Skip to content

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

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

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06806150
Acronym
INSPIRE
Enrollment
450
Registered
2025-02-03
Start date
2026-04-15
Completion date
2027-08-15
Last updated
2026-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burnout, Professional, Emotional Exhaustion, Emotions, Satisfaction, Personal, Wellness, Psychological

Keywords

Psychological resilience, Positive Psychology

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.

Interventions

BEHAVIORALINSPIRE 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.

BEHAVIORALINSPIRE 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.

Sponsors

University of Bern
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

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.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Emotional Exhaustion3 months post-interventionEmotional Exhaustion subscale of the MBI-HSS

Secondary

MeasureTime frameDescription
Change in Emotional ExhaustionBaseline to 2 weeks, 1 month, 6 months, 1 yearEmotional Exhaustion subscale of the MBI-HSS
Change in DepersonalizationBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 yearDepersonalization subscale of the MBI-HSS
Change in Personal AccomplishmentBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 yearPersonal accomplishment subscale of the MBI-HSS
Change in Physician wellbeingBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 yearPhysician Wellness Inventory (PWI)
Change in Job SatisfactionBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 yearPhysician Job Satisfaction Scale
Change in comfort with End-of-Life CommunicationBaseline to 1 month, 3 months, 6 months, 1 yearCommunication about End of Life Survey
Change in MindfulnessBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 yearMindful Attention Awareness Scale (MAAS-Trait)
Change in Compassionate CareBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 yearSanta Clara Brief Compassion Scale
Change in Emotion RegulationBaseline to 1 month, 3 months, 6 months, 1 yearEmotion Regulation Questionnaire (ERQ)
Change in Positive and Negative AffectBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 yearPositive and Negative Affect Schedule (PANAS)
Change in AuthenticityBaseline to 3 months, 6 months, 1 yearInauthenticity Scale
ResilienceBaseline to 2 weeks, 1 month, 3 months, 6 months, 1 year2-item Connor-Davidson resilience scale

Countries

Switzerland

Contacts

CONTACTSofia C Zambrano, PhD
sofia.zambrano@unibe.ch+41 31 684 57 76
CONTACTRobert Staeck, MSc
robert.staeck@unibe.ch
PRINCIPAL_INVESTIGATORSofia C Zambrano, PhD

University of Bern

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026