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The Influence of Exercise on Neuroplasticity and Motor Learning After Stroke

The Influence of Acute Bouts of Aerobic Exercise on Neuroplasticity and Motor Learning After Stroke

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02980796
Acronym
EX-ML3
Enrollment
104
Registered
2016-12-02
Start date
2016-11-30
Completion date
2022-08-31
Last updated
2017-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise, Rest, Stroke

Keywords

Brain, MRI, Exercise, Rehabilitation, TMS

Brief summary

Participants will complete 11 sessions. These include screening, 5 sessions where exercise or rest (according to group assignment) are paired with practice of a motor task, MRI and Transcranial Magnetic Stimulation (TMS) before and after the intervention will be used to assess neuroplasticity (ability for the brain to reorganize and create new connections).

Detailed description

All participants will complete baseline sessions: 1) sub-maximal exercise test to ensure safe participation in aerobic exercise (testing session \[s\] 1); and 2) magnetic resonance imaging (MRI) to assess brain structure and function, and 3) clinical assessments of motor function and activity. The MRI and clinical tests will be completed on s2. Between the exercise test and MRI sessions individuals will wear accelerometers for 3 days to index usual activity levels. A custom computer program will then assign participants quasi-randomly to either the rest or exercise groups stratified on age, sex, and baseline motor function. Cortical excitability will be assessed before and after either a single session of priming aerobic exercise, or rest, by group (s3). Next, priming exercise will be paired with skilled motor practice for 5 sessions (s4-8). Practice sessions will be separated by 48 hours. Importantly motor learning will be assessed via delayed, no-exercise retention tests 24-hours (s9) and 30-days (s11) after the last practice session. Activity levels (3 day accelerometry), TMS and MRI measures will be re-assessed after the second retention test (s10).

Interventions

BEHAVIORALExercise

Each experimental day participants will complete an acute bout of exercise on a recumbent bike.

BEHAVIORALPractice

Each experimental day participants will complete a session of skilled motor practice.

Sponsors

University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Between the ages of 40 - 85 * Had a stroke at least 12 months ago * OR are a healthy adult who does not have a history of neurodegenerative disorders * Have the ability to understand English

Exclusion criteria

* Contraindication to brain stimulation (such as a history of seizure or epilepsy) * Contraindication to MRI (such as a pacemaker, metal in the eyes / brain or fear of enclosed spaces) * Neurodegenerative disorder ( such as Parkinson disease, Alzheimers disease or Multiple Sclerosis) * Contraindications to exercise

Design outcomes

Primary

MeasureTime frameDescription
Change response time during a novel motor task.Baseline, After Intervention (2 weeks), 30-day follow-upSerial targeting task
Wolf Motor Function Task RateBaseline, After Intervention (2 weeks), 30-day follow-upStandardized test of arm motor function

Secondary

MeasureTime frameDescription
Transcallosal InhibitionBaseline, After Intervention (2 weeks), 30-day follow-upIpsilateral silent period
Functional magnetic resonance imaging (fMRI)Baseline, After Intervention (2 weeks), 30-day follow-upResting state fMRI
Structural magnetic resonance imaging - diffusionBaseline, After Intervention (2 weeks), 30-day follow-upDiffusion weighted fractional anisotrophy
Arm Use RatioBaseline, After Intervention (2 weeks), 30-day follow-upAccelerometry
Structural magnetic resonance imaging - myelinBaseline, After Intervention (2 weeks), 30-day follow-upMyelin water fraction

Countries

Canada

Contacts

Primary ContactAsha Toner, BSc
asha.toner@ubc.ca604-828-6303
Backup ContactJason Neva, PhD
jason.neva@ubc.ca604-827-3369

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026