AzTrials
AzTrials

StrokeInHIbNCT01371409

Interhemispheric Inhibitory Interactions

A study testing continuous theta burst stimulation in people with Stroke, run by Canadian Institutes of Health Research (CIHR) at 1 site in Canada.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial 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. Read more about this study

Who is it for?
Ages 40 to 75 years
Conditions the study is for
Stroke
What is being tested?
continuous theta burst stimulation
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
49 participants
Where
1 siteCanada
Study dates
Apr 2011to Jun 2016
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • aged 40-75
  • single, MCA territory stroke
  • at least 6 months post stroke
  • Fugl-Meyer (upper extremity) score of 15-55

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • University of British Columbia

    Vancouver, British Columbia, V6T 2B5

Other trials in Canada

About this study

Official title: Interhemispheric Contributions to Neuroplasticity and Motor Learning After Stroke

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.

Read the 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.

Conditions
Stroke
Being tested
continuous theta burst stimulation
Keywords
Stroke, TMS, Paired Pulse, EEG, Motor Learning
Medical subject headings
Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • continuous theta burst stimulationOther

    Also called transcranial magnetic stimulation

    80% active motor threshold, 600 pulses

Study groups in NCT01371409
Study groupRoleWhat they receive
active cTBSExperimentalNot described
Receives: Other: continuous theta burst stimulation
Sham cTBSSham comparatorNot described
Receives: Other: continuous theta burst stimulation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Response Time

    Response time on a custom designed serial tracking program

    Measured: change from baseline to day 6

Secondary outcomes (6)
  1. Wolf Motor

    standardized measure of upper limb function

    Measured: change from baseline to day 6

  2. Limb Position Matching

    Limb position matching using custom designed software

    Measured: change from baseline to day 6

  3. Intracortical Inhibition

    Intracortical Inhibition as measured by paired pulse transcranial magnetic stimulation

    Measured: change from baseline to day 6

  4. Movement Time

    movement time on custom designed serial tracking program

    Measured: change from baseline to day 6

  5. Movement Trajectory

    Movement trajectory on a custom designed serial tracking program

    Measured: change from baseline to day 6

  6. Intracortical facilitation

    Intracortical facilitation as measured by paired pulse transcranial magnetic stimulation

    Measured: change from baseline to day 6

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Jun 2011 (estimated)
  2. Study startApr 2011
  3. Primary completionFeb 2014
  4. Study completionJun 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
49 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01371409
Sponsor's protocol ID
H09-00368
Other IDs
CIHR
Acronym
InHIb
Status last verified
Jun 2016
First submitted
2 Jun 2011
Last updated
28 Jun 2016
Results posted
No
Data monitoring committee
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing continuous theta burst stimulation in people with Stroke, run by Canadian Institutes of Health Research (CIHR) at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Jun 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Response Time (time frame: change from baseline to day 6). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jun 2016.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in