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NCT06964581Recruiting

Cognitive Rehabilitation of Deficits in Patients With Multiple Sclerosis

Cognitive Rehabilitation of Deficits in Patients With Multiple Sclerosis: Proposal for an Integrated Cognitive Treatment in a Telematic Format

Source: ClinicalTrials.gov · Last updated 9 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
30 Apr 2025
Start date
8 Feb 2023
Primary completion date
22 Apr 2025
Lead sponsor
Universita di Verona
NCT number
NCT06964581

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 8 Feb 2023 to the primary completion date, 22 Apr 2025
  • 1 site 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.

Prior treatment

  • Alcohol and/or drug abuse;

Other illness

  • Presence of other neurological conditions;
  • Psychiatric disorders in medical history;

Other

  • Presence of uncorrected severe visual deficits.

Who the study is looking for

  • Diagnosis of relapsing-remitting multiple sclerosis (RRMS), or primary progressive (PPMS) or secondary progressive (SPMS), defined by at least 3-6 months.
  • Age between 18 and 65 years.
  • Expanded Disability Status Scale (EDSS) between 3 and 5 to include patients with overall neurological disability from mild to moderate.
  • Presence of one or more of the following cognitive disorders (reported by the patient and subsequently confirmed through the Oxford Cognitive Screen-OCS):
  • Memory disorders
  • Attention disorders
  • Executive function disorders
  • Availability of internet at the patient's home necessary for the tele-rehabilitation procedures.
  • Adequate visual and auditory abilities to use the rehabilitation device.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Azienda Ospedaliera Universitaria Integrata Verona - UOC di Neuroriabilitazione
Coordinator of this site? Confirm its status
VeronaItalyRecruiting

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