NCT05997082

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
26

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Aug 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
7 days until next milestone

Study Start

First participant enrolled

August 17, 2023

Completed
1 day until next milestone

First Posted

Study publicly available on registry

August 18, 2023

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2024

Completed
Last Updated

December 27, 2024

Status Verified

December 1, 2024

Enrollment Period

7 months

First QC Date

August 10, 2023

Last Update Submit

December 23, 2024

Conditions

Keywords

Mindful Self-CompassionCompassion-Based InterventionMeditationOnline InterventionRehabilitation ProvidersPhysiatrists

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

EXPERIMENTAL

Participants in the intervention will participate in the 6-week mindfulness self-compassion course delivered online.

Other: Mindfulness Self-Compassion Course

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).

Participants in the intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Burnout, ProfessionalCompassion Fatigue

Condition Hierarchy (Ancestors)

Occupational StressOccupational DiseasesBurnout, PsychologicalStress, PsychologicalBehavioral SymptomsBehaviorMental FatigueFatigueSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Robert Simpson, Md, PhD

    Sunnybrook Research Institute

    PRINCIPAL INVESTIGATOR

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

Locations