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Stress, Psychological clinical trials

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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: 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.

NCT ID: NCT00498030 Completed - Insulin Resistance Clinical Trials

Predicting Insulin Resistance in American Indian Youth

Start date: December 5, 2005
Phase:
Study type: Observational

The purpose of this study is to identify risks that may contribute to increased insulin resistance which may help explain some of the increased incidence of type 2 diabetes in American Indian Youth, at the Rosebud reservation ages 5 to 18 years old. If specific positive indicators of insulin resistance are present, individuals are recruited back in one year for repeat of all measures.

NCT ID: NCT00451126 Completed - Clinical trials for Psychological Stress

Moderating Impact of Various Emotion Personality Factors on Salivary Cortisol Response to a TSST

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Start date: October 2005
Phase: N/A
Study type: Observational

With the aim of evaluating the putative impacts of emotion related personality factors on physical and mental disease and the mechanisms of these impacts, 58 students were submitted to a social stress test (Trier Social Stress Test) and salivary cortisol samples were taken. The subjects were also submitted to several personality trait inventory, that evaluated respectively Alexithymia, Emotional Intelligence, Resilience and the Five Factor Model of Personality. The moderating impact of these factors on the cortisol response were analysed

NCT ID: NCT00442884 Completed - Type 2 Diabetes Clinical Trials

Effect of Acute Psychological Stress on Glucose Concentrations in Patients With Type 2 Diabetes

Start date: February 2006
Phase: N/A
Study type: Interventional

The study is designed to evaluate the effects of acute psychological stress on blood glucose levels. We will study one group of patients in the fasting state on a control day and a stress test day, another group will undergo the same protocol in the postprandial state.

NCT ID: NCT00381927 Completed - Breast Cancer Clinical Trials

Effect of Counseling on Psychological Stress Amongst Women Felt to be at High Risk for Breast Cancer Development

Start date: August 2003
Phase: N/A
Study type: Observational

To evaluate 1) the extent of patient overestimation of breast cancer development risk in subjects referred to a physician-based high-risk breast clinic; 2) the ability of physician counseling to improve patient risk perception and reduce psychological distress; 3) to identify factors relevant in clinical practice associated with increased distress and risk perception.

NCT ID: NCT00377130 Completed - Cancer Clinical Trials

Stress Management Therapy in Patients Receiving Chemotherapy for Cancer

Start date: December 2006
Phase: N/A
Study type: Interventional

RATIONALE: A stress-management program may improve quality of life and reduce anxiety and depression in patients receiving chemotherapy for cancer. PURPOSE: This randomized clinical trial is studying how well stress management therapy works in patients receiving chemotherapy for cancer.