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Stress clinical trials

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NCT ID: NCT03728062 Completed - Stress Clinical Trials

Mindfulness Meditation Versus Physical Exercise: Comparing Effects on Stress and Immunocompetence

Start date: September 4, 2017
Phase: N/A
Study type: Interventional

The objective of this research project is to examine if including mindfulness meditation or physical exercise at lunch break improve workers' recovery from work stress. Therefore, 72 workers included either mindfulness meditation or physical exercise during their lunchbreaks for a month in order to find out if these recovery strategies have more favorable outcomes than usually spent lunch breaks concerning: a) psychological detachment, b) perceived stress, c) general health, d) burnout, e) fatigue, f) quality of sleep, g) cortisol awakening response and h) immunocompetence.

NCT ID: NCT03709225 Not yet recruiting - Anxiety Clinical Trials

Mindfulness-Music Intervention for Adolescents and Young Adults With Cancer

MAYA
Start date: November 1, 2018
Phase: N/A
Study type: Interventional

This study is evaluating how well a music therapy program works to improve anxiety and stress in adolescents and young adults receiving cancer treatment.

NCT ID: NCT03704779 Not yet recruiting - Stress Clinical Trials

Effectiveness of a Multimodal Mindfulness Program to Alleviate Graduate Student Stress

Start date: February 2019
Phase: N/A
Study type: Interventional

The purpose of this pilot study is to develop and assess a multimodal mindfulness activity program for physical and occupational therapy students intended to teach management of stressors impacting educational performance. This study will use a two group, randomized controlled design in which approximately 25 students will be randomized to an intervention group and 25 to a control group. Intervention will be implemented in an 8-week period with pre- and post-study measures administered at 1-week prior to and 1-week following intervention.

NCT ID: NCT03688854 Completed - Stress Clinical Trials

The Role of Short Chain Fatty Acids in Microbiota-gut-brain Axis

SCFA-AP
Start date: January 4, 2018
Phase: N/A
Study type: Interventional

The role of short chain fatty acids (SCFA) in the microbiota-gut-brain axis is examined in a sample of healthy volunteers. SCFA are the major products of bacterial fermentation of dietary fiber in the colon, and are hypothesised to mediate the bidrectional communication between the gut and the residing microbiota on the one hand, and the central nervous system on the other hand. We perform a 1-week intervention with SCFA and measure their effects on a range of affective outcomes in healthy male volunteers.

NCT ID: NCT03687450 Not yet recruiting - Depression Clinical Trials

An Evaluation of Changes in Psychological Health to a Yoga Program for Medical Residents

Start date: September 2018
Phase: N/A
Study type: Interventional

The investigators aim to initiate and complete the first investigation of the effect of a yoga-based program on resident physicians' psychological health using a randomized controlled trial to assess feasibility of the program in this population and measure outcomes across several domains. To meet the goals of the proposed project the investigators have identified 3 specific aims: Specific Aim 1: Assess the acceptability and feasibility of the yoga program through measuring participation and conducting standardized interviews with a subset of yoga participants. Specific Aim 12: Evaluate the effect of the yoga program on resident physicians' stress, burnout, resilience, mindfulness, mood, depression, anxiety, and sleep quality using quantitative self-report measures. Specific Aim 3. Examine whether outcome measures were perceived as relevant to the participants' work environment and were not burdensome as to the length and content of the program.

NCT ID: NCT03673579 Recruiting - Stress Clinical Trials

Clinical Evaluation of the "NICU Clinical Decision Support Dashboard" - MHSB

Start date: June 14, 2018
Phase: N/A
Study type: Interventional

This study evaluates the use of a NICU clinical integration system (Dashboard and accessories) in improving the quality of care delivered, patient health outcomes, and parent and clinician satisfaction. Clinicians will be asked to follow their current standard of care practices with the aid of this technology. About half of participants will receive care in NICU rooms with the Dashboard installed while the other half will receive standard care without the Dashboard.

NCT ID: NCT03673566 Not yet recruiting - Stress Clinical Trials

Clinical Evaluation of the "NICU Clinical Decision Support Dashboard" - CHMCO

Start date: March 2019
Phase: N/A
Study type: Interventional

This study evaluates the use of a NICU clinical integration system (Dashboard and accessories) in improving the quality of care delivered, patient health outcomes, and parent and clinician satisfaction. Clinicians will be asked to follow their current standard of care practices with the aid of this technology. About half of participants will receive care in NICU rooms with the Dashboard installed while the other half will receive standard care without the Dashboard.

NCT ID: NCT03671317 Not yet recruiting - Pain Clinical Trials

Medical Clowns for Pediatric Blood Draw

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The research objective of this proposed clinical trial is to determine the efficacy of a medical clowning intervention for pediatric patients undergoing venipuncture. Efficacy is defined in terms of decreasing anxiety, pain, and crying duration, and increasing the pace and ease of the procedure. The study population includes pediatric patients between the ages of four to ten who must undergo venipuncture at the LAC + USC Outpatient Clinic. The subjects will be randomized into two groups. The control subjects will receive no intervention during blood draw, while the intervention subjects will receive medical clown intervention during blood draw. The clowns will interact with one patient at a time, engaging in play with the patient and caretakers during all parts of the procedure. Duration of crying and the duration of the entire procedure, the patient's level of pain and anxiety, the caretaker's level of anxiety, need for restraining devices (papoose) and the efficiency of the procedure will be measured. In order to perform the survey and self-assessment procedures, we will implement the use of measurement scales including the Faces Pain Scale, State-Trait Anxiety Inventory Form Y-1, Visual Analog Scale, and Children's Anxiety and Pain Scale. The data will be analyzed using descriptive statistics.

NCT ID: NCT03669016 Recruiting - Stress Clinical Trials

MIndfulness for Students

Mindfulstud
Start date: August 22, 2018
Phase: N/A
Study type: Interventional

The aim of the study is to find out, weather the students' wellbeing and functional ability can be enhanced by two different type of mindfulness interventions: 1) face-to-face group-based training, and 2) internet-based training based in mindfulness and acceptance and commitment therapy. Study results may be used to decide whether it is worth offering mindfulness training for medical faculty students, and what kind of training would be most suitable and effective in the medical education context.

NCT ID: NCT03664362 Recruiting - Stress Clinical Trials

The BSHAPE Intervention Program for Safety and Health of Survivors of Cumulative Trauma

BSHAPE
Start date: October 10, 2018
Phase: N/A
Study type: Interventional

The goal of the BSHAPE study is to test a trauma informed, culturally tailored, multicomponent program entitled BSHAPE (Being Safe, Healthy, And Positively Empowered) for immigrant survivors of cumulative trauma.