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A study comparing Rapid Cycle Deliberate Practice and traditional Simulation on nurses' performance in a simulated scenario

A Randomised Controlled Trial Comparing Rapid Cycle Deliberate Practice (RCDP) and Traditional Immersive Simulation (TIS) On Nurses' Resuscitation Performance in a Simulated Scenario

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001065482
Enrollment
230
Registered
2025-09-29
Start date
2025-10-01
Completion date
2026-04-01
Last updated
2025-10-06

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

Conditions

None listed

Brief summary

This study aims to find out which simulation training method helps nurses perform better during a simulated resuscitation. It compares two approaches: Rapid Cycle Deliberate Practice (RCDP), which involves short, repeated practice with immediate feedback, and Traditional Immersive Simulation (TIS), which uses longer, more realistic scenarios and formal debriefing feedback. The main goal is to see which method results in better resuscitation performance such as faster delivery of defibrillation and higher quality chest compressions. We hypothesize that nurses trained with RCDP will perform this critical step more quickly than those trained with TIS.

Interventions

Participants allocated to the intervention arm will receive Rapid Cycle Deliberate Practice (RCDP) as an education method for resuscitation training. In this intervention arm, participants will receive training over one hour, Face to Face, on one allocated day: - 5-minute pre brief and Basic Life Support confidence survey - 20-minute RCDP resuscitation training session - Participants work through a clinical scenario which is broken up into small sections. During each section participants prac

Participants allocated to the intervention arm will receive Rapid Cycle Deliberate Practice (RCDP) as an education method for resuscitation training. In this intervention arm, participants will receive training over one hour, Face to Face, on one allocated day: - 5-minute pre brief and Basic Life Support confidence survey - 20-minute RCDP resuscitation training session - Participants work through a clinical scenario which is broken up into small sections. During each section participants practice clinical skills (e.g. CPR, Defibrillation, and Airway skills and are provided with immediate feedback and debriefing. Sections are then repeated until skill mastery is achieved. - 5-minute NASA TLX - Participants will complete the NASA TLX tool immediately after the RCDP training session. The NASA TLX is a tool used to assess self perceived workload. It measures six dimensions: mental demand, physical demand, temporal demand, performance, effort, and frustration. This tool will assist in assessing cognitive load of training received. NASA TLX sourced from NASA Human Systems Integration Division. - 10-minute uninterrupted clinical scenario. Participants work through a full clinical scenario (e.g. cardiac arrest scenario) using a manikin. The scenario runs without instructor interruption to capture team resuscitation performance (e.g. CPR quality, timely defibrillation), - 20 minute debrief. * Informational materials that would be used include: - Scenario guides (includes simulated clinical notes for participants to use during their simulation). Designed specifically for this study. - Facilitator guides (instructions for running simulations/training sessions). Designed specifically for this study. - Debriefing tool to facilitate debriefing. Sourced from St George Hospital and Debreif2Learn.org - Basic Life Support education poster. Sourced from the Australian Resuscitation Council * Physical materials: - Laerdal QCPR Mannequin - Simulated defibrillator - Realiti Sourced from iSimulate - Clinical equipment (resuscitation equipment - Airway equipment) The training sessions within this intervention arm will be delivered by Nursing educators who have been trained in RCDP method. The location of the intervention will be in a purpose-built education center e.g. Clinical Skills Centre within an acute in-patient hospital. Adherence to the intervention will be through direct observation. Researchers will be using facilitator guides during training sessions to ensure intervention adherence occurs.

Sponsors

South Eastern Sydney Area Health Service
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used) (Investigator)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Nurses employed in an acute care in patient hospital

Exclusion criteria

1. Unable to give consent 2. Nurses who have previously received RCDP resuscitation training 3. Registered Midwife (direct entry midwife)

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026