Evidence map›Paper›PMID 38783001›Full record

ArticleNPJ digital medicine2024

Early adverse physiological event detection using commercial wearables: challenges and opportunities.

Jesse Phipps, Bryant Passage, Kaan Sel, Jonathan Martinez, Milad Saadat, Teddy Koker, Natalie Damaso, Shakti Davis, Jeffrey Palmer, Kajal Claypool and 3 more

Abstract read
In one paragraph

Article in NPJ digital medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Wearable penile devices: the TechRing.Translational andrology and urology · 2025
    Article
  6. Review
  7. Article
  8. Review
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

13 authors.

Jesse Phipps *Department of Computer Science and Engineering, Texas A&M University, College Station, TX, USA.
Bryant Passage *Department of Computer Science and Engineering, Texas A&M University, College Station, TX, USA.ORCID http://orcid.org/0009-0003-7378-4037
Kaan SelLaboratory for Information and Decision Systems, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-3862-8616
Jonathan MartinezDepartment of Computer Science and Engineering, Texas A&M University, College Station, TX, USA.
Milad SaadatDepartment of Electrical and Computer Engineering, Texas A&M University, College Station, TX, USA.
Teddy KokerLincoln Laboratory, Massachusetts Institute of Technology, Lexington, MA, USA.ORCID http://orcid.org/0000-0001-8861-9788
Natalie DamasoLincoln Laboratory, Massachusetts Institute of Technology, Lexington, MA, USA.
Shakti DavisLincoln Laboratory, Massachusetts Institute of Technology, Lexington, MA, USA.ORCID http://orcid.org/0000-0001-5987-5918
Jeffrey PalmerLincoln Laboratory, Massachusetts Institute of Technology, Lexington, MA, USA.ORCID http://orcid.org/0000-0001-8919-1285
Kajal ClaypoolLincoln Laboratory, Massachusetts Institute of Technology, Lexington, MA, USA.
Christopher KileyDefense Threat Reduction Agency, Fort Belvoir, VA, USA.
Roderic I PettigrewSchool of Engineering Medicine, Texas A&M University, Houston, TX, USA.ORCID http://orcid.org/0000-0003-0320-8600
Roozbeh JafariDepartment of Computer Science and Engineering, Texas A&M University, College Station, TX, USA. roozbeh.jafari@ll.mit.edu.ORCID http://orcid.org/0000-0002-6358-0458

Funding

MIT | Lincoln Laboratory, Massachusetts Institute of Technology (Lincoln Laboratory) 7000544217MIT | Lincoln Laboratory, Massachusetts Institute of Technology (Lincoln Laboratory) 7100544217United States Department of Defense | Defense Threat Reduction Agency (DTRA) HDTRA1240085
6 · The paper itself

Abstract

Data from commercial off-the-shelf (COTS) wearables leveraged with machine learning algorithms provide an unprecedented potential for the early detection of adverse physiological events. However, several challenges inhibit this potential, including (1) heterogeneity among and within participants that make scaling detection algorithms to a general population less precise, (2) confounders that lead to incorrect assumptions regarding a participant's healthy state, (3) noise in the data at the sensor level that limits the sensitivity of detection algorithms, and (4) imprecision in self-reported labels that misrepresent the true data values associated with a given physiological event. The goal of this study was two-fold: (1) to characterize the performance of such algorithms in the presence of these challenges and provide insights to researchers on limitations and opportunities, and (2) to subsequently devise algorithms to address each challenge and offer insights on future opportunities for advancement. Our proposed algorithms include techniques that build on determining suitable baselines for each participant to capture important physiological changes and label correction techniques as it pertains to participant-reported identifiers. Our work is validated on potentially one of the largest datasets available, obtained with 8000+ participants and 1.3+ million hours of wearable data captured from Oura smart rings. Leveraging this extensive dataset, we achieve pre-symptomatic detection of COVID-19 with a performance receiver operator characteristic (ROC) area under the curve (AUC) of 0.725 without correction techniques, 0.739 with baseline correction, 0.740 with baseline correction and label correction on the training set, and 0.777 with baseline correction and label correction on both the training and the test set. Using the same respective paradigms, we achieve ROC AUCs of 0.919, 0.938, 0.943 and 0.994 for the detection of self-reported fever, and 0.574, 0.611, 0.601, and 0.635 for detection of self-reported shortness of breath. These techniques offer improvements across almost all metrics and events, including PR AUC, sensitivity at 75% specificity, and precision at 75% recall. The ring allows continuous monitoring for detection of event onset, and we further demonstrate an improvement in the early detection of COVID-19 from an average of 3.5 days to an average of 4.1 days before a reported positive test result.

Identifiers

PMID38783001
PMCPMC11116498

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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.