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Burnout, Psychological clinical trials

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NCT ID: NCT04738448 Completed - Clinical trials for Burnout, Professional

Examining the Effects of Art Therapy in Reducing Burnout in Healthcare Providers

Start date: February 15, 2021
Phase: N/A
Study type: Interventional

In this study, the investigators aim to examine the effects of art therapy in reducing burnout in healthcare providers. Using the Maslach Burnout Inventory Human Services Survey for Medical Personnel, the investigators will measure burnout in Medical University of South Carolina (MUSC) providers before and after the administration of a 4-week art therapy group.

NCT ID: NCT04728126 Not yet recruiting - Menopause Clinical Trials

Menopausal Symptoms and Burnout: Comparison of Occupational Health Issue Among Health Professionals in UMC Hospitals

Start date: September 2021
Phase:
Study type: Observational

This study aims at evaluating the burnout in women healthcare providers (physicians and nurses) Kazakhstan settings, and to investigate the potential parameters that play a role in increasing the risk of burnout. This study would apply the Oldenburg Burnout Inventory (OBI) in a sample of menopausal healthcare providers belonging to the University Medical Center (UMC) - quaternary healthcare institution in Nur-Sultan, Kazakhstan.

NCT ID: NCT04723797 Recruiting - Physical Activity Clinical Trials

The Effect of a Physical Activity Program on Burnout Risk Among Secondary School Teachers

Start date: February 15, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effect of a 6 weeks physical activity program on burnout risk in secondary school teachers. Also, the difference between the effects of moderate en vigorous-intensity physical activity will be investigated.

NCT ID: NCT04712461 Recruiting - Mental Health Issue Clinical Trials

Implementation Supports to Reduce Burnout in Therapists Delivering Child Trauma EBPs

SUPPORTS
Start date: January 1, 2023
Phase: N/A
Study type: Interventional

The majority of children exposed to early adversity and trauma do not have access to sustainably delivered evidence-based mental health programs (EBPs), despite the growing prevalence of large-scale multiple-EBP implementation efforts aimed at increasing access to these services. The objective of this proposal is to develop and test a package of implementation strategies designed to promote the sustained delivery of child trauma EBPs by reducing provider turnover through targeting the associated mechanisms of provider burnout and organizational psychological safety climate. Findings will have a significant public health impact by informing efforts to increase the sustained availability of child trauma EBPs, thereby improving outcomes for children exposed to trauma.

NCT ID: NCT04697030 Completed - Covid-19 Pandemic Clinical Trials

Burnout Among Adolescent Population During Covid-19 Lockdown in Pakistan

Start date: September 15, 2020
Phase:
Study type: Observational

The lethal severe acute respiratory syndrome coronavirus 2 (SARS-COV2) which caused the COVID-19 pandemic starting at the end of 2019 has affected the lives of children and adolescents globally. world adopted the lockdown to prevent spread of the infection and protect the population. lockdown suspended out of home activities of almost everyone, along with health benefits, yielding some side effects as well including burnout. The burnout includes physical and emotional burnout, physical burnout refers to the lack of interest in any physical activity to the point of a rebel and the emotional burnout of teenagers refers to a syndrome including features such as behavior changes, thinking change, feeling change, health change leading to stress and other pathological disturbances. Together the external and internal factors lead to overall personality destruction. It was an observational study with a sample size of 443 participants.

NCT ID: NCT04690452 Completed - Depression Clinical Trials

Evaluation of the Efficacy and Mechanisms of Change of Compassion Cultivation Training in Medical Students

Start date: December 11, 2020
Phase: N/A
Study type: Interventional

The aim of this randomized, waitlist controlled trial is to examine the efficacy of the Compassion Cultivation Training (CCT©) in reducing psychological distress (i.e., stress, anxiety and depression) and burnout symptoms while improving psychological well-being medical students. The second goal of the study is to examine whether mindfulness and compassion-related variables as well as emotional-cognitive emotional regulation processes mediate the psychological distress and well-being changes. The effects of the CCT© program will be measured by means of self-report questionnaires involving different domains (mindfulness, compassion, distress, and well-being measures) at different time points (pre-intervention, inter-session assessment, post-intervention, 2-month and 6-month follow-up).

NCT ID: NCT04665505 Not yet recruiting - Clinical trials for Burnout, Professional

Resource Optimization in the Intensive Care Unit Setting

Start date: September 2024
Phase: N/A
Study type: Interventional

The purpose of the study is to facilitate cost-effective, high quality care within the the ICUs of two Ottawa teaching hospitals through educational workshops and nurse scheduling optimization.

NCT ID: NCT04645290 Enrolling by invitation - Caregivers Clinical Trials

Efficacy of a Multicomponent and Interdisciplinary Intervention on the Care Ability and Burden of Family Caregivers of People With Chronic Cardiocerebrovascular Diseases

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

The purpose of this intervention is to improve the caregiving ability of family caregivers of people with cardiovascular diseases and therefore reduce burden caregiver through face-to-face, virtual interdisciplinary educational actions (B-learning) and with simulation support. The study will have two groups, one who will receive the intervention and the other with regular treatment.

NCT ID: NCT04635540 Enrolling by invitation - Parkinson Disease Clinical Trials

Decreased Empathy and Emotion Recognition in Patients With Neurodegenerative Disease

Empathy
Start date: July 22, 2019
Phase: N/A
Study type: Interventional

This study evaluates an educational brochure tailored to caregivers of people with Alzheimer's disease, Parkinson's disease dementia, Lewy body disease, frontotemporal dementia, and vascular disease dementia. The goal of the brochure is educating caregivers about the decreased ability to detect emotion and decreased empathy that can be seen in dementia, increasing caregiver competence in providing care, and teaching caregivers ways to manage over time that lessens burden and improves quality of life.

NCT ID: NCT04632368 Completed - Clinical trials for Stress, Psychological

Targeting the Health Care Provider (HCP) Burnout Crisis During the COVID-19 Pandemic

Start date: November 20, 2020
Phase: N/A
Study type: Interventional

This single blind, randomized, controlled trial (RCT) evaluates, a nonpharmacological intervention, TM (Transcendental Meditation) for improving burnout (, as measured by self-reporting (survey), physiologic, and neuro-functional imaging studies in health care providers (HCPs) when practiced over 3 months' time. The investigators define HCPs as any physician, physician trainee, nurse, physician assistant, nurse practitioner or respiratory therapist. HCPs will be screened by a single-item stress scale and Columbia Suicide Severity Rating Scale (CSSRS) to understand their stress level and exclusion criteria respectively. The Global Severity Index of the Brief Symptom Inventory (BSI)-18 Global Severity score will be used as the primary outcome for pre- and post-TM training (baseline, 1 vs. 3 months). In addition, the investigators will evaluate physiological markers of stress and cardiovascular resiliency such as 1) changes (pre/post-treatment) in heart rate variability (HRV) through wearables, 2) Galvanic Skin Response (GSR) - changes in sweat gland activity that result from changes in an emotional state. fMRI will be performed by the Duke Brain Imaging and Analysis Center (BIAC) on a subset of participants to evaluate changes A specifically developed mobile app will aid data collection as well as reminders for providers to aid compliance for meditation