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Stress clinical trials

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NCT ID: NCT02088294 Completed - Obesity Clinical Trials

Guided Imagery Lifestyle Intervention to Promote Health and Prevent Diabetes in Youth

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

The childhood obesity epidemic, which falls disproportionately on Latino adolescents, represents a major public health threat to the current generation of youth, and therefore to the health of the nation overall. This project directly addresses the role of psychosocial stress in promoting obesity and metabolic disease risk, and investigates the role of the mind-body CAM intervention of guided imagery in both reducing stress and promoting healthy lifestyle behaviors that could dramatically improve the metabolic health of today's youth.

NCT ID: NCT02062762 Completed - Depression Clinical Trials

Internet-based Stress Reduction Training for Students

IBSR-stud
Start date: February 2014
Phase: N/A
Study type: Interventional

The main objective of the current study is to evaluate whether a mindfulness based intervention delivered online can provide an effective resource for increasing psychological well-being among students. In addition, explore potential mechanisms through which the training lead to improvements by means of mediational analyses, with hypothesized variables like positive/negative affect and attention regulation.

NCT ID: NCT02060422 Completed - Epilepsy Clinical Trials

Mindfulness-based Psychotherapy for Drug-resistant Epilepsy

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

Psychological problems are prevalent among patients with drug-resistant epilepsy. The bi-directional interaction between psychological well-being and seizure have been recognized in recent years. Reduction of psychological stress has the potential to improve seizure manifestation. The present study uses an assessor-blinded prospective randomized controlled trial to evaluate the efficacy of a mindfulness-based psychotherapy and an attentional-placebo social support on improving psychological well-being, seizure control and cognitive performance among adult patients with drug-resistant epilepsy.

NCT ID: NCT02047682 Completed - Stress Clinical Trials

Implementation of Physical Exercise at the Workplace (IRMA10) - Occupational Load

IRMA10
Start date: February 2014
Phase: N/A
Study type: Interventional

Static postures, repetitive work tasks, and work stress increase the risk for musculoskeletal disorders and sickness absence. Objective measurements of occupational loadings - EMG for muscular activity, EEG for cognitive activity, ECG for cardiovascular activity and heart rate variability, actigraphy for bodily movements - may provide useful early indicators of muscular, cognitive and cardiovascular overload. The aim of this study is to investigate the effect of an individually tailored bio-psycho-social intervention strategy versus "usual care" ergonomics and standard physical exercises (reference group) on these risk factors in lab technicians with a history of work-related musculoskeletal pain.

NCT ID: NCT02047669 Completed - Stress Clinical Trials

Implementation of Physical Exercise at the Workplace (IRMA09) - Laboratory Technicians

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

Musculoskeletal disorders and stress of employees remain a major problem in many occupations. The aim of this study is to investigate the effect of an individually tailored bio-psycho-social intervention strategy versus "usual care" ergonomics and standard physical exercises (reference group) on musculoskeletal pain, work disability, and stress in lab technicians with a history of work-related musculoskeletal pain.

NCT ID: NCT02022449 Completed - Depression Clinical Trials

Stress Management Intervention for Mothers of Children With Cancer

CTC
Start date: September 2010
Phase: N/A
Study type: Interventional

To explore maternal biological (activation of the hypothalamic-pituitary-adrenal axis) and behavioral (smoking, sleep behavior, exercise and alcohol use) pathways of intervention-related decreases in inflammation. Hypothesis: The intervention group will show decreased levels of cortisol and improved health behaviors from pre- to post-intervention when compared with the control group. We will also explore whether intervention-related changes in these parameters predict symptoms of illness. Exploratory Aim 2. To explore psychological pathways of intervention-related decreases in distress among mothers, including the perception of social support and the use of behavioral coping strategies that are components of the intervention. Hypothesis: Increases in perceived social support and use of active behavioral coping strategies will be associated with intervention-related decreases in symptoms of depression, anxiety and psychological stress.

NCT ID: NCT02020265 Active, not recruiting - Depression Clinical Trials

fMRI Based EEG Neurofeedback as a Method of Enhancing Emotional Resilience Among Soldiers

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

EEG protocols exist for reducing stress and improve PTSD symptoms (A/T EEG protocols, Peniston, 1993, Hammond, 2005) however; our innovative EEG-NF LMI approach intends to be more amygdala/stress specific and therefore more efficient. Three groups of soldiers, while in operational activity will go through 24 sessions of 3 different methods of EEG-NF; our newly developed NF via MLI, a standard procedure for NF via A/T and a placebo NF. Difference between the groups in regard to their emotion regulation capability will be tested by fMRI with regard to amygdala activation following EEG-NF LMI as well as two stress challenge tests.

NCT ID: NCT02013401 Completed - Stress Clinical Trials

Transmission of Mother-Infant Stress Communication

MIBLS
Start date: October 2013
Phase:
Study type: Observational

The central aim of this study is to assess mother-infant communication via behavioral, physiological, and affective indices under conditions where distal stressors may not be directly detectable by the infant.

NCT ID: NCT01993082 Completed - Aging Clinical Trials

Fitness, Cellular Aging, and Caregiver Stress Study

FAST
Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether an aerobic training intervention will alter markers of immune cell aging, improve exercise capacity and blood pressure and decrease psychological distress over 24 weeks in 32 caregivers compared to 32 age-matched wait list control caregivers.

NCT ID: NCT01981538 Completed - Stress Clinical Trials

Web-based Patient Reported Outcome Measurement Information System (PROMIS ) to Explore Burden and Stress in Cancer Caregivers (BaSiC2)

Start date: November 7, 2013
Phase:
Study type: Observational

Background: - Caring for a loved one is often stressful. Some studies show it may affect health and emotions. Researchers want to know more about this but do not know the best way to gather data. They want to know if an online survey is a good way to gather data from caregivers of people receiving cancer treatment at the NIH Clinical Center. They want to know if there are differences among caregivers depending on the type of cancer treatment the family member or friend is receiving. They want to use this data to improve support programs for caregivers. Objectives: - To see if an online study is a good way to get data from caregivers of people with cancer. Eligibility: - Adults 18 years old and older who are taking care of a cancer patient at the NIHCC. Design: - The study period begins when the family member or friend begins a new cancer treatment and continues for 6 months afterward. - Participants will complete an online survey 3-4 times. This will include questions about caregiving, stress, emotions, and spirituality. The survey can be taken anywhere on a computer. It will take about 30 45 minutes each time. - Participants will also answer general questions about themselves and their health. This will be done over the phone with the study team. It will take 5 minutes.