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The INSPIRE Study: INvestigation of Swiss Physicians Inner-life, Resilience, and Emotions

Not Applicable
Not yet recruiting
Conditions
Burnout, Professional
Emotional Exhaustion
Emotions
Wellness, Psychological
Satisfaction, 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
Inclusion Criteria
  1. Be a practicing physician in Switzerland
  2. Working at least 40% in a clinical capacity
  3. Be willing and able to provide informed consent
  4. Expecting to be professionally active until 2028
Exclusion Criteria
  1. Retired physician or physician seeking retirement within 3 years from first participation in the study
  2. 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
NameTimeMethod
Change from baseline in Emotional Exhaustion3 months post-intervention

Emotional Exhaustion subscale of the MBI-HSS

Secondary Outcome Measures
NameTimeMethod
Change in Emotional ExhaustionBaseline to 2 weeks, 1 month, 6 months, 1 year

Emotional Exhaustion subscale of the MBI-HSS

Change in DepersonalizationBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

Depersonalization subscale of the MBI-HSS

Change in Personal AccomplishmentBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

Personal accomplishment subscale of the MBI-HSS

Change in Physician wellbeingBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

Physician Wellness Inventory (PWI)

Change in Job SatisfactionBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

Physician Job Satisfaction Scale

Change in comfort with End-of-Life CommunicationBaseline to 1 month, 3 months, 6 months, 1 year

Communication about End of Life Survey

Change in MindfulnessBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

Mindful Attention Awareness Scale (MAAS-Trait)

Change in Compassionate CareBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

Santa Clara Brief Compassion Scale

Change in Emotion RegulationBaseline to 1 month, 3 months, 6 months, 1 year

Emotion Regulation Questionnaire (ERQ)

Change in Positive and Negative AffectBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

Positive and Negative Affect Schedule (PANAS)

ResilienceBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

2-item Connor-Davidson resilience scale

Change in AuthenticityBaseline to 3 months, 6 months, 1 year

Inauthenticity Scale

Trial Locations

Locations (1)

University of Bern

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Bern, Switzerland

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