Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID06964581

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

Led by Universita di Verona · Updated on 2025-05-09

60

Participants Needed

1

Research Sites

23 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating cognitive rehabilitation methods for patients diagnosed with Multiple Sclerosis (MS), including relapsing-remitting, primary progressive, or secondary progressive types. The study aims to determine if a computer-based cognitive treatment delivered remotely through telerehabilitation is not less effective than the same treatment given in person. It also examines how these approaches affect attention, memory, executive functions, and daily living aspects such as cognitive fatigue, quality of life, and mood in people with MS. Participants receive three hours per week of cognitive rehabilitation using a computerized device tailored to their needs. One group completes the treatment independently at home via telerehabilitation, while the other attends in-person sessions where a therapist activates and guides the use of the device. This randomized, single-blind trial compares these two delivery methods over an eight-week treatment period. During the study, patients undergo several cognitive and functional tests before treatment, after eight weeks of therapy, and two months following treatment completion. These include assessments of attention, memory, executive function, fatigue, quality of life, and mood. Researchers use these measures to evaluate the effectiveness and long-term impact of the two rehabilitation approaches. The total participation duration includes treatment and follow-up assessments to monitor sustained benefits.

CONDITIONS

Brief Title

Cognitive Rehabilitation of Deficits in Patients With Multiple Sclerosis

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of relapsing-remitting, primary progressive, or secondary progressive multiple sclerosis for at least 3 to 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 the Oxford Cognitive Screen
  • Access to internet at home for telerehabilitation
  • Adequate vision and hearing to use the rehabilitation device
Not Eligible

You will not qualify if you...

  • Other neurological conditions
  • History of psychiatric disorders
  • Alcohol or drug abuse
  • Severe uncorrected visual impairments

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 8 weeks

Participants receive cognitive rehabilitation treatment either remotely via telerehabilitation or in-person using a computerized device. Each treatment involves three hours of cognitive exercises per week tailored to individual needs.

Weekly visits for up to 8 weeks

Follow-up

Duration - 2 months

Participants are monitored two months after the end of treatment to assess cognitive function and quality of life.

1 follow-up visit (in-person)

Trial Site Locations

Total: 1 location

1

Azienda Ospedaliera Universitaria Integrata Verona - UOC di Neuroriabilitazione

Verona, verona, Italy, 37134

Actively Recruiting

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Research Team

V

Valentina Varalta, Doctor

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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