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Psychological Stress clinical trials

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NCT ID: NCT02502227 Completed - Mindfulness Clinical Trials

Mechanisms of Mindfulness Training and Stress Reduction

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

This study is a three-arm randomized controlled trial of a mindfulness stress reduction intervention, with the aim of dismantling the experience-monitoring and nonjudgmental-acceptance elements of mindfulness programs to determine the active treatment component. In addition to enhancing understanding of mechanisms underlying the effects of mindfulness interventions, identifying the therapeutic constituent(s) could inform development of targeted interventions as well as provide strategies to optimize adherence.

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: 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.

NCT ID: NCT02075424 Completed - Clinical trials for Psychological Stress

Descriptive Study of Biological Stress and Perceived Stress at the Center 15

RegulStress
Start date: March 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to describe biological stress (cortisolemia) and perceived stress in Emergency Call Center Operators and Doctors while processing a center 15 call.

NCT ID: NCT01997008 Completed - Depression Clinical Trials

Optimizing Resilience and Coping in HIV Via Internet Delivery

ORCHID
Start date: May 2014
Phase: N/A
Study type: Interventional

This is a feasibility/pilot test of a set of positive affect skills provided online to HIV positive people with elevated depressive symptoms - a Center for Epidemiological Studies Depression Scale D (CES-D) score > 10. The investigators will test the feasibility of recruitment, retention and acceptability of these skills in an online delivery format, determine feasibility and acceptability of daily emotion assessments via text messaging and assess efficacy of these skills for improving psychological well-being this population.