# Within-person prediction of depressive symptom change using year-long Screenome data and CES-D assessments

Source: [Within-person prediction of depressive symptom change using year-long Screenome data and CES-D assessments](<https://www.sota2.com/research/paper/69f03f1855a3c32af89fa09a>)

Collection index: [llms.txt](<https://www.sota2.com/research/llms.txt>)

Data updated: 2026-04-29T05:00:05.003Z

Authors: Merve Cerit, Andrea Mock, Vryan Almanon Feliciano, Thomas N. Robinson, Byron Reeves, Nilam Ram, Nick Haber

Published: 2026-04-24T22:00:36.000Z

## Abstract

Predicting whether an individual's depressive symptoms will worsen, remain stable, or improve over the coming weeks can enable earlier and more targeted care, yet prospective within-person trajectory prediction remains largely unaddressed in digital phenotyping. We combine fortnightly CES-D assessments with over 100 million screenshots captured every five seconds via the Stanford Screenomics platform from 96 adults followed for approximately one year (M = 20.9, SD = 3.9 assessments per participant, 2,002 total observations). We frame prediction as a within-person classification task: whether symptoms will worsen, remain stable, or improve over the subsequent fortnight, operationalized in three ways to capture clinically meaningful change. Under temporal holdout, XGBoost achieves an AUC of 0.906 for crossings of established CES-D severity bands and 0.755 for change relative to each participant's own within-person variability, generalizing to unseen individuals (AUC = 0.821). Each person's typical symptom level was the only statistically significant predictor above the most recent CES-D score; without it, the most consequential worsening transitions go undetected. Screenome-derived behavioral features revealed prodromal patterns of worsening, including escalating social media use, fragmented device engagement, and changes in overnight activity, with substantial individual heterogeneity. These findings establish a proof-of-concept foundation for monitoring systems that could identify individuals approaching clinical deterioration before symptoms reach a crisis point.

## Recorded benchmark results

A research result applies to its stated dataset, split, metric and evaluation configuration. Compare like-for-like settings, preserve the metric's unit and direction, and distinguish paper-reported results from independent reproduction. The best result recorded here is not a claim of exhaustive, current global coverage.

- [Symptom trajectory classification on CES-D personalized threshold label (test)](<https://www.sota2.com/research/sota/symptom-trajectory-classification-on-ces-d-personalized-threshold-label-test.md>): Symptom trajectory classification; CES-D personalized threshold label N = 411; 10% worsening, 12% improving, 78% stable (test); Balanced Accuracy: 62.

- [Within-person depression trajectory classification on CES-D severity crossing label N = 411 (test)](<https://www.sota2.com/research/sota/within-person-depression-trajectory-classification-on-ces-d-severity-crossing-label-n-411-test.md>): Within-person depression trajectory classification; CES-D severity crossing label N = 411 (test); Balanced Accuracy: 84.2.

## Original sources and implementation

[Original paper](<https://arxiv.org/abs/2604.23040>)

[PDF](<https://arxiv.org/pdf/2604.23040.pdf>)
