Skip to main content
Clinical Trials/NCT03679468
NCT03679468
Completed
Not Applicable

Improving Cognition in People With Progressive Multiple Sclerosis: A Multi-Arm, Randomized, Blinded, Sham-Controlled Trial of Cognitive Rehabilitation and Aerobic Exercise.

Sunnybrook Health Sciences Centre1 site in 1 country309 target enrollmentMarch 18, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Multiple Sclerosis, Primary Progressive
Sponsor
Sunnybrook Health Sciences Centre
Enrollment
309
Locations
1
Primary Endpoint
Change from baseline cognitive Information processing speed at 12 weeks and 6 months
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Given that up to 70% of people with secondary progressive MS are cognitively impaired, the search for effective treatments is considered a priority by people living with the disease. This proposal will address the effectiveness of cognitive rehabilitation (CR) and exercise, either alone, or in combination in this regard. A team of MS researchers has been assembled from the USA, Canada, the United Kingdom, Italy, Denmark, Germany and Belgium for this. A total of 360 people with progressive MS will make up the sample. Brain MRIs will be undertaken in a third of the sample before and after the 12 weeks of treatment to document the functional changes that are expected to occur with symptom improvement.

Detailed Description

Aim: The broad aim of this proposal is to evaluate a multidisciplinary and multi-modal approach to rehabilitation in people with progressive MS. Cognitive rehabilitation and aerobic exercise will be evaluated individually and in combinations to address cognitive dysfunction as the primary outcome variable. Over 20 years have passed since the introduction of the first disease modifying treatment, interferon beta-1betaseron (b), for multiple sclerosis (MS).Since then 13 treatments have been approved and made it onto the market. All are for relapsing-remitting disease (RRMS), apart from mitoxantrone which is limited to progressive disease with relapses, Interferon-beta-1b, which is for secondary progressive disease (SPMS), but does not delay disability progression and Ocrelizumab for primary progressive MS only. Thus, for a sizeable proportion of people with MS there is no therapeutic option to slow progression. This raises the question, how are patients with primary and secondary progressive MS (PPMS and SPMS) to be helped? While research is underway to find a medication that holds promise of halting further deterioration in a disease that has already entered a progressive stage, patients and their clinicians are left with basically symptomatic treatments. Hypothesis: The investigators hypothesize that CR and aerobic exercise are effective treatments for cognitive impairment (processing speed deficits) in people with progressive MS. In particular a combination of these two treatment given twice weekly over 12 weeks is more effective than each individual treatment given alone or as sham. The investigators further hypothesize that improvements in processing speed will be matched on functional MRI (fMRI) by enhanced neural activity in networks associated with information processing speed.

Registry
clinicaltrials.gov
Start Date
March 18, 2019
End Date
February 3, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Anthony Feinstein

Professor, department of psychiatry, University of Toronto

Sunnybrook Health Sciences Centre

Eligibility Criteria

Inclusion Criteria

  • Have a confirmed diagnosis of progressive Multiple Sclerosis
  • Visual Acuity of 20/70
  • Language comprehension, to ensure subjects have the ability to understand instructions

Exclusion Criteria

  • Wheelchair dependent (EDSS \> 7.0)
  • History of central nervous system disease other than progressive MS
  • Steroids use within the past 3 months
  • Regular aerobic training (eg. bi-cycling, running, swimming or rowing)
  • Unwilling to travel to study sites for rehabilitation 2 times a week for 3 months

Outcomes

Primary Outcomes

Change from baseline cognitive Information processing speed at 12 weeks and 6 months

Time Frame: Baseline, 12 weeks, and 6 month

The Symbol Digit Modalities Test (SDMT) will be used to measure cognitive information processing speed The SDMT is a simple matching task that requires the participant to refer to a reference key, in order to correctly match a geometric symbol with the corresponding number. Participant will be under a 90 second time constraint to quickly and correctly match each pair. Test will be administered at index assessment, 12 weeks following cognitive rehab/ aerobic exercise, and at 6 months to examine cognitive retention

Secondary Outcomes

  • Change from baseline cognitive verbal memory at 12 weeks and 6 months(Baseline, 12 weeks, & 6 month)
  • Change from baseline anxiety & depression, at 12 weeks and 6 months(Baseline, 12 weeks, and 6 month)
  • Change from baseline fatigue, at 12 weeks and 6 months(Baseline, 12 weeks, and 6 month)
  • Change from baseline perceived deficits, at 12 weeks and 6 months(Baseline, 12 weeks, and 6 month)
  • Change from baseline quality of life, at 12 weeks and 6 months(Baseline, 12 weeks, and 6 month)
  • Change from baseline depression, at 12 weeks and 6 months(Baseline, 12 weeks, and 6 month)
  • Change from baseline global function, at 12 weeks and 6 months(Baseline, 12 weeks, and 6 month)
  • Change from baseline cognitive visual memory at 12 weeks and 6 months(Baseline, 12 weeks, & 6 month)
  • Change from baseline impact of Multiple Sclerosis, at 12 weeks and 6 months(Baseline, 12 weeks, and 6 month)
  • Change from baseline subjective impact of walking, at 12 weeks and 6 months(Baseline, 12 weeks, and 6 month)

Study Sites (1)

Loading locations...

Similar Trials