Actively Recruiting

All Genders
NCT07069010

Burnout Syndrome in the Intensive Care Unit Before and During a Palliative Care Trial

Led by University of Athens · Updated on 2025-08-01

100

Participants Needed

1

Research Sites

115 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

One hundred ICU doctors, nurses and psychologists from the 28 units participating in the EPIC stepped-wedge trial (ClinicalTrials.gov NCT06605079) will each complete the same four-part survey twice-once during their unit's usual-care phase and again during the EPIC tele-palliative-care intervention. The questionnaire begins with Part A, gathering demographic and professional details such as age, gender, family status, education, role, years of ICU service, shift patterns, leave days and any prior palliative-care or ethics training. Part B then probes 22 workplace stressors and ethical dilemmas-resource constraints, family pressures, moral conflicts, emotional distancing from colleagues, perceived control over decisions and work-life balance-using a five-point frequency scale. Part C merges a 19-item Maslach Burnout Inventory subset (emotional exhaustion, depersonalization, personal accomplishment) on a seven-point frequency scale with a 16-item Oldenburg Burnout Inventory subset (exhaustion, disengagement) on a four-point agreement scale. Finally, Part D employs Neff's 16-item Self-Compassion Scale-rated from almost never to almost always-to assess self-kindness, common humanity, mindfulness, self-judgment, isolation and over-identification. Within-subject, repeated-measures analyses of total and subscale scores will quantify how EPIC's blended-learning curriculum and standardized teleconsultations shift clinician burnout profiles and self-compassion over time.

CONDITIONS

Official Title

Burnout Syndrome in the Intensive Care Unit Before and During a Palliative Care Trial

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • ICU clinicians (nurses, physicians, advanced practice providers) actively caring for critically ill patients
  • Employed in participating ICUs for 653 months prior to study start
  • Willing to complete both pre- and during-intervention surveys
  • Consent to participate in educational tele-palliative care trial
Not Eligible

You will not qualify if you...

  • Locum tenens or temporary staff not continuously assigned to the unit
  • Clinicians on leave (medical, parental, or extended leave) during either survey period
  • Prior enrollment in similar palliative care training within past 6 months

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

National and Kapodistrian University of Athens

Athens, Greece

Actively Recruiting

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Research Team

S

Spyros D Mentzelopoulos, Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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