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Trial · NCT07898891

Generative AI and Gamified Simulation-Based Train-the-Trainer Basic Life Support Training for High School Teachers in Vietnam

NCT07898891, Not applicable, Not yet recruiting, Eastern International University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Generative AI and Gamified Simulation-Based Train-the-Trainer Basic Life Support Training for High School Teachers in Vietnam. Trials, record NCT07898891. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07898891

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Generative AI and Gamified Simulation-Based Train-the-Trainer Basic Life Support Training for High School Teachers in Vietnam
NCT number
NCT07898891
Status
Not yet recruiting
Phases
Not applicable
Enrollment
56 participants, estimated
Lead sponsor
Eastern International University
Conditions
Cardiac Arrest, Cardiopulmonary Resuscitation
Interventions
Generative AI and Gamified Simulation-Based Train-the-Trainer BLS Programme, Conventional Instructor-Led Simulation-Based BLS Training
First posted
2026-10-27
Last updated
2026-10-27

Source ClinicalTrials.gov

Registered outcomes5

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryBLS Performance Score (BLS Performance Checklist)Baseline (T1, 3-7 days before training, before randomization), immediately after the training day (T2, same day), and 3 months after training (T3, 12 +/- 2 weeks)
BLS performance measured with the researcher-developed 15-item BLS Performance Checklist (Tool 1) based on the 2020 AHA Guidelines, covering recognition of cardiac arrest, activation of the emergency response system, high-quality CPR and AED use, in one standardized scenario on a WorldPoint CPR Taylor manikin with feedback monitor in Blind Mode. Each item is scored 0 or 1; total score 0-15, higher scores indicate better performance. Scored live by trained assessors blinded to group allocation.
SecondaryBLS Knowledge ScoreBaseline (T1, 3-7 days before training, before randomization), immediately after the training day (T2, same day), and 3 months after training (T3, 12 +/- 2 weeks)BLS Knowledge Questionnaire (Tool 2, Part 2): 15 multiple-choice items based on the 2020 AHA Guidelines. Total score 0-15; higher scores indicate better knowledge.
SecondaryAttitudes Toward BLS ScoreBaseline (T1, 3-7 days before training, before randomization), immediately after the training day (T2, same day), and 3 months after training (T3, 12 +/- 2 weeks)Attitudes toward BLS Scale (Tool 2, Part 3): 10 Likert-type items on a five-point response format. Total score 10-50; higher scores indicate more positive attitudes toward BLS.
SecondarySelf-Efficacy in Performing BLS ScoreBaseline (T1, 3-7 days before training, before randomization), immediately after the training day (T2, same day), and 3 months after training (T3, 12 +/- 2 weeks)
Self-Efficacy in Performing BLS Scale (Tool 2, Part 4): 10 items on a five-point response format, aligned with Bandura's Social Learning Theory. Total score 10-50; higher scores indicate greater self-efficacy.
SecondaryBLS Teaching Skills Score (BLS Teaching Skills Assessment)Immediately after the training day (T2, same day) and 3 months after training (T3, 12 +/- 2 weeks)
BLS Teaching Skills Assessment (Tool 3): 10-item rubric across five domains (content accuracy, demonstration skills, facilitation skills, learner engagement, feedback skills), each item scored 0-2; total score 0-20, higher scores indicate better teaching skills. Rated from video of a 5-7 minute micro-teaching session by an assessor blinded to group allocation.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07898891

GET https://conductscience.org/api/trials/v1/NCT07898891/registered