NCT07155460

Brief Summary

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.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for not_applicable healthy-volunteers

Timeline
1mo left

Started Jan 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress82%
Jan 2026Jun 2026

First Submitted

Initial submission to the registry

August 19, 2025

Completed
16 days until next milestone

First Posted

Study publicly available on registry

September 4, 2025

Completed
4 months until next milestone

Study Start

First participant enrolled

January 15, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Expected
Last Updated

January 20, 2026

Status Verified

January 1, 2026

Enrollment Period

3 months

First QC Date

August 19, 2025

Last Update Submit

January 15, 2026

Conditions

Keywords

Surface ElectroMyoGraphy (sEMG)K-Nearest Neighbor classification algorithm (KNN)Nearest Centroids classification algorithm (NC)Random Forest classification algorithm (RF)Stochastic Gradient Descent classification algorithm (SGD)High Dimensional Computing (HDC)

Outcome Measures

Primary Outcomes (1)

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

    Calculation of gesture recognition rate expressed in percentage of gesture recognition

    3 hours

Secondary Outcomes (3)

  • Real-time gesture recognition (latency <100ms)

    3 hours

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

    3 hours

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

    3 hours

Study Arms (1)

HDC-GCog

EXPERIMENTAL

High Dimensional Computing Gesture Recognition

Device: HDC-GCog

Interventions

HDC-GCogDEVICE

Surface electromyography records

HDC-GCog

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Clinatec Cea/Chuga

Grenoble, 38054, France

Location

Related Publications (4)

  • 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)

    BACKGROUND
  • Salerno, A., Barraud, S. (2025). Novel and efficient hyperdimensional encoding of surface electromyography signals for hand gesture recognition, Biosensor 2025.

    BACKGROUND
  • 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

    BACKGROUND
  • 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

    BACKGROUND

Central Study Contacts

Daniel ANGLADE, MD, PhD

CONTACT

Caroline SANDRE-BALLESTER, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Model Details: The Primary Purpose of this clinical trial is to test a prototype device for feasibility and not health outcomes.This study is conducted to confirm the design and operating specifications of a device before beginning a full clinical trial.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 19, 2025

First Posted

September 4, 2025

Study Start

January 15, 2026

Primary Completion

April 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

January 20, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations