Multiple Sclerosis Clinical Trial
— AERCONNOfficial title:
Randomized Controlled Trial Investigating the Effects of a Standardized Aerobic Exercise Intervention on Cognitive Function and Brain Connectivity in Relapsing-remitting Multiple Sclerosis
| Verified date | June 2017 |
| Source | Universitätsklinikum Hamburg-Eppendorf |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Cognitive dysfunction is frequent in patients with multiple sclerosis (MS) and to date,
there are no available treatments to improve cognition in this patient population. Some
evidence from animal studies and small clinical trials suggest that aerobic exercise might
beneficially affect cognitive function in MS. The aim of this randomized-controlled trial is
to explore if an aerobic exercise training program can enhance cognition in MS. In addition,
we will employ neuroimaging markers to determine if exercise alters measures of brain
structure and function.
Patients will be randomly assigned to either a 3-months exercise program (bicycle ergometry,
2-3 session per week) or a waitlist control group. The primary endpoint of the study is a
test of verbal learning and memory. Secondary endpoints include neuroimaging markers of
functional and structural connectivity in the brain. We hypothesize that exercise will
improve verbal learning and memory and beneficially affect measures of brain connectivity.
| Status | Completed |
| Enrollment | 68 |
| Est. completion date | November 2016 |
| Est. primary completion date | May 2016 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility |
Inclusion Criteria: - Relapsing-remitting multiple sclerosis according to McDonald criteria - Currently in remission - Disease duration < 10 years - Low to moderate physical disability (EDSS 0-3.5) - On stable immunotherapy (>3 months) or without any planned treatment for the next year Exclusion Criteria: - Patients who are not able to understand the study concept due to severe cognitive deficits or psychiatric comorbidity - Patients currently taking psychoactive drugs - Patients unable to undergo aerobic exercise training for medical reasons - Patients with active disease or uncertain stability under current immunomodulatory therapy (as judged by the treating neurologist) - Patients with implants or body modifications (e.g. dental implants, piercings, tattoos, pacemakers etc.) which might interfere with MEG and MRI assessments - Patients unable to travel to the study center 2-3 times a week for the duration of the study |
| Country | Name | City | State |
|---|---|---|---|
| Germany | University Hospital Hamburg-Eppendorf | Hamburg |
| Lead Sponsor | Collaborator |
|---|---|
| Universitätsklinikum Hamburg-Eppendorf | German Federal Ministry of Education and Research |
Germany,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | Change in Patient-Reported Outcomes | Patient-reported outcomes will be assessed for depressive symptoms (IDS-30SR), fatigue (FSMC), quality of life (HAQUAMS), and walking (MSWS-12) | Baseline and at Month 3 (end of intervention) | |
| Other | Change in Walking Ability | Walking ability will be assessed using the six-minute-walk test (6MWT) as well as Actibelt accelerometry | Baseline and at Month 3 (end of intervention) | |
| Primary | Change in Verbal Learning and Memory | Verbal Learning and Memory will be assessed with the Verbal Learning and Memory Test (VLMT) | Baseline and at Month 3 (end of intervention) | |
| Secondary | Change in Functional Connectivity | Functional connectivity of CNS networks will be assessed by resting-state functional magnetic resonance imaging (rs fMRI) and resting-state magnetoencephalography (rs MEG) | Baseline and at Month 3 (end of intervention) | |
| Secondary | Change in Structural Connectivity | Structural connectivity and integrity of CNS networks will be assessed by diffusion tensor imaging (DTI) as well as measures of gray matter density using magnetic resonance imaging (MRI) | Baseline and at Month 3 (end of intervention) | |
| Secondary | Change in Neuropsychological Function | Neuropsychological function will be assessed using a standardized battery covering the following domains: visuospatial learning and memory, attention, processing speed, working memory, and social cognition | Baseline and at Month 3 (end of intervention) |
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