Evidence map›Paper›PMID 42463554›Full record

ArticleBehavior research methods2026

Standardized synchronization and validation pipeline for physiological biomarkers across multiple devices.

Selin Acan, Clàudia Valenzuela-Pascual, Filippo Corponi, Bryan M Li, Diego Hidalgo-Mazzei, Dick Thijssen, Gideon Vos, Stefan Bogaerts, Erno Hermans, Mitra Baratchi and 2 more

Abstract read
In one paragraph

Article in Behavior research methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Selin Acan *Donders Institute for Brain, Cognition, and Behaviour, Radboud University, Kapittelweg 29, 6525 EN, Nijmegen, The Netherlands. selin.acan@ru.nl.ORCID https://orcid.org/0009-0007-1223-7178
Clàudia Valenzuela-Pascual *Department of Psychiatry and Psychology, Hospital Clínic de Barcelona, Barcelona, Catalonia, Spain.
Filippo CorponiSchool of Informatics, University of Edinburgh, Dugald Stewart Building, 10 Crichton St, Edinburgh, EH8 9AB, UK.
Bryan M LiSchool of Informatics, University of Edinburgh, Dugald Stewart Building, 10 Crichton St, Edinburgh, EH8 9AB, UK.
Diego Hidalgo-MazzeiDepartment of Psychiatry and Psychology, Hospital Clínic de Barcelona, Barcelona, Catalonia, Spain.
Dick ThijssenDepartment of Medical Biosciences, Radboud University Medical Center (Radboudumc), Geert Grooteplein 28, 6525, GA, Nijmegen, The Netherlands.
Gideon VosJames Cook University, 18 Joan St, Mornington, QLD, 4825, Australia.
Stefan BogaertsScience and Treatment Innovation, Fivoor, 3014 AE, Rotterdam, The Netherlands.
Erno HermansDonders Institute for Brain, Cognition, and Behaviour, Radboud University, Kapittelweg 29, 6525 EN, Nijmegen, The Netherlands.
Mitra BaratchiLeiden University, Rapenburg 70, 2311 EZ, Leiden, The Netherlands.
Martin DreslerDonders Institute for Brain, Cognition, and Behaviour, Radboud University, Kapittelweg 29, 6525 EN, Nijmegen, The Netherlands.
Peter De LooffBehavioural Science Institute, Radboud University, 6525 GD, Nijmegen, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wearable devices enable continuous monitoring of physiological signals in real-world settings, yet a standardized approach for synchronizing signals across devices remains lacking. We present a generalizable, user-friendly pipeline that enables synchronization of any two devices capturing the same physiological signals, without requiring coding expertise. The pipeline performs resampling, dynamic time warping alignment, amplitude correction via wavelet transforms, and signal standardization, followed by agreement analyses at both waveform and feature levels. To demonstrate its validity, we applied the pipeline to a case study comparing two research-grade devices, the Empatica E4 and the EmbracePlus, using up to 48 h of concurrent recordings from 31 participants. We compared signal-level agreement across waveform similarity, amplitude distribution, spectral content, and extracted features between the two research-grade devices to determine their interchangeability for longitudinal and multi-site studies. Specifically, we aimed to determine how well these devices agree at the signal level and to identify which physiological signals are most robust to device-specific variability. Four signals were examined (blood volume pulse, electrodermal activity, accelerometry, and temperature) using NeuroKit2 and FLIRT. We computed Pearson and concordance correlation coefficients, Bland-Altman bias and limits of agreement, root mean squared error (RMSE), KL divergence, spectral coherence, mutual information, and feature-level correlations using NeuroKit2 and FLIRT. Results showed near-perfect agreement for BVP (concordance correlation coefficient (CCC) ≈ 1.0; coherence ≤ 0.98) and phasic EDA features (CCC 0.85-0.99), whereas tonic EDA, temperature, and accelerometry exhibited systematic amplitude biases (EmbracePlus lower) and axis-dependent variability (Z-axis CCC = 0.85; Y-axis = 0.19). Relative signal dynamics were preserved across devices despite differences in absolute levels. These findings support integration of BVP, EDA, and TEMP data across E4 and EmbracePlus with proper preprocessing, while highlighting calibration needs for movement signals.

Indexed as

Signal Processing, Computer-AssistedWearable Electronic DevicesAccelerometryBiomarkersGalvanic Skin ResponseHumansMonitoring, PhysiologicReproducibility of ResultsBiomarkersAlignmentCross-platform interoperabilityEmbracePlusEmpatica E4Statistical analysisSynchronizationWearables

Identifiers

PMID42463554
PMCPMC13375695

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.