Change in surgical performance due to communication.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00031952

Enrollment

Registered

2023-05-30

Start date

2023-06-14

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

Surgical training

Interventions

Group 1: Laparoscopic suturing and knotting without communication (control) Group 2: laparoscopic suturing and knotting during small talk Group 3: laparoscopic suturing and knotting during simulation

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Study of human medicine in the clinical study section

Exclusion criteria

Exclusion criteria: more than 2h laparoscopic previous experience

Design outcomes

Primary

Measure	Time frame
The primary endpoint is the difference in the quality and efficiency (time) of the exercises performed as a function of the confounding factors. This is to be evaluated in comparison to the control run. Established evaluation scores (e.g. operation-specific OSATS scores) are used for the assessment.	—

Secondary

Measure	Time frame
Secondary endpoint is finding the most disruptive form of communication	—

Countries

Germany

Contacts

Public ContactMona Schmidt

Klinik und Poliklinik für Geburtshilfe und Frauengesundheit, Universitätsmedizin Mainz

mona.schmidt@unimedizin-mainz.de06131170

Outcome results

None listed

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