The INSPIRE Study: INvestigation of Swiss Physicians Inner-life, Resilience, and Emotions
NCT ID: NCT06806150
Last Updated: 2025-09-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
450 participants
INTERVENTIONAL
2025-10-15
2027-03-15
Brief Summary
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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
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
TRIPLE
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.
Study Groups
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Intervention 1 - General Positive Psychology Reflection
Participants engage in an 8-day web-based intervention involving positive psychology exercises focused on general life situations.
INSPIRE Life Reflection
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.
Intervention 2 - Work-Specific Positive Psychology Reflection
Participants engage in the same 8-day web-based intervention, but the focus is specifically on positive reflections related to work and patient interactions.
INSPIRE Work Reflection
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.
Control group
Participants complete assessments but do not receive the intervention.
No interventions assigned to this group
Interventions
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INSPIRE Life Reflection
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.
INSPIRE Work Reflection
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
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Inclusion Criteria
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
2. Physician unable to participate in one of the study languages: English, German, or French
18 Years
ALL
Yes
Sponsors
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University of Bern
OTHER
Responsible Party
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Principal Investigators
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Sofia C Zambrano, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Bern
Locations
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University of Bern
Bern, , Switzerland
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2023-00963
Identifier Type: -
Identifier Source: org_study_id
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