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Burnout, Psychological clinical trials

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NCT ID: NCT05977894 Enrolling by invitation - Clinical trials for Burnout, Professional

Floatation Experience in Nurses and Physicians

Start date: October 28, 2023
Phase:
Study type: Observational

The goal of this observational study is to monitor the floatation experience and continue the program as long as deemed important. The main question it aims to answer is: will inventory wellbeing scores increase according to the number of floatation sessions accrued? Nurses (registered, practitioner, and anesthetist) and physicians, employed at St. Elizabeth Youngstown Trauma Center, Mercy Health, will be welcomed to participate in the floatation experience. Participants will be given an option to complete the Wellbeing Inventory survey prior to each floatation session.

NCT ID: NCT05956470 Completed - Depression Clinical Trials

A Comprehensive Wellness Program (SKY) to Mitigate Physician Burnout

SKY
Start date: November 11, 2021
Phase: N/A
Study type: Interventional

The primary objective of the study was to determine whether the yoga-based breathing and meditation program SKY could improve wellness indicators in currently practicing physicians. The hypothesis of this study is that SKY is effective in reducing anxiety and depression, increasing subjective optimism, and reducing physician burnout in healthy, actively practicing physicians.

NCT ID: NCT05949216 Not yet recruiting - Stress Clinical Trials

The Impact of Musical Engagement on Medical Resident Well-being

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

It is common knowledge that music has a positive impact on human well-being. It is also well-known that medical residents are frequently stressed and burnt out. With these two thoughts in mind, the investigators want to explore how participating in a musical engagement program may positively impact medical resident well-being. The investigators hope to do this by hosting four informal musical engagement sessions with medical residents, which will involve playing instruments, improvising, and reading sheet music. To study the impact that this program has on participants, investigators will ask participants to complete a survey. The investigators hope to find that participants are positively impacted by participation in the study, in terms of factors like stress reduction and minimized burnout symptoms. Hopefully, the study results may inform residency program curriculum designers in the future may incorporate music into wellness programming.

NCT ID: NCT05942469 Not yet recruiting - Depression Clinical Trials

Fostering Optimal Regulation of Emotion for Prevention of Secondary Trauma (FOREST)

FOREST
Start date: June 1, 2024
Phase: N/A
Study type: Interventional

FOREST is a positive emotion skills program designed to target mental health and coping needs for frontline violence prevention workers at READI Chicago. Ten skills are taught over a period of nine months during existing meetings and wellness activities, as well as in online modules in READI's Learning Management System (LMS). Through infusing the FOREST skills throughout READI, we hope to inspire organizational culture change that will emphasize the importance of wellbeing and enhance resilience, therefore reducing burnout and turnover.

NCT ID: NCT05938556 Recruiting - Clinical trials for Burnout, Professional

Coaching for Advanced Practice Providers

Start date: July 14, 2023
Phase: N/A
Study type: Interventional

This study aims to determine if online coaching is feasible in advanced practice providers (APP) and can impact burnout. The study will recruit APPs from Children's Healthcare of Atlanta (CHOA), Emory, Colorado University (CU), and their affiliate hospitals through online consent sent via email. Interventions will include online video coaching, written coaching, and self-coaching through self-study material.

NCT ID: NCT05929430 Recruiting - Clinical trials for Mental Health Wellness

Mindfulness in University Students. ATENEU Program

ATENEU
Start date: November 2, 2023
Phase: N/A
Study type: Interventional

The study aims to examine the effects of a mindfulness-based intervention and a mindfulness-based intervention with virtual reality on occupational balance and on the reduction of psychological distress in university students (i.e. stress, anxiety and depression). The specific objectives will be to examine the effects of the intervention on other variables related to mental health, psychological functioning and occupations, and their maintenance at three months.

NCT ID: NCT05907538 Recruiting - Fibromyalgia Clinical Trials

Interoception in Patients With Medically Unexplained Symptoms

Start date: July 25, 2022
Phase:
Study type: Observational

The goal of this observational study is to learn about interoception in patients with stress related syndromes (overstrain, burnout; SRS) and functional disorder (fibromyalgia/ chronic fatigue syndrome; FD). The main questions it aims to answer are: - Is there a significant difference in interoception between patients with SRS and healthy controls? - Is there a significant difference in interoception between patients with FD and healthy controls? - Is there a significant difference in interoception between patients with SRS and FD? The participants will perform the respiratory occlusion discrimination task and have to fill out some questionnaires. Researchers will compare healthy controls to see if there is a significant difference.

NCT ID: NCT05905991 Completed - Burnout Clinical Trials

Enhanced Stress Resilience Training for Critical Care Nurses

Start date: April 25, 2023
Phase: N/A
Study type: Interventional

Job stress and burnout are significant problems affecting physical health, emotional well-being, job performance, and retention of nurses. Enhanced Stress Resilience Training (ESRT) is a theory-driven, evidence-based intervention to increase stress resilience and decrease burnout among clinicians. This study is a randomized waitlist-controlled trial to examine the efficacy, feasibility, and long-term sustainability of the 5-week ESRT intervention to improve psychosocial and occupational well-being of critical care nurses.

NCT ID: NCT05884073 Not yet recruiting - Burnout, Caregiver Clinical Trials

Exercise for Oncology Care Professionals

C4C+
Start date: September 1, 2024
Phase: N/A
Study type: Interventional

The goal of this preference-based pilot study will be to assess the feasibility, acceptability, and impact of a 12-week exercise intervention on oncology care provider burnout, compassion fatigue, and well-being. Participants will be divided into one of three exercise groups. Group assignment will be based on participant preference. Group 1: Supervised circuit-based resistance exercise (2 days/week) Group 2: Supervised circuit-based resistance exercise (2 days/week) + moderate-to-high intensity home-based walking/light jogging program (3 days/week) Group 3: Self-paced home-based walking program (3 days/week)

NCT ID: NCT05833269 Recruiting - Burnout Clinical Trials

Intercare, Mindfulness and Compassion Based Intervention for Parental Burnout

Start date: December 22, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to test the effectiveness of an adapted mindfulness and compassion-based intervention (IBAP) in reducing parental burnout in Chilean mothers who telework while living with children under 18 years old. The main questions it aims to answer are: - Can the intervention reduce symptoms of parental burnout in the short term (3 months) and medium-term (6 and 9 months) compared to the control group? - Can the intervention improve work engagement in the intervention group compared to the control group? Participants will be randomly assigned to either the intervention group or the active control group. The intervention group will receive the IBAP program while the active control group will receive a relaxation audio guide. Both group will receive parental burnout educational material, invitation to a Whatsapp group and a weekly email reminders. Parental Burnout (PBA) will be measured at baseline, 3, 6, and 9 months, and work engagement will be measured at the same time points. Researchers will compare the intervention group to the active control group to see if the IBM program is more effective in reducing parental burnout and improving work engagement,