@inproceedings{al-smadi-2026-automated,
title = "Automated Detection of Dosing Errors in Clinical Trial Narratives: A Multi-Modal Feature Engineering Approach with {L}ight{GBM}",
author = "AL-Smadi, Mohammad",
editor = "Gupta, Deepak and
Thompson, Paul and
Ananiadou, Sophia and
Demner-Fushman, Dina",
booktitle = "Proceedings of the Third Workshop on Patient-Oriented Language Processing ({CL}4{H}ealth) @ {LREC} 2026",
month = may,
year = "2026",
address = "Palma, Mallorca (Spain)",
publisher = "ELRA Language Resources Association (ELRA)",
url = "https://aclanthology.org/2026.cl4health-1.29/",
doi = "10.63317/2kuc94aqpqj8",
pages = "333--343",
abstract = "Clinical trials require strict adherence to medication protocols, yet dosing errors remain a persistent challenge affecting patient safety and trial integrity. We present an automated system for detecting dosing errors in unstructured clinical trial narratives using gradient boosting with comprehensive multi-modal feature engineering. Our approach combines 3,451 features spanning traditional NLP (TF-IDF, character n-grams), dense semantic embeddings (all-MiniLM-L6-v2), domain-specific medical patterns, and transformer-based scores (BiomedBERT, DeBERTa-v3), used to train a LightGBM model. Features are extracted from nine complementary text fields (median 5,400 characters per sample) ensuring complete coverage across all 42,112 clinical trial narratives. On the CT-DEB benchmark dataset with severe class imbalance (4.9{\%} positive rate), we achieve 0.8725 test ROC-AUC through 5-fold ensemble averaging (cross-validation: 0.8833 {\ensuremath{\pm}} 0.0091 AUC). Systematic ablation studies reveal that removing sentence embeddings causes the largest performance degradation (2.39{\%}), demonstrating their critical role despite contributing only 37.07{\%} of total feature importance. Feature efficiency analysis demonstrates that selecting the top 500-1000 features yields optimal performance (0.886-0.887 AUC), outperforming the full 3,451-feature set (0.879 AUC) through effective noise reduction. Our findings highlight the importance of feature selection as a regularization technique and demonstrate that sparse lexical features remain complementary to dense representations for specialized clinical text classification under severe class imbalance."
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<abstract>Clinical trials require strict adherence to medication protocols, yet dosing errors remain a persistent challenge affecting patient safety and trial integrity. We present an automated system for detecting dosing errors in unstructured clinical trial narratives using gradient boosting with comprehensive multi-modal feature engineering. Our approach combines 3,451 features spanning traditional NLP (TF-IDF, character n-grams), dense semantic embeddings (all-MiniLM-L6-v2), domain-specific medical patterns, and transformer-based scores (BiomedBERT, DeBERTa-v3), used to train a LightGBM model. Features are extracted from nine complementary text fields (median 5,400 characters per sample) ensuring complete coverage across all 42,112 clinical trial narratives. On the CT-DEB benchmark dataset with severe class imbalance (4.9% positive rate), we achieve 0.8725 test ROC-AUC through 5-fold ensemble averaging (cross-validation: 0.8833 \ensuremath\pm 0.0091 AUC). Systematic ablation studies reveal that removing sentence embeddings causes the largest performance degradation (2.39%), demonstrating their critical role despite contributing only 37.07% of total feature importance. Feature efficiency analysis demonstrates that selecting the top 500-1000 features yields optimal performance (0.886-0.887 AUC), outperforming the full 3,451-feature set (0.879 AUC) through effective noise reduction. Our findings highlight the importance of feature selection as a regularization technique and demonstrate that sparse lexical features remain complementary to dense representations for specialized clinical text classification under severe class imbalance.</abstract>
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%0 Conference Proceedings
%T Automated Detection of Dosing Errors in Clinical Trial Narratives: A Multi-Modal Feature Engineering Approach with LightGBM
%A AL-Smadi, Mohammad
%Y Gupta, Deepak
%Y Thompson, Paul
%Y Ananiadou, Sophia
%Y Demner-Fushman, Dina
%S Proceedings of the Third Workshop on Patient-Oriented Language Processing (CL4Health) @ LREC 2026
%D 2026
%8 May
%I ELRA Language Resources Association (ELRA)
%C Palma, Mallorca (Spain)
%F al-smadi-2026-automated
%X Clinical trials require strict adherence to medication protocols, yet dosing errors remain a persistent challenge affecting patient safety and trial integrity. We present an automated system for detecting dosing errors in unstructured clinical trial narratives using gradient boosting with comprehensive multi-modal feature engineering. Our approach combines 3,451 features spanning traditional NLP (TF-IDF, character n-grams), dense semantic embeddings (all-MiniLM-L6-v2), domain-specific medical patterns, and transformer-based scores (BiomedBERT, DeBERTa-v3), used to train a LightGBM model. Features are extracted from nine complementary text fields (median 5,400 characters per sample) ensuring complete coverage across all 42,112 clinical trial narratives. On the CT-DEB benchmark dataset with severe class imbalance (4.9% positive rate), we achieve 0.8725 test ROC-AUC through 5-fold ensemble averaging (cross-validation: 0.8833 \ensuremath\pm 0.0091 AUC). Systematic ablation studies reveal that removing sentence embeddings causes the largest performance degradation (2.39%), demonstrating their critical role despite contributing only 37.07% of total feature importance. Feature efficiency analysis demonstrates that selecting the top 500-1000 features yields optimal performance (0.886-0.887 AUC), outperforming the full 3,451-feature set (0.879 AUC) through effective noise reduction. Our findings highlight the importance of feature selection as a regularization technique and demonstrate that sparse lexical features remain complementary to dense representations for specialized clinical text classification under severe class imbalance.
%R 10.63317/2kuc94aqpqj8
%U https://aclanthology.org/2026.cl4health-1.29/
%U https://doi.org/10.63317/2kuc94aqpqj8
%P 333-343
Markdown (Informal)
[Automated Detection of Dosing Errors in Clinical Trial Narratives: A Multi-Modal Feature Engineering Approach with LightGBM](https://aclanthology.org/2026.cl4health-1.29/) (AL-Smadi, CL4Health 2026)
ACL