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Comparison of Vigorous Versus Low Intensity Cool Room Treadmill Training in People With Multiple Sclerosis

Primary Purpose

Multiple Sclerosis, Neurological Rehabilitation, Exercise

Status
Not yet recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Body-weight supported treadmill training in a room cooled to 16°C
Sponsored by
Memorial University of Newfoundland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • people with a confirmed diagnosis of relapsing-remitting or progressive MS
  • older than 18 and less than 70 years of age
  • able to walk at least 10 meters with use of walking aids (Expanded Disability Status Scale (EDSS) <7.0)
  • must be stable without relapse for at least 90 days

Exclusion Criteria:

  • currently attending physical rehabilitation
  • functional community ambulators (gait speed>120 cm/s)
  • a relapse of MS

Sites / Locations

  • Memorial University of Newfoundland

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Low Intensity Group

Vigorous Intensity Group

Arm Description

Less than 40% Heart Rate Reserve

More than 60% Heart Rate Reserve

Outcomes

Primary Outcome Measures

Fast walking speed
Gait velocity (cm/s) measured while walking at fast pace

Secondary Outcome Measures

Spatiotemporal parameters of gait measured while walking at self-selected pace
Walkway outputs include step length and width (cm), double support time (%), symmetry (ratio between affected and less-affected sides)
Maximal oxygen consumption during graded exercise test
VO2max
Multiple Sclerosis Impact Scale-29
The Multiple Sclerosis Impact Scale-29 provides physical and psychological sub-scales. Using a Likert scale, participants indicate the degree to which problems, such as 'moving about' and 'balance' affect them from 'not at all' to 'extremely'.
Fatigue Severity Scale
A 9-item questionnaire, which assesses the severity of fatigue with items scored on a 7-point scale, '1 = strongly disagree' and '7 = strongly agree'. The minimum and maximum score possible are 9 and 63 respectively. Another reporting method is the mean of all scores from all 9-items, with minimum and maximum score possible being 1 and 7 respectively.
Hospital Anxiety and Depression Scale
A self-reported rating scale of severity of mood symptoms ranging from 0-21 with higher score indicating more symptoms.
Montreal Cognitive Assessment
Measures overall cognitive function with score ranging from 0 to 30 with higher scores indicating higher executive function
Symbol Digit Modality Test
Cognitive impairment
Transcranial Magnetic Stimulation
Corticospinal excitability
Serum Insulin-like growth factor-1 (IGF-1)
Resting and exercise-induced serum levels of IGF-1 in response to the 12-week exercise intervention
Structural and functional brain changes on Magnetic Resonance Imaging (MRI)
Standardized protocol recommended by the Canadian Dementia Imaging Group (https://www.cdip-pcid.ca/) which includes T1 and T2-weighted structural images, diffusion tensor imaging, and resting state connectivity.

Full Information

First Posted
November 19, 2019
Last Updated
March 16, 2023
Sponsor
Memorial University of Newfoundland
Collaborators
Multiple Sclerosis Society of Canada
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1. Study Identification

Unique Protocol Identification Number
NCT04175054
Brief Title
Comparison of Vigorous Versus Low Intensity Cool Room Treadmill Training in People With Multiple Sclerosis
Official Title
Training to Restore Walking and Promote Nervous System Repair in Multiple Sclerosis: RCT to Determine the Importance of Intensity
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 2023 (Anticipated)
Primary Completion Date
February 2025 (Anticipated)
Study Completion Date
February 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Memorial University of Newfoundland
Collaborators
Multiple Sclerosis Society of Canada

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
New research in animal models of MS suggests that greater training intensity is required to restore lost functions. We have developed and tested vigorous intensity cool room treadmill training that people with MS who have fatigue and heat-sensitivity can tolerate. This study will focus on the appropriate dosage of training.
Detailed Description
Our previous research showed that vigorous aerobic training in a room cooled to 16°C can improve walking and measures of brain plasticity among people with MS related walking disability, especially in those who had fatigue and heat sensitivity. As a next step, we will compare our novel vigorous intensity cool room treadmill training to low intensity cool room treadmill walking and determine whether intensity is important in order to improve brain repair and restore walking among people with MS. Our first objective is to compare the effects of 12 weeks of vigorous versus low intensity training on walking. Our second objective is to determine whether treadmill training alters indicators of brain repair. We hypothesize that the cool room vigorous training will result in greater increases in walking and less fatigue, which will be sustained at follow-up. We also hypothesize that improvements will align with less brain inhibition (shortened CSP measured using Transcranial Magnetic Stimulation) and greater upregulation of the neurotrophin IGF-1.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Neurological Rehabilitation, Exercise, Neuronal Plasticity, Cooling

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is an assessor-blinded Randomized Controlled Trial.
Masking
Outcomes Assessor
Masking Description
The outcome assessor will be blinded to group allocation, and will not be involved in conducting the training intervention.
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Low Intensity Group
Arm Type
Active Comparator
Arm Description
Less than 40% Heart Rate Reserve
Arm Title
Vigorous Intensity Group
Arm Type
Experimental
Arm Description
More than 60% Heart Rate Reserve
Intervention Type
Other
Intervention Name(s)
Body-weight supported treadmill training in a room cooled to 16°C
Intervention Description
Exercise will be performed on a treadmill using an overhead harness for safety in a temperature controlled-room at 16°C with 1:1 supervision. The high intensity group will maintain vigorous intensity with a target workload >60% of heart rate reserve for 30 min (plus 5min warm up and 5min cool down) while the low-intensity group will walk at mild intensity (<40% heart rate reserve) for the same duration. Heart rate, blood pressure, and rating of perceived exertion will be recorded throughout to monitor for potential adverse events and to ensure that target training zone heart rates are maintained. The intervention is 3 times per week for 12 weeks, with a 3-month run-in observational period to confirm disease stability, and 3-month follow-up to determine the sustainability of effects.
Primary Outcome Measure Information:
Title
Fast walking speed
Description
Gait velocity (cm/s) measured while walking at fast pace
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Spatiotemporal parameters of gait measured while walking at self-selected pace
Description
Walkway outputs include step length and width (cm), double support time (%), symmetry (ratio between affected and less-affected sides)
Time Frame
Following completion of the 12-week exercise intervention and 3-months post-exercise intervention
Title
Maximal oxygen consumption during graded exercise test
Description
VO2max
Time Frame
Following completion of the 12-week exercise intervention and 3-months post-exercise intervention
Title
Multiple Sclerosis Impact Scale-29
Description
The Multiple Sclerosis Impact Scale-29 provides physical and psychological sub-scales. Using a Likert scale, participants indicate the degree to which problems, such as 'moving about' and 'balance' affect them from 'not at all' to 'extremely'.
Time Frame
Following completion of the 12-week exercise intervention and 3-months post-exercise intervention
Title
Fatigue Severity Scale
Description
A 9-item questionnaire, which assesses the severity of fatigue with items scored on a 7-point scale, '1 = strongly disagree' and '7 = strongly agree'. The minimum and maximum score possible are 9 and 63 respectively. Another reporting method is the mean of all scores from all 9-items, with minimum and maximum score possible being 1 and 7 respectively.
Time Frame
Following completion of the 12-week exercise intervention and 3-months post-exercise intervention
Title
Hospital Anxiety and Depression Scale
Description
A self-reported rating scale of severity of mood symptoms ranging from 0-21 with higher score indicating more symptoms.
Time Frame
Following completion of the 12-week exercise intervention and 3-months post-exercise intervention
Title
Montreal Cognitive Assessment
Description
Measures overall cognitive function with score ranging from 0 to 30 with higher scores indicating higher executive function
Time Frame
Following completion of the 12-week exercise intervention and 3-months post-exercise intervention
Title
Symbol Digit Modality Test
Description
Cognitive impairment
Time Frame
Following completion of the 12-week exercise intervention and 3-months post-exercise intervention
Title
Transcranial Magnetic Stimulation
Description
Corticospinal excitability
Time Frame
Following completion of the 12-week exercise intervention and 3-months post-exercise intervention
Title
Serum Insulin-like growth factor-1 (IGF-1)
Description
Resting and exercise-induced serum levels of IGF-1 in response to the 12-week exercise intervention
Time Frame
Following completion of the 12-week exercise intervention and 3-months post-exercise intervention
Title
Structural and functional brain changes on Magnetic Resonance Imaging (MRI)
Description
Standardized protocol recommended by the Canadian Dementia Imaging Group (https://www.cdip-pcid.ca/) which includes T1 and T2-weighted structural images, diffusion tensor imaging, and resting state connectivity.
Time Frame
Following completion of the 12-week exercise intervention and 3-months post-exercise intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: people with a confirmed diagnosis of relapsing-remitting or progressive MS older than 18 and less than 70 years of age able to walk at least 10 meters with use of walking aids (Expanded Disability Status Scale (EDSS) <7.0) must be stable without relapse for at least 90 days Exclusion Criteria: currently attending physical rehabilitation functional community ambulators (gait speed>120 cm/s) a relapse of MS
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michelle Ploughman
Phone
709-777-2099
Email
michelle.ploughman@med.mun.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Marie Curtis
Phone
709-777-2082
Email
marie.curtis@mun.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michelle Ploughman, PhD
Organizational Affiliation
Memorial University of Newfoundland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Memorial University of Newfoundland
City
St. John's
State/Province
Newfoundland and Labrador
ZIP/Postal Code
A1A 1E5
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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Comparison of Vigorous Versus Low Intensity Cool Room Treadmill Training in People With Multiple Sclerosis

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