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Effectiveness of Simulation Based Training in Implementing One Hour Bundle Sepsis

The Role of Simulation-Based Training to Improve Team Performance in Implementing One Sepsis Hour Bundle in Intensive Care Unit

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05076721
Enrollment
40
Registered
2021-10-13
Start date
2020-08-22
Completion date
2020-10-24
Last updated
2021-10-13

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

Conditions

Medical Education, Sepsis, Simulation Training

Keywords

medical education, simulation training, sepsis, high-fidelity manikin, one-hour bundle sepsis

Brief summary

This study aimed to compare simulation training with conventional training (case-based discussion only) to improve team performance in implementing one-hour sepsis bundle in the intensive care unit

Detailed description

This was an experimental randomized single-blind study to examine the role of simulation-based training in improving team performance in conducting sepsis management. Subjects were sixteen doctors and twenty-four nurses working in the intensive care unit. The subjects were randomly divided into two treatment groups: the discussion group and the simulation group. Each treatment group was further divided into four small groups consisting of two doctors and three nurses. Prior to the training, every subject received a pretest for cognitive evaluation and a posttest at the end of the training. The performance of both groups in implementing one-hour sepsis bundle was assessed by solving a sepsis case in high fidelity manikin.

Interventions

OTHERSimulation training

The participants in the simulation group will receive simulation training with high-fidelity manikin to practice and implement one-hour bundle sepsis

OTHERCase-based discussion training

The participants in the conventional group will only do a case-based discussion in implementing one-hour bundle sepsis

Sponsors

Indonesia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Doctors working in Dr. Cipto Mangunkusumo Public Hospital's ICU * Nurses working in Dr. Cipto Mangunkusumo Public Hospital's ICU

Exclusion criteria

* Doctors and nurses who are not fit or healthy to undergo this training

Design outcomes

Primary

MeasureTime frameDescription
Differences in score of skills in implementing one-hour bundle sepsis in the intensive care unit assessed with checklist which were designed by four anesthesiologist-intensivistsupon study completion, in 1 dayMeasured by checklist which were designed by four anesthesiologist-intensivists before the study was conducted and validated by Aiken coefficient. The Aiken coefficient for this checklist were all \>0.3 which is declared valid.

Secondary

MeasureTime frameDescription
Differences in intrateam communication's score in implementing one hour sepsis bundle assessed with checklist which were designed by four anesthsiologist-intensivistsupon study completion, in 1 dayMeasured by checklist which were designed by four anesthesiologist-intensivists before the study was conducted and validated by Aiken coefficient. The Aiken coefficient for this checklist were all \>0.3 which is declared valid.

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026