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Psychological Stress clinical trials

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NCT ID: NCT01964820 Completed - Depression Clinical Trials

Online Positive Emotion Skills Intervention for Symptoms of Depression

MARIGOLD
Start date: July 2014
Phase: N/A
Study type: Interventional

Major depressive disorder affects over 120 million people worldwide. Only 50% of Americans with depression receive adequate treatment, and one-third of those receiving treatment do not benefit. In this pilot project investigators will bring together two approaches that have the promise to reach large numbers of depression sufferers: a skills-based intervention for increasing positive affect and experiences in depressed individuals, delivered in an inexpensive self-paced mobile format. The study will make use of smartphone technology to improve conventional outcome measurement via in-the-moment emotion sampling and mobile assessment of heart rate variability, a predictor of cardiac health that may mediate some of the health effects of depression. The aims are: 1) Retool the existing web-based positive emotion intervention for use on smartphones, with innovative exercises that help participants bring the skills they are learning into real- life situations; 2) Measure heart rate variability and emotions using existing smartphone software; and 3) Perform a randomized pilot trial of the mobile intervention on individuals with clinical depression recruited online.

NCT ID: NCT01796054 Completed - Depression Clinical Trials

Stress Free Now, a Mind-body Reduction Program for Nurses

SFN-Nurses
Start date: February 2013
Phase: N/A
Study type: Interventional

Mindful meditation sessions have been associated with an improvement in mindfulness, perceived stress, psychological well-being, anxiety, hostility, and depression. Meditation has been associated with a decrease in autonomic sympathetic activity, heart rate, oxygen consumption and energy expenditure. Randomized controlled trials of online mindfulness and relaxation programs have been studied in patients with conditions such as irritable bowel syndrome, headache, depression, fibromyalgia, and insomnia. Nurses may benefit from such programs given levels of job stress. This study will determine whether an online stress reduction program that incorporates meditation with and without concomitant group support reduces burnout among nurses, including emotional exhaustion and depersonalization. The proposed research study will utilize Stress Free Now, an online stress reduction program developed by Cleveland Clinic Wellness Institute.

NCT ID: NCT01784796 Completed - Stroke Clinical Trials

Mindful Hearts Study: Mindfulness to Reduce Stress

Start date: July 1, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine how a stress reduction program, called Mindfulness Based Stress Reduction (MBSR), compared to a health education program, improves well being and reduces the risk of heart disease in women Veterans. Recruitment completed.

NCT ID: NCT01738256 Completed - Overweight Clinical Trials

Study of Effectiveness of Different Lifestyle Interventions for Health and Wellbeing

Start date: August 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effectiveness and applicability of different interventions designed for enhancing overall wellbeing. Lifestyle changes, as well as psychological and physiological health variables are assessed. The interventions are based on the principles of cognitive behavioural therapy, and delivered either face-to-face, via mobile phone application, or Internet.

NCT ID: NCT01683617 Completed - Clinical trials for Psychological Stress

Management and Treatment of Stress-related Disorders (INTERSTRESS)

INTERSTRESS
Start date: May 2012
Phase: N/A
Study type: Interventional

Psychological stress occurs when an individual perceives that environmental demands tax or exceed his or her adaptive capacity. In this view, stressful experiences are conceptualized as person-environment transactions, whose result is dependent on the impact of the external stimulus. This is mediated by the person's appraisal of the significance of the stimulus, of the personal, social and cultural resources available and of the efficacy of the coping efforts. Extreme levels of stress can have a negative influence on one's professional life and can disrupt both the social and personal life of an individual. Stress can also cause different physiological and psychological disorders such as anxiety, chronic headaches, depression, withdrawal symptoms, nausea, phobias, blood pressure problems, heart impairments and others. Stress Management Therapy can help to overcome counter effects of stress. Usually various techniques are used including relaxation, interaction, biofeedback and Cognitive Behavior Therapy methods. According to the Cochrane Database of Systematic Reviews the best validated approach covering both stress management and stress treatment is the Cognitive Behavioral Therapy (CBT) approach. The trouble with stress is that it is very personal. Thus, stress-related disorders depend a great deal on how the person experiencing a stressor is put together —psychologically and physically. So the focus for assessment, prediction and treatment has to be the person's situated experience. To overcome the above limitations, the INTERSTRESS project suggests the adoption of a new paradigm for e-health - Interreality - that integrates contextualized assessment and treatment within a hybrid environment, bridging physical and virtual world. From the clinical point of view the INTERSTRESS solution may offer the following innovations to current traditional protocols for stress management: - Objective and quantitative assessment of user's stress level using biosensors and behavioral analysis; - Provision of warnings and motivating feedbacks to improve self awareness, compliance and long term outcome; - Decision Support System (DSS) for treatment planning through data fusion and detection algorithms.

NCT ID: NCT01519895 Completed - Clinical trials for Psychological Stress

Effectiveness of Telephone Intervention for Colorectal Cancer Caregivers

Start date: June 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the effectiveness of the telephone intervention program for caregivers of colorectal cancer.

NCT ID: NCT01488422 Completed - Stress Clinical Trials

Neural Correlates of Stress Reduction

Start date: December 2011
Phase: N/A
Study type: Interventional

This study will identify neural mechanisms associated with changes in emotion regulation following participation in stress reduction programs.

NCT ID: NCT01406028 Completed - Clinical trials for Psychological Stress

Does Emotional Support Decrease In Vitro Fertilization Stress?

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

In vitro fertilization for infertility has been associated with a significant amount of treatment related stress for patients. In addition,stress levels increase between embryo transfer and pregnancy test, during this waiting period. The investigators evaluated whether or not brief interventions by phone by trained social workers influenced stress levels. Our data showed that these interventions did not change levels, but confirmed that stress did increase during this time and that patients report wanting additional emotional support to improve stress during this period.

NCT ID: NCT01176188 Completed - Clinical trials for Psychological Stress

A Nursing Intervention to Enhance Child Comfort and Psychological Well-Being During and Following PICU Hospitalization

Start date: August 2010
Phase: Phase 1
Study type: Interventional

Children who become critically ill and require Pediatric Intensive Care Unit (PICU)hospitalization may develop negative psychological outcomes following discharge. This pilot study will test a nursing intervention that seeks to promote child comfort, sleep and psychological well-being during and following PICU hospitalization. Study objectives are to: 1. test the feasibility and acceptability of a PICU comfort care intervention that can be administered by nursing staff 2. examine the feasibility and acceptability of data collection procedures 3. pilot test outcome measures 4. determine effect sizes to inform sample size calculation for a future multi-centred randomized controlled trial (RCT). The intervention will take place in the PICU, and consists of a parental soothing activity followed by a quiet period in which earmuffs are placed over the child's ears to block noise. Children's sleep time and comfort level will be monitored in the PICU, and the investigators will follow them for 3 months post-discharge to examine the effects of the intervention on psychological well-being.

NCT ID: NCT01110343 Completed - Depression Clinical Trials

Conventional vs Mindfulness Intervention in Parents of Children With Disabilities

PSIP
Start date: February 2010
Phase: N/A
Study type: Interventional

This application compares the effectiveness of a conventional Parent Group intervention to Mindfulness- Based Stress Reduction (MBSR) in parents of children with autism spectrum disorders (ASD) and other disabilities. Parent groups are widely-used to provide information, emotional support, education and advocacy. MBSR is efficacious for people with medical, psychiatric or other concerns, and teaches stress reduction through mindfulness training and practice. In contrast to conventional parent groups, the investigators' studies suggest that mindfulness-based interventions may be particularly effective in reducing stress and improving the health and mental health of parents of children with disabilities. The investigators will assess parent factors that may correlate with intervention efficacy in the 2 treatment arms.