Actively Recruiting
Cognitive Rehabilitation of Deficits in Patients With Multiple Sclerosis
Led by Universita di Verona · Updated on 2025-05-09
60
Participants Needed
1
Research Sites
137 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Non-Inferiority Study, Post-Market Clinical Investigation with a Device, Single-Blind Randomized Controlled Trial in a Cohort of Patients Diagnosed with Multiple Sclerosis (MS). The aim of the study is to assess whether a computer-based cognitive treatment delivered via telerehabilitation produces effects from T0 to T1 that are not inferior to those of an in-person treatment on sustained attention in a cohort of patients with MS. The secondary objective is to evaluate the effects of telerehabilitation compared to the same treatment delivered in person on attentional shifting, memory, executive functions, and daily functioning (including cognitive fatigue, quality of life, and mood) in patients with MS.
CONDITIONS
Official Title
Cognitive Rehabilitation of Deficits in Patients With Multiple Sclerosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of relapsing-remitting, primary progressive, or secondary progressive multiple sclerosis for at least 3-6 months
- Age between 18 and 65 years
- Expanded Disability Status Scale (EDSS) score between 3 and 5 indicating mild to moderate neurological disability
- Presence of memory, attention, or executive function disorders confirmed by Oxford Cognitive Screen (OCS)
- Availability of internet at home for telerehabilitation
- Adequate visual and auditory abilities to use the rehabilitation device
You will not qualify if you...
- Other neurological conditions
- History of psychiatric disorders
- Alcohol or drug abuse
- Severe visual deficits that are not corrected
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Azienda Ospedaliera Universitaria Integrata Verona - UOC di Neuroriabilitazione
Verona, verona, Italy, 37134
Actively Recruiting
Research Team
V
Valentina Varalta, Doctor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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