Foundation models have recently extended beyond natural language and vision to timeseries domains, including physiological signals. However, progress in electrodermal activity (EDA) modeling is hindered by the absence of large-scale, curated, and openly accessible datasets. EDA reflects sympathetic nervous system activity and is widely used to infer cognitive load, stress, and engagement. Yet very few wearable devices provide continuous, unobtrusive sensing, and the only large-scale archive to date is proprietary. To address this gap, we compile EDAMAME, a collection of EDA traces from 24 public datasets, comprising more than 25,000 hours from 634 users. Using this resource, we train UME, the first dedicated foundation model for EDA. In eight out of ten scenarios, UME outperforms baselines and matches generalist timeseries foundation models while using 20x fewer computational resources. Our findings, however, also highlight the intrinsic challenges of EDA modeling, motivating further research to unlock its full potential. All datasets, model weights, and code are released to support further research.
Figures & tables
Foundation model
train data
Ref.
Signal(s)
Params.
Avail.
Dataset(s)
Data type
Hours (k)
Users
Avail.
Clinical data
[ 72 ]
PPG
∼ 30 - 150 M
Open source
VitalDB [ 57 ]
Clinical
∼ 17
∼ 6k
✓
MIMIC-III [ 51 ]
Clinical
∼ 20
∼ 6k
✓
MESA [ 94 ]
Clinical
∼ 20
∼ 2k
✓
[ 32 ]
PPG
∼ 1-8 M
Code only
[ 32 ]
Clinical
∼ 300
∼ 29k
✓
Table 1: Overview of selected foundation models for physiological data and the datasets used to train them.
Dataset Name
Duration (h)
# Users
Scenario
Environment
APSync [ 39 ]
168
27
Real-world Stress
Wild
BIG IDEAS [ 11 ]
2607
16
Daily Living
Wild
BiHeartS [ 2 ]
2911
11
Sleep Monitoring
Wild
DREAMT [ 92 ]
882
100
Daily Living
Wild
Dynamics in the workplace [ 61 ]
1813
42
Workplace Analysis
Wild
EmpaticaE4Stress [ 20 ]
5
29
Stress/Emotion Induction
Lab
Table 2: Summary of the datasets included in the training split. The collection spans diverse physiological scenarios and environments.
Figure 1: Example of six EDA signals (randomly drawn). Each signal is from a different dataset, each for one of the six scenarios.
Figure 2: Ridgeline plot with distribution of EDA values from each dataset. The colors represent the six scenarios each dataset was collected in. The plot has been truncated, for visualization’s sake, in the range 0−2.5μS . The original range was 0−40μS (the E4’s max theoretical value is 100μS ).
Figure 3: Number of users and data per user across the EDAMAME collection of datasets. Marker size is proportional to the size of the dataset (in terms of hours of EDA data).
Figure 4: Overview of the train and downstream evaluation process we used for the UME foundation model. For reference, we report a sketch of the EfficientNet architecture, which we use as backbone for UME.
Dataset
Binary Tasks
APSync
Low/High Engagement
HeartS
Sleep/Wake
USILaughs
Cog. Load/Relaxation
WESAD
High/Low Arousal, High/Low Valence (self-report)
Nurses’ Stress
Low/High Stress
DREAMT
Sleep/Wake
Table 3: Summary of Datasets and Associated Binary Tasks
Figure 5: Pairplot with comparison between UME and the baseline features for the selected downstream tasks. Colors represent the two validation methods, TA and LOPO.
Dummy
Handcrafted (HC)
Generalist Foundation
Ours
Dataset
Binary Task
Gen.
EDA-spec.
Mantis
MOMENT
Chronos
UME
Balanced accuracy standarderror
Time-Aware cross-validation (TA)
APSYNC
Low/High engagement
.45.20
.80.10
.80.10
.86.07
.4716
.61.20
.89.11
Dreamt
Deep Sleep/REM
.48.02
.55.05
.59.04
.64.03
.6501
.6302
.63.05
Dreamt
Sleep/Wake
.50.01
.65.02
.69.01
.73.01
.6901
.7301
.70.01
Table 4: Results of binary classification experiments across datasets and tasks, in terms of balanced accuracy standarderror . Reported are results for both TA and LOPO cross-validation methods. Acronyms: Gen. HC stands for generic handcrafted features ; EDA HC stands for EDA-specific handcrafted features .
Figure 6: Computational complexity analysis. (a) Average (across 20 samples) per-sample computation time for a 60-second window of EDA data for all three components (phasic, tonic, and original signal). Note: hc stands for handcrafted ; generic handcrafted features are not shown as they require negligible computation time. (b) GFLOPs for the different foundation models.
Appendix figures & tables12 assets
Supplementary material from the paper’s appendix.
Appendix
Dataset Name
License
BiHeartS [ 2 ]
✓- data share agreement
BIG IDEAS [ 11 ]
✓- with original license (ODC-BY 1)
Dynamics in the workplace [ 61 ]
✓- data share agreement
EmpaticaE4Stress [ 20 ]
✓- (CCBY 4) with original license
EPM-E4 [ 37 ]
✓- (CCBY 4) with original license
LAUREATE [ 55 ]
✓- data share agreement
Appendix
Table A.1: Summary of datasets with their corresponding data-sharing agreements. This table includes all datasets, including citations and the "Reshareable" column, for inclusion in the appendix.
Model / Feature Set
Model Size
Feature Dim. ( d )
Handcrafted Methods
Generic HC
N/A
12
EDA-specific HC
N/A
45
Generalist Foundation Models
Mantis [ 35 ]
∼ 8 M
768
Chronos [ 9 ]
∼ 200 M
1536
Appendix
Table A.2: Overview of the models and feature sets used in the experimental evaluation. We report the model size (number of trainable parameters) and the dimensionality of the feature space ( d ) used for linear probing.
Feature
Mathematical Notation or Formula
Feature Set(s)
Time-domain
Mean
N1∑i=1Nxi
Generic & EDA-specific
Minimum
min(x1,x2,…,xN)
Generic & EDA-specific
Maximum
max(x1,x2,…,xN)
Generic & EDA-specific
Standard Deviation
N−11∑i=1N(xi−xˉ)2
Generic & EDA-specific
Dynamic Range
max(x1,x2,…,xN)−min(x1,x2,…,xN)
EDA-specific only
Appendix
Table A.3: Mathematical formulations for the 15 base hand-crafted features extracted from EDA time series signals ( x ) of length N . All features are computed independently for the tonic, phasic, and original EDA components. The "Feature Set(s)" column indicates whether the feature was used in the Generic baseline (12 total features) or the EDA-specific baseline (45 total features).
Hyperparameter
Values
Regularization strength ( C )
0.01, 0.1, 1, 10
Solver
lbfgs, liblinear
Penalty
L2
Max iterations
10000
Class weight
balanced
Appendix
Table A.4: Hyperparameter Grid for Logistic Regression
Table A.5: Summary of Electrodermal Activity (EDA) Data Augmentations used to train the UME foundation model. The table details both EDA-specific transforms designed to isolate physiological components or simulate artifacts, and generic time series transforms. The set is the same proposed by Matton et al. [64] .
Figure B.1: Example of EDA signal reconstruction using MAE.
Figure B.2: Validation loss during training for different configurations of masking and masking weight.
Figure B.3:
Figure 19
Extractor
CPU Time (mean) [ms]
CPU Time (SE) [ms]
MOMENT (128M)
4823.53
161.11
Chronos (28M)
721.34
28.91
Mantis (8M)
350.23
39.06
UME (1M)
184.56
3.12
EDA-specific hc
35.39
1.40
generic hc
0.09
0.01
Appendix
Table C.1: CPU Performance Comparison of Extractors
Dataset
Binary Task
Model
Metrics
Balanced Acc.
MCC
F1
Dreamt
Deep Sleep/REM
Dummy
0.73±0.05
−0.01±0.01
0.16±0.06
Gen. HC
0.64±0.07
0.00±0.03
0.10±0.06
EDA-spec. HC
0.54±0.05
0.02±0.03
0.19±0.07
Mantis
0.59±0.05
0.02±0.04
0.18±0.07
MOMENT
0.64±0.03
0.06±0.03
0.21±0.07
Appendix
Table C.2: Results of binary classification experiments, using the Leave One Participant Out (LOPO) cross-validation. Results shown as metric ± standard error .
Dataset
Binary Task
Model
Metrics
Balanced Acc.
MCC
F1
Dreamt
Deep Sleep/REM
Dummy
0.51±0.01
0.01±0.01
0.20±0.06
Gen. HC
0.55±0.10
0.09±0.20
0.28±0.13
EDA-spec. HC
0.59±0.08
0.16±0.13
0.37±0.13
Mantis
0.64±0.07
0.22±0.11
0.40±0.12
MOMENT
0.65±0.04
0.24±0.07
0.42±0.10
Appendix
Table C.3: Results of binary classification experiments for Time-Aware (TA) cross-validation. Results shown as metric ± standard error . Experiments whose result is reported as OoM (out of memory) means that the required memory size for the embeddings computation exceeded the computational resources available.
Foundation models (FMs) are increasingly being developed for general time series and physiological signals, yet their transferability to downstream physiological tasks remains poorly understood. This question is particularly challenging for electromyography (EMG), where signal distributions vary substantially across users, sensing configurations, acquisition hardware, and downstream tasks. We introduce EMG-FM-Bench, a systematic benchmark for studying foundation-model transfer and adaptation on EMG. EMG-FM-Bench unifies 20 public datasets with over 1 million EMG segments and evaluates nine pretrained foundation models across four questions: how pretrained models perform when frozen or fully fine-tuned, how much pretraining helps compared with training the same model from scratch, how well models generalize to new users with limited labeled data, and how performance changes across different EMG tasks. Across the benchmark, linear probing provides useful information about pretrained representations, but full fine-tuning can substantially change downstream EMG performance. Comparing each pretrained model with the same model trained from scratch shows that the benefit of pretraining varies substantially across models and is not universal. Performance decreases when models are evaluated on new users, while five-shot adaptation improves macro-F1 in 70.2% of evaluated model-dataset combinations but recovers only part of the lost performance. Model performance is highly consistent between upper- and lower-limb classification and remains strongly correlated with continuous EMG-to-text decoding. Together, these results provide a systematic view of when pretrained time-series models transfer effectively to EMG and how their performance depends on fine-tuning, user variation, and downstream task.
Tianhao Wu, Jiawei Yu, Xiangdong Hu +8
University of Georgia · University of Oklahoma · University of Massachusetts Amherst
Wrist electrodermal activity (EDA) differs in amplitude from one person to the next, so affect-recognition models normalize their input before classification. Studies that test such models on held-out subjects seldom report where the normalization statistics come from, yet statistics computed from the held-out subject's own recording give the model information that a device does not have when it is first worn. We asked how this choice alters the measured benefit of pretraining. A compact convolutional network, SAFE-EDA, was pretrained on expert artifact annotations from 43 subjects and compared with the same network trained from scratch on the Wearable Stress and Affect Detection (WESAD) dataset (15 subjects, leave-one-subject-out), with two normalization sources crossed with four window hops. When the statistics came only from training subjects, pretraining raised macro-F1 by 0.078 to 0.227; when they came from the held-out user's full recording, the gain fell to between 0.020 and 0.050 and was no longer significant. Artifact supervision was far more useful than self-supervised pretraining on the same recordings (0.078 versus 0.008). Across 13 configurations in two datasets, the pretrained network was better in 12, but on the second dataset (26 subjects) per-user normalization increased the gain instead of reducing it, so the interaction depends on the data. Only five of 50 published WESAD studies state which data were used for normalization. Reporting this choice is necessary to separate first-use performance from performance after calibration.
Haochen Chai, Xinbi Luo, Zining Liu +1
College of Medicine and Biological Information Engineering, Northeastern University, Shenyang, China
Foundation models (FMs) promise to extract unified representations that generalize across downstream tasks. They have emerged across fields, including electroencephalography (EEG), but it is less clear how effective they are in this particular field. Published evaluations differ in datasets, in the EEG-specific preprocessing that might influence reported results, and in the reported metrics, frequently obscuring the clinical relevance in EEG. We introduce NeuroAtlas, the largest EEG benchmark to date: 42 datasets and 260k hours covering clinical EEG (epilepsy, sleep medicine, brain age estimation) and brain-computer interfaces, and include multiple datasets per task along with bespoke clinical evaluation metrics. Besides evaluating EEG-FMs with respect to supervised baselines, we present results from generic time-series FMs. We report three findings. First, EEG-specific FMs do not consistently outperform time-series FMs, which have neither EEG-focused architectures nor been pretrained on EEG. Second, standard machine learning metrics are insufficient to assess clinical utility: thus, we thoroughly evaluate more appropriate measures such as the quality of event-level decision-making, hypnogram-derived features, and the brain-age gap in the domains of epilepsy, sleep, and brain age, respectively. Third, model rankings and performance can vary substantially within domains. We conclude that pretrained models perform largely on par, with only narrow advantages for a few, and that current models do not yet deliver on the promise of an out-of-the-box unified EEG model. NeuroAtlas exposes this gap and provides the datasets and metrics for the next generation of unified EEG FMs.
Konstantinos Kontras, Trui Osselaer, Stylianos G. Mouslech +12