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NCT Number: NCT06806150

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

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Bern

Bern, 3012, Switzerland

Location contact

Robert Staeck, MSc

CONTACT

[email protected]

Sofia C Zambrano, PhD

CONTACT

[email protected]

Sofia C Zambrano, PhD

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

INSPIRE Life Reflection

Behavioral

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

Behavioral

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.

Primary outcomes

  1. Change from baseline in Emotional Exhaustion

    Time frame: 3 months post-intervention

    Emotional Exhaustion subscale of the MBI-HSS

Secondary outcomes

  1. Change in Emotional Exhaustion

    Time frame: Baseline to 2 weeks, 1 month, 6 months, 1 year

    Emotional Exhaustion subscale of the MBI-HSS

  2. Change in Depersonalization

    Time frame: Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

    Depersonalization subscale of the MBI-HSS

  3. Change in Personal Accomplishment

    Time frame: Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

    Personal accomplishment subscale of the MBI-HSS

  4. Change in Physician wellbeing

    Time frame: Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

    Physician Wellness Inventory (PWI)

  5. Change in Job Satisfaction

    Time frame: Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

    Physician Job Satisfaction Scale

  6. Change in comfort with End-of-Life Communication

    Time frame: Baseline to 1 month, 3 months, 6 months, 1 year

    Communication about End of Life Survey

  7. Change in Mindfulness

    Time frame: Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

    Mindful Attention Awareness Scale (MAAS-Trait)

  8. Change in Compassionate Care

    Time frame: Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

    Santa Clara Brief Compassion Scale

  9. Change in Emotion Regulation

    Time frame: Baseline to 1 month, 3 months, 6 months, 1 year

    Emotion Regulation Questionnaire (ERQ)

  10. Change in Positive and Negative Affect

    Time frame: Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

    Positive and Negative Affect Schedule (PANAS)

  11. Change in Authenticity

    Time frame: Baseline to 3 months, 6 months, 1 year

    Inauthenticity Scale

  12. Resilience

    Time frame: Baseline to 2 weeks, 1 month, 3 months, 6 months, 1 year

    2-item Connor-Davidson resilience scale

Other outcomes

  1. Perceived impact of the INSPIRE Interventions

    Time frame: Within 6 months post-intervention

    Qualitative interviews with a subset of trial participants to understand perceived impact of the INSPIRE interventions.

  2. Acceptability of the INSPIRE Interventions

    Time frame: Within 6 months post-intervention

    Qualitative interviews with a subset of trial participants to understand acceptability of the INSPIRE interventions.

Study contacts

Contact information is provided by the study sponsor or research team.

Robert Staeck, MSc

CONTACT

[email protected]

Sofia C Zambrano, PhD

CONTACT

[email protected]

+41 31 684 57 76

Sponsors and collaborators

Lead sponsor

University of Bern

Other

Registry information

Acronym: INSPIRE

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Feb 3, 2025
Registry last updated
Feb 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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