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Stress clinical trials

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NCT ID: NCT02744573 Completed - Pain Clinical Trials

Evaluation Of The Analgesia Nociception Index vs. Surgical Pleth Index Under General And Regional Anaesthesia

Start date: September 2011
Phase: N/A
Study type: Observational

There is a lack of sufficient analgesia monitoring apart from surrogate parameters. The analgesia nociception index (ANI) shall be evaluated under general and regional anaesthesia.

NCT ID: NCT02741973 Completed - Stress Clinical Trials

Yoga in School Sports - a Pilot Study in Germany

Start date: March 2016
Phase: N/A
Study type: Interventional

The aim of this trial is a first evaluation of the effectiveness of yoga as alternative for school sports to evaluate potential effects in stress reduction and concomitant psychological parameters.

NCT ID: NCT02736292 Completed - Stress Clinical Trials

Mindfulness Practice for Healthcare Professionals in Training

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

A newly developed intervention, Mindfulness Based Practices for Health Care Professionals in Training: Clinical Applications, will be piloted to determine the feasibility, acceptability, accessibility, and preliminary effects within this population.

NCT ID: NCT02736136 Completed - Depression Clinical Trials

An Early Intervention to Increase Maternal Self-efficacy After Preterm Birth

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Start date: August 2016
Phase: N/A
Study type: Interventional

This study aims to investigate the effects of an early intervention (joint observation and video feedback) on maternal parenting self-efficacy following a premature birth. Mothers who have given birth to a very premature baby will be randomly allocated to either the early intervention or usual care whilst the infant is still hospitalized. Participants will be followed up at one month and six months. It is predicted that participants who received the early intervention will report higher maternal parenting self-efficacy than those who are not.

NCT ID: NCT02729363 Completed - Pain Clinical Trials

The Feasibility of the PAINReportIt Guided Relaxation Intervention-Outpatient

Start date: April 2016
Phase: N/A
Study type: Interventional

Our goal is to improve the self-management of pain and stress in adult outpatients with sickle cell disease (SCD) by determining the feasibility of a self-managed guided relaxation (GR) stress reduction intervention using a tablet-based mobile device. Currently, opioid analgesics are primarily used to treat SCD pain while self-managed behavioral modalities such as GR, are rarely used. Little is known about the effects or mechanisms of GR on pain and stress, in adults with SCD. Emerging evidence from the hypothalamic pituitary adrenal (HPA) axis theory offer insights for understanding the mechanisms. Adding GR as a supplement to analgesic therapies will address the paucity of self-management strategies for controlling pain in SCD. GR is a simple and cost-effective non-drug intervention that could reduce pain and stress in outpatients with SCD. GR is an intervention where outpatients with SCD are directed to listen to and view audio-visual recordings while they visualize themselves being immersed in that scene.

NCT ID: NCT02726724 Completed - Stress Clinical Trials

Does the Presence of Observers Influence the Success of the Neonatal Endotracheal Intubation?

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

The Endotracheal intubation (ETI) of a neonate is a procedure that usually attracts a large number of observers. The fear of being judged by others could cause an increased level of stress, especially on the junior trainees. Little research has focused on the effect of the audience on the level of stress and therefore, on the success rate of complicated procedures in neonatal intensive care. Hypothesis:Investigators hypothesize that time to successful intubation (in seconds) will be longer with the presence of observers.

NCT ID: NCT02723227 Completed - Stress Clinical Trials

The Impact of Family Financial Support on Parental Stress

Start date: March 2016
Phase: N/A
Study type: Interventional

The investigators have partnered with financial coaching organizations to establish what the investigators have termed a "Medical-Financial Partnership (MFP)" that offers financial coaching to improve financial and mental health. The investigators will evaluate the MFP's impact on family economic strain and parental stress.

NCT ID: NCT02705235 Completed - Pregnancy Clinical Trials

Stress, Coping and Health Behaviors in Pregnancy

Start date: January 2016
Phase:
Study type: Observational

Stress is an important determinant of pregnancy health behaviors, maternal physiology and maternal-infant health outcomes. The purpose of this study is to explain the relationship between dimensions of lifetime stress and the stress hormone cortisol in pregnant women. Additionally, the study will examine how coping styles help pregnant women to better manage stress and improve their health behaviors to achieve the goal of having a healthy baby.

NCT ID: NCT02670421 Completed - Stress Clinical Trials

Stress Management Intervention in Women's Heart Clinic, Heart SMART Program

Start date: March 2016
Phase: N/A
Study type: Interventional

Will the intervention (Heart SMART program) be feasible in moderate or high stress patients, who are referred to the Women's Heart and Preventive Cardiology clinics at Mayo Clinic?

NCT ID: NCT02660307 Completed - Stress Clinical Trials

A Stress Reduction Program for Companies

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

This protocol proposes a well-being program based in stress reduction program for employees of a company. objectives: To evaluate the effects of a stress reduction program with a specific orientation for workers and taught to them within their companies. Methods: Participants with stress complaints were recruited and randomized into two groups: group 1 (G1) received the intervention while group 2 (G2) did not. Both groups were evaluated before the intervention (time 1 - T1); again after the eight weeks of the program for G1 (time 2 - T2); and then at the end of a second eight-week period during which G2 received the intervention and G1 was simply instructed to maintain the practice they had learned without further instruction (time 3- T3).