Telerehabilitation Decision Support System: Pilot Testing Protocol

NCT07079787 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2025-07-23

No results posted yet for this study

Summary

This study follows the successfully completed HOLOBalance project which was funded by the EU Horizon 2020 scheme. TheHOLOBalance platform delivers exercises demonstrated via a hologram of the physiotherapist and corrected in real time by the hologram prompts based on performance monitoring via sensors. Further information is available at: https://holobalance.eu/. HOLOBalance was developed as a comprehensive rehabilitation protocol for individualised remote (tele)rehabilitation balance physiotherapy programme. It includes different multisensory balance and gait exercises, physical activity and memory training and exergames (video games which are also exercises) to improve balance function in older adults. The system can thus assess and remotely monitor how users are performing the exercises.

This pilot testing of a multisite randomised control trial (TeleRehab DSS, short for TeleRehabilitation Decision Support System) aims to investigating the usability and feasibility among a smaller sample population at each clinical site, identifying any technical bugs, and/or clinical procedural flaws to be remedied before delivery of the full-scale RCT.

Conditions

  • Stroke
  • Mild Cognitive Impairment (MCI)
  • Vestibular Disease
  • Long Covid-19

Interventions

DEVICE

TeleRehab DSS Pilot Test

Participants will perform an individualised multisensory balance rehabilitation program via augmented reality, while wearing motion sensors. The program will consist of multisensory balance exercises, cognitive games, and exergames. All participants will perform 2 sessions per week, carried in at each clinical site, over the course of 3-week.s

Sponsors & Collaborators

  • National and Kapodistrian University of Athens

    collaborator OTHER
  • University Medical Center Freiburg

    collaborator OTHER
  • King Chulalongkorn Memorial Hospital

    collaborator OTHER
  • Secretaria Regional de Saúde e Proteção Civil da Região Autónoma da Madeira

    collaborator UNKNOWN
  • Institute of Communications and Computer Systems, Athens, Greece

    collaborator OTHER
  • University of Ioannina

    collaborator OTHER
  • Vilabs

    collaborator UNKNOWN
  • BioIRC

    collaborator UNKNOWN
  • Activage

    collaborator UNKNOWN
  • Institue De Desenvolvimento De Novas Technologiassociacao

    collaborator UNKNOWN
  • Quantitas SRL

    collaborator UNKNOWN
  • Instituto para o Desenvolvimento e Inovação

    collaborator UNKNOWN
  • BRIDG

    collaborator UNKNOWN
  • University College, London

    lead OTHER

Principal Investigators

  • Doris-Eva Bamiou, PhD · University College, London

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-07-25
Primary Completion
2025-08-18
Completion
2025-08-29

Countries

  • Germany
  • Greece
  • Portugal
  • Thailand
  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

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 NCT07079787 on ClinicalTrials.gov