About this trial
This observational study aims to monitor functional status and identify potential declines in the functioning of medically fragile patients with neurological and/or orthopedic conditions, representing an added value for ensuring appropriate patient management. This approach improves system efficiency and supports a proactive strategy that promotes the appropriate use of resources.
Eligibility criteria
Qualifiers
Adult medically fragile patients with one of the following neurological conditions: mild-to-moderate stroke (Rankin ≤ 3), Multiple Sclerosis (EDSS ≤ 6.5), Parkinson's disease or parkinsonisms, neuromuscular diseases; or orthopedic conditions: femur, pelvis, or humerus fracture.
Able to walk independently, with or without assistive devices.
Adequate cognitive function (MMSE ≥ 24).
Patient or caregiver owns and can use a mobile device with internet/data connection.
Disqualifiers
Patients with severe neurological or orthopedic conditions who cannot walk independently, even with assistive devices.
Patients with moderate or severe cognitive impairment (MMSE < 24).
Patients with Barthel Index > 60.
Patients or caregivers unable to use a mobile device or without internet/data connection.
Trial design
Treatments tested in this trial
- Telemedicine-Based Functional Monitoring
Treatment groups
Sponsors and collaborators
Azienda Sanitaria Locale CN2 Alba-Bra
Lead sponsor
Casa di Cura La Residenza di Rodello (CN, Italy)
Collaborator