Evidence map›Paper›PMID 41079692›Full record

ArticleFrontiers in digital health2025

Establishing a real-time biomarker-to-LLM interface: a modular pipeline for HRV signal acquisition, processing, and physiological state interpretation via generative AI.

Morris Gellisch, Boris Burr

Abstract read
In one paragraph

Article in Frontiers in digital health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

2 authors.

Morris GellischCenter for Medical Education, Ruhr University Bochum, Bochum, Germany.
Boris BurrDepartment of Neuroanatomy and Molecular Brain Research, Medical Faculty, Ruhr University Bochum, Bochum, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Large language models are capable of summarizing research, supporting clinical reasoning, and engaging in coherent conversations. However, their inputs are limited to user-generated text, which reflects subjective reports, delayed responses, and consciously filtered impressions. Integrating physiological signals provides a clear additional value, as it allows language models to consider real-time indicators of autonomic state alongside linguistic input, thereby enabling more adaptive and context-sensitive interactions in learning, decision-making, and healthcare. Therefore, we present a streamlined architecture for routing real-time heart rate variability data from a wearable sensor directly into a generative AI environment. Methods: Using a validated heart rate variability sensor, we decoded Bluetooth-transmitted R-R intervals via a custom Python script and derived core heart rate variability metrics (HR, RMSSD, SDNN, LF/HF ratio, pNN50) in real time. These values were published via REST and WebSocket endpoints through a FastAPI backend, making them continuously accessible to external applications-including OpenAI's GPT models. Results: A live data pipeline from autonomic input to conversational output. A language model that does not just talk back, but responds to real-time physiological shifts in natural language. In multiple proof-of-concept scenarios, ChatGPT accessed real-time HRV data, performed descriptive analyses, generated visualizations, and adapted its feedback in response to autonomic shifts induced by low and high cognitive load. Discussion: This system represents an early prototype of bioadaptive AI, in which physiological signals are incorporated as part of the model's input context.

Indexed as

affective computingbiofeedback-enhanced LLM interactionembodied AIphysiologically coupled language modelsstress detection via AI

Identifiers

PMID41079692
PMCPMC12512671

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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.