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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05543655
Other study ID # 49RC22_0241
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 2022
Est. completion date April 2023

Study information

Verified date September 2022
Source University Hospital, Angers
Contact Axelle CHAVANON
Phone 0665806935
Email Axelle.Chavanon@chu-angers.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date April 2023
Est. primary completion date April 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
high fidelity simulation
Each half-day training session will begin with a reminder of the context and general objectives of the training. Nurses will complete the self-assessment and knowledge tests. The nurses, each in turn, will start the scenario and will immediately assess the workload felt, by the Nasa-TLX grid. During these high-fidelity simulation sessions, an "error cart" workshop will allow all the other nurses to summon up their knowledge on safety tools upstream of the administration procedure. The session begins with a briefing and ends with a debriefing.

Locations

Country Name City State
France Simulation center All'Sims; University Hospital of Angers Angers

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary The effectiveness of simulation-based training on safe drug administration for nurses in conventional services in terms of the number of good steps achieved among the 10 proposed by the HAS Difference between the two assessments of the number of good steps performed during the process three month
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