Diffusion Model-based Activity Completion for AI Motion Capture from Videos

AI-based motion capture is an emerging technology that offers a cost-effective alternative to traditional motion capture systems. However, current AI motion capture methods rely entirely on observed video sequences, similar to conventional motion capture. This means that all human actions must be predefined, and movements outside the observed sequences are not possible. To address this limitation, we aim to apply AI motion capture to virtual humans, where flexible actions beyond the observed sequences are required. We assume that while many action fragments exist in the training data, the transitions between them may be missing. To bridge these gaps, we propose a diffusion-model-based action completion technique that generates complementary human motion sequences, ensuring smooth and continuous movements. By introducing a gate module and a position-time embedding module, our approach achieves competitive results on the Human3.6M dataset. Our experimental results show that (1) MDC-Net outperforms existing methods in ADE, FDE, and MMADE but is slightly less accurate in MMFDE, (2) MDC-Net has a smaller model size (16.84M) compared to HumanMAC (28.40M), and (3) MDC-Net generates more natural and coherent motion sequences. Additionally, we propose a method for extracting sensor data, including acceleration and angular velocity, from human motion sequences.

Image Classification Using a Diffusion Model as a Pre-Training Model

In this paper, we propose a diffusion model that integrates a representation-conditioning mechanism, where the representations derived from a Vision Transformer (ViT) are used to condition the internal process of a Transformer-based diffusion model. This approach enables representation-conditioned data generation, addressing the challenge of requiring large-scale labeled datasets by leveraging self-supervised learning on unlabeled data. We evaluate our method through a zero-shot classification task for hematoma detection in brain imaging. Compared to the strong contrastive learning baseline, DINOv2, our method achieves a notable improvement of +6.15% in accuracy and +13.60% in F1-score, demonstrating its effectiveness in image classification.