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Stress clinical trials

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NCT ID: NCT00624520 Terminated - Stress Clinical Trials

Mental Stress Reduction in Defibrillator Patients

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the effectiveness of a 10 week program of Stress Management versus control Patient Education sessions on cardiac responses to mental stress in veterans with Implantable Cardioverter-Defibrillators

NCT ID: NCT00615082 Completed - Dementia Clinical Trials

The Balance Study Balancing Life and Reducing Stress For Those Providing Elder Care

Balance
Start date: February 2007
Phase: N/A
Study type: Interventional

The primary goals of this exploratory/developmental (R21) study are to evaluate the feasibility and acceptability of a MBSR intervention for caregivers of patients with dementia, and to estimate the effectiveness of program outcomes on standardized measures of perceived stress, psychological distress and caregiver burden. We will randomize 60 caregivers 1:1 to participate in: 1.) an intervention arm consisting of a MBSR program that includes 8 weeks of group instruction in mindfulness meditation techniques followed by home practice, or 2.) an active control arm consisting of a standard 8 week Community Caregiver Education and Support (CESS) program.

NCT ID: NCT00611936 Completed - Stress Clinical Trials

Effects of Atomoxetine Treatment in Humans

Start date: June 2006
Phase: Phase 1/Phase 2
Study type: Interventional

A total of 18 healthy volunteers will participate in this four-week, within-groups, double-blind, placebo-controlled study. The study has two phases separated by a 4 to 15-day washout period. Subjects will be randomly assigned to receive either 40 mg atomoxetine or placebo. For Phase I, subjects will be assigned to atomoxetine or placebo for 4 days. After receiving medication or placebo for three days, subjects will have a 6-hour laboratory session, where responses to physical and psychological stress of a 20 mg/70 kg (20 mg maximum) dose of d-amphetamine will be measured. Several physiological, hormonal, and subjective outcome measures will be obtained during the experimental sessions. Subjects will then have a 4-15 day washout period and will be crossed over to the alternative treatment for Phase II.

NCT ID: NCT00536159 Completed - Stress Clinical Trials

Medicaid Enhanced Prenatal/Postnatal Services Using a Nurse-Community Health Worker Team

Start date: January 1997
Phase: N/A
Study type: Interventional

Our objective was to test whether there were advantages to Nurse-CHW team home visiting designed to combine the strengths of both visitors, with a focus on maternal stress and mental health, when compared with standard of Community Care (CC) that included professional home visitors in a state-sponsored Medicaid program. We conducted the study under usual community conditions in a population of women eligible for state-sponsored Medicaid programs. We predicted that during pregnancy and infancy, women in the Nurse-CHW team intervention would report 1) less perceived stress; 2) fewer depressive symptoms; and 3) increased levels of psychosocial resources (self-esteem, mastery, and social support) than women in CC. Benefits were expected to be most pronounced for women with low psychosocial resources and high stress at enrollment.

NCT ID: NCT00485927 Recruiting - Stress Clinical Trials

The Effects of Stress on the Clinical Performance of Residents in Simulated Trauma Scenarios

Start date: April 2007
Phase: N/A
Study type: Interventional

Medical practice & training are inherently stressful situations. However, the effects of stress on educational & clinical performance are not well defined. The purpose of the current study is to examine the effects of stress on performance of residents in simulated trauma scenarios. The hypothesis is: 1) acutely stressful scenarios will be appraised as threat by residents and result in elevations of heart rate and salivary cortisol; 2) increased subjective & physiological stress will result in impairments in performance; and 3) greater stress responses will result in greater clinical impairments.

NCT ID: NCT00482404 Completed - Stress Clinical Trials

Effects of Romantic Affection on Blood Chemistry and Immune Parameters

Start date: February 2007
Phase: Phase 0
Study type: Interventional

This trial tests the hypothesis that increasing nonverbal affection in romantic relationships will improve blood lipid parameters (total cholesterol, high and low density lipoproteins, triglycerides), blood glucose, and immune parameters (C-reactive protein and antibodies to latent Epstein-Barr virus). 52 healthy cohabiting romantic couples took part. In half of the couples, one partner increased the frequency of romantic kissing with the other partner during the six-week trial. The other couples received no such instruction. Blood tests performed before and after the trial were used to assess the health outcomes.

NCT ID: NCT00468572 Completed - Stress Clinical Trials

Using Affectionate Communication as a Response to Acute Stress

Start date: February 2007
Phase: N/A
Study type: Interventional

This study will examine the effects of tending to significant social relationships on managing and reducing stress.

NCT ID: NCT00429117 Withdrawn - Stress Clinical Trials

Interest in Spirituality and Oncology: Is It An International Phenomenon?

Start date: January 2007
Phase: N/A
Study type: Observational

Primary Objective: -To assess correlations between spiritual and religious beliefs and physician burnout using the Work Related Stress Inventory. Secondary Objectives: - To assess relationships between a physician's spiritual/religious beliefs and age, race, sex, marital status, and nationality. - To explore differences in survey responses among oncologists from different countries: Duke University Religion Index (DUREL), Hoge (Intrinsic religiosity scale), Templer's Death Anxiety Scale, Locus of Control Scale, Work Related Strain Inventory, and non-validated case scenarios. - To correlate survey responses to management of specific patient case situations.

NCT ID: NCT00375531 Withdrawn - Stress Clinical Trials

Use of Mindfulness Meditation With Iraqi/Afghanistan War Veterans

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

Objectives: The primary objective of this study is to conduct a randomized pilot study on the efficacy of Mindfulness Meditation (MfM) on sleep in post war Iraqi/Afghanistan veterans with PTSD. It is hypothesized that the change in sleep (measured by actigraphy), sleep self report measures, and PTSD symptoms (measured by the PTSD Checklist) from baseline, 8 weeks and 12 weeks will be greater for veterans with PTSD who are treated with MfM, controlling for pretreatment values and other clinical and demographic factors. A secondary objective will investigate whether there is an improvement in psychological wellness (measured by optimism, perceived wellness, and spirituality) following MfM treatments. It is hypothesized that change in optimism, perceived wellness, and spirituality from baseline, 8 weeks and 12 weeks will improve in veterans with PTSD who are treated with MfM, controlling for pretreatment values and other clinical and demographic factors. Physiological measures of actigraphy in the home will be done at baseline, eight weeks, and twelve weeks. Subjective measure of sleep include measurements of sleep and quality of life(FOSQ) and subjective sleep quality (PSQI). Other self-report measures that will examine psychological wellness include the Life Orientation Test (LOT), the Perceived Wellness Survey (PWS) and the Spirituality Assessment Scale (SAS).

NCT ID: NCT00362284 Completed - Depression Clinical Trials

Comprehensive Support for Alzheimer's Disease Caregivers

Start date: September 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effectiveness of a comprehensive counseling and support intervention for people who care for parents with Alzheimer's disease (AD) or other dementias on outcomes such as stress, depression and ability to postpone or avoid nursing home placement.