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Stress clinical trials

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NCT ID: NCT00734721 Completed - Stress Clinical Trials

Assessment of Psychological Strain and Perioperative Fear in Intravitreal Injections

FIVA
Start date: December 1, 2007
Phase: Phase 2
Study type: Interventional

1. Intravitreal injection can induce perioperative stress for the patients. 2. Different factors can modulate the pre-operative fear and physiologic reaction.

NCT ID: NCT00700349 Completed - Depression Clinical Trials

Evaluation of Impacts of Access to Credit and Loan Size for Microcredit Clients in South Africa

Start date: September 2004
Phase: N/A
Study type: Interventional

This study involves randomization of individuals who were initially rejected from a micro-lending organization in South Africa. Subjects were placed into two arms: (1) not receiving a loan; (2) being reconsidered for a "second look." Of those in the second arm, 53% were then selected by the organization's loan officers to receive a standard loan for first-time borrowers. Mental health and financial data were collected at one timepoint: approximately 6-12 months after the subjects first applied for the loan.

NCT ID: NCT00696852 Completed - Depression Clinical Trials

Mindfulness, Yoga, and Cardiovascular Disease

Start date: June 2008
Phase: N/A
Study type: Interventional

In this study, we will conduct a preliminary, yet comprehensive evaluation of Mindfulness and Yoga, as compared to an exercise and education-based stress-reduction program. and simultaneous evaluation of the effect of an 8 week program of Mindfulness, 12 weeks of Yoga practice, and 12 weeks of an exercise and education-based program. 105 otherwise healthy individuals, who have cardiovascular risk factors and mild to moderate stress or anxiety will be randomly assigned to one of the three intervention groups: an 8 week program of Mindfulness, 12 week program of Yoga practice, and 12 week exercise and education-based group program. All subjects will perform daily practice that will continue after the weekly sessions end, allowing a follow up assessment at 24 weeks. Self-reported mood and psychological distress and physiological indicators of function of the ANS and stress hormones will be assessed at baseline, 8 weeks, 12 weeks and 24 weeks. Blood and urine samples will be collected at baseline and 8 weeks to determine levels inflammatory and atherosclerosis markers. We anticipate that the study will provide information on the efficacy of the Mindfulness and Yoga interventions as stress-reduction practices, variability in potential markers for activation of the brain/cardiovascular system connections, and preliminary estimates of effect size for each of these markers. Thus, the study will provide the data needed for designing a future study that will rigorously address these questions in a larger, randomized trial of Mindfulness and Yoga in patients with cardiovascular risk.

NCT ID: NCT00685282 Completed - Infertility Clinical Trials

The Effect of Stress on DNA Integrity and the Effect of Cognitive Behavioral Therapy on Stress and Infertility in Women

Start date: November 2008
Phase: N/A
Study type: Interventional

The general hypothesis of the research is that stress decreases fertility and that Cognitive Behavioral Therapy will reduce stress and increase fertility. Secondarily, we hypothesize that stress has a detrimental effect on DNA integrity and that stress reduction will reduce DNA damage in the cell.

NCT ID: NCT00641394 Completed - Depression Clinical Trials

The Effect of Psychotherapy on Stress Biochemistry: An RCT of Psychotherapy and Emotional Freedom Techniques (EFT)

Start date: April 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether there is a change in levels of cortisol, a key stress hormone, during the course of a psychotherapy session. The two forms of psychotherapy compared are Cognitive Behavioral Therapy (CBT) and Emotional Freedom Techniques (EFT). A no treatment control group provides a baseline measure. The change in cortisol level is compared between the start and end of a one hour session.

NCT ID: NCT00636129 Completed - Stress Clinical Trials

Biochemical and Physiological Changes Associated With Differing Durations of Relaxation Response Training

Start date: December 2006
Phase: N/A
Study type: Observational

We are looking at the effects of Stress Management and Relaxation Response training on stress hormones (like adrenalin and cortisol), immune function and physiology (heart rate, breathing rate, muscle tension).

NCT ID: NCT00633737 Completed - Surgery Clinical Trials

The Effects of Stress Reduction on Surgical Wound Healing

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether a stress reduction intervention prior to surgery can improve wound healing and recovery.The investigators hypothesise that patients who receive a psychological stress reduction intervention prior to surgery will report lower stress and higher perceived control, have lower stress hormones, better wound healing and better self-reported recovery than patients who receive standard care alone.

NCT ID: NCT00632684 Completed - Stress Clinical Trials

Effectiveness of an Adaptive Treatment Model for At-risk Family Caregivers

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

This study will develop and evaluate the effectiveness of an adaptive treatment model for reducing the stress of, and burden on, family members caring for a person with dementia.

NCT ID: NCT00625807 Completed - Stress Clinical Trials

Comparison of Two Behavioral Treatments for Stress Reduction

Start date: January 2008
Phase: N/A
Study type: Interventional

Currently there are 2 popular stress reduction courses that are widely used in the US. Although they use somewhat similar techniques, it is currently unknown whether or not they work the same way, or if they are similarly effective at reducing stress. The study will directly compare these 2 courses. Participants will undergo approximately 4-5 hours of testing before and after each 8-week course.

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.