ArticleScientific reports2026
Interpretable depressive symptoms screening via statistical reasoning-augmented large language models using wearable and environmental data.
Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
Abstract
Early assessment of depressive symptoms is essential for scalable and personalized mental health care. We developed a hybrid clinical decision support system (CDSS) that combines interpretable logistic regression with fine-tuned large language models (LLMs) to classify depressive symptom status using wearable-derived behavior, clinical features, and environmental exposures. This study aimed to develop a hybrid clinical decision support system by fine‑tuning a GPT‑based large language model with odds ratio-derived statistical reasoning to classify depressive symptom status from wearable‑derived behavioral metrics, clinical characteristics, and environmental exposures. We compared the diagnostic accuracy, interpretability, and operational efficiency of this OR‑based fine‑tuned model against both traditional nomogram‑based statistical models and label‑supervised fine‑tuned LLM approaches. We further evaluated the incremental predictive value of wearable‑derived behavioral features beyond readily available demographic and clinical variables using matched feature-set comparisons. We analyzed data from 2437 adults at Chonnam National University Hospital, South Korea (August 2021-January 2023) who wore wrist actigraphy devices continuously for 7 days. Depressive symptoms were assessed using PHQ-9, with a score ≥ 10 indicating higher symptom burden. We extracted temporal behavioral features including morning steps (06:00-12:00), non-daylight steps, and vigorous physical activity minutes, stratified by weekday/weekend. Meteorological data (temperature, precipitation) were integrated with behavioral metrics. Multivariable logistic regression identified significant predictors with odds ratios (ORs). Five LLMs (GPT-4o, o3-mini, Claude 3.5-sonnet, Gemini 2.0-flash, Llama 3.3) were evaluated under zero-shot conditions. The GPT-based model was selected for supervised fine-tuning using two strategies: label-based (binary outcome only) and OR-based (embedding statistical reasoning into prompts). The system was deployed as a chatbot interface. Among 2437 participants (mean age 60.2 years, 67.5% female), 317 (13.0%) were classified as having elevated depressive symptoms (PHQ-9 ≥ 10). Prespecified incremental-value analyses using matched feature sets (clinical-only, wearable-only, and combined) demonstrated that wearable-derived behavioral features provided additive predictive value beyond demographic and clinical variables. In the OR-based fine-tuned LLM framework, balanced accuracy increased from 0.635 (clinical-only) to 0.735 (wearable-only) to 0.787 (combined) on weekdays, and from 0.589 to 0.647 to 0.680 on weekends. In the nomogram framework, adding wearable features to the clinical model significantly improved risk reclassification (continuous NRI: 0.469, p < 0.001 on weekdays; 0.372, p = 0.002 on weekends) and integrated discrimination improvement (IDI: 0.037, p < 0.001 on weekdays; 0.018, p = 0.002 on weekends). The combined OR-based fine-tuned model achieved 90.3% accuracy and 94.5% specificity on weekdays and 88.8% accuracy and 96.4% specificity on weekends, outperforming both nomogram and label-based fine-tuned models. This hybrid framework demonstrates that odds ratio-anchored fine-tuning can improve classification performance while preserving predictor traceability for PHQ-9-defined elevated depressive symptoms. Wearable-derived behavioral features provided statistically significant incremental predictive value beyond demographic and clinical variables, with larger gains observed on weekdays than on weekends. Prospective external validation across diverse populations is required before clinical implementation.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.