# Data-driven design guide for vibrotactile display layouts by continuous mapping

**Authors:** Max vom Stein, Maximilian Hoppe, Niclas Rieger, Kai-Dietrich Wolf

PMC · DOI: 10.1038/s41598-025-25416-3 · Scientific Reports · 2025-11-12

## TL;DR

This paper provides data-driven guidelines for designing vibrotactile displays by analyzing spatial sensitivity across different body areas.

## Contribution

The study introduces a novel automated framework using Bayesian adaptive estimation to generate continuous psychometric functions for vibrotactile display design.

## Key findings

- Existing vibrotactile datasets are scattered and inconsistent.
- There is a pronounced horizontal anisotropy near the body midline.
- A marked sensitivity gradient is observed along the lower back.

## Abstract

Tactile displays are emerging as vital components across fields such as medical technology, assistive technology, virtual reality, infotech and gaming, yet their design remains hampered by an inadequate psychophysical foundation. In this work, we critically assess current tactile display research, uncovering gaps in spatial acuity data, and introduce robust, data-driven layout guidelines for vibrotactile displays (VTDs). We collected high‐resolution vibrotactile data from 33 participants across five large‐area body sites using a novel, fully automated experimental framework that employs Bayesian adaptive parameter estimation to generate continuous psychometric functions. This approach allows us to derive thresholds at any recognition rate, thereby overcoming the limitations of traditional, discrete measures. Our findings reveal that existing datasets are scattered and inconsistent, demonstrate a pronounced horizontal anisotropy especially near the body midline and expose a marked sensitivity gradient along the lower back. These insights provide a validated psychophysical basis for VTD development, paving the way for more reliable, user‐centric designs in next‐generation tactile interfaces.

The online version contains supplementary material available at 10.1038/s41598-025-25416-3.

## Full-text entities

- **Genes:** STS (steroid sulfatase) [NCBI Gene 412] {aka ARSC, ARSC1, ASC, ES, SSDD, XLI}, PLAG1 (PLAG1 zinc finger) [NCBI Gene 5324] {aka PSA, SGPA, SRS4, ZNF912}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, SV2A (synaptic vesicle glycoprotein 2A) [NCBI Gene 9900] {aka DEE113, SLC22B1, SV2}
- **Diseases:** diabetes (MESH:D003920), phantom sensations (MESH:D010591), RDD (MESH:D010468), cognitive disorders (MESH:D003072), dyslexia (MESH:D004410), learning disabilities (MESH:D007859), central nervous system disorders (MESH:D002493), dermatitis (MESH:D003872), carpal tunnel syndrome (MESH:D002349), fatigue (MESH:D005221), attention deficits (MESH:D001289)
- **Chemicals:** MPFh (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12612159/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12612159/full.md

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Source: https://tomesphere.com/paper/PMC12612159