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Impact of Simulation-Based Training on the Safety of Medication Administration (SIM-SAM)

U

University Hospital, Angers

Status

Completed

Conditions

Nurse Training
Simulation
Health Knowledge, Attitudes, Practice

Treatments

Other: high fidelity simulation

Study type

Interventional

Funder types

Other

Identifiers

NCT05543655
49RC22_0241

Details and patient eligibility

About

Task interruption is part of professional life. The healthcare world is not exempt from this phenomenon. Task interruptions lead to errors and increase the risks in managing patients.

Medication administration is the critical step, in that it is the final step to stop medication errors produced upstream. It therefore requires the full attention of any healthcare professional.

In the field of health, simulation has become an innovative educational tool allowing experiential learning and reflective practice.

The general aim of this study is to objectivize the value of simulation-based training as regards medication administration when task interruptions occur.

Enrollment

25 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Nurses from conventional medical and surgical departments participating in the training
  • people agreeing to participate in the study

Exclusion criteria

  • Person refusing the processing of their data

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

simulated
Experimental group
Description:
The 'Simulation training', using high fidelity simulation with a simulated patient, is composed of 2 training sessions of 3 hours each. The training will include a high-fidelity scenario whose events will be adapted to medication administration in conventional care services. This scenario is developed by a multidisciplinary team of healthcare professionals, experts in simulation and risk management
Treatment:
Other: high fidelity simulation

Trial contacts and locations

1

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Central trial contact

DRCI Promotion Interne; Axelle CHAVANON

Data sourced from clinicaltrials.gov

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