Modulation of Brain Plasticity After Perinatal Stroke "PLASTIC CHAMPS"

Active, not recruiting

Phase 2/3 Results N/A

Trial Description

Newborn stroke is the leading cause of a common type of cerebral palsy (CP) that affects thousands of Canadian children and families. Treatments for CP are generally ineffective, and have traditionally focused on the weak body rather than the injured brain. Understanding how the newborn brain responds to injuries like stroke (plasticity) carries the greatest potential for better treatments. We propose to study the ability of two interventions to modulate brain plasticity toward better function in children with stroke-induced CP. One is a rehabilitation method called constraint-induced movement therapy (CIMT), the other is a type of non-invasive brain stimulation called transcranial magnetic stimulation (TMS). TMS is safe and comfortable for children and we recently showed it could improve motor function in children with stroke.
We will perform a special study to test both treatments simultaneously. Children 7-18 years with stroke-induced CP will be recruited into the study from across Alberta. Each child will randomly receive either TMS, CIMT, both, or neither each day for two weeks while attending our new HemiKids Power Camp for motor learning. Improvements will be measured by trained therapists over 1 year. TMS will also measure brain plasticity, both initially and following treatment. Our lead investigator is an expert in both newborn stroke and TMS and has assembled an experienced team of accomplished collaborators to ensure the completion of this important work. This will be the largest study of children with CP examined in this manner. This will be the first clinical trial of non-invasive brain stimulation (TMS) in CP, the largest trial of CIMT (and the first exclusive to newborn stroke), and the first study allowing the direct comparison of two different therapies. In establishing the first dedicated pediatric TMS laboratory in Canada, we will be the first to measure plasticity changes in newborn stroke, advancing new treatments of this previously untreatable and disabling disease.
Patient recruitment is currently underway at Alberta Children's Hospital. Application is currently underway to expand recruitment to Northern Alberta through the Glenrose Rehabilitation Hospital and Stollery Children's Hospital, to enable patients from Northern Alberta greater opportunity to participate as subjects in this study.

Detailed Description

Perinatal stroke is the leading cause of the most common term-born cerebral palsy: hemiplegic CP (HCP). With morbidity spanning all aspects of a child's life and lasting for decades, global impact is large. Mechanisms are poorly understood and prevention strategies remain elusive. Treatments are limited, leading to loss of hope in children and families that merits exploration of new interventions. Constraint-induced movement therapy (CIMT) may benefit but proper clinical trials are required. The investigators clinical-radiographic classifications have established perinatal stroke syndromes correlating with neurological outcome. Most common are: (1) arterial ischemic stroke of the middle cerebral artery (AIS-MCA) featuring cortical and subcortical damage acquired at birth and (2) periventricular venous infarction (PVI), a novel subcortical injury acquired in utero. These syndromes differ in the essential variables for plastic organization after perinatal injury: location and timing. In addition, recent animal and human studies suggest they may share a similar maladaptive plasticity whereby motor control of the weak side is "installed" in the non-lesioned hemisphere during development. Despite the ideal plasticity model such focal injury in a young brain provides, studies have been limited and suffer from small numbers of older patients with heterogeneous lesions. The value of studying plastic organization will be realized upon translation into meaningful patient benefits.
Transcranial magnetic stimulation (TMS) offers non-invasive measurement of the neurophysiological brain properties underlying neuroplasticity. Repetitive TMS (rTMS) may modulate such systems with therapeutic effect. the investigators recently demonstrated the ability of rTMS to improve motor function in children with chronic stroke. Advances in perinatal brain injury and neurodevelopment are, for the first time, affording novel windows of opportunity for interventions to direct plastic organization toward better outcomes. Via the Alberta Perinatal Stroke Project (APSP), the investigators propose a clinical trial of two interventions to improve function in HCP while measuring the fundamental neurophysiological properties at play.
Aim 1. Determine if rTMS and CIMT can improve motor function in HCP. Hypothesis: Two weeks of daily rTMS improves motor function at 30 days.
Aim 2. Define the neurophysiology of motor organization in strokeā€induced HCP at baseline and following rTMS and CIMT.
Hypothesis: rTMS and CIMT reduce excitability of the non-lesioned motor cortex.
Population-based studies through the Alberta Perinatal Stroke Project (APSP) are establishing the largest perinatal stroke cohort to date. The investigators will complete a factorial 2 x 2 randomized clinical trial to determine the ability of daily rTMS and CIMT to improve motor function in children with HCP. Families will attend a child-centered, custom-designed intensive motor learning rehabilitation program (KidsCan Power Camp) for 2 weeks. Outcomes include validated measures of motor function and CP quality of life. The investigators will simultaneously measure the neurophysiology of plastic organization using TMS including cortical excitability, interhemispheric inhibition, and short interval intracortical inhibition. Baseline measures will define organization patterns while post-interventional measurement will evaluate the neurophysiological effects of rTMS and CIMT. Four groups of 16 children each (n=64) will be studied over 24 months with interim safety analysis after 10 and 32 patients.
Successful completion is assured by principle investigator experience in perinatal stroke and TMS and the collaborative support of world leaders in pediatric and adult stroke, TMS, basic neuroscience, and physiatry/rehabilitation. Understanding perinatal stroke plasticity and discovering methods to modulate it toward better outcomes carries a large impact, greatest for children with CP and their families.

Conditions

Interventions

  • Repetitive Transcranial Magnetic Stimulation (rTMS) Device
    Intervention Desc: TMS can affect discrete functional ares of motor cortex offering non-invasive, painless mapping and modulation of motor systems. Inhibitory rTMS (1Hz)has been shown to safely lower motor cortex excitability in normal patients as well as adult and pediatric stroke patients. Dose is 20 minutes per day (1200 stimulations) x 10 days administered over the non-lesioned M1.
    ARM 1: Kind: Experimental
    Label: rTMS and CIMT
    Description: This group will receive both rTMS and CIMT.
    ARM 2: Kind: Experimental
    Label: rTMS and no CIMT
    Description: This group will receive rTMS only.
  • Constraint-induced movement therapy (CIMT) Behavioral
    Intervention Desc: CIMT uses gentle restraint of the fully functional upper extremity to promote functional gains in the affected upper extremity. CIMT is well established to be safe and is likely effective in children with hemiplegic cerebral palsy, many of whom have perinatal stroke as studied here. A custom-fitted, bivalved cast is applied and worn for >90% of waking hours for the 2 weeks of active treatment according to protocol with daily assessments for comfort.
    ARM 1: Kind: Experimental
    Label: rTMS and CIMT
    Description: This group will receive both rTMS and CIMT.
    ARM 2: Kind: Experimental
    Label: Sham and CIMT
    Description: This group will receive CIMT and sham rTMS.

Trial Design

  • Allocation: Randomized
  • Masking: Double Blind (Subject, Caregiver, Outcomes Assessor)
  • Purpose: Treatment
  • Endpoint: Safety/Efficacy Study
  • Intervention: Factorial Assignment

Outcomes

Type Measure Time Frame Safety Issue
Primary Canadian Occupational Performance Measure (COPM). Completed 2 weeks or less before treatment day 1 Yes
Primary Canadian Occupational Performance Measure (COPM) Completed day 5 after treatment day 10 Yes
Secondary PedsQL Cerebral Palsy Module version 3.0 Young child report (ages 5-7), Child report (ages 8-12), Teen report (ages 8-12) Completed 2 weeks or less before treatment day 1 Yes
Secondary Pediatric Stroke Outcome Measure Short Neuro Exam Child Version (>2 years)(PSOM) Completed before treatment day 1 No
Secondary PedsQL Cerebral Palsy Module version 3.0 Parent Report for young child(ages 5-7), Parent Report for Child(ages 8-12), Parent report for teen(ages 8-12) Completed 2 weeks or less before treatment day 1 Yes
Secondary SHUEE (Shriners Hospital Upper Extremity Evaluation) Completed 2 weeks or less prior to treatment day 1 Yes
Secondary Box and Blocks Test Completed 2 weeks or less before treatment day 1 Yes
Secondary TMS Tolerability Measure Completed 2 weeks or less before treatment day 1 Yes
Secondary Grip and Pinch Strength Measures (GS, PS) Completed 2 weeks or less before treatment day 1 Yes
Secondary Assisting Hand Assessment (AHA) Completed 2 weeks or less before treatment day 1 Yes
Secondary Melbourne Assessment of Unilateral Upper Limb Function (MAUULF) Completed 2 weeks or less before treatment day 1 Yes
Secondary ABILHAND-Kids -Manual ability measure Completed 2 weeks or less before treatment day 1 Yes
Secondary The Revised Pediatric Motor Activity Log and the Tween Motor Activity Log (PMAL / TMAL) Completed 2 weeks or less before treatment day 1 Yes
Secondary Biometrics Data Sheet Completed each day during the 10 day camp program Yes
Secondary Paediatric Stroke Outcome Measure Short Neuro Exam (PSOM-SNE)-Child Version (Children Aged 2yrs and Older) Completed before treatment day 1 No
Secondary Home Program Log Completed by each participant everyday during treatments days 1-10 No
Secondary Camp Evaluation Form Completed by participants on Day 10 of treatment No

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