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Effects of Aerobic Exercise During the Early Rehabilitation After Ischemic Stroke (EXERTION)

Primary Purpose

Ischemic Stroke, Stroke Rehabilitation

Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Walking Exercise
Sponsored by
University Hospital Muenster
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Ischemic Stroke focused on measuring Motor Function, Aerobic Exercise, Immune System, Cognition

Eligibility Criteria

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

Inclusion Criteria: initial NIHSS or NIHSS determined at the moment of maximum deterioration 1-18 age > 18 ischemic stroke pre-stroke independence sufficient motivation / patient's desire to cooperate / exercise for 3-5x/week for 30-45 min Exclusion Criteria: transient ischemic attack premorbid motor disability / musculoskeletal injury / severe arthritis impairing degree of movement balance and transfer function that requires assistance cardiac disease not allowing to perform aerobic training inability to give informed consent

Sites / Locations

  • University Hospital MünsterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Exercise Group

No Exercise Group

Arm Description

Participants will exert a heart rate controlled aerobic walking training 3-5 times per week for 30-45 minutes per training. This exercise as well as the daily amount of steps will be assessed via smartwatch.

Participants receive no demands regarding the daily exercise. Their daily amount of steps will be assessed via smartwach.

Outcomes

Primary Outcome Measures

Motor function
Recovery of motor function is assessed by fugl-meyer assessment (FMA). The FMA-UE (upper extremity) is measured in a score with a maximum of 66 points for motor function, the FMA-LE (lower extremity) extends up to a sum score of 34 points for motor function.

Secondary Outcome Measures

Cognition
A MoCA (Montreal Cognitive Assessment) is performed. The evaluation takes place via the calculation of demographically corrected standard values (the z-value): https://www.mocatest.ch/de/standardwerte/standardwerte-online-berechnen. In addition, the SDMT (Symbol Digites Modality Test) is performed. The evaluation takes places via evaluation of the sum score in a age and education adjusted manner as stated in the following publication: Kiely KM et al. Arch Clin Neuropsychol. 2014.
Fatigue
The effect of aerobic exercise on fatigue after ischemic stroke will be assessed by neuropsychological testing. The FSMC (Fatigue Scale for Motor and Cognitive Functions) is performed. A total score is calculated after the patient has completed the questionnaire. These cut-off values have been validated by Penner et al, 2009, Mult Scler. 2009.
Physical Comfort
The HADS-S (Hospital Anxiety and Depression Scale; German Version) is performed. The score consists of 14 items, 7 each for depression and anxiety which are arranged in alternating order. After the patient has completed the questionnaire, two dimension are analyzed via building to sub-scores. The cut-off values are derived from Herrmann-Lingen, C., Buss, U., & Snaith, R. P. (2011). Furthermore, physical comfort is assessed by the WHODAS (World Health Organization Disability Assessment Schedule). The 12-item questionnaire is self-administered and we focus on the symptoms during the last 14 days. Each item/question is assigned a value from 0 to 4 and a sum score is calculated. The score is interpreted adjusted to age, gender and physical condition as proposed in the following publication: Andrews G, et al. PLoS One. 2009.
Flow cytometry analysis of cryoasservated peripheral blood mononuclear cells (PBMC)
Blood sampling is performed at baseline and on day 90 after study inclusion. In our analysis, we focus on the major leukocyte subtypes. Of these, effector functions such as cytokine production, differentiation and activation levels, and expression of regulatory molecules will also be determined. The major measurement by flow cytometry analysis will be the percentage of the expressed target in the interventional cohort compared to the control group.
Structural axonal changes
Fibre tract density is assessed by cerebral magnetic resonance imaging (MRI-DTI).

Full Information

First Posted
December 20, 2022
Last Updated
April 6, 2023
Sponsor
University Hospital Muenster
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1. Study Identification

Unique Protocol Identification Number
NCT05690165
Brief Title
Effects of Aerobic Exercise During the Early Rehabilitation After Ischemic Stroke
Acronym
EXERTION
Official Title
Aerobic Exercise in the the Early Stroke Rehabilitation - Effects on Motor Function, Cognition, Physical Comfort and the Immune System
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 26, 2022 (Actual)
Primary Completion Date
October 1, 2025 (Anticipated)
Study Completion Date
October 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital Muenster

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
The goal of this clinical trial is to study the effects of aerobic exercise during the early rehabilitation after ischemic stroke. The main questions it aims to answer are: How is the recovery of motor function affected by regularly walking during the first 90 days after an ischemic stroke? Does regularly walking during the first 90 days after ischemic stroke affect cognition, physical comfort and the immune system? Participants will exert a heart rate controlled walking programme of walking 3-5 times 30-45 minutes per week. Researchers will compare the recovery of the walking group to a control group without any demands regarding physical exercise.
Detailed Description
From animal experiments we know that wheel running has a positive impact on functional recovery after experimental stroke. We aim to translate this observations from our animal experiments into the clinic. Therefore, patients will be included shortly after ischemic stroke and start an aerobic exercise programme during the first 14 days after the event. At baseline visit the participants receive a neuropsychological testing with the focus on cognition, fatigue and depressive symptoms. Furthermore, we perform blood sampling for analysis of the activation state of the peripheral immune system. The patients receive a lactate ergometry with measurement of the 3 mmol lactate threshold to define the optimal heart rate range for their walking exercise. We perform the fugl-meyer assessment for the upper and the lower extremity. For correlation with training-induced structural changes participants receive cerebral magnetic resonance imaging to assess the density of axonal fibre tracts (assessed by MRI-DTI). During the following 90 days participants in the intervention group are instructed to walk 3-5 times for 30-45 minutes per week and control the exercise intensity by optical heart rate measurement via smartwatch. The daily step count will be protocolled by the intervention and the control group. Participants will measure their resting heart rate in the morning before getting up to prevent overexercising. The assessments of the baseline visit will be repeated after 90 days.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Stroke, Stroke Rehabilitation
Keywords
Motor Function, Aerobic Exercise, Immune System, Cognition

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Exercise Group
Arm Type
Experimental
Arm Description
Participants will exert a heart rate controlled aerobic walking training 3-5 times per week for 30-45 minutes per training. This exercise as well as the daily amount of steps will be assessed via smartwatch.
Arm Title
No Exercise Group
Arm Type
No Intervention
Arm Description
Participants receive no demands regarding the daily exercise. Their daily amount of steps will be assessed via smartwach.
Intervention Type
Behavioral
Intervention Name(s)
Walking Exercise
Intervention Description
Heart rate controlled walking exercise
Primary Outcome Measure Information:
Title
Motor function
Description
Recovery of motor function is assessed by fugl-meyer assessment (FMA). The FMA-UE (upper extremity) is measured in a score with a maximum of 66 points for motor function, the FMA-LE (lower extremity) extends up to a sum score of 34 points for motor function.
Time Frame
90 days
Secondary Outcome Measure Information:
Title
Cognition
Description
A MoCA (Montreal Cognitive Assessment) is performed. The evaluation takes place via the calculation of demographically corrected standard values (the z-value): https://www.mocatest.ch/de/standardwerte/standardwerte-online-berechnen. In addition, the SDMT (Symbol Digites Modality Test) is performed. The evaluation takes places via evaluation of the sum score in a age and education adjusted manner as stated in the following publication: Kiely KM et al. Arch Clin Neuropsychol. 2014.
Time Frame
90 days
Title
Fatigue
Description
The effect of aerobic exercise on fatigue after ischemic stroke will be assessed by neuropsychological testing. The FSMC (Fatigue Scale for Motor and Cognitive Functions) is performed. A total score is calculated after the patient has completed the questionnaire. These cut-off values have been validated by Penner et al, 2009, Mult Scler. 2009.
Time Frame
90 days
Title
Physical Comfort
Description
The HADS-S (Hospital Anxiety and Depression Scale; German Version) is performed. The score consists of 14 items, 7 each for depression and anxiety which are arranged in alternating order. After the patient has completed the questionnaire, two dimension are analyzed via building to sub-scores. The cut-off values are derived from Herrmann-Lingen, C., Buss, U., & Snaith, R. P. (2011). Furthermore, physical comfort is assessed by the WHODAS (World Health Organization Disability Assessment Schedule). The 12-item questionnaire is self-administered and we focus on the symptoms during the last 14 days. Each item/question is assigned a value from 0 to 4 and a sum score is calculated. The score is interpreted adjusted to age, gender and physical condition as proposed in the following publication: Andrews G, et al. PLoS One. 2009.
Time Frame
90 days
Title
Flow cytometry analysis of cryoasservated peripheral blood mononuclear cells (PBMC)
Description
Blood sampling is performed at baseline and on day 90 after study inclusion. In our analysis, we focus on the major leukocyte subtypes. Of these, effector functions such as cytokine production, differentiation and activation levels, and expression of regulatory molecules will also be determined. The major measurement by flow cytometry analysis will be the percentage of the expressed target in the interventional cohort compared to the control group.
Time Frame
90 days
Title
Structural axonal changes
Description
Fibre tract density is assessed by cerebral magnetic resonance imaging (MRI-DTI).
Time Frame
90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: initial NIHSS or NIHSS determined at the moment of maximum deterioration 1-18 age > 18 ischemic stroke pre-stroke independence sufficient motivation / patient's desire to cooperate / exercise for 3-5x/week for 30-45 min Exclusion Criteria: transient ischemic attack premorbid motor disability / musculoskeletal injury / severe arthritis impairing degree of movement balance and transfer function that requires assistance cardiac disease not allowing to perform aerobic training inability to give informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Antje Schmidt-Pogoda, MD
Phone
+49 (0) 251-8341155
Email
antje.schmidt-pogoda@ukmuenster.de
First Name & Middle Initial & Last Name or Official Title & Degree
Frederike A Straeten, MD
Email
frederike.straeten@ukmuenster.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antje Schmidt-Pogoda, MD
Organizational Affiliation
University Hospital Muenster
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Münster
City
Münster
State/Province
Northrine-Westphalia
ZIP/Postal Code
D-48149
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Antje Schmidt-Pogoda, MD
Phone
+49 (0) 251-8341155
Email
antje.schmidt-pogoda@ukmuenster.de
First Name & Middle Initial & Last Name & Degree
Frederike A Straeten, MD
Email
frederike.straeten@ukmuenster.de

12. IPD Sharing Statement

Plan to Share IPD
No

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Effects of Aerobic Exercise During the Early Rehabilitation After Ischemic Stroke

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