Feasibility of a custom tailored, evidence-based, theory-informed, intervention to prevent burnout and reduce stress for healthcare professionals: Protocol for a single-arm trial

Conditions

Z73

Schiele JK, Schröter M, Berschick J, Steinmetz M, Bogdanski M, Jankow S, Stritter W, Kessler CS, Seifert G, Koch AK.

2025-09-16

Feasibility of a tailored, combined intervention with mind-body elements to prevent burnout in healthcare professionals (LAGOM) in a mixed-methods multicenter single-arm trial

Marleen Schröter, Anna K. Koch, Julia Berschick, Julia Katharina Schiele, Martin Bogdanski et al. (10 authors)

Scientific Reports2025-07-28

10.1038/s41598-025-12543-0

Feasibility of a custom-tailored, evidence-based, theory-informed, intervention to prevent burnout and reduce stress for healthcare professionals: protocol for a single-arm trial

Marleen Schröter, Julia Berschick, Anna K. Koch, Julia Katharina Schiele, Martin Bogdanski et al. (9 authors)

Pilot and Feasibility Studies2024-11-073 citations

10.1186/s40814-024-01553-w

A custom tailored, evidence-based, theory-informed intervention for healthcare professionals to prevent burnout (LAGOM): study protocol for a pragmatic randomized controlled trial.

Koch AK, Schröter M, Berschick J, Schiele JK, Bogdanski M, Steinmetz M, Stritter W, Voss A, Seifert G, Kessler CS.

2024-09-273 citations

10.1186/s13063-024-08491-1

Interventions

Group 1: LAGOM program The LAGOM program will take place over a period of 9 weeks, consisting of 2-hour sessions at the beginning and end of the program respectively, as well as 7x90min sessions (one

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Working as healthcare professionals actively practicing medicine or nursing at the Charité – university hospital Berlin or the Immanuel Hospital, Wannsee, Germany Gave written informed consent Proficient in German language

Exclusion criteria

Exclusion criteria: Not actively practicing medicine or nursing Pregnancy Clinically diagnosed burnout syndrome according to ICD-11 (QD85 “Burnout”)

Design outcomes

Primary

Measure	Time frame
The main objectives of this study are to evaluate (1) the feasibility and accceptability of the trial procedures (recruitment, attrition, completeness of data collection, assessment process, procotol adherence, adherence of participants, adverse events), and (2) the feasibility and acceptability of the intervention content and structure (satisfaction, utility, knowledge, application to practice, organizational results).	—

Measure

Time frame

The main objectives of this study are to evaluate (1) the feasibility and accceptability of the trial procedures (recruitment, attrition, completeness of data collection, assessment process, procotol adherence, adherence of participants, adverse events), and (2) the feasibility and acceptability of the intervention content and structure (satisfaction, utility, knowledge, application to practice, organizational results).

—

Secondary

Measure	Time frame
explorative effectiveness evaluation (MBI, BSW-5-REV, break habits) biosignal analysis	—

Countries

Germany

Contacts

Public ContactMelanie Steinmetz

Charité Universitätsmedizin Berlin

melanie.steinmetz@charite.de+49 30 450 566288

Outcome results

None listed