Multiple Sclerosis: Associated Cardiometabolic Risks and Impact of Exercise Therapy

NCT ID: NCT02466165

Last Updated: 2017-06-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-02-28

Study Completion Date

2015-12-31

Brief Summary

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Multiple Sclerosis (MS) is the most common chronic inflammatory neurological disorder in young adults. Due to heterogeneous symptoms, MS patients are often more inactive than healthy controls, resulting in an inactivity related physiological profile. In healthy people, physical inactivity can contribute to the development of an increased cardiometabolic risk state including the combined presence of cardiovascular risk factors (increased cholesterol, elevated blood pressure, body fat, glucose intolerance/insulin resistance, inflammation and reduced heart function/autonomic control). In other populations, these secondary health complications can be, in part, reduced by physical exercise, which is often used as the primary treatment strategy. Since the impact of exercise on cardiovascular risk factors in MS is unknown the present project first aims to explore this in a pilot trial and a controlled research setting (during 12 weeks). A better understanding of the above described risk factors and underlying physiological mechanisms will reduce the incidence of preventable comorbidities in MS and will further improve the multidisciplinary treatment of MS patients and MS rehabilitation in particular. Interestingly, the investigators already reported an elevated prevalence of impaired glucose tolerance in MS, but it is not clear whether the cardiometabolic state in MS is also impaired. Therefore, in a second part, the researchers will explore whether MS patients present a higher risk to develop cardiovascular diseases, as measured by the assessment of various cardiovascular risk factors, compared to healthy controls.

Detailed Description

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In a first part, various cardiovascular risk factors will be determined in a group of MS patients (n=\~16). These patients will be enrolled in a pilot trail, investigating the feasability and impact of a high intense interval exercise intervention (12 weeks high intensity interval training). After 12 weeks, baseline cardiovascular risk measurements will be repeated to determine the impact of high intensity interval training on these risk factors in MS.

In a second part, these cardiovascular risk factors in a larger group of MS patients (n=\~50) will be compared to healthy controls (n=\~25), in order to determine whether MS patients show an increased prevalence of cardiovascular risk factors, and thus an elevated risk to develop cardiovascular diseases.

In total, a group of 80 subjects (MS patients and HC) will be investigated throughout this study, with only MS patients participating in the pilot trial/exercise intervention.

Measurements of cardiovascular risk factors will include:

* body composition (DEXA)
* blood pressure and heart rate (Omron M4-I)
* whole body glucose disposal (oral glucose tolerance test)
* blood analysis: insulin, total cholesterol, high- density lipoprotein, low-density lipoprotein, plasma triglycerides, C-reactive protein and glycosylated haemoglobin.

Furthermore, a maximal exercise test (determination maximal heart rate, workload, lactate concentrations, etc) and an isometric/isokinetic strength test will be performed to determine the impact of the rehabilitation program in MS patients.

Conditions

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Multiple Sclerosis Healthy Controls

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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MS patients intervention group

the feasibilty and influence of high intense interval exercise on the cardiometabolic risk state in MS patients will be investigated in a pilot trial.

Group Type EXPERIMENTAL

Physical exercise

Intervention Type BEHAVIORAL

healthy controls

To identify whether MS patients have a higher cardiometabolic risk state than healthy controls, this project discovers the prevalence of cardiometabolic risk factors (dyslipidemia, hypertension, body fat, glucose tolerance/IR, inflammation and heart function), in MS and referent subjects.

Group Type NO_INTERVENTION

No interventions assigned to this group

larger group of MS patients

To identify whether MS patients have a higher cardiometabolic risk state than healthy controls, this project discovers the prevalence of cardiometabolic risk factors (dyslipidemia, hypertension, body fat, glucose tolerance/IR, inflammation and heart function), in MS and referent subjects.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Physical exercise

Intervention Type BEHAVIORAL

Other Intervention Names

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combined (endurance and resistance) exercise programme

Eligibility Criteria

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Inclusion Criteria

Healthy controls:

* male/female
* 18 years
* written informed consent (Declaration of Helsinki and ethical committee guidelines)

MS patients:

* cfr healthy controls criteria, in addition:
* Diagnosed MS according to the McDonald criteria
* Expanded Disability Status Scale (EDSS) between 1 and 7
* Being available for the complete study course

Exclusion Criteria

* other disorders
* pregnancy
* participation in another study
* MS exacerbation 6 months prior to the start.
* for the MS patients: contra-indication to perform physical exercise
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Bert Op't Eijnde

OTHER

Sponsor Role lead

Responsible Party

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Bert Op't Eijnde

PhD

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Bert O Eijnde, Ph.D.

Role: STUDY_CHAIR

Hasselt University, REVAL/BIOMED

Locations

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REVAL

Diepenbeek, , Belgium

Site Status

Jessa hospital

Hasselt, , Belgium

Site Status

Countries

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Belgium

Other Identifiers

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MS-CMR

Identifier Type: -

Identifier Source: org_study_id

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