AI-Assisted Anaerobic Threshold Interpretation in Cardiopulmonary Exercise Testing (PACE-Reader)
A Randomized Two-Period Crossover Reader Study of Artificial Intelligence-Assisted Anaerobic Threshold Interpretation in Cardiopulmonary Exercise Testing
This prospective randomized two-period crossover reader study will evaluate whether assistance from a frozen artificial intelligence model improves physicians' interpretation of the anaerobic threshold (AT) in cardiopulmonary exercise testing (CPET). Sixteen physicians, including 8 senior and 8 junior readers, will each interpret 150 de-identified CPET examinations once without AI assistance and once with AI assistance. The primary outcome is the within-physician difference in absolute AT localization error between the assisted and unassisted conditions. Secondary outcomes include signed timing error, agreement on whether AT is present, estimates within 15 and 30 seconds of the reference, inter-reader reliability, interpretation time, and whether the effect of AI assistance differs by physician seniority.
Aperçu de l'étude
Statut
Les conditions
Description détaillée
The 150 de-identified CPET examinations will be divided into two non-overlapping case libraries, X and Y, with 75 examinations in each library. The libraries will be balanced, as far as feasible, by clinical severity and acquisition characteristics. None of the reader-study examinations will be used for model training, hyperparameter selection, or checkpoint selection.
Within each seniority stratum, physicians will be randomized in a 1:1 ratio to Sequence A or Sequence B. In period 1, Sequence A will interpret library X without AI assistance and library Y with AI assistance; Sequence B will receive the opposite conditions. Following a 14 ± 3 day washout, the assistance conditions will be reversed in period 2. Case order will be randomized within each period, and new blinded task identifiers will be assigned in period 2. Thus, every physician will interpret every examination once without AI assistance and once with AI assistance, yielding 4,800 interpretations.
In the assisted condition, the interface will display the frozen model's predicted AT time. In the unassisted condition, no model output will be shown. Readers will be masked to case source, routine-report and reference-standard labels, other readers' annotations, and their own annotations from the previous period. For each examination, the reader will classify AT as confirmed, not reached, or unable to confirm. When AT is confirmed, the reader will record the AT time and the interpretive method used. Interpretation time will also be recorded.
The reference standard will be prespecified from unassisted senior-physician annotations. AT will be considered present when at least 6 of 8 senior physicians confirm it, and the reference AT time will be the median of the confirming senior estimates. AT will be considered not reached when at least 6 of 8 senior physicians make that classification. Discordant cases will undergo adjudication by an additional senior physician who is masked to model output and reader identity. For analyses of senior readers, a leave-one-reader-out reference will be used.
The primary analysis will compare absolute AT localization error between assisted and unassisted interpretations using a crossed mixed-effects model. Fixed effects will include assistance condition, physician seniority, the assistance-by-seniority interaction, period, randomized sequence, and case library. Random intercepts will be included for physician and examination. Estimates will be reported with 95% confidence intervals. No simulated or pilot-result data will be included in the prospective study analysis.
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Cong Wang, MD, PhD
- Numéro de téléphone: +86-21-64041990
- E-mail: wang.cong1@zs-hospital.sh.cn
Lieux d'étude
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Chine, 200032
- Zhongshan Hospital, Fudan University
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Contact:
- Cong Wang, MD, PhD
- Numéro de téléphone: +86-21-64041990
- E-mail: wang.cong1@zs-hospital.sh.cn
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Age 18 years or older.
- Licensed physician or physician enrolled in a recognized postgraduate clinical training program at the study institution.
- Eligible for one of the two prespecified seniority strata: senior physicians are attending physicians or above with at least 5 years of independent CPET interpretation experience; junior physicians are residents or specialty trainees with less than 5 years of independent CPET interpretation experience.
- Able to interpret CPET examinations and use the study interface after standardized orientation.
- Willing and able to complete both study periods and the prespecified washout interval.
- Provides written informed consent.
Exclusion Criteria:
- Direct involvement in development, training, hyperparameter selection, or checkpoint selection of the PACE-Former model.
- Prior access to the study case libraries, reference-standard annotations, or model outputs for the study examinations.
- Unable to complete the required interpretation tasks or the 14 ± 3 day washout interval.
- Withdrawal of consent before completion of study procedures.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Diagnostique
- Répartition: Randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Sequence A
Period 1: library X interpreted without AI assistance and library Y interpreted with AI assistance. Period 2, after a 14 ± 3 day washout: library X interpreted with AI assistance and library Y interpreted without AI assistance. |
A frozen PACE-Former model provides a predicted anaerobic threshold time within the CPET review interface. Physicians retain responsibility for the final classification and AT time annotation. No other model output or reference label is displayed. The physician reviews the same de-identified CPET data using the study interface without display of any model prediction or AI-generated suggestion and independently classifies AT status and records the AT time when confirmed. |
|
Expérimental: Sequence B
Period 1: library X interpreted with AI assistance and library Y interpreted without AI assistance. Period 2, after a 14 ± 3 day washout: library X interpreted without AI assistance and library Y interpreted with AI assistance. |
A frozen PACE-Former model provides a predicted anaerobic threshold time within the CPET review interface. Physicians retain responsibility for the final classification and AT time annotation. No other model output or reference label is displayed. The physician reviews the same de-identified CPET data using the study interface without display of any model prediction or AI-generated suggestion and independently classifies AT status and records the AT time when confirmed. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Difference in Absolute Anaerobic Threshold Localization Error
Délai: Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
Absolute difference, in seconds, between the physician-selected AT time and the prespecified expert reference AT time. The primary estimand is the within-physician difference between AI-assisted and unassisted interpretations, analyzed across the same examinations using a crossed mixed-effects model. |
Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Signed Anaerobic Threshold Localization Error
Délai: Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
Signed difference, in seconds, between the physician-selected AT time and the prespecified expert reference AT time. Negative values indicate earlier placement and positive values indicate later placement relative to the reference. |
Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
|
Proportion of Anaerobic Threshold Estimates Within 15 Seconds of the Reference
Délai: Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
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Proportion of interpretable examinations for which the physician-selected AT time is within 15 seconds, in either direction, of the prespecified expert reference AT time. |
Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
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Proportion of Anaerobic Threshold Estimates Within 30 Seconds of the Reference
Délai: Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
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Proportion of interpretable examinations for which the physician-selected AT time is within 30 seconds, in either direction, of the prespecified expert reference AT time. |
Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
|
Agreement With the Reference Anaerobic Threshold Status
Délai: Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
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Agreement between the physician classification (AT confirmed, AT not reached, or unable to confirm) and the prespecified expert reference classification. Results will be summarized as overall agreement and condition-specific classification performance. |
Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
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Inter-Reader Reliability
Délai: Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
Reliability among physicians for AT timing and AT-status classification under AI-assisted and unassisted conditions, summarized using appropriate intraclass correlation and chance-corrected agreement statistics with 95% confidence intervals. |
Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
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Interpretation Time per Examination
Délai: Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
Elapsed time, in seconds, from opening the blinded CPET task to submission of the physician's AT classification and, when applicable, the selected AT time. |
Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
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Interaction Between AI Assistance and Physician Seniority
Délai: Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
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Difference in the effect of AI assistance between senior and junior physicians, estimated from the prespecified assistance-by-seniority interaction term in the crossed mixed-effects model for absolute AT localization error. |
Recorded immediately after each case interpretation and analyzed after completion of both study periods, up to 2 months
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Cong Wang, MD, PhD, Fudan University
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Autres numéros d'identification d'étude
- PACE-AT-READER-01
Plan pour les données individuelles des participants (IPD)
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Informations sur les médicaments et les dispositifs, documents d'étude
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