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Compassion Fatigue clinical trials

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NCT ID: NCT04396600 Enrolling by invitation - Anxiety Clinical Trials

The Professional Peer Resilience Initiative

PPRI
Start date: June 8, 2020
Phase:
Study type: Observational

The Professional Peer Resilience Initiative (PPRI) study is an observational study aimed at understanding how symptoms of traumatic stress and resilience evolve over time in the University of Minnesota (UMN) healthcare workforce during the coronavirus disease 2019 (COVID-19) pandemic. The study is being conducted concurrently with a UMN peer support program called the MinnRAP program and will remotely administer quality of life and mental health surveys to healthcare workers before they start the MinnRAP program and throughout their participation in the program.

NCT ID: NCT04372303 Completed - Compassion Fatigue Clinical Trials

Effect of a Compassion Fatigue Resiliency Program

Start date: January 8, 2017
Phase: N/A
Study type: Interventional

This study aimed to conduct a short- and long-term Compassion Fatigue Resiliency Program and compare its impact on nurses' professional quality of life, perceived stress and resilience. The research was conducted between January 2017 and January 2019 as a randomized controlled trial. The sample comprised 125 oncology-hematology nurses randomly assigned to a Experimental I (short-term Compassion Fatigue Resiliency Program), Experimental II (long-term Compassion Fatigue Resiliency Program) or control group. Data was collected using Personal Information Form, Professional Quality of Life Scale-IV (ProQOL-IV), Perceived Stress Scale, and Resilience Scale for Adults. Measurements were obtained during pre- and post-test and at three-, six- and twelve-month follow-ups. Research hypotheses were analyzed using multilevel models.

NCT ID: NCT04368676 Terminated - Clinical trials for Psychological Trauma

Breath Regulation and Yogic Exercise An Online Therapy for Calm and Happiness During the COVID-19 Pandemic

BREATH
Start date: June 25, 2020
Phase: Early Phase 1
Study type: Interventional

This study will examine the feasibility of conducting an online Randomized Controlled Trial (RCT) in frontline hospital and long term care healthcare staff in managing COVID-19 patients in London, ON. The study will randomize participants to Sudarshan Kriya Yoga (SKY) or a Health Enhancement Program (HEP).

NCT ID: NCT04122534 Completed - Clinical trials for Occupational-based Secondary Trauma

Somatic Mindfulness Training for a Healthy Workforce: Student Pilot Sample

Start date: September 5, 2019
Phase: N/A
Study type: Interventional

This pilot study evaluates a somatic mindfulness training. Reductions in mental and physical health correlates of secondary trauma are assessed using a pretest-posttest design.

NCT ID: NCT03914898 Completed - Compassion Fatigue Clinical Trials

Effect of Nurse-Led Intervention Programme Professional Quality of Life and Psychological Distress in Nurses

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

Nurses are at risk in terms of burnout and empathic fatigue. Therefore, efforts to protect the mental health of nurses are very important. It is stated that the studies conducted are mostly descriptive and not interventional. In addition, the evidence levels of interventional studies are low.

NCT ID: NCT03212417 Completed - Normal Volunteer Clinical Trials

Education as an Intervention of Compassion Fatigue

Start date: June 6, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact education has on reducing compassion fatigue in Oncology Clinical Research Nurses.

NCT ID: NCT03070249 Completed - Compassion Fatigue Clinical Trials

Compassion Fatigue in ED Providers

Start date: April 13, 2017
Phase: N/A
Study type: Observational

This study will assess compassion fatigue among healthcare providers in a single emergency department (ED) using the Professional Quality of Life (ProQoL) scale.

NCT ID: NCT03017469 Completed - Clinical trials for Stress, Psychological

Achieving Resilience in Acute Care Nurses (ARISE).

Start date: February 21, 2017
Phase: N/A
Study type: Interventional

Nurses are exposed to myriad stressors, both in the workplace and in their everyday lives, which can lead to adverse personal and professional outcomes. While workplace stress cannot be eliminated, nurses can learn techniques to build resilience, mitigate stress, and decrease fatigue. Organizational employee health, wellness, and assistance programs are all intentioned to provide this type of support; however, nurses often lack awareness of options and opportunities, and access can be a challenge. The purpose of the proposed study is to assess the outcomes of a multi-modal intervention and toolkit, ARISE, designed to enhance resilience and promote awareness of organizational resources for health, wellness, and employee assistance. We will evaluate the impact of participation in ARISE on resilience and other outcomes in nurses in critical care and trauma settings. As a Best Practice Spotlight Organization designated by the Registered Nurses Association of Ontario (RNAO), this project will incorporate relevant recommendations from Best Practice Guidelines (BPG) related to Workplace Health, Safety, and Well-being of the Nurse; and Preventing and Mitigating Nurse Fatigue in Health Care.

NCT ID: NCT02521571 Completed - Clinical trials for Secondary Traumatic Stress

The Resilience Alliance

Start date: December 2011
Phase: N/A
Study type: Interventional

The Resilience Alliance is a skill-based staff development intervention for child protective staff that focuses on improving job satisfaction, resilience, optimism and social support, while decreasing attrition, stress reactivity and burnout. The investigators believe that the intervention will enhance the capacity of child welfare workers to care for themselves, which will result in them providing better care for the children and families involved with the child welfare system. The Resiliance Alliance will be implemented in two child protective offices, Manhattan Zone C and Brooklyn Zone B. Staff from two additional offices (Staten Island Zone A and Brooklyn Zone C) will serve as a control group. A web-based survey will be administered in the group receiving the Resiliance Alliance intervention prior to intervention, at completion of the intervention, and 3 months post completion. The control group will be given a two-part training (3 hours in total) on secondary traumatic stress. The control group will then be asked to complete the same survey as the intervention group.

NCT ID: NCT02191345 Completed - Stress Clinical Trials

The Effectiveness of Guided Imagery for a Nonprofit's Employees

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

Primary Aim A. To determine if listening to prerecorded guided imagery 3 times per week for 4 weeks will reduce state anxiety, perceived stress, burnout, compassion fatigue, and vicarious trauma in Fronltine Service staff. Primary Aim B. To determine if staff will continue to listen to guided imagery after the first 4 weeks of the study is over.