A Mindful Self-compassion Based Intervention for Specialist Rehabilitation Providers
Mindful Self-compassion, Compassion Fatigue, Secondary Traumatic Stress, and Burnout Among Specialist Rehabilitation Providers - a Mixed Methods Study Protocol
1 other identifier
interventional
26
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Aug 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 10, 2023
CompletedStudy Start
First participant enrolled
August 17, 2023
CompletedFirst Posted
Study publicly available on registry
August 18, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2024
CompletedDecember 27, 2024
December 1, 2024
7 months
August 10, 2023
December 23, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Professional Quality of Life Scale (ProQOL) Version 5
Measures the positive and negative effects of one's compassion for those that they help rehabilitate.
Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention
Secondary Outcomes (6)
Relational Compassion Scale
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
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
Perceived Stress Scale
Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention
- +1 more secondary outcomes
Study Arms (1)
Participants in the intervention
EXPERIMENTALParticipants in the intervention will participate in the 6-week mindfulness self-compassion course delivered online.
Interventions
This course is designed to reduce burnout and compassion fatigue among specialist rehabilitation providers. Course materials are adapted from the Center for Mindful Self-Compassion (CMSC).
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
St. John's Rehab (Sunnybrook Health Sciences Centre)
Toronto, Ontario, M3H2L4, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Robert Simpson, Md, PhD
Sunnybrook Research Institute
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Masking Details
- No masking since there is only 1 group.
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Physiatrist and Associate Scientist
Study Record Dates
First Submitted
August 10, 2023
First Posted
August 18, 2023
Study Start
August 17, 2023
Primary Completion
March 1, 2024
Study Completion
May 1, 2024
Last Updated
December 27, 2024
Record last verified: 2024-12