Electroencephalogram (EEG)-based emotion recognition has garnered significant attention in brain–computer interface research and healthcare applications. While deep learning models have been extensively studied, most are designed for classification tasks and struggle to accurately predict continuous emotional scores in regression settings. In this paper, we introduce EEG-RegNet, a novel deep neural network tailored for precise emotional score prediction across the continuous valence–arousal–dominance (VAD) space. EEG-RegNet tackles two core challenges: extracting subject-independent, emotion-relevant EEG features and mapping these features to fine-grained, continuous emotional scores. The model leverages 2D convolutional neural networks (CNNs) for spatial feature extraction and a 1D CNN for temporal dynamics, providing robust spatiotemporal modeling. A key innovation is the hybrid loss function, which integrates mean squared error (MSE) and cross-entropy (CE) with a Bernoulli penalty to enhance probability estimation and address sparsity in the emotional space. Extensive experiments on the DEAP dataset show that EEG-RegNet achieves state-of-the-art results in continuous emotional score prediction and attains 95% accuracy in fine-grained emotion classification, highlighting its scalability and precision in emotion recognition.

Large-scale Visual-Language Models have demonstrated powerful adaptability in video recognition tasks. However, existing methods typically rely on fine-tuning or text prompt tuning. In this paper, we propose a visual-only prompting method that employs watermark and trademark prompts to bridge the distribution gap of spatial-temporal video data with Visual-Language Models. Our watermark prompts, designed by a trainable prompt generator, are customized for each video clip. Unlike conventional visual prompts that often exhibit noise signals, watermark prompts are intentionally designed to be imperceptible, ensuring they are not misinterpreted as an adversarial attack. The trademark prompts, bespoke for each video domain, establish the identity of specific video types. Integrating watermark prompts into video frames and prepending trademark prompts to per-frame embeddings significantly boosts the capability of the Visual-Language Model to understand video. Notably, our approach improves the adaptability of the CLIP model to various video action recognition datasets, achieving performance gains of 16.8%, 18.4%, and 13.8% on HMDB-51, UCF-101, and the egocentric dataset EPIC-Kitchen-100, respectively. Additionally, our visual-only prompting method demonstrates competitive performance compared with existing fine-tuning and adaptation methods while requiring fewer learnable parameters. Moreover, through extensive ablation studies, we find the optimal balance between imperceptibility and adaptability. Code will be made available.

Accurate early screening of Alzheimer’s disease (AD) is crucial, yet traditional diagnostic methods are often limited by invasiveness or high costs. Therefore, there is a critical need for non-invasive biomarkers that enable precise and accessible screening. In this study, we propose a multi-modal digital biomarker framework designed to accurately detect AD by evaluating impairments across multiple cognitive domains, such as language, working memory, and visuospatial attention. By leveraging voice and video data, our approach significantly enhances user accessibility and real-world applicability. We validated the proposed framework using a dataset of 128 participants, comprising 77 healthy controls (HCs) and 51 patients with AD. While individual cognitive tasks yielded F1-scores ranging from 69.23% to 77.78% and sensitivities from 69.23% to 80.77%, our ensemble strategy significantly enhanced detection performance, achieving an F1-score of 83.64% and a sensitivity of 88.46%. These findings confirm that the proposed multi-modal digital biomarker framework, enhanced via ensembling, provides a highly accurate, scalable, and practical solution for the non-invasive screening and detection of AD.