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Clinical Trial ROBERT® - Project Active Training

NCT04304976 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2021-02-21

No results posted yet for this study

Summary

The overall purpose with this clinical trial is to, monitor and secure ROBERT®'s clinical performance and safety in a clinical environment in the regional hospital North Denmark, Neuro Unit North. The purpose of the study is to investigate if ROBERT® has the ability to 1. Perform guided active training. 2. Perform resistance based active training. And validate the safety of ROBERT® in a clinical environment.

Conditions

  • Apoplexy; Stroke
  • Spinal Cord Injuries
  • Safety
  • Usability

Interventions

DEVICE

ROBERT®

Robotic Rehabilitation intervention ROBERT®, designed for early, and supplementary therapy of patients.

Sponsors & Collaborators

  • Lifescience-Robotics

    lead INDUSTRY

Principal Investigators

  • Helle Rovsing Jørgensen, Therapist · Neuro Unit Nord, Denmark

Study Design

Allocation
NON_RANDOMIZED
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-11-27
Primary Completion
2020-01-16
Completion
2020-04-21

Countries

  • Denmark

Study Locations

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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 NCT04304976 on ClinicalTrials.gov