designed to improve symptoms in adults with mild levels of stress, depression, and anxiety. The study will take place at Madigan Army Medical Center. Primary outcomes include usage data including time, frequency and duration of app use, participant satisfaction with the game, and comments and suggestions regarding participants' experiences using the Sinasprite game over a 12-week period. Participants will download Litesprite's game, Sinasprite, onto their personal smartphone. Elements of cognitive-behavioral therapies like cognitive strategies, diaphragmatic breathing, and visualization are embedded in the game enabling participants to learn to achieve the desired healthy habits. The game's goal is to help Socks the Fox become a Zen Master. Over six weeks, players help Socks to progress by describing and categorizing their concerns, entrusting Socks to "hold" these concerns, and engaging in bonding activities with Socks, such as fishing and meditation. The investigators currently have a prototype and have been told by insurance firms, providers, and self-funded employers that they need to see validated results from a pilot study that shows feasibility with subjects in the target audience before they can consider a commercial roll out. Participants will complete questions related to mood, stress, and well-being at baseline, 6 weeks, and 12 weeks. Data will be evaluated in real-time and reports of participant progress will be provided to the participant's provider, with the participant's consent. Data and feedback from this pilot study will be used to update the design and inform the technical development team to further refine the game experience in preparation for a larger randomized controlled trial evaluating the effectiveness of Sinasprite.

NCT ID: NCT02902159 Recruiting - Depression Clinical Trials

RCT of the Effectiveness of Big White Wall Compared to Other Online Support

REBOOT
Start date: September 2016
Phase: N/A
Study type: Interventional

A randomised controlled trial to compare the effect on wellbeing of an online peer review website (Big White Wall) compared to freely available online information (NHS Moodzone) for people with depression and anxiety.

NCT ID: NCT02831153 Recruiting - Depression Clinical Trials

Evaluation of Emotional Status and Coronary Flow Characteristics by TIMI Frame Count Method

STRAIN-TIMI
Start date: July 2016
Phase: N/A
Study type: Interventional

This study evaluates the effects of emotional status on coronary flow in patients undergoing elective coronary angiography. Patients whom undergoing elective coronary angiography will fulfill the Beck Anxiety Inventory, Beck Depression Inventory, State-Trait Anxiety Inventory, Hospital Anxiety and Depression Scale. State Anxiety Inventory will be fulfilled both before the intervention and after 1 hour the patients learned the results of the coronary angiography. The other scales will be performed after 1 hour the patients learned their results. Coronary flow will be assessed by TIMI (Thrombolysis In Myocardial Infarction) frame count method.

NCT ID: NCT02804009 Recruiting - Anxiety Clinical Trials

Elective Coronary Angiography and Anxiety Study

ANGST
Start date: November 2015
Phase: N/A
Study type: Observational

Anxiety will be assessed from two aspects, the somatic and emotional. ANGST aims to determine how anxiety correlates with psychological parameters (personality traits, coping strategies and depressive symptoms) and with the outcome of elective coronary angiography (CA).

NCT ID: NCT02704442 Recruiting - Anxiety Clinical Trials

Does Anxiety in Children on the Day of Surgery Impact Compliance in the Ophthalmology Clinic?

Start date: February 2016
Phase:
Study type: Observational

The hypothesis is that pediatric patients with increased levels of anxiety on the day of surgery, in particular at point of anesthetic induction, will demonstrate decreased compliance with assessment in ophthalmology clinic postoperatively.