High Dimensional Computing Gesture Recognition (HDC-GCog)

January 15, 2026 updated by: University Hospital, Grenoble

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.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

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.

Study Type

Interventional

Enrollment (Estimated)

10

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

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).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: HDC-GCog
High Dimensional Computing Gesture Recognition
Surface electromyography records

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
3 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
3 hours
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 hours
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
3 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Salerno, A., Barraud, S. (2024). Evaluation and implementation of High-Dimensionnal Computing for gesture recognition using sEMG signals. Proceedings of the 2024 International Conference on Control, Automation and Diagnosis (ICCAD)
  • Salerno, A., Barraud, S. (2025). Novel and efficient hyperdimensional encoding of surface electromyography signals for hand gesture recognition, Biosensor 2025.
  • A. Sultana, F. Ahmed, Md. S. Alam, A systematic review on surface electromyography-based classification system for identifying hand and finger movements, Healthcare Analytics, 3, 100126, 2022, DOI:10.1016/j.health.2022.100126
  • Sgambato, B. G., Castellano, G. (2022). Performance comparison of different classifiers applied to gesture recognition from sEMG signals. In Bastos-Filho, T. F., de Oliveira Caldeira, E. M., Frizera-Neto, A. (Eds.), XXVII Brazilian Congress on Biomedical Engineering. CBEB 2020. IFMBE Proceedings, Vol. 83. Springer, Cham

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

January 15, 2026

Primary Completion (Estimated)

April 1, 2026

Study Completion (Estimated)

June 1, 2026

Study Registration Dates

First Submitted

August 19, 2025

First Submitted That Met QC Criteria

August 26, 2025

First Posted (Estimated)

September 4, 2025

Study Record Updates

Last Update Posted (Actual)

January 20, 2026

Last Update Submitted That Met QC Criteria

January 15, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Healthy Volunteers

Clinical Trials on HDC-GCog

Subscribe