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Clinical Thinking and Decision-making Skills in Anesthesia ResidentsNCT07735871

Application of the Four-Dimensional Driven Teaching Model (Version 3) to Anesthesia Training

A study testing VANT intervention and Traditional Structured Teaching intervention in people with Clinical Thinking and Decision-making Skills in Anesthesia Residents, run by China International Neuroscience Institution.

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

The goal of this clinical trial is to learn if the "Visual-Auditory-Tactile-Numerical" (VANT) four-dimensional integrated teaching model improves clinical thinking and decision-making skills in second-year anesthesia residents. Read more about this study

Who is it for?
Ages 20 to 40 years
What is being tested?
VANT intervention and Traditional Structured Teaching intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
No sites listed yet
Study dates
25 Jul 2026to 22 Oct 2026
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 20 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • All participants were in their second year of standardized residency training in anesthesiology, had completed basic anesthesia rotations, and possessed fundamental operational skills suitable for advanced clinical thinking training.

Who cannot join

  • unwillingness to complete the full training and assessment protocol

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

XinYa Wang, Dr contact

01083199270

1055885750@qq.com

Yi Huang, Dr contact

01083199321

1104406602@qq.com

About this study

Official title: Application of the Four-Dimensional Driven Teaching Model (Version 3) to Anesthesia Training: A Multicenter Study

The goal of this clinical trial is to learn if the "Visual-Auditory-Tactile-Numerical" (VANT) four-dimensional integrated teaching model improves clinical thinking and decision-making skills in second-year anesthesia residents. The main questions it aims to answer are:

  • Does the VANT teaching model improve structured clinical thinking scores (measured by the Anesthesia Clinical Thinking Process Scale) compared to traditional teaching methods?
  • Does the VANT teaching model enhance crisis management performance, including accuracy of primary management and critical decision time, in high-fidelity simulation scenarios?
  • Does the VANT teaching model lead to better long-term knowledge retention (at 1 month) and ability to apply learned skills to new clinical situations (at 3 months)? Researchers will compare the VANT four-dimensional integrated teaching group to a traditional structured teaching group to see if the VANT model produces greater improvements in clinical reasoning, crisis response, and knowledge transfer.
Read more

Participants will:

  • Complete a 4-week training program (16 credit hours total) in either the VANT group or the traditional teaching group
  • In the VANT group, engage in multisensory immersive learning involving visual displays (physiological curves and brain network animations), auditory case narratives, tactile manikin manipulation with real-time feedback, and numerical modeling using PK/PD simulation software
  • In the control group, participate in traditional structured teaching including theoretical lectures, case discussions, and simulation practice with basic feedback
  • Complete clinical thinking assessments before training, immediately after, and at 1 month and 3 months post-training
  • Participate in a high-fidelity crisis simulation scenario to evaluate real-time decision-making ability
  • Complete questionnaires about their learning experience and cognitive load
Read the detailed description

The goal of this clinical trial is to learn if the "Visual-Auditory-Tactile-Numerical" (VANT) four-dimensional integrated teaching model improves clinical thinking and decision-making skills in second-year anesthesia residents. The main questions it aims to answer are:

  • Does the VANT teaching model improve structured clinical thinking scores (measured by the Anesthesia Clinical Thinking Process Scale) compared to traditional teaching methods?
  • Does the VANT teaching model enhance crisis management performance, including accuracy of primary management and critical decision time, in high-fidelity simulation scenarios?
  • Does the VANT teaching model lead to better long-term knowledge retention (at 1 month) and ability to apply learned skills to new clinical situations (at 3 months)? Researchers will compare the VANT four-dimensional integrated teaching group to a traditional structured teaching group to see if the VANT model produces greater improvements in clinical reasoning, crisis response, and knowledge transfer.

Participants will:

  • Complete a 4-week training program (16 credit hours total) in either the VANT group or the traditional teaching group
  • In the VANT group, engage in multisensory immersive learning involving visual displays (physiological curves and brain network animations), auditory case narratives, tactile manikin manipulation with real-time feedback, and numerical modeling using PK/PD simulation software
  • In the control group, participate in traditional structured teaching including theoretical lectures, case discussions, and simulation practice with basic feedback
  • Complete clinical thinking assessments before training, immediately after, and at 1 month and 3 months post-training
  • Participate in a high-fidelity crisis simulation scenario to evaluate real-time decision-making ability
  • Complete questionnaires about their learning experience and cognitive load
Being tested
VANT intervention, Traditional Structured Teaching intervention
Keywords
Four-dimensional integrated teaching model

What participants receive

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

  • VANT interventionOther

    Also called Teaching model intervention

    (Four-Dimensional Integrated Immersive Teaching): The "Visual-Auditory-Numerical-Tactile" (VANT) four-dimensional driven teaching model was implemented in a dedicated immersive simulation classroom equipped with multimodal teaching devices. The teaching procedure followed the sequential order of the four dimensions: ① Visual Insight. ② Auditory Embedding. ③ Numerical Validation. ④Tactile Interaction

  • Traditional Structured Teaching interventionOther

    This group adopted a structured teaching model consistent with most domestic anesthesia teaching practices, with total credit hours exactly matching the experimental group. The teaching content also centered on the same core case, the organizational format was:①Theoretical Lectures (4 hours).②Case Discussions (6 hours).③Simulation Practice (6 hours).

Study groups in NCT07735871
Study groupRoleWhat they receive
VANT GROUPExperimental(Four-Dimensional Integrated Immersive Teaching): The "Visual-Auditory-Numerical-Tactile" (VANT) four-dimensional driven teaching model was implemented in a dedicated immersive simulation classroom equipped with multimodal teaching devices. The teaching procedure followed the sequential order of the four dimensions: ① Visual Insight. ② Auditory Embedding. ③ Numerical Validation. ④Tactile Interaction
Receives: Other: VANT intervention
Control GroupActive comparatorControl Group (Traditional Structured Teaching): This group adopted a structured teaching model consistent with most domestic anesthesia teaching practices, with total credit hours exactly matching the experimental group. The teaching content also centered on the same core case, the organizational format was:①Theoretical Lectures (4 hours).②Case Discussions (6 hours).③Simulation Practice (6 hours). The control group received a structured teaching model consistent with conventional didactic practice in our center, which follows a linear 'theory-discussion-practice' sequence without the integrated multisensory or real-time quantitative feedback loops.
Receives: Other: Traditional Structured Teaching intervention

What is being measured

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

  1. Assessment of Anesthesia Clinical Thinking Process

    A modified version of the Anesthesia Clinical Thinking Process Scale (ACTPS), which had been validated for reliability and validity (Cronbach's α = 0.873), was used to evaluate the clinical thinking process before the teaching session, immediately after, and at one month post-teaching. The scale consists of 12 items across four dimensions: breadth of information integration, depth of problem identification, reasonableness of plan generation, and comprehensiveness of expected and alternative plans. Each item is rated on a 7-point Likert scale, with a total score of 84 converted to a percentage scale.

    Measured: pre-teaching (baseline), immediately post-teaching, and one month post-teaching

Secondary outcomes (5)
  1. High-Fidelity Scenario-Based Assessment:Accuracy rate of the primary response (whether the judgment and initial measures aligned with guidelines/expert consensus);

    High-Fidelity Scenario-Based Assessment:Accuracy rate of the primary response (whether the judgment and initial measures aligned with guidelines/expert consensus);In high-fidelity scenarios, four critical decision points are established based on scenario-triggered events. Each decision point is scored independently according to the criteria below, with no mutual influence among them. The scores from the four decision points are summed to produce the "Integrated Management Competency Score" for the scenario (maximum score: 12 points). The final total score corresponds to a competency tier (e.g., 10-12 = Excellent, 7-9 = Proficient, 4-6 = Basic, 0-3 = Needs Improvement).

    Measured: Immediately post-teaching

  2. High-Fidelity Scenario-Based Assessment(Second):Critical decision time (time from scenario start to the first correct intervention)

    High-Fidelity Scenario-Based Assessment(Second):Critical decision time (time from scenario start to the first correct intervention);Compare the times recorded by the timers in the two groups at the first measurement point.

    Measured: Immediately post-teaching

  3. Mid- to Long-Term Knowledge Retention and Transfer Application Testing:Knowledge retention rate

    Knowledge retention rate: A closed-book test consisting of 20 standardized multiple-choice questions (1 point each, total 20 points), parallel in content to the teaching cases but with different scenarios, was administered at one month post-teaching. The retention rate was calculated as (actual score / maximum score × 100%).

    Measured: at 1 month and 3 months post-teaching

  4. Mid- to Long-Term Knowledge Retention and Transfer Application Testing:Transfer application ability

    Transfer application ability at three months: A new virtual case not presented during teaching was introduced. Participants were required to complete four tasks: selection of monitoring indicators, design of anesthesia and analgesia regimens, planning of adverse event countermeasures, and justification for regimen adjustments (each task scored 0-25, total 100 points). Two senior clinicians blinded to group allocation independently rated the performance, and the average score was taken as the transfer application score.

    Measured: at 1 month and 3 months post-teaching

  5. Subjective Learning Experience and Cognitive Load

    The Paas Self-Rating Scale of Cognitive Load were used to measure participants' mental load, mental demand, and effort immediately after key teaching sessions.

    Measured: immediately post-teaching

Timeline

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

  1. First posted30 Jul 2026
  2. Study start25 Jul 2026 (estimated)
  3. Primary completion19 Oct 2026 (estimated)
  4. Study completion22 Oct 2026 (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
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
40 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07735871
Sponsor's protocol ID
CINI -ZYLX-2026[0622]
Status last verified
Jul 2026
First submitted
15 Jul 2026
Last updated
30 Jul 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing VANT intervention and Traditional Structured Teaching intervention in people with Clinical Thinking and Decision-making Skills in Anesthesia Residents, run by China International Neuroscience Institution.

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 1 inclusion and 1 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 30 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

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 XinYa Wang, Dr (01083199270, 1055885750@qq.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assessment of Anesthesia Clinical Thinking Process (time frame: pre-teaching (baseline), immediately post-teaching, and one month post-teaching). 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 30 Jul 2026.

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