Key result
Shuffle-rPPGNet achieves low mean absolute error for heart rate variability measurement across datasets.
Why the study?
Relatively few studies exist on remote heart rate variability measurement, and existing deep neural network methods are computationally intensive due to high complexity.
Shuffle-rPPGNet provides an efficient and accurate deep learning method for remote heart rate variability measurement from facial videos.
Promising for remote HRV assessment; leaves open prospective clinical validation before practice adoption.
In the field of remote physiological indicator measurement, there are relatively few studies on measuring heart rate variability (HRV). Moreover, some methods using deep neural networks are computationally intensive due to high network complexity. In this article, a HRV measurement method is proposed based on an efficient 3-D convolutional neural network (3DCNN) model defined as Shuffle-rPPGNet. The basic idea of the proposed method is to extract more precise remote photoplethysmography (rPPG) signals from facial videos by this model and then calculate relevant indicators of HRV through the post-processed rPPG signals. Shuffle-rPPGNet uses a lightweight network structure named ShuffleNetV2 as a baseline to construct an efficient 3DCNN with additional parts including 3-D global context, 3-D channel shuffle, and up-sample blocks. The proposed method has been evaluated on two public datasets, i.e., UBFC-rPPG and PURE datasets. The results show that the proposed method has a better performance in HRV measurement compared to the state-of-the-art methods. Especially, the mean absolute errors (MAEs) of the average values of the normal-to-normal interval (NNI) sequence reach 2.35 and 6.62, respectively, on these two public datasets.
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Kuang et al. (2023) studied Heart rate variability measurement. Shuffle-rPPGNet vs. State-of-the-art methods was evaluated on Mean absolute errors (MAEs) of the average values of the normal-to-normal interval (NNI) sequence. Shuffle-rPPGNet achieved mean absolute errors of 2.35 and 6.62 for the average values of the normal-to-normal interval sequence on the UBFC-rPPG and PURE datasets, respectively.
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