Stress reduction in an university anesthesia department due to an interventions program according to MBSR measured by subjective and objective parameters

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

DRKS

Registry ID

DRKS00012306

Enrollment

Registered

2017-05-03

Start date

2017-04-08

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Z73

Interventions

Group 1: All subjects recieve an intervention once a week for a six week period at the end of a working day (4 times 90 minutes and 2 times 60 minutes). During these six intervention sessions all subj

Eligibility

Sex/Gender

All

Age

24 Years to 67 Years

Inclusion criteria

Inclusion criteria: Female and male anesthesiologists working in an University department of anesthesia

Exclusion criteria

Exclusion criteria: Ongoing corticoid therapy, hypo- or hypercortisolism, late preganancy in third trimenon, cardiac arrhythmia, antiarrhythmic therapy

Design outcomes

Primary

Measure	Time frame
Improvement of the subjective measurable stress parameters by the following questionaires: WHO-5 Wellbeing Scale, MBI-22 Maslach Burn out Index, PSS-10 Perceived Stress Scale, RS-11 Resilience Scale. Improvement of the objective measurable stress parameters by heart rate variability, after a resting phase and after short body exercise, and hair cortisol concentation. Mesaurements are made before interventions, after intervention, three and six months after intervention period.	—

Measure

Time frame

Improvement of the subjective measurable stress parameters by the following questionaires: WHO-5 Wellbeing Scale, MBI-22 Maslach Burn out Index, PSS-10 Perceived Stress Scale, RS-11 Resilience Scale. Improvement of the objective measurable stress parameters by heart rate variability, after a resting phase and after short body exercise, and hair cortisol concentation. Mesaurements are made before interventions, after intervention, three and six months after intervention period.

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Countries

Germany

Contacts

Public ContactBenjamin Gerber

Universitätsklinikum MannheimKlinik für Anästhesiologie und Operative Intensivmedizin, Schmerzzentrum

benjamin.gerber@umm.de0621 383 2608

Outcome results

None listed

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