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Exercise Booster Sessions in People With Multiple Sclerosis

Primary Purpose

Multiple Sclerosis

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Systematic aerobic training
Systematic resistance training
Aerobic training booster sessions
Resistance training booster sessions
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring Exercise, Rehabilitation

Eligibility Criteria

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

Inclusion Criteria:

  • A definite diagnosis of MS, according to the McDonald criteria
  • Walking <650m on 6MWT.
  • Exercising ≤ two sessions per week of moderate-to-high intensity during the past six months.

Exclusion Criteria:

  • Comprise comorbidities (cardiovascular-, respiratory-, orthopedic- or other neurological diseases.)

Sites / Locations

  • Aarhus UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

No Intervention

Arm Label

Aerobic training booster group

Aerobic training control group

Resistance training booster group

Resistance training control group

Control group

Arm Description

Will receive 12 weeks of aerobic training followed by booster sessions + standard care in the 40 follow up period

Will receive 12 weeks of aerobic training followed by standard care in the 40 follow up period

Will receive 12 weeks of resistance training training followed by booster sessions + standard care in the 40 follow up period

Will receive 12 weeks of resistance training followed by standard care in the 40 follow up period

Will receive standard care throughout the study

Outcomes

Primary Outcome Measures

Change in functional capacity measured as a composite score of the six minute walk test and the 5x sit to stand test (5STS).
The six minute walk test it the distance covered during a six-minute maximal walking test. The 5STS is the time used to stand up from a chair and sit again five times.

Secondary Outcome Measures

Change in functional capacity measured by the Six spot step test (SSST)
SSST is a measure of walking ability, balance and coordination. Measured as the time to complete the six-spot course.
Change in functional capacity measured by the Multiple Sclerosis Functional Composite (MSFC)
Composite score from Timed 25-Feet Walk Test (T25FWT), 9-Hole Peg Test (9HPT), Paced Auditory Serial Addition Test (PASAT)

Full Information

First Posted
May 26, 2021
Last Updated
November 5, 2021
Sponsor
University of Aarhus
Collaborators
Oxford Brookes University
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1. Study Identification

Unique Protocol Identification Number
NCT04913012
Brief Title
Exercise Booster Sessions in People With Multiple Sclerosis
Official Title
Sustainability of Exercise Therapy by the Use of Exercise Booster Sessions in People With Multiple Sclerosis.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2021 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
June 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
Oxford Brookes University

4. Oversight

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

5. Study Description

Brief Summary
This study wants to investigate whether exercise booster sessions applied in the follow-up period after an exercise intervention can increase the sustainability of exercise induced effects in persons with multiple sclerosis. The study will be a randomized, multi-site, controlled trial. Participants will from the beginning be allocated to either aerobic training group, resistance training group or control group. After a 12 week exercise intervention, the exercise groups will be additionally randomized to receive either exercise booster sessions + standard care or just standard care in the 40 week follow up period. It is hypothesized that exercise booster sessions can increase the sustainability of exercise induced effects.
Detailed Description
MS is a chronic, autoimmune, and inflammatory disease of the central nervous system, exemplified through marked demyelination and axonal loss. As a result, symptoms such as fatigue, numbness, weakness, depression, walking difficulties and spasticity frequently appear. Although there is no cure for MS, several disease-modifying therapies are available. These can potentially slow the progression of disabilities and reduce the overall disease burden. This is of great interest from both an individual perspective, where increased disability is associated with a lowered health-related quality of life, and from a societal perspective, where increased disability is associated with larger costs. Over the past decades exercise has been shown to be safe, tolerable and beneficial in persons with MS (PwMS). Hence, it is known to be an effective way of treating symptoms such as fatigue7, muscle weakness, walking impairments and depression. As with other chronic diseases, exercise for PwMS has been proposed as "medicine". However, in order to benefit from the positive effects of any kind of treatment (i.e. most medical drugs or exercise) one has to adhere to the prescriptions of the treatment (i.e. dose and timing). Despite all the potential benefits of exercise therapy for PwMS, one of the major challenges relate to long-term maintenance of exercise efforts. An emerging concept that may hold the potential to increase the sustainability of exercise therapy is supervised "exercise booster sessions" (i.e. training sessions provided regularly throughout the follow-up period, to sustain effects of the preceding exercise intervention). These can be placed regularly during the follow-up period, where patients attend a number of supervised high-intensity exercise sessions, hereby trying to boost the effects of the preceding exercise intervention. Furthermore, exercise booster sessions can potentially motivate the patient to keep exercising throughout the follow up period. However, the optimal way of utilizing this concept is still not fully understood, and has not yet been tried in neurological patients. Therefore, the main purpose of the present study is to investigate how exercise booster sessions combined with usual care performed over a period of 40 weeks affects the sustainability of effects on functional capacity induced by a 12-week exercise intervention. It is hypothesized that participants receiving exercise booster sessions + usual care during follow up will have a better functional capacity at follow up, than the participants receiving usual care only. The study will be a randomized, multi-site, controlled trial. Participants will from the beginning be allocated to either aerobic training group, resistance training group or control group. After a 12 week exercise intervention, the exercise groups will be additionally randomized to receive either exercise booster sessions + standard care or just standard care in the 40 week follow up period. The 12 week exercise intervention will consist of 2-3 weekly supervised exercise sessions. The training will be planned by exercise physiologists and performed in a progressive manner. To allow handling of a large number of participants, who is also geographically spread, the exercise intervention will be locally anchored, but at the same time supervised by student employees and controlled by internet- and telephonic communication. Participants allocated to exercise booster sessions will receive two sessions every fifth week during the follow up period. The power calculation is based on the primary purpose of the study which is to investigate the effect of frequently applied exercise booster sessions. To set the estimated number of participants, a two-sample two-sided power calculation has been conducted. Based on previous studies, a mean difference on functional capacity between the group receiving usual care and the group receiving exercise booster sessions + usual care, regardless of exercise intervention, is expected to be 6% with a standard deviation (SD) of ±10%. The level of significance was set as 5% and a statistical power of 80%. According to the power calculation each group shall contain 60 participants (expected drop-out rate of 30 % is included). The results of these studies can have great clinical implications in many ways. If we find that by adding exercise booster sessions in a follow up period, one can maintain, or maybe even improve, functional capacity over a long period, this would be a novel finding making ground for new rehabilitation opportunities

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Exercise, Rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Aerobic training booster group
Arm Type
Experimental
Arm Description
Will receive 12 weeks of aerobic training followed by booster sessions + standard care in the 40 follow up period
Arm Title
Aerobic training control group
Arm Type
Active Comparator
Arm Description
Will receive 12 weeks of aerobic training followed by standard care in the 40 follow up period
Arm Title
Resistance training booster group
Arm Type
Experimental
Arm Description
Will receive 12 weeks of resistance training training followed by booster sessions + standard care in the 40 follow up period
Arm Title
Resistance training control group
Arm Type
Active Comparator
Arm Description
Will receive 12 weeks of resistance training followed by standard care in the 40 follow up period
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Will receive standard care throughout the study
Intervention Type
Combination Product
Intervention Name(s)
Systematic aerobic training
Intervention Description
Two-three weekly supervised aerobic exercise sessions for 12 weeks. The training will be planned by exercise physiologists, and performed in a progressive manner.
Intervention Type
Combination Product
Intervention Name(s)
Systematic resistance training
Intervention Description
Two-three weekly supervised resistance exercise sessions for 12 weeks. The training will be planned by exercise physiologists, and performed in a progressive manner.
Intervention Type
Combination Product
Intervention Name(s)
Aerobic training booster sessions
Intervention Description
Supervised aerobic training booster sessions delivered in the follow up period (two sessions every fifth week).
Intervention Type
Combination Product
Intervention Name(s)
Resistance training booster sessions
Intervention Description
Supervised resistance training booster sessions in the follow up period (two sessions every fifth week).
Primary Outcome Measure Information:
Title
Change in functional capacity measured as a composite score of the six minute walk test and the 5x sit to stand test (5STS).
Description
The six minute walk test it the distance covered during a six-minute maximal walking test. The 5STS is the time used to stand up from a chair and sit again five times.
Time Frame
Baseline,12 weeks and 52 weeks.
Secondary Outcome Measure Information:
Title
Change in functional capacity measured by the Six spot step test (SSST)
Description
SSST is a measure of walking ability, balance and coordination. Measured as the time to complete the six-spot course.
Time Frame
Baseline, 12 weeks and 52 weeks.
Title
Change in functional capacity measured by the Multiple Sclerosis Functional Composite (MSFC)
Description
Composite score from Timed 25-Feet Walk Test (T25FWT), 9-Hole Peg Test (9HPT), Paced Auditory Serial Addition Test (PASAT)
Time Frame
Baseline, 12 weeks and 52 weeks.
Other Pre-specified Outcome Measures:
Title
Change in physical activity, accelerometry
Description
Measurement of level of physical activity by wearing a accelerometer for 7 days at each time point. Measured in counts/min.
Time Frame
Baseline, 12 weeks and 52 weeks.
Title
Change in aerobic capacity
Description
Maximal oxygen uptake test on bike ergometer, measured by indirect calorimetry.
Time Frame
Baseline, 12 weeks and 52 weeks.
Title
Change in Multiple Sclerosis Walking Scale 12 (MSWS-12)
Description
Questionnaire assessing the impact of the disease on walking. Each question is scored from 1-5 and then summed and transformed to a 0-100 scale. Higher scores indicate a greater impact on walking.
Time Frame
Baseline, 12 weeks and 52 weeks.
Title
Change in Modified Fatigue Impact Scale (MFIS)
Description
Questionnaire assessing the effects of fatigue on physical, cognitive and psychosocial functioning. The score of the MFIS is the sum of the scores for the 21 items. A higher score represents a higher impact of fatigue, in general or in relation to one of the above mentioned areas.
Time Frame
Baseline, 12 weeks and 52 weeks.
Title
Change in Short Form Health Survey 36 (SF-36)
Description
Questionnaire assessing health status. The SF-36 consists of eight subscales, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability.
Time Frame
Baseline, 12 weeks and 52 weeks.
Title
Change in Hospital anxiety and depression scale (HADS)
Description
Questionnaire assessing anxiety and depression. It consists of two subscales (anxiety and depression), and should be scored separately. A higher score indicates a higher degree of anxiety and depression.
Time Frame
Baseline, 12 weeks and 52 weeks.
Title
Change in self reported physical activity measured by the Baecke questionnaire.
Description
Questionnaire assessing the self reported amount of physical activity. This questionnaire quantifies the habitual physical activity level in three indexes: occupational (at work), sport (structured exercise) and leisure (leisure time). Each index is scored from 1 to 5, with 5 indicating the highest level of physical activity
Time Frame
Baseline, 12 weeks and 52 weeks.
Title
Change in maximal strength
Description
Maximal strength measurement measured in the knee extensors by isokinetic dynamometry.
Time Frame
Baseline, 12 weeks and 52 weeks.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A definite diagnosis of MS, according to the McDonald criteria Walking <650m on 6MWT. Exercising ≤ two sessions per week of moderate-to-high intensity during the past six months. Exclusion Criteria: Comprise comorbidities (cardiovascular-, respiratory-, orthopedic- or other neurological diseases.)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Laurits Taul-Madsen, MSc.
Phone
+45 61656063
Email
ltm@ph.au.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Laurits Taul-Madsen, MSc.
Organizational Affiliation
University of Aarhus
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aarhus University
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laurits Taul-Madsen, MSc.
Phone
61656063
Email
ltm@ph.au.dk

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All data will be stored in The Danish National Archives after completion of the project, and data can be accessed through request to The Danish National Archives.
IPD Sharing Time Frame
The data will become available after completion of the project, expectedly May 2024. The Danish National Archives stores data without a time frame (forever).
IPD Sharing Access Criteria
Sharing of data can happen upon request to The Danish National Archives.
Citations:
PubMed Identifier
18970977
Citation
Compston A, Coles A. Multiple sclerosis. Lancet. 2008 Oct 25;372(9648):1502-17. doi: 10.1016/S0140-6736(08)61620-7.
Results Reference
background
PubMed Identifier
15571060
Citation
Calabresi PA. Diagnosis and management of multiple sclerosis. Am Fam Physician. 2004 Nov 15;70(10):1935-44.
Results Reference
background
PubMed Identifier
24880538
Citation
Pilutti LA, Platta ME, Motl RW, Latimer-Cheung AE. The safety of exercise training in multiple sclerosis: a systematic review. J Neurol Sci. 2014 Aug 15;343(1-2):3-7. doi: 10.1016/j.jns.2014.05.016. Epub 2014 May 15.
Results Reference
result
PubMed Identifier
23669008
Citation
Latimer-Cheung AE, Pilutti LA, Hicks AL, Martin Ginis KA, Fenuta AM, MacKibbon KA, Motl RW. Effects of exercise training on fitness, mobility, fatigue, and health-related quality of life among adults with multiple sclerosis: a systematic review to inform guideline development. Arch Phys Med Rehabil. 2013 Sep;94(9):1800-1828.e3. doi: 10.1016/j.apmr.2013.04.020. Epub 2013 May 10.
Results Reference
result
PubMed Identifier
26606383
Citation
Pedersen BK, Saltin B. Exercise as medicine - evidence for prescribing exercise as therapy in 26 different chronic diseases. Scand J Med Sci Sports. 2015 Dec;25 Suppl 3:1-72. doi: 10.1111/sms.12581.
Results Reference
result
PubMed Identifier
28607693
Citation
Heesen C, Bruce J, Gearing R, Moss-Morris R, Weinmann J, Hamalainen P, Motl R, Dalgas U, Kos D, Visioli F, Feys P, Solari A, Finlayson M, Eliasson L, Matthews V, Bogossian A, Liethmann K, Kopke S, Bissell P. Adherence to behavioural interventions in multiple sclerosis: Follow-up meeting report (AD@MS-2). Mult Scler J Exp Transl Clin. 2015 May 12;1:2055217315585333. doi: 10.1177/2055217315585333. eCollection 2015 Jan-Dec.
Results Reference
result
PubMed Identifier
19884575
Citation
Dalgas U, Stenager E, Jakobsen J, Petersen T, Hansen HJ, Knudsen C, Overgaard K, Ingemann-Hansen T. Resistance training improves muscle strength and functional capacity in multiple sclerosis. Neurology. 2009 Nov 3;73(18):1478-84. doi: 10.1212/WNL.0b013e3181bf98b4.
Results Reference
result
PubMed Identifier
21247971
Citation
Collett J, Dawes H, Meaney A, Sackley C, Barker K, Wade D, Izardi H, Bateman J, Duda J, Buckingham E. Exercise for multiple sclerosis: a single-blind randomized trial comparing three exercise intensities. Mult Scler. 2011 May;17(5):594-603. doi: 10.1177/1352458510391836. Epub 2011 Jan 19.
Results Reference
result
PubMed Identifier
25257612
Citation
Kjolhede T, Vissing K, de Place L, Pedersen BG, Ringgaard S, Stenager E, Petersen T, Dalgas U. Neuromuscular adaptations to long-term progressive resistance training translates to improved functional capacity for people with multiple sclerosis and is maintained at follow-up. Mult Scler. 2015 Apr;21(5):599-611. doi: 10.1177/1352458514549402. Epub 2014 Sep 25.
Results Reference
result

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Exercise Booster Sessions in People With Multiple Sclerosis

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