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NCT06881979Recruiting

High-Tech Rehabilitation Pathway for Chronic Adult Neuromuscular Diseases - Fit4MedRob-Chronic MND Project

Clinical Protocol for a Pragmatic Trial on a High-Tech Rehabilitation Pathway for Chronic Adult Neuromuscular Diseases (Fit4MedRob-Chronic MND Project)

Source: ClinicalTrials.gov · Last updated 4 Nov 2026

Brief summary (registry, in English)

The primary objective is to demonstrate, in a population of chronic neuromuscular disease the non-inferiority of a rehabilitation treatment integrated with robotic and/or technological devices compared to traditional rehabilitation treatment in the level of fatigue. The main question it aims to answer is: Are high-tech rehabilitation interventions, including robotic systems, virtual reality, and stabilometric platforms, not inferior to traditional rehabilitation methods in improving balance, motor function, fatigue levels, sarcopenia, cognitive engagement, and overall quality of life in patients with chronic neuromuscular diseases (NMDs)? Researchers will compare a robotic treatment group, that consists in an high-tech rehabilitation, with a control group, that will receive the traditional rehabilitative treatment.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
11 Mar 2025
Start date
28 Apr 2025
Primary completion date
Nov 2026
Lead sponsor
Istituti Clinici Scientifici Maugeri SpA
NCT number
NCT06881979

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 28 Apr 2025 to the primary completion date, Nov 2026
  • 7 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with unstable medical conditions (e.g. severe cardiovascular diseases, such as "New York Heart Association" - NYHA=4, respiratory distress not compensated by ventilation) that could interfere, in the clinician's judgment, with their ability to safely participate in the study or to perform the assessments related to the protocol.

Other

  • Patients currently participating in other clinical trials that could interfere with this study.
  • Pregnant women.

Who the study is looking for

  • Patients with a confirmed diagnosis of chronic neuromuscular diseases (e.g. ALS, CIDP, CMT)
  • Patient able to walk independently or with assistance
  • Patients capable of understanding and adhering to the study protocol.
  • Patients who have provided informed consent to participate in the study

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
IRCCS Azienda Ospedaliera Universitaria San Martino - Genova
Coordinator of this site? Confirm its status
GenovaItalyNot yet recruiting
Istituti Clinici Scientifici Maugeri IRCCS, Milan Institute
Coordinator of this site? Confirm its status
MilanItalyRecruiting
Azienda Ospedaliero - Universitaria di Modena
Coordinator of this site? Confirm its status
ModenaItalyNot yet recruiting
Istituti Clinici Scientifici Maugeri
Coordinator of this site? Confirm its status
MontescanoItalyNot yet recruiting
Istituti Clinici Scientifici Maugeri IRCCS
Coordinator of this site? Confirm its status
PaviaItalyNot yet recruiting
Fondazione Don Carlo Gnocchi ONLUS
Coordinator of this site? Confirm its status
RomaItalyNot yet recruiting
Istituti Clinici Scientifici Maugeri IRCCS
Coordinator of this site? Confirm its status
Telese TermeItalyNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.