Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06489145

Multi-domain Improvements in High-TEchnology Rehabilitation Programs for Post-stroke Patients

Led by University of Milano Bicocca · Updated on 2024-12-09

80

Participants Needed

1

Research Sites

66 weeks

Total Duration

On this page

Sponsors

U

University of Milano Bicocca

Lead Sponsor

U

University of Milan

Collaborating Sponsor

AI-Summary

What this Trial Is About

Through a multi-method, multi-informant, and patient-centred approach, the study aims to investigate the experience of use and the effectiveness of rehabilitation technology (robotics and virtual reality - VR) in post-stroke patients and their caregivers and therapists

CONDITIONS

Official Title

Multi-domain Improvements in High-TEchnology Rehabilitation Programs for Post-stroke Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Acute stroke event within 12 months before treatment
  • Age over 18 years
  • Acceptable muscle weakness as measured by Motricity Index
  • Spasticity compatible with limb function (Modified Ashworth Scale score less than 2)
  • Mental health sufficient to understand study and complete questionnaires
  • Caregivers who continuously assist a patient at least half a day
  • Physiotherapists assisting patients during entire intervention period
  • Physiotherapists with experience using rehabilitation technology for post-stroke patients (Study 2)
Not Eligible

You will not qualify if you...

  • Severe clinical conditions such as cognitive impairment (MMSE score less than 24), severe apraxia, complete upper limb paralysis, severe sensory disorders, joint fractures or dislocations
  • Not eligible for exoskeleton device use based on device technical requirements
  • Inability or difficulty completing self-report measures in Italian or illiteracy
  • History or recent psychiatric conditions affecting data reliability
  • Refusal or withdrawal of consent
  • Caregivers unable to understand Italian or illiterate
  • Physiotherapists not assisting patients throughout entire intervention period
  • Physiotherapists refusing or withdrawing consent (Study 2)

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

University of Milano-Bicocca

Milan, Italy, 20126

Actively Recruiting

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Research Team

M

Marco D'Addario, PhD

CONTACT

F

Francesco Zanatta, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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