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Stress, Psychological clinical trials

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NCT ID: NCT00962273 Terminated - Clinical trials for Psychological Stress

The Pandemic Stress Vaccine: A Resource to Enhance the Resilience of Healthcare Workers Facing an Infectious Outbreak

Start date: October 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effects of an interactive, computerized learning resource designed to increase resilience in hospital-based health care workers preparing for an influenza pandemic. The effects of the learning resource will be compared to a non-interactive learning resource condition and a control condition. It is hypothesized that (a) online pandemic-related education reduces absenteeism and interpersonal problems for healthcare workers (HCWs), and improves their pandemic self-efficacy in the short and long-term, and (b) an interactive format for online education is necessary for its benefits.

NCT ID: NCT00954902 Completed - Clinical trials for Psychological Stress

Effects of Antioxidants on Cardiovascular Risk Measures (Spice Study)

Spice
Start date: August 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether feeding highly antioxidant spices of providing these same antioxidants as capsules is able to affect cardiovascular risk measures. Because this is a new area of research, the investigators will use many measures to assess this question including blood markers, tests of blood vessel health, measures of blood pressure responses, measures of clotting activity, and other inflammation measures.

NCT ID: NCT00924456 Completed - Clinical trials for Psychological Stress

A Clinical Trial of the Transcendental Meditation (TM) Program on Blood Pressure, Psychological Distress, and Coping

AU
Start date: January 2006
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to show that the Transcendental Meditation program can decrease blood pressure in young adults (college students) and is associated with decreased psychological distress and coping ability.

NCT ID: NCT00887614 Completed - Sleep Clinical Trials

Mindfulness, Emotional Well-being, and Sleep Quality

Start date: July 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether participating in a Mindfulness-Based Stress Reduction (MBSR) program increases mindful attention and awareness, and whether anticipated changes in mindfulness relate to improved emotional well-being, sleep quality, physical symptoms of stress, sense of spirituality, and quality of life following MBSR.

NCT ID: NCT00844896 Completed - Clinical trials for Stress, Psychological

Intervention to Reduce Stress in 0-5 Year Olds With Burns

Start date: May 2008
Phase: N/A
Study type: Interventional

The objectives of this study are to test and validate a simple, feasible intervention to reduce pediatric burn traumatic stress in 0-5 year old children and their parents. We have refined and implemented an early post-burn psychosocial assessment and intervention for stress reduction for young children and their parents based on the "DEF" Protocol (Distress, Emotional Support, Family) from NCTSN's 'Pediatric Medical Toolkit for Health Care Providers,' and a burn specific version of the COPE (Creating Opportunities for Parent Empowerment)intervention. It is hypothesized that the combined DEF + COPE Intervention will be simple to implement and use under both experimental and real world conditions. The proof of the latter hypothesis will be that staff at Shriners Hospitals for Children-Boston will willingly incorporate it into routine care by the end of the project. We will evaluate, using an RCT design, the DEF + COPE Intervention by comparing outcomes for subjects who are randomly assigned to receive it with outcomes for subjects who are assigned to receive the DEF Intervention only. It is hypothesized that children in the DEF + COPE Intervention Group will show significantly greater decreases over time in pain and anxiety ratings, heart rate, PTSD total symptom scores and physiological symptom scores (such as heart rate and heart rate variability from baseline to follow up) than will children in the DEF-only group. Similarly, it is hypothesized that parents assigned to the DEF + COPE group will show significantly decreased scores on the Stanford PTSD measure.

NCT ID: NCT00661271 Completed - Clinical trials for Stress, Psychological

Mindfulness-based Stress Reduction for Urban Youth

Start date: September 2007
Phase: N/A
Study type: Interventional

Our uncontrolled study of mindfulness-based stress reduction (MBSR) for urban youth suggests benefits in mental health and quality of life outcomes. To evaluate further the specific effects of MBSR, we are conducting a small randomized controlled trial of the MBSR program compared with a health education program.

NCT ID: NCT00624520 Terminated - Stress Clinical Trials

Mental Stress Reduction in Defibrillator Patients

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the effectiveness of a 10 week program of Stress Management versus control Patient Education sessions on cardiac responses to mental stress in veterans with Implantable Cardioverter-Defibrillators

NCT ID: NCT00621738 Completed - Healthy Clinical Trials

Effect of Mental Stress on Platelet Function in Healthy Subject

Start date: December 2007
Phase: Phase 1
Study type: Observational

Psychological stress is an independent cardiovascular risk factor. Activation of platelets plays an important role in atherosclerosis development and it could one of the mechanisms linking psychological stress and cardiovascular diseases

NCT ID: NCT00538707 Completed - Mental Stress Clinical Trials

Effect of Mental Stress on Platelet Function

Start date: September 2007
Phase: N/A
Study type: Interventional

The aim of the project is to study the acute and chronic effect of mental stress on platelet adhesion and aggregation in two population composed of normal subjects at different ages

NCT ID: NCT00516555 Completed - Clinical trials for Stress, Psychological

EBIS: The Eindhoven Breech Intervention Study

Start date: October 2007
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate whether successful external cephalic version is associated with maternal thyroid function and mood state in pregnant women with breech presentation at term. The relationship between successful external cephalic version and neonatal thyroid function will also be investigated. A possible beneficial effect of successful external cephalic version on the development of congenital hip dysplasia will be evaluated.