A Mindful Self-compassion Based Intervention for Specialist Rehabilitation Providers

Sponsor
Sunnybrook Health Sciences Centre (Other)
Overall Status
Recruiting
CT.gov ID
NCT05997082
Collaborator
(none)
30
1
1
6
5

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Mindfulness Self-Compassion Course
N/A

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, plus daily pre-recorded meditations. 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Masking Description:
No masking since there is only 1 group.
Primary Purpose:
Supportive Care
Official Title:
Mindful Self-compassion, Compassion Fatigue, Secondary Traumatic Stress, and Burnout Among Specialist Rehabilitation Providers - a Mixed Methods Study Protocol
Anticipated Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Nov 1, 2023
Anticipated Study Completion Date :
Feb 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Participants in the intervention

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

Other: Mindfulness Self-Compassion Course
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).

Outcome Measures

Primary Outcome Measures

  1. Professional Quality of Life Scale (ProQOL) Version 5 [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 Outcome Measures

  1. Relational Compassion Scale [Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention]

    Measure's ones tendencies for receiving and providing relational compassion.

  2. Self-Compassion Scale - Short Form [Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention]

    Measures how one typically acts towards themselves in difficult times.

  3. The Brief Interpersonal Reactivity Index [Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention.]

    Measures the different ways that people may think about their lives.

  4. 5 Facet Mindfulness Questionnaire: Short Form [Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention]

    Measures one's tendencies to engage in mindfulness practices.

  5. Perceived Stress Scale [Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention]

    Measures one's thoughts and feelings pertaining to stress.

  6. Difficulties in Emotion Regulation Scale - Short Form [Baseline, post-intervention (6 weeks after baseline), and 3 months post-intervention]

    Measures emotion regulation.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. John's Rehab (Sunnybrook Health Sciences Centre) Toronto Ontario Canada M3H2L4

Sponsors and Collaborators

  • Sunnybrook Health Sciences Centre

Investigators

  • Principal Investigator: Robert Simpson, Md, PhD, Sunnybrook Research Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Robert Simpson, Physiatrist and Associate Scientist, Sunnybrook Health Sciences Centre
ClinicalTrials.gov Identifier:
NCT05997082
Other Study ID Numbers:
  • 5492
First Posted:
Aug 18, 2023
Last Update Posted:
Aug 18, 2023
Last Verified:
Aug 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dr. Robert Simpson, Physiatrist and Associate Scientist, Sunnybrook Health Sciences Centre
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 18, 2023