The INSPIRE Study: INvestigation of Swiss Physicians Inner-life, Resilience, and Emotions
- Conditions
- Burnout, ProfessionalEmotional ExhaustionEmotionsWellness, PsychologicalSatisfaction, Personal
- Registration Number
- NCT06806150
- Lead Sponsor
- University of Bern
- Brief Summary
The goal of this clinical trial, nested within an observational cohort study, is to evaluate whether two positive psychology web-based interventions can reduce emotional exhaustion and improve overall well-being in practicing physicians in Switzerland. The main questions it aims to answer are:
Does participation in positive psychology interventions reduce emotional exhaustion at three months post-intervention? How do these interventions impact physician wellness, job satisfaction, comfort with end-of-life communication and other aspects of physicians' emotional well-being?
Researchers will compare the effects of two intervention arms (general reflection vs. work-specific reflection) to a control group to determine whether focusing on work-specific aspects leads to greater improvements in emotional exhaustion and job-related outcomes.
Participants will:
* Complete an 8-day intervention consisting of positive psychology activities delivered online.
* Complete baseline and follow-up assessments over the study period
- Detailed Description
Burnout, emotional exhaustion, and moral distress are widespread among physicians, negatively impacting patient care, job satisfaction, and physician retention in the workforce. While interventions targeting burnout exist, many require significant time commitments or institutional support, limiting accessibility.
Positive psychology interventions, which emphasize strengths-based approaches such as self-reflection, gratitude, and self-compassion, have shown promise in enhancing resilience and well-being.
The INSPIRE study is a randomized controlled trial (RCT) nested within an observational cohort using a Trial within Cohort (TwiC) design. It evaluates two web-based positive psychology interventions aimed at reducing emotional exhaustion and improving physician well-being.
A subset of cohort participants is randomized into one of three arms: a control group, a general life reflection intervention, or a work-focused reflection intervention. The interventions consist of an 8-day structured self-reflection program delivered online.
The study employs automated randomization, triple masking (participants, investigators, and outcome assessors), and longitudinal assessments over one year. Findings will inform the scalability of low-burden interventions for physician burnout prevention.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 450
- Be a practicing physician in Switzerland
- Working at least 40% in a clinical capacity
- Be willing and able to provide informed consent
- Expecting to be professionally active until 2028
- Retired physician or physician seeking retirement within 3 years from first participation in the study
- Physician unable to participate in one of the study languages: English, German, or French
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Change from baseline in Emotional Exhaustion 3 months post-intervention Emotional Exhaustion subscale of the MBI-HSS
- Secondary Outcome Measures
Name Time Method Change in Emotional Exhaustion Baseline to 2 weeks, 1 month, 6 months, 1 year Emotional Exhaustion subscale of the MBI-HSS
Change in Depersonalization Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year Depersonalization subscale of the MBI-HSS
Change in Personal Accomplishment Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year Personal accomplishment subscale of the MBI-HSS
Change in Physician wellbeing Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year Physician Wellness Inventory (PWI)
Change in Job Satisfaction Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year Physician Job Satisfaction Scale
Change in comfort with End-of-Life Communication Baseline to 1 month, 3 months, 6 months, 1 year Communication about End of Life Survey
Change in Mindfulness Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year Mindful Attention Awareness Scale (MAAS-Trait)
Change in Compassionate Care Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year Santa Clara Brief Compassion Scale
Change in Emotion Regulation Baseline to 1 month, 3 months, 6 months, 1 year Emotion Regulation Questionnaire (ERQ)
Change in Positive and Negative Affect Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year Positive and Negative Affect Schedule (PANAS)
Resilience Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year 2-item Connor-Davidson resilience scale
Change in Authenticity Baseline to 3 months, 6 months, 1 year Inauthenticity Scale
Related Research Topics
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Trial Locations
- Locations (1)
University of Bern
šØšBern, Switzerland