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Trial · NCT07903467

Generative AI-Assisted Personalized Feedback for Laparoscopic Skill Learning in Medical Undergraduates

NCT07903467, Not applicable, Not yet recruiting, Yang Xiaodong

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Generative AI-Assisted Personalized Feedback for Laparoscopic Skill Learning in Medical Undergraduates. Trials, record NCT07903467. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07903467

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Trial

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

Title
Generative AI-Assisted Personalized Feedback for Laparoscopic Skill Learning in Medical Undergraduates
NCT number
NCT07903467
Status
Not yet recruiting
Phases
Not applicable
Enrollment
40 participants, estimated
Lead sponsor
Yang Xiaodong
Conditions
Medical Education
Interventions
Generative AI-Assisted Personalized Feedback, Structured Template-Based Feedback
First posted
2026-10-29
Last updated
2026-10-30

Source ClinicalTrials.gov

Registered outcomes10

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

ListOutcomeTime frameDescription
PrimaryFundamentals of Laparoscopic Surgery Precision Cutting-Derived Objective Score (PCOS) at T4Immediately after completion of the cutting training phase (T4), approximately 4 weeks after baseline.
Precision cutting performance will be assessed using the study-defined Precision Cutting Objective Score derived from the Fundamentals of Laparoscopic Surgery task. PCOS = max(0, 300 - T - 100 × Aerror/Atarget), where T is completion time in seconds, Aerror is the exclusive-or area between the target and actual cutting contours, and Atarget is the target area. Scores range from 0 to 300; higher scores indicate better performance. Incomplete tasks or completion times of 300 seconds or longer receive 0. Technically unevaluable assessments are treated as missing. This is a research score, not an official FLS certification score.
SecondaryFundamentals of Laparoscopic Surgery Peg Transfer-Derived Objective Score (PTOS) at T2Immediately after completion of the transfer training phase (T2), approximately 2 weeks after baseline.
Peg transfer performance will be assessed using the study-defined Peg Transfer Objective Score derived from the Fundamentals of Laparoscopic Surgery task. PTOS = max(0, 300 - T - 100 × Nlost/6), where T is completion time in seconds and Nlost is the number of irretrievable objects. Scores range from 0 to 300; higher scores indicate better performance. Incomplete tasks or completion times of 300 seconds or longer receive 0. Recoverable drops do not incur an additional direct penalty. Technically unevaluable assessments are treated as missing. This is a research score, not an official FLS certification score.
SecondaryTransfer Training Task Performance Assessed With the Task-Specific Behaviorally Anchored Rating Scale (TS-BARS)Baseline (T0), approximately week 1 (T1), and approximately week 2 (T2).
Learning progression on the 14-ball transfer training task will be assessed using the study-specific Task-Specific Behaviorally Anchored Rating Scale. Seven domains are scored from 0 to 5, yielding a total score of 0-35; higher scores indicate better technical performance. The mean of two independent masked assessors' valid total scores will be used after any required discrepancy review. Repeated total scores will characterize the training trajectory.
SecondaryCutting Training Task Performance Assessed With the Task-Specific Behaviorally Anchored Rating Scale (TS-BARS)Approximately week 2 (T2), week 3 (T3), and week 4 (T4) after baseline.
Learning progression on the study-developed shape-cutting training task will be assessed using the study-specific Task-Specific Behaviorally Anchored Rating Scale. Seven domains are scored from 0 to 5, yielding a total score of 0-35; higher scores indicate better technical performance. The mean of two independent masked assessors' valid total scores will be used after any required discrepancy review. Repeated total scores will characterize the training trajectory.
OtherPrecision Cutting Skill Retention Assessed With the Precision Cutting Objective Score (PCOS) at T5T5, 4-8 weeks after T4, approximately 8-12 weeks after baseline.
Retention will be assessed by repeating the Fundamentals of Laparoscopic Surgery Precision Cutting task and calculating the study-defined Precision Cutting Objective Score: max(0, 300 - completion time in seconds - 100 × error area/target area). Scores range from 0 to 300; higher scores indicate better retained performance. The same completion, time-limit, and evaluability rules used for the T4 assessment will apply.
OtherPeg Transfer Skill Retention Assessed With the Peg Transfer Objective Score (PTOS) at T5T5, 4-8 weeks after T4, approximately 8-12 weeks after baseline.
Retention will be assessed by repeating the Fundamentals of Laparoscopic Surgery Peg Transfer task and calculating the study-defined Peg Transfer Objective Score: max(0, 300 - completion time in seconds - 100 × number of irretrievable objects/6). Scores range from 0 to 300; higher scores indicate better retained performance. The same completion, time-limit, and evaluability rules used for the T2 assessment will apply.
OtherTransfer Training Self-Assessment Absolute Calibration Error Relative to TS-BARS Ratings at T2At the end of the transfer training phase (T2), approximately 2 weeks after baseline.
Self-assessment accuracy will be quantified as the mean absolute difference between the learner's domain-level self-ratings and the corresponding mean ratings from two independent assessors using the Task-Specific Behaviorally Anchored Rating Scale for the transfer training task. Each comparable domain is rated from 0 to 5. Absolute calibration error ranges from 0 to 5; lower values indicate more accurate self-assessment.
OtherCutting Training Self-Assessment Absolute Calibration Error Relative to TS-BARS Ratings at T4At the end of the cutting training phase (T4), approximately 4 weeks after baseline.
Self-assessment accuracy will be quantified as the mean absolute difference between the learner's domain-level self-ratings and the corresponding mean ratings from two independent assessors using the Task-Specific Behaviorally Anchored Rating Scale for the cutting training task. Each comparable domain is rated from 0 to 5. Absolute calibration error ranges from 0 to 5; lower values indicate more accurate self-assessment.
OtherStudy-Specific Feedback Satisfaction and Acceptability Questionnaire Item ScoresAt the end of the transfer phase (T2, approximately week 2) and cutting phase (T4, approximately week 4).
Learners' perceptions of the feedback actually received will be assessed using the study-specific, source-neutral, eight-item Feedback Satisfaction and Acceptability Questionnaire. Each item is scored from 1 to 5, with higher scores indicating greater satisfaction or acceptability after any prespecified reverse coding. Item scores will be reported separately at each assessment. The questionnaire will not identify the feedback source or ask about AI-specific acceptance.
OtherStudy-Specific Feedback Quality Rating Rubric Domain Scores for Paired AI and Template CandidatesAt four feedback-generation events based on baseline (T0) and approximately weeks 1, 2, and 3 (T1-T3) assessments.
First-attempt, unedited AI and template feedback candidates generated from identical frozen inputs will be evaluated offline by two independent source-masked raters using the study-specific Feedback Quality Rating Rubric. Domains are grounding, prioritization, specificity, actionability, goal clarity, longitudinal coherence, and information economy. Each domain is rated from 1 to 5; higher scores indicate better quality. The mean of the two raters' scores will be reported separately for each domain. Longitudinal coherence is assessed only for second-feedback events within each task phase. Undelivered candidates are used only for the offline comparison and are not linked to learner reception or subsequent performance.

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.

Papers4

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
6876333BACKGROUNDPubMed
14694297BACKGROUNDPubMed
20103076BACKGROUNDPubMed
41671848BACKGROUNDPubMed

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.

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