A custom tailored, evidence-based, theory-informed, intervention for healthcare professionals to reduce symptoms of burnout (LAGOM): a pragmatic randomized controlled trial

A custom tailored, evidence-based, theory-informed, intervention for healthcare professionals to reduce symptoms of burnout (LAGOM): a pragmatic randomized controlled trial - LAGOM

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00034060

Enrollment

Registered

2024-05-31

Start date

2024-06-04

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

Z73.0

Interventions

Group 1: LAGOM program The LAGOM program will take place over a period of 9 weeks and will consist of 3 hour sessions at the beginning and end of the program and 7 x 90 minute sessions (one session p

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: working healthcare professionals of one of the two study locations who actively practice medicine or nursing; signed, written declaration of consent is required; sufficient knowledge of German language

Exclusion criteria

Exclusion criteria: Currently clinically diagnosed burnout syndrome according to ICD-11; purely administrative position; pregnancy

Design outcomes

Primary

Measure	Time frame
emotional exhaustion, measured by the Maslach Burnout Inventory	—

Secondary

Measure	Time frame
depersonalization, personal accomplishment, subjective stress, mental well-being, self-care, self-efficacy, working conditions, mindfulness, and adverse events	—

Countries

Germany

Contacts

Public ContactMarleen Schröter

Charité Universitätsmedizin Berlin

marleen.schroeter@charite.de+49 30 450 566288

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Apr 4, 2026