Evidence map›Paper›PMID 40460422›Full record

Observational studyJMIR formative research2025

Idiographic Lapse Prediction With State Space Modeling: Algorithm Development and Validation Study.

Eric Pulick, John Curtin, Yonatan Mintz

Abstract readValidation StudyObservational Study
In one paragraph

Observational study in JMIR formative research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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  3. Observational
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

3 authors.

Eric PulickDepartment of Industrial and Systems Engineering, College of Engineering, University of Wisconsin-Madison, Madison, WI, United States.ORCID 0009-0003-9636-6233
John CurtinDepartment of Psychology, College of Letters & Science, University of Wisconsin-Madison, Madison, WI, United States.ORCID 0000-0002-3286-938X
Yonatan MintzDepartment of Industrial and Systems Engineering, College of Engineering, University of Wisconsin-Madison, Madison, WI, United States.ORCID 0000-0002-0670-1794

Funding

Contextualized daily prediction of lapse risk in opioid use disorder by digital phenotypingR01DA047315 · NIDA · UNIVERSITY OF WISCONSIN-MADISON · PI CURTIN, JOHN J., SHAH, DHAVAN · 2019 to 2023
$3.4M
Dynamic, real-time prediction of alcohol use lapse using mHealth technologiesR01AA024391 · NIAAA · UNIVERSITY OF WISCONSIN-MADISON · PI CURTIN, JOHN J. · 2015 to 2019
$1.9M
National Science Foundation 2041428NIAAA NIH HHS R01 AA024391NIDA NIH HHS R01 DA047315
6 · The paper itself

Abstract

backgroundMany mental health conditions (eg, substance use or panic disorders) involve long-term patient assessment and treatment. Growing evidence suggests that the progression and presentation of these conditions may be highly individualized. Digital sensing and predictive modeling can augment scarce clinician resources to expand and personalize patient care. We discuss techniques to process patient data into risk predictions, for instance, the lapse risk for a patient with alcohol use disorder (AUD). Of particular interest are idiographic approaches that fit personalized models to each patient.

objectiveThis study bridges 2 active research areas in mental health: risk prediction and time-series idiographic modeling. Existing work in risk prediction has focused on machine learning (ML) classifier approaches, typically trained at the population level. In contrast, psychological explanatory modeling has relied on idiographic time-series techniques. We propose state space modeling, an idiographic time-series modeling framework, as an alternative to ML classifiers for patient risk prediction.

methodsWe used a 3-month observational study of participants (N=148) in early recovery from AUD. Using once-daily ecological momentary assessment (EMA), we trained idiographic state space models (SSMs) and compared their predictive performance to logistic regression and gradient-boosted ML classifiers. Performance was evaluated using the area under the receiver operating characteristic curve (AUROC) for 3 prediction tasks: same-day lapse, lapse within 3 days, and lapse within 7 days. To mimic real-world use, we evaluated changes in AUROC when models were given access to increasing amounts of a participant's EMA data (15, 30, 45, 60, and 75 days). We used Bayesian hierarchical modeling to compare SSMs to the benchmark ML techniques, specifically analyzing posterior estimates of mean model AUROC.

resultsPosterior estimates strongly suggested that SSMs had the best mean AUROC performance in all 3 prediction tasks with ≥30 days of participant EMA data. With 15 days of data, results varied by task. Median posterior probabilities that SSMs had the best performance with ≥30 days of participant data for same-day lapse, lapse within 3 days, and lapse within 7 days were 0.997 (IQR 0.877-0.999), 0.999 (IQR 0.992-0.999), and 0.998 (IQR 0.955-0.999), respectively. With 15 days of data, these median posterior probabilities were 0.732, <0.001, and <0.001, respectively.

conclusionsThe study findings suggest that SSMs may be a compelling alternative to traditional ML approaches for risk prediction. SSMs support idiographic model fitting, even for rare outcomes, and can offer better predictive performance than existing ML approaches. Further, SSMs estimate a model for a patient's time-series behavior, making them ideal for stepping beyond risk prediction to frameworks for optimal treatment selection (eg, administered using a digital therapeutic platform). Although AUD was used as a case study, this SSM framework can be readily applied to risk prediction tasks for other mental health conditions.

Indexed as

AlcoholismAlgorithmsAdultEcological Momentary AssessmentFemaleHumansMachine LearningMaleMiddle AgedRisk Assessmentalcohol use disorderdigital healthdigital therapeuticsmental healthmHealthmobile healthpersonalized medicinesubstance use disorder

Identifiers

PMID40460422
PMCPMC12174888

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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.