Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07155460

High Dimensional Computing Gesture Recognition

The primary objective of this study is the Improvement of gesture recognition and classification accuracy through the use of the HDC algorithm compared to other classification methods (KNN, RF, SGD, NC). The recognition rate will be expressed by the sensitivity and specificity of gesture recognition. The model will be trained on a portion of the dataset and tested on the remaining part to avoid any bias.

The secondaries objectives are the :

* Improvement of gesture recognition accuracy with our HDC algorithm compared to other standard models. * Calculation of gesture recognition rates depending on the number of electrodes used and their position. * Subject's assessment of device comfort rated above 6 on a 10-level visual analog scale. * Subject's assessment of ease of performing the gesture rated above 6 on a 10-level visual analog scale.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

This project aims to work on gesture recognition based on surface electromyography (EMG) recorded on the forearm. The CEA is currently developing a learning algorithm based on hyperdimensional computing designed to improve the accuracy and latency of gesture recognition. Unlike conventional computing methods, the developed approach relies on (pseudo) random hypervectors. This brings significant advantages: a simple algorithm with a well-defined set of arithmetic operations, extremely robust to noise and errors, with fast, one-pass learning that could ultimately benefit from a memory-centric architecture with a high degree of parallelism.

This research could lead to multiple applications, such as video gaming or the metaverse, but also strongly interests the healthcare field, for example in robotic prostheses, tele-surgery applications, or simply medical training using virtual reality applications.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy, right-handed volunteer subject,
  • Male or female,
  • Age between 18 and 65 years inclusive,
  • BMI < 30 kg/m²,
  • Minimum forearm circumference less than 15 cm,
  • Subjects agree to shaving or trimming of the right forearm.
  • Agreement to the study non-opposition form,
  • Subject affiliated with a social security scheme,
  • Registered in the national database of individuals who participate in biomedical research

Exclusion criteria

  • Subject with a known motor problem in the right forearm and hand,
  • Known allergy or intolerance to one of the electrode components,
  • Presence of a lesion in the measurement area,
  • Subject with an active medical implant (e.g. pacemaker, cochlear implant, etc.),
  • Subject wearing a contraceptive implant in the measurement area.
  • Female subject aware of pregnancy at the time of measurement,
  • Subject refusing to shave or trim the area or whose body hair precludes shaving or trimming the area,
  • Presence of a pathology likely to alter the EMG.
  • Persons referred to in Articles L1121-5 to L1121-8 of the Public Health Code (corresponds to all protected persons: pregnant women, women in labour, breastfeeding mothers, persons deprived of their liberty by judicial or administrative decision, persons receiving psychiatric care under Articles L. 3212-1 and L. 3213-1 who do not fall under the provisions of Article L. 1121-8, persons admitted to a health or social establishment for purposes other than research, minors, persons subject to a legal protection measure or unable to express their consent).

Treatment and study plan

HDC-GCog

Device

Surface electromyography records

Primary outcomes

  1. Gesture recognition rate using a device composed of 32 high-frequency surface EMG electrodes

    Time frame: 3 hours

    Calculation of gesture recognition rate expressed in percentage of gesture recognition

Secondary outcomes

  1. Real-time gesture recognition (latency <100ms)

    Time frame: 3 hours

    Measurement of the improved gesture recognition rate with our HDC algorithm compared to other common models

  2. Validation of the positioning and number of electrodes used for EMG acquisition in order to maximize gesture recognition rates

    Time frame: 3 hours

    Calculation of gesture recognition rates based on the number of electrodes used and their position

  3. Analysis of the subject's feedback regarding the ease of performing the gestures (in the form of a questionnaire)

    Time frame: 3 hours

    Subject's rating of device comfort as greater than 6 on a 10-point visual analogue scale

Study contacts

Contact information is provided by the study sponsor or research team.

Caroline SANDRE-BALLESTER, PhD

CONTACT

[email protected]

04 38 78 28 51

Daniel ANGLADE, MD, PhD

CONTACT

[email protected]

04 38 78 17 46

Sponsors and collaborators

Lead sponsor

University Hospital, Grenoble

Other

Collaborators

  • CLINATEC
  • Commissariat à l'Energie Atomique (CEA) Grenoble

Registry information

Acronym: HDC-GCog

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Sep 4, 2025
Registry last updated
Jan 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.