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Psychological Stress clinical trials

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NCT ID: NCT02445950 Completed - Clinical trials for Psychological Stress

With-Me - Technology-Aided Phone Coaching for Occupational Health Study

Start date: November 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to examine whether the technology (web-based coaching, profiling and suggestion tool) brings added value to the traditional phone coaching in occupational health context. The interventions are phone counseling interventions. The other intervention exploits additionally a specific web-based coaching, profiling and suggestion tool.

NCT ID: NCT02438514 Terminated - Clinical trials for Psychological Stress

Biological Biomarkers in MOMS Partnership

Start date: November 2014
Phase:
Study type: Observational

The investigators propose to evaluate the potential utility of stress-related biomarkers obtained via dried blood spots (DBS) and retinal scans by collecting new data from mothers and children within the New Haven MOMS Partnership, a well-established community-partnered research setting. The proposed research could greatly advance the application of stress-related biomarkers within community-based research by increasing our understanding of how stress, trauma, and depression influence biology in childhood and adulthood, as measured using minimally-invasive approaches.

NCT ID: NCT02433431 Recruiting - Mindfulness Clinical Trials

Mechanisms of Mindfulness and Stress Resilience: A Mobile App Mindfulness Training Study

Start date: February 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to test the active components of mindfulness meditation for reducing psychological stress and improving biomarkers of health. This study compares the effects of three brief trainings: (1) training in both present-moment attention and mindful acceptance, (2) training in present-focused attention, and (3) an active psychological training with no mindfulness content.

NCT ID: NCT02432339 Recruiting - Clinical trials for Psychological Stress

Effects of an Immunosuppressant Mycophenolate Mofetil or MMF on the Urinary Sodium Excretion Response to Mental Stress

MMF
Start date: April 22, 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine if stopping the stress induced increase in inflammation will prevent sodium retention which in turn increases blood pressure. Each subject will test two separate times. One week, they will be taking a daily dose of mycophenolate mofetil (MMF), the other week they will be taking a placebo.

NCT ID: NCT02417051 Completed - Clinical trials for Psychological Stress

The Efficacy of a Brief Resilience Training Program for Hurricane Sandy Disaster Responders

Start date: April 2015
Phase: N/A
Study type: Interventional

The goal of this project is to adapt and test the efficacy of the National Institute of Environmental Health and Safety (NIEHS) Disaster Worker Resilience Training (DWRT) Program for Superstorm Sandy responders. The DWRT is a brief, 4-5 hour training program designed to improve resilience for stress reactions in active emergency responders. A total of 120 participants will be recruited. 60 will receive the DWRT, and 60 will be assigned to a waitlist control condition. A three-month assessment period will be utilized to enable us to evaluate the effects of the intervention. Participants assigned to the waitlist condition will be offered the option to participant in the course following completion of the 3 month wait period. It is hypothesized that, participants attending the DWRT program, as compared to those in the waitlist condition, will show increased resilience at three months post-intervention as indicated by lower perceived stress, greater posttraumatic growth, more positive health behaviors (e.g., sleep, nutrition, exercise), and fewer new PTSD and depression symptoms. It is predicted that participants attending the DWRT program, as compared to those in the waitlist condition, will demonstrate greater awareness of the mental health effects of disasters, including the symptoms of PTSD and depression. It is predicted that, participants attending the DWRT program, as compared to those in the waitlist condition, will endorse more positive attitudes towards mental health care, including willingness to seek treatment if needed.

NCT ID: NCT02394899 Completed - Sickle Cell Disease Clinical Trials

Improving Parental Psychosocial Functioning and Early Developmental Outcomes in Children With Sickle Cell Disease

Start date: October 2014
Phase: N/A
Study type: Interventional

There are all significant risk factors for poor early cognitive development and, as such, neurocognitive deficits have been demonstrated in pre-school children with sickle cell disease (SCD). This project assesses the efficacy of using an evidence-based early stimulation program, combined with components to help parents cope with stress, delivered during six routine monthly clinic visits to parents of children with sickle cell disease. It is hoped that this innovation will improve parental psychological outcomes, as well as child developmental outcomes.

NCT ID: NCT02378610 Completed - Clinical trials for Psychological Stress

Relationship Between the Gut Microbiota and Stress

Start date: February 2015
Phase: N/A
Study type: Observational

The relationship between the gut microbiota and stress is poorly studied in humans. In this study we aim to look for if stressed persons have different levels of key bacterial groups compared to the levels in non-stressed persons.

NCT ID: NCT02378597 Completed - Clinical trials for Psychological Stress

Resiliency Program for Medical Interpreters

CARE
Start date: January 2014
Phase: Phase 1/Phase 2
Study type: Interventional

To develop and test a 4-session program to teach resiliency skills to Medical Interpreters.

NCT ID: NCT02339363 Completed - Anxiety Clinical Trials

Effects of Sitting Meditation and Hatha Yoga in Adolescents

Start date: March 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The present study was a randomized controlled trial that explored the feasibility, acceptability, and effectiveness of short-term mindfulness training among adolescents. The primary purpose was to investigate the effectiveness of two main Mindfulness-Based Stress Reduction components—sitting meditation and hatha yoga—on working memory, stress, anxiety and mindfulness. The influence of daily home practice compliance on intervention outcomes was also examined.

NCT ID: NCT02196142 Completed - Clinical trials for Psychological Stress

Acute Effects of Cortisol on Alcohol Craving in Alcohol Dependence

CAR-Bern 2013
Start date: November 2014
Phase: Phase 3
Study type: Interventional

To investigate the effects of cortisol on alcohol craving and stress reactivity in alcohol addicted subjects. Randomized, double-blind, placebo-controlled, cross-over, single administration of study medication. Study hypothesis: Cortisol has an inhibiting effect on alcohol craving and stress reactivity in alcohol dependent subjects.