Interhemispheric Inhibitory Interactions (InHIb)
Primary Purpose
Stroke
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
continuous theta burst stimulation
Sponsored by

About this trial
This is an interventional treatment trial for Stroke focused on measuring Stroke, TMS, Paired Pulse, EEG, Motor Learning
Eligibility Criteria
Inclusion Criteria:
- aged 40-75
- single, MCA territory stroke
- at least 6 months post stroke
- Fugl-Meyer (upper extremity) score of 15-55
Exclusion Criteria:
- absence of TMS motor evoked potential
- score <24 on the Montreal Cognitive Assessment
- history of seizure/epilepsy, head trauma, major psychiatric diagnosis
- aphasic (score <13 on Frenchay Aphasia Screen)
- contraindications to TMS/MRI
Sites / Locations
- University of British Columbia
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
active cTBS
Sham cTBS
Arm Description
Outcomes
Primary Outcome Measures
Response Time
Response time on a custom designed serial tracking program
Secondary Outcome Measures
Wolf Motor
standardized measure of upper limb function
Limb Position Matching
Limb position matching using custom designed software
Intracortical Inhibition
Intracortical Inhibition as measured by paired pulse transcranial magnetic stimulation
Movement Time
movement time on custom designed serial tracking program
Movement Trajectory
Movement trajectory on a custom designed serial tracking program
Intracortical facilitation
Intracortical facilitation as measured by paired pulse transcranial magnetic stimulation
Full Information
NCT ID
NCT01371409
First Posted
June 2, 2011
Last Updated
June 27, 2016
Sponsor
Canadian Institutes of Health Research (CIHR)
1. Study Identification
Unique Protocol Identification Number
NCT01371409
Brief Title
Interhemispheric Inhibitory Interactions
Acronym
InHIb
Official Title
Interhemispheric Contributions to Neuroplasticity and Motor Learning After Stroke
Study Type
Interventional
2. Study Status
Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
June 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Canadian Institutes of Health Research (CIHR)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
After a stroke the excitability of the brain decreases on the stroke side and increases on the opposite, non-stroke side. These changes make use of the stroke-affected arm difficult and slow recovery. Rehabilitation exercises that increase arm use after stroke help increase brain excitability, but the net effect of this approach is low. New therapies are needed that restore more equal levels of brain excitability between the two sides. Brain stimulation is a noninvasive way to affect activity the excitability of brain cells. Pairing brain stimulation with exercises that require patients to learn new movements may help the brain to learn. Using stimulation that reduces activity in the side opposite to the stroke can increase activity on the stroke -affected side, through connections between the two brain hemispheres. The purpose of this study is to test if brain stimulation on the side opposite to the stroke, paired with arm movement exercises, can help patients learn new arm movements and improve arm function.
In this study people with stroke will receive brain stimulation over two different areas on the side of the brain opposite to the stroke: 1) those areas responsible for movement and 2) those responsible for sensation. These experiments will test both the short and long term effects of brain stimulation on patients' learning and arm function and will allow us to identify which area of the brain best improves learning and arm function. These experiments have the potential to improve the effectiveness of rehabilitation after stroke. The proposed study is among the first to test stimulation over the side of the brain opposite to the stroke damage and at multiple sites. This unique approach may help stimulate the development of new methods for stroke rehabilitation.
Detailed Description
The overall objective of this proposal is to examine the efficacy of new approaches to stroke recovery based on recent reports of interhemispheric contributions to neuroplastic change and motor skill learning. After stroke, cortical excitability is decreased in the ipsilesional and increased in the contralesional primary motor cortices (M1). Combined, these changes hamper hemiparetic arm use and impede functional recovery. Increasing hemiparetic arm use elevates the excitability of the ipsilesional cortex and improves function. Importantly, skilled motor practice raises cortical excitability to an even greater extent than merely increasing generalized use. However, the impact of increasing cortical excitability on recovery of function after stroke is limited, perhaps because the rate of change associated with both increasing use and learning new motor skills is low.
Repetitive transcranial magnetic stimulation (rTMS) is a noninvasive method of brain stimulation. In humans, rTMS applied at high frequencies can increase cortical excitability; conversely, at low frequencies it can decrease cortical excitability. While rTMS in isolation can change cortical excitability after stroke its impact on neuroplastic change is small, likely reflecting a lack of consolidation in the absence of paired motor behaviour. Modulating the activity in a given neural network with brain stimulation prior to motor skill practice may in essence prime the system and enhance the neuroplastic effects associated with learning new motor skills. Yet to date, few studies have paired rTMS with practice of a novel motor task and assessed changes in motor function or behaviour.
Intuitively, it seems simplest to employ high frequency rTMS in the ipsilesional cortex to enhance cortical excitability. However, because of the difficulty of locating stimulation targets in the damaged hemisphere, low-frequency rTMS applied over the contralesional cortex may be the better approach. Though the direct effect of low-frequency rTMS in the human cortex is to suppress activity in the stimulated region it also indirectly enhances distant activity. Low-frequency rTMS over M1 increases cortical activity in the contralateral M1 homologue. We recently extended this finding to the primary sensory cortex (S1); demonstrating that low-frequency rTMS over left S1 increased excitability in (i.e., disinhibited) right S1. Therefore, suppressing the contralesional cortex to enhance ipsilesional cortical activity may facilitate a neural environment that is conducive for neuroplastic change.
Taken together these data suggest that inhibitory brain stimulation over the contralesional cortex, paired with skilled motor practice, may offer a new approach for stroke rehabilitation. To better understand whether this approach has merit, we propose to test two specific aims in separate experiments.
Specific Aim: To test the cumulative effects of repeated sessions that pair brain stimulation over M1c versus S1c with skilled motor practice in individuals with stroke.
We will assess hemiparetic arm motor and sensory function, motor performance/ motor skill acquisition (repeated sequence response times), cortical excitability, and neuroelectric activity in individuals with chronic sub-cortical stroke. Pre-brain stimulation measures will be compared with those obtained after 5 days of training paired with brain stimulation at a separate no-rTMS retention test to assess the cumulative effects of brain stimulation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Stroke, TMS, Paired Pulse, EEG, Motor Learning
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
49 (Actual)
8. Arms, Groups, and Interventions
Arm Title
active cTBS
Arm Type
Experimental
Arm Title
Sham cTBS
Arm Type
Sham Comparator
Intervention Type
Other
Intervention Name(s)
continuous theta burst stimulation
Other Intervention Name(s)
transcranial magnetic stimulation
Intervention Description
80% active motor threshold, 600 pulses
Primary Outcome Measure Information:
Title
Response Time
Description
Response time on a custom designed serial tracking program
Time Frame
change from baseline to day 6
Secondary Outcome Measure Information:
Title
Wolf Motor
Description
standardized measure of upper limb function
Time Frame
change from baseline to day 6
Title
Limb Position Matching
Description
Limb position matching using custom designed software
Time Frame
change from baseline to day 6
Title
Intracortical Inhibition
Description
Intracortical Inhibition as measured by paired pulse transcranial magnetic stimulation
Time Frame
change from baseline to day 6
Title
Movement Time
Description
movement time on custom designed serial tracking program
Time Frame
change from baseline to day 6
Title
Movement Trajectory
Description
Movement trajectory on a custom designed serial tracking program
Time Frame
change from baseline to day 6
Title
Intracortical facilitation
Description
Intracortical facilitation as measured by paired pulse transcranial magnetic stimulation
Time Frame
change from baseline to day 6
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
aged 40-75
single, MCA territory stroke
at least 6 months post stroke
Fugl-Meyer (upper extremity) score of 15-55
Exclusion Criteria:
absence of TMS motor evoked potential
score <24 on the Montreal Cognitive Assessment
history of seizure/epilepsy, head trauma, major psychiatric diagnosis
aphasic (score <13 on Frenchay Aphasia Screen)
contraindications to TMS/MRI
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lara A Boyd, PT, PhD
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of British Columbia
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6T 2B5
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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