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This paper proposes an architectural framework for neurodiversity-aware multimodal affective computing that prioritizes construct validity over simple discrimination in automated assessments. By distinguishing between population-relative deviations and adverse functioning, the approach aims to prevent mislabeling behavioral variations as deficits without claiming immediate clinical superiority or presenting a trained model. The work establishes auditable requirements for interpretability, privacy, and human decision boundaries specifically for machine learning systems used in neurodevelopmental contexts.
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Neurodiversity-Aware Multimodal Affective Computing for Neurodevelopmental Assessment: From Norm-Referenced Classification to Context-Sensitive Decision Support

arXiv2 min de cititArticolul și perspectiva sunt în engleză.

arXiv:2610.04705v1 Announce Type: cross Abstract: Automated neurodevelopmental assessment increasingly combines computer vision, speech, eye tracking, physiology, and machine learning, yet multimodality and discrimination do not establish construct validity, clinical usefulness, or appropriate interpretation of behavioral variation. We propose a testable architecture for neurodiversity-aware multimodal affective computing in which population-relative deviation is not treated as sufficient evidence of adverse functioning. This conceptual article reports neither a new participant-level study nor a trained predictive system, and no predictive or clinical superiority is claimed. The framework keeps observable signals, modality quality and availability, context, population-relative information, pooled within-person references and, when sufficiently supported, context-conditioned within person references, and predictive uncertainty distinguishable throughout inference. It defines structured decision-support outputs and auditable requirements for target validity, temporal integrity, contextual leakage, missing-modality robustness, calibration, subgroup evaluation, interpretability, privacy, and human decision boundaries. The contribution is architectural rather than algorithmic: it specifies empirically testable constraints that can be instantiated with different multimodal learning methods. Autism provides the principal motivating evidence base, without assuming unchanged transfer to other neurodevelopmental conditions.

Abstract:Automated neurodevelopmental assessment increasingly combines computer vision, speech, eye tracking, physiology, and machine learning, yet multimodality and discrimination do not establish construct validity, clinical usefulness, or appropriate interpretation of behavioral variation. We propose a testable architecture for neurodiversity-aware multimodal affective computing in which population-relative deviation is not treated as sufficient evidence of adverse functioning. This conceptual article reports neither a new participant-level study nor a trained predictive system, and no predictive or clinical superiority is claimed. The framework keeps observable signals, modality quality and availability, context, population-relative information, pooled within-person references and, when sufficiently supported, context-conditioned within person references, and predictive uncertainty distinguishable throughout inference. It defines structured decision-support outputs and auditable requirements for target validity, temporal integrity, contextual leakage, missing-modality robustness, calibration, subgroup evaluation, interpretability, privacy, and human decision boundaries. The contribution is architectural rather than algorithmic: it specifies empirically testable constraints that can be instantiated with different multimodal learning methods. Autism provides the principal motivating evidence base, without assuming unchanged transfer to other neurodevelopmental conditions.

Human-Computer Interaction (cs.HC); Artificial Intelligence (cs.AI)

arXiv:2610.04705 [cs.HC]

(or arXiv:2610.04705v1 [cs.HC] for this version)

https://doi.org/10.48550/arXiv.2610.04705 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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