The INSPIRE Study: INvestigation of Swiss Physicians Inner-life, Resilience, and Emotions
INSPIRE
1 other identifier
interventional
450
1 country
1
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 31, 2025
CompletedFirst Posted
Study publicly available on registry
February 3, 2025
CompletedStudy Start
First participant enrolled
April 15, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 15, 2027
February 13, 2026
February 1, 2026
9 months
January 31, 2025
February 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from baseline in Emotional Exhaustion
Emotional Exhaustion subscale of the MBI-HSS
3 months post-intervention
Secondary Outcomes (12)
Change in Emotional Exhaustion
Baseline to 2 weeks, 1 month, 6 months, 1 year
Change in Depersonalization
Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year
Change in Personal Accomplishment
Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year
Change in Physician wellbeing
Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year
Change in Job Satisfaction
Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year
- +7 more secondary outcomes
Other Outcomes (2)
Perceived impact of the INSPIRE Interventions
Within 6 months post-intervention
Acceptability of the INSPIRE Interventions
Within 6 months post-intervention
Study Arms (3)
Intervention 1 - General Positive Psychology Reflection
EXPERIMENTALParticipants engage in an 8-day web-based intervention involving positive psychology exercises focused on general life situations.
Intervention 2 - Work-Specific Positive Psychology Reflection
EXPERIMENTALParticipants engage in the same 8-day web-based intervention, but the focus is specifically on positive reflections related to work and patient interactions.
Control group
NO INTERVENTIONParticipants complete assessments but do not receive the intervention.
Interventions
An 8-day web-based positive psychology intervention encouraging participants to reflect on positive aspects of their daily lives. Activities include gratitude exercises, self-compassion writing, and recognizing meaningful moments.
An 8-day web-based positive psychology intervention encouraging participants to reflect on positive aspects of their work experiences. Activities include gratitude exercises, self-compassion writing, and recognizing meaningful professional interactions.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Bern
Bern, 3012, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Sofia C Zambrano, PhD
University of Bern
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- Participants: Control participants are aware of the trial but do not know they are assigned to the control arm, as they are treated as part of the larger cohort and do not receive the intervention. Investigators: Investigators are masked because recruitment and assignment are automated, ensuring they do not know which participants are in the intervention or control arms. Outcome Assessors: Researchers analyzing the data remain blinded to group allocation to minimize bias in data interpretation.
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 31, 2025
First Posted
February 3, 2025
Study Start
April 15, 2026
Primary Completion (Estimated)
January 15, 2027
Study Completion (Estimated)
August 15, 2027
Last Updated
February 13, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Time Frame
- 18 months after publication of primary results and will remain accessible for at least 5 years
- Access Criteria
- Researchers can request access by submitting a proposal to the study investigators. Access will be granted to qualified researchers for scientifically valid analyses, subject to data-sharing agreements and ethical considerations.
De-identified individual participant data (IPD) will be made available for research purposes upon request. Data will include survey responses and outcome measures but will exclude any personally identifiable information