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arXiv:2611.16647 · v1

InertiaMPDD: Multimodal Personalized Depression Detection via Emotional Inertia-Inspired Dynamics Modeling

首次提交 2026-11-12 19:22
版本更新 2026-11-12 19:22
雷达观测 2026-11-13 14:15
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摘要

Multimodal depression screening estimates risk from speech, visual behavior and language. Current methods mainly predict labels, with limited evidence of departures from a non-depressed reference. Recording-level supervision also leaves fine-grained emotional dynamics unannotated. Motivated by emotional inertia, the persistence of affect, InertiaMPDD learns healthy next-state patterns using a world-model-inspired latent predictor. Using pretrained multimodal representations, it predicts from observed history and context. Reference deviation, residual decay rate and a Jacobian spectral descriptor form reference-derived emotional dynamics descriptors, evaluated as candidate proxy biomarkers for standalone screening and personalized decision correction. Across five cohorts from four datasets, fusion reaches 98.41% F1 on D-Vlog and 84.98% on LMVD. Standalone descriptors outperform fixed additive fusion on MPDD but discriminate weakly on AVEC2014. These findings distinguish reference informativeness from fusion benefit and reveal context-dependent utility.

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v1 · 2026-11-12 19:22 · 最新观测版本

InertiaMPDD: Multimodal Personalized Depression Detection via Emotional Inertia-Inspired Dynamics Modeling

Multimodal depression screening estimates risk from speech, visual behavior and language. Current methods mainly predict labels, with limited evidence of departures from a non-depressed reference. Recording-level supervision also leaves fine-grained emotional dynamics unannotated. Motivated by emotional inertia, the persistence of affect, InertiaMPDD learns healthy next-state patterns using a world-model-inspired latent predictor. Using pretrained multimodal representations, it predicts from observed history and context. Reference deviation, residual decay rate and a Jacobian spectral descriptor form reference-derived emotional dynamics descriptors, evaluated as candidate proxy biomarkers for standalone screening and personalized decision correction. Across five cohorts from four datasets, fusion reaches 98.41% F1 on D-Vlog and 84.98% on LMVD. Standalone descriptors outperform fixed additive fusion on MPDD but discriminate weakly on AVEC2014. These findings distinguish reference informativeness from fusion benefit and reveal context-dependent utility.

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