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Stress clinical trials

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NCT ID: NCT04722549 Completed - Stress Clinical Trials

Effects of Butyrate on Affective Processes

Start date: February 8, 2021
Phase: N/A
Study type: Interventional

The effects of butyrate on psychobiological processes are examined in a sample of healthy volunteers.

NCT ID: NCT04722367 Completed - Stress Clinical Trials

Being Present With Art: The Impact of Mindful Engagement With Art on Awareness and Connection

Start date: September 28, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to observe and measure the impact of mindfulness and art pedagogy on stress levels amongst students.

NCT ID: NCT04721379 Recruiting - Anxiety Clinical Trials

Effect of Heartfulness Meditation on Brain Waves and How Calm One Feels During Meditation

Start date: July 31, 2021
Phase: N/A
Study type: Interventional

Objectives: 1. To assess the EEG patterns and EKG recordings of participants with no meditation experience with simply closing the eyes for 10 minutes followed by relaxing for 30 minutes. 2. To assess the EEG patterns and EKG recordings of participants with no meditation experience by simply closing the eyes for 10 minutes and then with guided Heartfulness relaxation and meditation for 30 minutes. 3. To assess the baseline anxiety score through GAD-7 questionnaire, subjective experience of all the participants through MEDEQ questionnaire that measures the depth of the meditation experience after the session and correlate with the EEG patterns of the brain and heart rate changes. EEG and EKG data from the groups will be analyzed by the sleep specialist. EKG device data for HRV and the EEG data will be correlated with the subjective depth of meditation experience in both the groups

NCT ID: NCT04713111 Completed - Covid19 Clinical Trials

Stress and Recovery in Frontline COVID-19 Workers

Start date: May 4, 2020
Phase: N/A
Study type: Interventional

The novel coronavirus (COVID-19) pandemic has caused an unprecedented stress on healthcare systems in affected countries, and in particular, on the healthcare workers at the frontline working directly with COVID-19 positive patients. Numerous lines of evidence support the damaging impact of stress on our immune systems which increases susceptibility to infection. Yet, the accurate measurement of immediate stress responses in real time and in naturalistic settings has so far been a challenge, limiting our understanding of how different facets of acute or sustained stress increases susceptibility. This study utilizes wearable technologies including an Oura smart ring as well as semi-continuous passive and active biometric measurements carried out using individuals' own smartphones equipped with applications to track and transmit key data to measure frontline workers stress and recovery during a uniquely stressful and high-risk work environment.

NCT ID: NCT04711694 Recruiting - Anxiety Clinical Trials

Mindfulness-Based Intervention for Adolescents

Mindfulteen
Start date: February 12, 2019
Phase: N/A
Study type: Interventional

The Mindfulteen Study is a 3-year long longitudinal cohort study with a nested randomized controlled trial, integrating neuroimaging, biological and clinical outcomes, and designed to evaluate the impact of a mindfulness-based intervention (MBI) on young adolescents. Young adolescents between 13 and 15 years with no history of current mental health disorder (with the exception for anxiety symptoms) or of psychotherapy are included and randomized to either early or late intervention (i.e. waiting list or control group), after being stratified between low or high anxiety group based on State and Trait Anxiety Inventory (STAI-T) score. Participants on the control group participate on MBI after completing the second assessment. The intervention is an 8-week long MBI adapted to adolescents. Primary outcomes are based on neuroimaging (structural and functional MRI) and secondary outcomes are clinical (self-reported questionnaires covering mostly emotion and stress reactivity and trait mindfulness) and biological (cortisol, inflammation markers and redox markers). Assessments are performed at baseline, immediately after intervention or waiting time and after 18 months of intervention.

NCT ID: NCT04706494 Completed - Stress Clinical Trials

A Study to Investigate the Efficacy of AlphaWave® L-Theanine on Stress

Start date: February 2, 2020
Phase: Phase 1
Study type: Interventional

AlphaWave® L-theanine will be compared against placebo to evaluate how the investigational study product effects on salivary cortisol, EEG readings, blood pressure, and heart rate in a moderately stressed and otherwise healthy adult population. It is hypothesized that participants taking the AlphaWave® L-theanine will have reduced stress levels as assessed by the parameters stated. Participants will be consuming the investigational study product or placebo in the clinic only.

NCT ID: NCT04705779 Active, not recruiting - Obesity Clinical Trials

The HARMONY Study: A Intervention to Reduce Cardiometabolic Risk in African American Women

Start date: May 20, 2021
Phase: N/A
Study type: Interventional

This study will test whether a culturally-tailored nutrition and exercise intervention designed for African-American women will lead to sustained improvements in exercise and healthy eating through improvements in self-management mediators: mindfulness, stress management, positive reappraisal, self-regulation, and self-efficacy.

NCT ID: NCT04702477 Completed - Diabetes Clinical Trials

Mindfulness Training and Group Counseling Among Prediabetes and Diabetes Patients

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

Examining a number of health outcomes in those with diabetes and prediabetes before and after a group-based mindfulness intervention.

NCT ID: NCT04700917 Recruiting - Depression Clinical Trials

Internet-Based Cognitive Behavioural Program for Managing Stress With IBD: An RCT

iCBT
Start date: March 16, 2021
Phase: N/A
Study type: Interventional

The study will examine the efficacy of an internet-based cognitive behavioural therapy (iCBT) for Inflammatory Bowel Disease (IBD) intervention to reduce stress, anxiety, and depression in individuals with IBD and comorbid clinically elevated t anxiety and/or depressive symptoms. The investigators will conduct a two-arm RCT comparing participants receiving the iCBT intervention (intervention group) and those receiving Treatment As Usual (TAU).

NCT ID: NCT04697173 Completed - Stress Clinical Trials

Bundle Consent and Expectation Setting in Pediatric Intensive Care Unit

Start date: January 13, 2021
Phase: N/A
Study type: Interventional

The purpose of this research study is to find out about how obtaining consent for procedures in the PICU affects parental/caregiver stress. The researchers think that alleviating some of the uncertainly of a PICU stay by discussing types of procedural support offered and obtaining informed consent prior to their immediate necessity may help decrease stress experienced by caregivers. This study will allow the researchers to learn more about it.