Study of Home Use of the Jaco Robotic Manipulation Device by Individuals With Tetraplegia

NCT07680361 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2026-07-02

No results posted yet for this study

Summary

For all individuals deprived of active and functional motor control of the upper limbs to perform grasping tasks, the restoration of a grasping function becomes a priority.

The population concerned is mainly represented by so-called functional tetraplegic individuals.

In this context, new technologies, and more particularly robotics, appear as a solution for substitution and compensation of motor impairment of the upper limb.

Assistive robotic manipulation today relies on three robot concepts that have led to commercially available products.

It is the robotic arms mounted on wheelchairs that have benefited the most from technological advances in assistive robotics over the past 15 years and from a more advanced industrial transfer than all other robotic devices. The two main ideas underlying their development are to offer, with a single robotic solution, what several technical and human aids could provide, and to allow the user to take along the "substitute" for their missing or impaired effector-namely the arm-into an unknown and non-configured environment.

The JACO arm, marketed by a Canadian company (KINOVA), now stands out on the market as one of the most promising arms in terms of functional contribution and ergonomics.

No published study has ever prospectively examined home uses related to this type of manipulator arm. Only an oral communication reports on this, suggesting, in 7 users, an impact in terms of functional gain and quality of life.

The idea that the use of the Jaco arm could reduce the time of professional caregiver intervention.

The present study aims to report on the potential uses of the Jaco robot at home, its appropriation in daily life, and its impact on psycho-social-family balance.

Conditions

Interventions

DEVICE

Use of the JACO robotic arm for a period of 2 months

1. Initial evaluation of the participant. 2. Presentation of the device and training of the participant in the use of the JACO arm. 3. Autonomous use of the JACO robotic arm for a 2-month period

Sponsors & Collaborators

  • Centre Bouffard Vercelli - USSAP

    collaborator OTHER
  • CEREMH, Avenue de l'Europe, Vélizy-Villacoublay, France

    collaborator UNKNOWN
  • Association APPROCHE

    lead OTHER

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-30
Primary Completion
2022-03-30
Completion
2023-04-21

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07680361 on ClinicalTrials.gov