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Exercise in Multiple Sclerosis: Effects on Cognitive Function and Brain Connectivity (AERCONN)

Primary Purpose

Multiple Sclerosis

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Aerobic Exercise
Sponsored by
Universitätsklinikum Hamburg-Eppendorf
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

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

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University Hospital Hamburg-Eppendorf

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Aerobic Exercise (12 Weeks)

Waitlist Control Group

Arm Description

Aerobic exercise on a bicycle ergometer, tailored to the individual's level of fitness. Duration: 12 weeks with 2-3 sessions per week.

No intervention (patients randomized to this group will be offered access to the training program after completion of the trial)

Outcomes

Primary Outcome Measures

Change in Verbal Learning and Memory
Verbal Learning and Memory will be assessed with the Verbal Learning and Memory Test (VLMT)

Secondary Outcome Measures

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)
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)
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

Full Information

First Posted
December 3, 2013
Last Updated
June 23, 2017
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
German Federal Ministry of Education and Research
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1. Study Identification

Unique Protocol Identification Number
NCT02005237
Brief Title
Exercise in Multiple Sclerosis: Effects on Cognitive Function and Brain Connectivity
Acronym
AERCONN
Official Title
Randomized Controlled Trial Investigating the Effects of a Standardized Aerobic Exercise Intervention on Cognitive Function and Brain Connectivity in Relapsing-remitting Multiple Sclerosis
Study Type
Interventional

2. Study Status

Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
December 2013 (undefined)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
German Federal Ministry of Education and Research

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
Background: 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. Aims: This study aims to explore the potential of an aerobic exercise program on brain structure and function in MS in a single-blind, randomized controlled phase IIa trial. We hypothesize that exercise will improve verbal learning and memory (primary endpoint) as well as induce changes in neuroimaging markers of structural and functional central nervous system (CNS) connectivity (secondary endpoints). Tertiary outcomes will include walking ability, motor function and coordination, as well as patient-based outcomes (depression, fatigue, and health-related quality of life). Design: This is a single-blind, randomized, controlled phase IIa trial with a parallel group design comparing 3 months of standardized aerobic exercise training (bicycle ergometry) to a waitlist control group (superiority framework). The allocation ratio of exercise to waitlist control is 1:1 with a sample size of n=60.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
68 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Aerobic Exercise (12 Weeks)
Arm Type
Experimental
Arm Description
Aerobic exercise on a bicycle ergometer, tailored to the individual's level of fitness. Duration: 12 weeks with 2-3 sessions per week.
Arm Title
Waitlist Control Group
Arm Type
No Intervention
Arm Description
No intervention (patients randomized to this group will be offered access to the training program after completion of the trial)
Intervention Type
Behavioral
Intervention Name(s)
Aerobic Exercise
Intervention Description
3-months exercise program tailored to the individual level of aerobic fitness. Patients will exercise on a bicycle ergometer (2-3 session per week) according to a predefined training plan with increasing duration and intensity
Primary Outcome Measure Information:
Title
Change in Verbal Learning and Memory
Description
Verbal Learning and Memory will be assessed with the Verbal Learning and Memory Test (VLMT)
Time Frame
Baseline and at Month 3 (end of intervention)
Secondary Outcome Measure Information:
Title
Change in Functional Connectivity
Description
Functional connectivity of CNS networks will be assessed by resting-state functional magnetic resonance imaging (rs fMRI) and resting-state magnetoencephalography (rs MEG)
Time Frame
Baseline and at Month 3 (end of intervention)
Title
Change in Structural Connectivity
Description
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)
Time Frame
Baseline and at Month 3 (end of intervention)
Title
Change in Neuropsychological Function
Description
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
Time Frame
Baseline and at Month 3 (end of intervention)
Other Pre-specified Outcome Measures:
Title
Change in Patient-Reported Outcomes
Description
Patient-reported outcomes will be assessed for depressive symptoms (IDS-30SR), fatigue (FSMC), quality of life (HAQUAMS), and walking (MSWS-12)
Time Frame
Baseline and at Month 3 (end of intervention)
Title
Change in Walking Ability
Description
Walking ability will be assessed using the six-minute-walk test (6MWT) as well as Actibelt accelerometry
Time Frame
Baseline and at Month 3 (end of intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stefan M Gold, PhD
Organizational Affiliation
Center for Molecular Neurobiology, University Hospital Hamburg Eppendorf
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Andreas K Engel, MD
Organizational Affiliation
Dept Neurophysiology, University Hospital Hamburg Eppendorf
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christoph Heesen, MD
Organizational Affiliation
Dept Neurology, University Hospital Hamburg Eppendorf
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Guido Nolte, PhD
Organizational Affiliation
Dept Neurophysiology, University Hospital Hamburg Eppendorf
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Karl-Heinz Schulz, MD, PhD
Organizational Affiliation
Dept Sports Medicine, University Hospital Hamburg Eppendorf
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Hamburg-Eppendorf
City
Hamburg
ZIP/Postal Code
20241
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
30581662
Citation
Baquet L, Hasselmann H, Patra S, Stellmann JP, Vettorazzi E, Engel AK, Rosenkranz SC, Poettgen J, Gold SM, Schulz KH, Heesen C. Short-term interval aerobic exercise training does not improve memory functioning in relapsing-remitting multiple sclerosis-a randomized controlled trial. PeerJ. 2018 Dec 12;6:e6037. doi: 10.7717/peerj.6037. eCollection 2018.
Results Reference
derived

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Exercise in Multiple Sclerosis: Effects on Cognitive Function and Brain Connectivity

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