Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06627387

A Low-Cost Balance Training Platform Using Augmented Reality in Neurorehabilitation: a Usability Study

Led by Hospital Universitari Vall d'Hebron Research Institute · Updated on 2024-10-04

15

Participants Needed

1

Research Sites

33 weeks

Total Duration

On this page

Sponsors

H

Hospital Universitari Vall d'Hebron Research Institute

Lead Sponsor

E

Eodyne Systems SL

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to assess the Usability, adherence, acceptance, and security of an augmented reality platform for balance training in patients with balance disorders due to degenerative injuries or cerebrovascular diseases. The main questions it aims to answer are: * Is the augmented reality system usable, acceptable, and safe with good adherence? * Does the system improve the balance in our population? * Participants will be asked to assist at Vall d'Hebrón Hospital, where patients will undergo balance training under the supervision of a physiotherapist three days a week for four weeks. * If the patients meet the inclusion criteria, the intervention will be extended for two more weeks at home.

CONDITIONS

Official Title

A Low-Cost Balance Training Platform Using Augmented Reality in Neurorehabilitation: a Usability Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Balance impairment due to cerebrovascular or neurodegenerative diseases
  • Ability to stand for 2 minutes without assistance
  • Berg scale score of 21 or higher
  • Age 18 years or older
  • Signed informed consent
  • Have a training partner for home exercises
  • No falls during hospital intervention
  • Adequate space at home for safe training
  • Familiarity with laptops, tablets, or smartphones
Not Eligible

You will not qualify if you...

  • Any condition that could compromise patient safety
  • Severe cognitive impairments preventing experiment participation (MoCA score below 19)
  • Sensory aphasia
  • Diagnosis of conduct disorders
  • Severe neglect
  • Spasticity level 4 in lower limb according to MAS

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hospital Vall D'Hebrón

Barcelona, Barcelona, Spain, 08035

Actively Recruiting

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Research Team

S

Susana Rodriguez Gonzalez, MD

CONTACT

M

Marta Fernandez-Lobera, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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