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Advanced Cardiac Life Support EducationNCT07862322

Effects of Two-Tier Test-Based Virtual Reality Instruction on ACLS Outcomes Among Clinical Nurses

A study testing Two-Tier Test-Based Virtual Reality Instruction and Traditional Interactive Virtual Reality Instruction in people with Advanced Cardiac Life Support Education, run by Taoyuan General Hospital at 1 site in Taiwan.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study aims to evaluate the effects of two-tier test-based virtual reality (VR) instruction on Advanced Cardiac Life Support (ACLS) learning outcomes among clinical nurses. Participants will be randomly assigned to either a two-tier test-based VR instruction group or a traditional interactive VR instruction group. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Advanced Cardiac Life Support Education
What is being tested?
Two-Tier Test-Based Virtual Reality Instruction and Traditional Interactive Virtual Reality Instruction
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteTaiwan
Study dates
Oct 2026to May 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Clinical nurses holding a valid nurse or registered nurse license.
  • Clinical nurses who have completed the hospital's emergency and resuscitation training courses.

Who cannot join

  • Newly employed nurses within the first 3 months of employment.
  • Instructors for the hospital's resuscitation training courses.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Cheng-Wei Chen, BSN contact

+886-972-608-263

g462113003@tmu.edu.tw

Taiwan1 site
  • Taoyuan General Hospital, Ministry of Health and Welfare

    Taoyuan, 33004

    Cheng-Wei Chen, BSN, +886-972-608-263, g462113003@tmu.edu.tw

    CHENG-WEI CHEN, BSN

Other trials in Taiwan

About this study

Official title: The Effects of Two-tier Test-based Virtual Reality Teaching on ACLS Knowledge and Resuscitation Self-efficacy Among Clinical Nurses

This study aims to evaluate the effects of two-tier test-based virtual reality (VR) instruction on Advanced Cardiac Life Support (ACLS) learning outcomes among clinical nurses. Participants will be randomly assigned to either a two-tier test-based VR instruction group or a traditional interactive VR instruction group. Both groups will use tablet-based, non-immersive VR to learn and practice ACLS-related clinical scenarios.

The study will assess ACLS knowledge, ACLS skills, resuscitation self-efficacy, critical reflection ability, and cognitive load. Assessments will be conducted before and after the intervention, with follow-up assessments conducted one month later to evaluate the retention of learning outcomes.

Read the detailed description

This study is a two-group randomized controlled trial designed to evaluate the effectiveness of two-tier test-based virtual reality (VR) instruction for Advanced Cardiac Life Support (ACLS) education among clinical nurses. A total of 100 clinical nurses will be randomly assigned in a 1:1 ratio to either the experimental group or the control group using computer-generated block randomization.

Both groups will receive tablet-based, non-immersive VR instruction using the same ACLS clinical scenario, learning content, equipment, and intervention duration. The VR scenario simulates the emergency management of a hospitalized patient and incorporates ACLS-related knowledge, clinical decision-making, and interactive questions with immediate feedback.

In the experimental group, participants will receive two-tier test-based VR instruction. Each embedded question consists of two levels: the first tier assesses ACLS knowledge or clinical decisions, and the second tier assesses the reasoning underlying the first-tier response. Both tiers use single-choice questions, and the system provides immediate feedback based on participants' responses. In the control group, participants will receive traditional interactive VR instruction using the same first-tier ACLS questions and immediate feedback but without the second-tier reasoning questions.

The study includes three assessment periods. Before the intervention, participants will complete assessments of ACLS knowledge, resuscitation self-efficacy, and critical reflection ability, along with demographic information. Immediately after the VR intervention, participants will complete assessments of ACLS knowledge, resuscitation self-efficacy, critical reflection ability, and cognitive load. Cognitive load will be assessed only after the intervention.

ACLS skills will be evaluated using a one-to-one, integrated simulation scenario rather than a multi-station assessment. Participants will be required to perform patient assessment, emergency response activation, cardiopulmonary resuscitation, ventilation, rhythm recognition, defibrillation, medication administration, and advanced airway management. A trained assessor will evaluate performance using a standardized scenario script and structured skills checklist without providing additional prompts or correctness feedback. To maintain consistency in assessment conditions, participants will undergo the post-intervention ACLS skills assessment on a scheduled assessment day after completion of the intervention phase, and the follow-up ACLS skills assessment will be conducted approximately one month later under the same standardized conditions.

At the one-month follow-up, ACLS knowledge, ACLS skills, resuscitation self-efficacy, and critical reflection ability will be reassessed to evaluate changes and retention of learning outcomes over time.

Being tested
Two-Tier Test-Based Virtual Reality Instruction, Traditional Interactive Virtual Reality Instruction
Keywords
Advanced Cardiac Life Support, Virtual Reality, Two-Tier Test, Nursing Education, Clinical Nurses

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Two-Tier Test-Based Virtual Reality InstructionBehavioural

    Participants will receive a single session of tablet-based, non-immersive virtual reality (VR) instruction lasting approximately 20-25 minutes. The VR program presents a simulated Advanced Cardiac Life Support (ACLS) scenario involving the emergency management of a hospitalized patient.

    Interactive two-tier test questions are embedded within the VR scenario. The first tier consists of single-choice questions assessing ACLS knowledge and clinical decision-making, and the second tier consists of single-choice questions assessing the reasoning underlying the first-tier responses. After participants respond, the system provides immediate feedback to support learning and reflection.

    The experimental and comparator interventions use the same tablet equipment, VR scenario, first-tier questions, core ACLS learning content, and intervention duration. The distinguishing feature of this intervention is the addition of second-tier reasoning questions.

  • Traditional Interactive Virtual Reality InstructionBehavioural

    Participants will receive a single session of tablet-based, non-immersive virtual reality (VR) instruction lasting approximately 20-25 minutes. The VR program presents a simulated Advanced Cardiac Life Support (ACLS) scenario involving the emergency management of a hospitalized patient.

    Single-tier, single-choice questions assessing ACLS knowledge and clinical decision-making are embedded within the VR scenario. After participants respond to each question, the system provides immediate feedback.

    The comparator and experimental interventions use the same tablet equipment, VR scenario, first-tier questions, core ACLS learning content, and intervention duration. The distinguishing feature of this intervention is that it does not include the second-tier reasoning questions used in the experimental intervention.

Study groups in NCT07862322
Study groupRoleWhat they receive
Two-Tier Test-Based Virtual Reality InstructionExperimentalParticipants in this arm will receive tablet-based, non-immersive virtual reality (VR) instruction using a simulated Advanced Cardiac Life Support (ACLS) clinical scenario. The VR instruction incorporates two-tier test questions. The first tier consists of single-choice questions assessing ACLS knowledge and clinical decision-making, while the second tier consists of single-choice questions assessing the reasoning underlying the first-tier responses. The system provides immediate feedback based on participants' responses. The VR instruction will last approximately 20-25 minutes.
Receives: Behavioral: Two-Tier Test-Based Virtual Reality Instruction
Traditional Interactive Virtual Reality InstructionActive comparatorParticipants in this arm will receive tablet-based, non-immersive virtual reality (VR) instruction using the same simulated Advanced Cardiac Life Support (ACLS) clinical scenario, learning content, equipment, and intervention duration as the experimental group. The VR instruction incorporates single-tier, single-choice questions assessing ACLS knowledge and clinical decision-making. The system provides immediate feedback after participants respond. Unlike the experimental group, this arm does not include second-tier questions assessing the reasoning underlying the first-tier responses. The VR instruction will last approximately 20-25 minutes.
Receives: Behavioral: Traditional Interactive Virtual Reality Instruction

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Advanced Cardiac Life Support Knowledge

    Advanced Cardiac Life Support (ACLS) knowledge will be assessed using researcher-developed 20-item single-choice tests. The baseline knowledge test assesses fundamental ACLS knowledge, including cardiopulmonary resuscitation procedures, electrocardiogram rhythm recognition, defibrillation, and emergency medications. The post-intervention knowledge test includes ACLS knowledge as well as clinical scenario-based questions assessing rhythm recognition, emergency response procedures, medication selection and use, team communication, and clinical decision-making. Each correct response receives 1 point, while an incorrect or unanswered item receives 0 points, resulting in a total score ranging from 0 to 20. Higher scores indicate greater ACLS knowledge. The same post-intervention knowledge test will be used at the one-month follow-up.

    Measured: Baseline, immediately after the intervention, and 1 month after the intervention

  2. Advanced Cardiac Life Support Skills

    Advanced Cardiac Life Support (ACLS) skills will be assessed using a researcher-developed 20-item structured skills performance checklist. The checklist evaluates the correct performance of ACLS procedures, including endotracheal intubation assistance, electrocardiogram rhythm recognition, defibrillation, cardiopulmonary resuscitation, and emergency medication-related assessment, decision-making, and technical performance. Each correctly performed item receives 1 point, while each incorrectly performed or omitted item receives 0 points, resulting in a total score ranging from 0 to 20. Higher scores indicate better ACLS skills performance.

    Measured: Post-intervention skills assessment and 1 month after the post-intervention skills assessment

Secondary outcomes (5)
  1. Resuscitation Self-Efficacy

    Resuscitation self-efficacy will be assessed using the 17-item Resuscitation Self-Efficacy Scale developed by Roh et al. (2012). The scale includes four domains: recognition, debriefing and recording, responding and rescuing, and reporting. Each item is rated on a 5-point Likert scale from 1 to 5, resulting in a total score ranging from 17 to 85. Higher total scores indicate greater resuscitation self-efficacy.

    Measured: Baseline, immediately after the intervention, and 1 month after the intervention

  2. Critical Reflection Competency

    Critical reflection competency will be assessed using the 19-item Critical Reflection Competency Scale developed by Shin et al. (2022). Each item is rated on a 5-point Likert scale from 1 to 5, resulting in a total score ranging from 19 to 95. Higher total scores indicate greater critical reflection competency.

    Measured: Baseline, immediately after the intervention, and 1 month after the intervention

  3. Intrinsic Cognitive Load

    3 items from the 10-item Cognitive Load Scale

    Measured: Immediately after the intervention

  4. Extraneous Cognitive Load

    3 items from the same 10-item Cognitive Load Scale

    Measured: Immediately after the intervention

  5. Germane Cognitive Load

    4 items from the same 10-item Cognitive Load Scale

    Measured: Immediately after the intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Oct 2026
  2. Study startOct 2026 (estimated)
  3. Primary completionMay 2027 (estimated)
  4. Study completionMay 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
Participants will be randomly assigned in a 1:1 ratio to either the two-tier test-based virtual reality instruction group or the traditional interactive virtual reality instruction group using computer-generated block randomization.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07862322
Sponsor's protocol ID
TYGH115056
Status last verified
Sep 2026
First submitted
1 Oct 2026
Last updated
7 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individual participant data will not be shared with other researchers because data sharing is not included in the current IRB-approved study protocol or informed consent. Study results will be reported only in aggregate form to protect participant confidentiality.

Questions about this trial

What is this clinical trial studying?

A study testing Two-Tier Test-Based Virtual Reality Instruction and Traditional Interactive Virtual Reality Instruction in people with Advanced Cardiac Life Support Education, run by Taoyuan General Hospital at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 7 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Cheng-Wei Chen, BSN (+886-972-608-263, g462113003@tmu.edu.tw), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Advanced Cardiac Life Support Knowledge (time frame: Baseline, immediately after the intervention, and 1 month after the intervention). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Oct 2026.

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