Multiple Sclerosis Clinical Trial

Computerized Cognitive Rehabilitation in MS Patients

Summary

This study examines a home-based computerized cognitive rehabilitation intervention in adults with multiple sclerosis compared to placebo (videogame). Patients are assessed through pre-and post neuropsychological testing.

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Full Description

Patients will be randomized to enter a 6 week course of computer based cognitive rehabilitation focused on improving attention, learning, and memory. Control patients will receive an alternative home-based computer program not designed for cognitive remediation but of the same duration.

The primary outcome will be performance on neuropsychological testing in the intervention sample compared to controls. Secondary outcomes will be the measures of self-efficacy, work productivity, quality of life, fatigue, depression, anxiety, and healthcare utilization. Healthcare utilization variables include annual total cost (current year and prior), number and cost of ER/hospital/outpatient visits, number of hospital visits, hospital length of stay, number preventive visits, total number claims, and number of new medications initiated. In addition, acute changes in neuropsychological testing induced by a bout of physical activity (i.e. self-paced walking during the Six-Minute Walk Test) will be examined, and that pattern of change will be compared between intervention and control groups at each data collection point.

Each subject will participate for a total of 6 months.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

1. Diagnosis of multiple sclerosis with cognitive complaint

Exclusion Criteria:

Patients unwilling to participate
Patients who cannot attend NPT sessions
Patients with severe cognitive impairment
Non-English speaking patients (testing materials are in English)
Patients with intact neuropsychological functioning at baseline on testing

Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

80

Study ID:

NCT03729713

Recruitment Status:

Recruiting

Sponsor:

Rutgers, The State University of New Jersey

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There is 1 Location for this study

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Robert Wood Johnson Medical School
New Brunswick New Jersey, 08091, United States More Info
Vikram Bhise, MD
Contact
732-235-7875
Vikram Bhise, MD
Principal Investigator

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Study is for people with:

Multiple Sclerosis

Estimated Enrollment:

80

Study ID:

NCT03729713

Recruitment Status:

Recruiting

Sponsor:


Rutgers, The State University of New Jersey

How clear is this clinincal trial information?

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