Burnout, Professional Clinical Trial
Official title:
Mindful Self-compassion, Compassion Fatigue, Secondary Traumatic Stress, and Burnout Among Specialist Rehabilitation Providers - a Mixed Methods Study Protocol
| Verified date | March 2024 |
| Source | Sunnybrook Health Sciences Centre |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
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.
| Status | Active, not recruiting |
| Enrollment | 26 |
| Est. completion date | March 2024 |
| Est. primary completion date | March 2024 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | 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 |
| Country | Name | City | State |
|---|---|---|---|
| Canada | St. John's Rehab (Sunnybrook Health Sciences Centre) | Toronto | Ontario |
| Lead Sponsor | Collaborator |
|---|---|
| Sunnybrook Health Sciences Centre |
Canada,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | 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 | Relational Compassion Scale | Measure's ones tendencies for receiving and providing relational compassion. | Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention | |
| Secondary | Self-Compassion Scale - Short Form | Measures how one typically acts towards themselves in difficult times. | Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention | |
| Secondary | The Brief Interpersonal Reactivity Index | Measures the different ways that people may think about their lives. | Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention. | |
| Secondary | 5 Facet Mindfulness Questionnaire: Short Form | Measures one's tendencies to engage in mindfulness practices. | Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention | |
| Secondary | Perceived Stress Scale | Measures one's thoughts and feelings pertaining to stress. | Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention | |
| Secondary | Difficulties in Emotion Regulation Scale - Short Form | Measures emotion regulation. | Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention |
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