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Robotic Rehabilitation and Brain Stimulation for Children With Hemiparetic Cerebral Palsy (RoboCP)

Primary Purpose

Hemiplegic Cerebral Palsy, Perinatal Stroke

Status
Unknown status
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Robot Rehabilitation + tDCS
Robotic Rehabilitation + sham tDCS
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemiplegic Cerebral Palsy focused on measuring robotic rehabilitation, tDCS, non-invasive brain stimulation

Eligibility Criteria

6 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • confirmed diagnosis of hemiparetic cerebral palsy due to unilateral perinatal stroke
  • age 6-18 years
  • Manual Ability Classification System (MACS) Level I-III
  • Modified Ashworth Score in shoulder and elbow <=3;
  • Visual acuity (corrected) better than 20/50 in both eyes
  • able to follow instructions and comply with protocol;
  • able to give consent/assent;
  • able to commit to all assessment and intervention sessions.

Exclusion Criteria:

  • significant contractures in the upper extremity;
  • other neurological conditions or active medical disease;
  • unstable epilepsy;
  • contraindications to tDCS;
  • botulinum toxin A injections in the upper extremity in the past 6 months;
  • upper extremity surgical intervention in past 6 months;
  • involvement in another interventional study.

Sites / Locations

  • Alberta Children's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Robot + tDCS

Robot + sham tDCS

Arm Description

10 sessions of 1.5 hrs of robotic therapy within a 3 week period, with 20 minutes of 1mA cathodal tDCS applied to the contralesional M1 area during first 20 minutes of robotic therapy. Robotic therapy will be conducted using the Kinarm Exoskeleton robot and use games to target unilateral and bilateral motor and sensory impairments.

10 sessions of 1.5 hrs of robotic therapy within a 3 week period with 20 minutes of SHAM tDCS applied during the first 20 minutes of the robotic therapy. As with experimental arm, electrode will be placed on contralesional M1. Current will ramp up and then immediately ramp down to simulate the cutaneous sensations felt with actual tDCS. Robotic therapy will be delivered with Kinarm Exoskeleton robot and use games to target unilateral and bilateral motor and sensory impairments.

Outcomes

Primary Outcome Measures

Reaching Accuracy
Change in reaching accuracy as measured by initial direction error on robotic visually guided reaching task.

Secondary Outcome Measures

Standardized robotic measures of motor and sensory performance
Robotic measures of spatiotemporal reaching (path length ratio, reaction time, movement speed, number of speed maximums), proprioception (variability in position matching) and bilateral object hitting task (number of balls hit with each hand). Each measure will be assessed as change from pre-assessment to immediate post-assessment
Assisting Hand Assessment
Performance on clinical assessment that determines how effectively the affected limb is used on tasks typically requiring both arms.
Box and Block Assessment
Measure of ability to reach, grasp and release that measures how many 1" cubes a child can move from one side of a box to another in 1 minute.
Purdue Pegboard
Measure of manual dexterity measured by how many small pegs a child can place in a pegboard in 30 seconds.

Full Information

First Posted
January 15, 2020
Last Updated
January 15, 2020
Sponsor
University of Calgary
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1. Study Identification

Unique Protocol Identification Number
NCT04233710
Brief Title
Robotic Rehabilitation and Brain Stimulation for Children With Hemiparetic Cerebral Palsy
Acronym
RoboCP
Official Title
Robotic Rehabilitation and Brain Stimulation for Children With Hemiparetic Cerebral Palsy
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 25, 2019 (Actual)
Primary Completion Date
December 31, 2020 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Calgary

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
This study evaluates the use of robotic rehabilitation with and without transcranial direct current stimulation (tDCS) to improve motor performance in children with hemiparetic cerebral palsy. Half of the participants will receive robotic rehabilitation and half will receive robotic rehabilitation with tDCS. We hypothesize that tDCS may augment the robotic therapy and show greater improvements than robotic therapy alone.
Detailed Description
The defining feature of hemiparetic cerebral palsy is motor impairments primarily on one side of the body. Robotic rehabilitation and non-invasive brain stimulation are both emerging technologies that may be beneficial in improving motor performance in individuals with hemiparetic cerebral palsy. Robotic rehabilitation can allow for hundreds of arm movements in the span of an hour, a level of concentrated repetitions that is not possible in traditional rehabilitation. Additionally, robotics can target specific deficits, such as coordinating both arms together, improving accuracy of reaching movements, or improving proprioception, while simultaneously giving the therapist and patient quantitative feedback on performance. Non-invasive brain stimulation using transcranial direct current stimulation (tDCS) can safely modulate activity in regions of the brain and has emerged as a tool to enhance motor learning in typically developing children and augment therapy in children with hemiparetic cerebral palsy. Children with hemiparetic cerebral palsy will be randomized to receive robotic rehabilitation with tDCS or robotic rehabilitation with sham-tDCS. Participants and the assessors will be blinded to the treatment. All children will complete 10 sessions within 3 weeks of 1.5 hours of robotic rehabilitation. The Kinarm Exoskeleton Robot will be used and children will play games with their affected arm or both arms to target different aspects of sensorimotor control. Children will simultaneously receive real or sham tDCS for the first 20 minutes of the session. tDCS will consist of 1 mA current with the cathode applied over the contralesional M1 area. All children will be assessed before and after the 10 session intervention period using robotic and clinical measures of motor and sensory performance, and at a 3 month follow up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemiplegic Cerebral Palsy, Perinatal Stroke
Keywords
robotic rehabilitation, tDCS, non-invasive brain stimulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Robot + tDCS
Arm Type
Experimental
Arm Description
10 sessions of 1.5 hrs of robotic therapy within a 3 week period, with 20 minutes of 1mA cathodal tDCS applied to the contralesional M1 area during first 20 minutes of robotic therapy. Robotic therapy will be conducted using the Kinarm Exoskeleton robot and use games to target unilateral and bilateral motor and sensory impairments.
Arm Title
Robot + sham tDCS
Arm Type
Sham Comparator
Arm Description
10 sessions of 1.5 hrs of robotic therapy within a 3 week period with 20 minutes of SHAM tDCS applied during the first 20 minutes of the robotic therapy. As with experimental arm, electrode will be placed on contralesional M1. Current will ramp up and then immediately ramp down to simulate the cutaneous sensations felt with actual tDCS. Robotic therapy will be delivered with Kinarm Exoskeleton robot and use games to target unilateral and bilateral motor and sensory impairments.
Intervention Type
Combination Product
Intervention Name(s)
Robot Rehabilitation + tDCS
Intervention Description
Robotic therapy with Kinarm Exoskeleton Robot and 1 mA cathodal tDCS applied to contralesional M1 for 20 minutes.
Intervention Type
Behavioral
Intervention Name(s)
Robotic Rehabilitation + sham tDCS
Intervention Description
Robotic therapy with Kinarm Exoskeleton Robot and sham tDCS.
Primary Outcome Measure Information:
Title
Reaching Accuracy
Description
Change in reaching accuracy as measured by initial direction error on robotic visually guided reaching task.
Time Frame
change between pre-assessment (within 1 week of starting intervention) and post-assessment (within 1 week of completing intervention)
Secondary Outcome Measure Information:
Title
Standardized robotic measures of motor and sensory performance
Description
Robotic measures of spatiotemporal reaching (path length ratio, reaction time, movement speed, number of speed maximums), proprioception (variability in position matching) and bilateral object hitting task (number of balls hit with each hand). Each measure will be assessed as change from pre-assessment to immediate post-assessment
Time Frame
change between pre-assessment (within 1 week of starting intervention) and post-assessment (within 1 week of completing intervention)
Title
Assisting Hand Assessment
Description
Performance on clinical assessment that determines how effectively the affected limb is used on tasks typically requiring both arms.
Time Frame
change between pre-assessment (within 1 week of starting intervention) and post-assessment (within 1 week of completing intervention)
Title
Box and Block Assessment
Description
Measure of ability to reach, grasp and release that measures how many 1" cubes a child can move from one side of a box to another in 1 minute.
Time Frame
change between pre-assessment (within 1 week of starting intervention) and post-assessment (within 1 week of completing intervention)
Title
Purdue Pegboard
Description
Measure of manual dexterity measured by how many small pegs a child can place in a pegboard in 30 seconds.
Time Frame
change between pre-assessment (within 1 week of starting intervention) and post-assessment (within 1 week of completing intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: confirmed diagnosis of hemiparetic cerebral palsy due to unilateral perinatal stroke age 6-18 years Manual Ability Classification System (MACS) Level I-III Modified Ashworth Score in shoulder and elbow <=3; Visual acuity (corrected) better than 20/50 in both eyes able to follow instructions and comply with protocol; able to give consent/assent; able to commit to all assessment and intervention sessions. Exclusion Criteria: significant contractures in the upper extremity; other neurological conditions or active medical disease; unstable epilepsy; contraindications to tDCS; botulinum toxin A injections in the upper extremity in the past 6 months; upper extremity surgical intervention in past 6 months; involvement in another interventional study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rachel L Hawe, DPT, PhD
Phone
403-944-1094
Email
rachel.hawe@ucalgary.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Sean P Dukelow, MD, PhD
Phone
403-944-5930
Email
spdukelo@ucalgary.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sean P Dukelow, MD, PhD
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
Facility Information:
Facility Name
Alberta Children's Hospital
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T3B 6A8
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rachel L Hawe, DPT, PhD
Phone
403-944-1094
Email
rachel.hawe@ucalgary.ca

12. IPD Sharing Statement

Citations:
PubMed Identifier
36188922
Citation
Raess L, Hawe RL, Metzler M, Zewdie E, Condliffe E, Dukelow SP, Kirton A. Robotic Rehabilitation and Transcranial Direct Current Stimulation in Children With Bilateral Cerebral Palsy. Front Rehabil Sci. 2022 Feb 25;3:843767. doi: 10.3389/fresc.2022.843767. eCollection 2022.
Results Reference
derived

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Robotic Rehabilitation and Brain Stimulation for Children With Hemiparetic Cerebral Palsy

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