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Not yet taking people in ItalyPhase 2

Home-based AI exercise program for people with multiple sclerosis

Tests an AI-guided home exercise system on walking in adults with multiple sclerosis.

Plain-language title generated from the registry record
Registry title: Implementation of an Advanced Telerehabilitation Solution for People With Multiple Sclerosis

Key facts

Where
Cagliari, ItalySee the site
Phase
Phase 2

Where in Italy

  • University of CagliariCagliari, ItalyNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Danish Multiple Sclerosis Hospitals
Trial code
NCT07310914
Record updated
30 December 2025
Original description
The overall purpose of the present study is to investigate the effect of an advanced telerehablitation system (TRS) in persons with multiple sclerosis on mobility. The advanced telerhabilitation system is based on AI components, and delivers instant feedback to the partcipants. If the project is successful, it can help optimize exercise for those persons with multiple sclerosis who are either not able or willing to travel to a clinical setting for exericse.Read full original descriptionShow less

Implementation of an Advanced Telerehabilitation Solution for People With Multiple Sclerosis

The overall purpose of the present study is to investigate the effect of an advanced telerehablitation system (TRS) in persons with multiple sclerosis on mobility. The advanced telerhabilitation system is based on AI components, and delivers instant feedback to the partcipants. If the project is successful, it can help optimize exercise for those persons with multiple sclerosis who are either not able or willing to travel to a clinical setting for exericse.

Inclusion: Definite diagnosis of MS according to the McDonald criteria (both relapse-remitting and progressive); Expanded Disability Status Scale (EDSS) score of 2.5 to 6.5 or Patient Determined Disability Score (PDDS) of 2 to 6, indicating preservation of at least some ambulatory function, that is, the ability to walk 20 meters or more, independently, with or without the use of an assistive device; Willingness to travel to the local study site for the evaluation sessions,; Internet platform availability.

Exclusion: comorbidities hindering participation in the study; Individuals who have had a documented relapse and/or corticoid treatment during the past three months will be excluded,; Individuals with severe cognitive deficits who cannot follow simple instructions and/or consent.

ClinicalTrials.gov NCT07310914