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Clinical Trials/NCT05997082
NCT05997082
Completed
Not Applicable

Mindful Self-compassion, Compassion Fatigue, Secondary Traumatic Stress, and Burnout Among Specialist Rehabilitation Providers - a Mixed Methods Study Protocol

Sunnybrook Health Sciences Centre1 site in 1 country26 target enrollmentAugust 17, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Burnout, Professional
Sponsor
Sunnybrook Health Sciences Centre
Enrollment
26
Locations
1
Primary Endpoint
Professional Quality of Life Scale (ProQOL) Version 5
Status
Completed
Last Updated
last year

Overview

Brief Summary

The goal of this clinical trial is to explore the impact of an online compassion-based intervention on burnout among specialist rehabilitation providers. Post-intervention interviews aim to gather information on: burnout and compassion, experiences with the intervention, barriers and facilitators to taking part, and suggestions for improving online course delivery.

Detailed Description

Burnout threatens the sustainability of compassionate care in rehabilitation. This project explores the impact of an online compassion-based intervention on burnout among specialist inpatient rehabilitation healthcare providers. Thirty specialist rehabilitation healthcare providers will be recruited to take part. The online intervention will include six weekly live one-hour sessions. Healthcare provider socio-demographic, practice, and wellness measures will be collected at baseline, post-course, and three months later. Qualitative interviews will be used to explore participant views on burnout and compassion, experiences with the intervention, barriers and facilitators to taking part, and suggestions for improving online course delivery. Up to two instructors and support persons will be invited to participate in qualitative interviews to explore their views for improving online course delivery.

Registry
clinicaltrials.gov
Start Date
August 17, 2023
End Date
May 1, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Robert Simpson

Physiatrist and Associate Scientist

Sunnybrook Health Sciences Centre

Eligibility Criteria

Inclusion Criteria

  • Employed substantively as a regulated health professional (e.g., physiatrist, nurse, allied health professional) by a specialist rehabilitation institute (e.g., Sunnybrook/St. John's Rehab, University Hospital Network, Providence Healthcare, Westpark Healthcare)
  • Over 18 years of age
  • Able to speak, read, and write in English
  • Willing to take part in the MSC course for up to the full 6-week duration
  • Willing to complete all study related questionnaires

Exclusion Criteria

  • Those already having completed a MSC (mindfulness-based stress reduction) course or mindfulness-based cognitive therapy within the past 12 months
  • Those employed as agency staff

Outcomes

Primary Outcomes

Professional Quality of Life Scale (ProQOL) Version 5

Time Frame: Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention

Measures the positive and negative effects of one's compassion for those that they help rehabilitate.

Secondary Outcomes

  • The Brief Interpersonal Reactivity Index(Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention.)
  • 5 Facet Mindfulness Questionnaire: Short Form(Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention)
  • Self-Compassion Scale - Short Form(Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention)
  • Relational Compassion Scale(Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention)
  • Perceived Stress Scale(Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention)
  • Difficulties in Emotion Regulation Scale - Short Form(Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention)

Study Sites (1)

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