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Remote Ischemic Conditioning for Cerebral Palsy
N/A
Recruiting
Led By Swati Surkar
Research Sponsored by East Carolina University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Manual Ability Classification System (MACS) levels I-III
Children diagnosed with unilateral cerebral palsy, ages 6-16 years
Must not have
Children with metal implants and incompatible medical devices for MRI scans
Children with absent active motor threshold
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline and 1 week
Summary
This trial tests a new treatment for children with one-sided cerebral palsy. It uses a blood pressure cuff to stop and start blood flow, combined with hand exercises, to help the brain learn new movements better. The goal is to improve hand and arm function in these children.
Who is the study for?
This trial is for children aged 6-16 with unilateral cerebral palsy, who can stack cups and follow instructions. They should be fairly independent in daily tasks (MACS levels I-III) and not have other developmental disabilities, seizures, metal implants, or be on certain medications.
What is being tested?
The study tests if remote ischemic conditioning (RIC), a new method that temporarily restricts blood flow to limbs, can improve hand coordination when combined with intensive bimanual skill training in children with unilateral cerebral palsy.
What are the potential side effects?
Potential side effects of RIC may include discomfort at the site where blood flow is restricted. The intensity of training could lead to muscle soreness or fatigue.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I can use my hands for daily tasks with little to some help.
Select...
My child, aged 6-16, has been diagnosed with unilateral cerebral palsy.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My child has metal implants or devices not safe for MRI.
Select...
My child cannot voluntarily move muscles.
Select...
My child has difficulties with thinking or communicating.
Select...
My child has a metabolic disorder, cancer, or water on the brain.
Select...
My child has heart, lung, or blood vessel problems.
Select...
My child has seizures and is taking medication for them.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline and 1 week
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and 1 week
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Assisting Hand Assessment
Change in Bimanual Task Performance
Change in Resting and Active Motor Thresholds
+1 moreSecondary study objectives
Change in Balance performance
Change in Box and Blocks Test (BBT)
Change in Hand grip and pinch strength
+5 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Remote Ischemic Conditioning (RIC)Experimental Treatment4 Interventions
RIC is achieved via blood pressure cuff inflation to at least 20 mmHg above systolic blood pressure to 250 mmHg on the more involved arm. RIC involves 5 cycles of 5 minutes blood pressure cuff inflation followed by alternating 5 minutes of cuff deflation and requires 45 minutes. RIC is performed on visits 2-6.
Intervention
* Hand Arm Bimanual Intensive Therapy (HABIT)
* Bimanual cup stacking training
* Balance training
Group II: Sham ConditioningPlacebo Group4 Interventions
Sham conditioning is achieved via blood pressure cuff inflation to 25 mmHg on the more involved arm. RIC involves 5 cycles of 5 minutes blood pressure cuff inflation followed by alternating 5 minutes of cuff deflation and requires 45 minutes. RIC is performed on visits 2-6.
Intervention
* Hand Arm Bimanual Intensive Therapy (HABIT)
* Bimanual cup stacking training
* Balance training
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Remote Ischemic Conditioning (RIC)
2015
Completed Phase 3
~410
Balance training
2014
Completed Phase 1
~820
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Cerebral Palsy (CP) such as Constraint-Induced Movement Therapy (CIMT), Bimanual Therapy, and Botulinum Neurotoxin (BoNT) injections work by enhancing motor function and promoting neuroplasticity. CIMT encourages the use of the affected limb by restraining the unaffected one, thereby improving motor and sensory function.
Bimanual Therapy focuses on coordinated use of both hands through structured activities. BoNT injections reduce muscle spasticity by blocking nerve signals, improving range of motion and function.
These treatments are vital for CP patients as they enhance neuroplasticity and motor skills, leading to greater independence and better quality of life.
Feasibility of High Repetition Upper Extremity Rehabilitation for Children with Unilateral Cerebral Palsy.The Most Cited Original Articles in Brain Imaging of Children With Cerebral Palsy: A Bibliometric Analysis Between 1984 and 2019.The effects of modified constraint-induced movement therapy combined with intensive bimanual training in children with brachial plexus birth injury: a retrospective data base study.
Feasibility of High Repetition Upper Extremity Rehabilitation for Children with Unilateral Cerebral Palsy.The Most Cited Original Articles in Brain Imaging of Children With Cerebral Palsy: A Bibliometric Analysis Between 1984 and 2019.The effects of modified constraint-induced movement therapy combined with intensive bimanual training in children with brachial plexus birth injury: a retrospective data base study.
Find a Location
Who is running the clinical trial?
East Carolina UniversityLead Sponsor
109 Previous Clinical Trials
39,153 Total Patients Enrolled
2 Trials studying Stroke
7,025 Patients Enrolled for Stroke
Swati SurkarPrincipal InvestigatorEast Carolina University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I can use my hands for daily tasks with little to some help.I am in regular school classes and can understand experiment instructions.Children with other conditions like autism or developmental coordination disorders.My child has metal implants or devices not safe for MRI.My child cannot voluntarily move muscles.My child has difficulties with thinking or communicating.My child has a metabolic disorder, cancer, or water on the brain.My child, aged 6-16, has been diagnosed with unilateral cerebral palsy.I can stack 3 cups in under 2 minutes.My child has heart, lung, or blood vessel problems.Children who are getting other treatments like rTMS and tDCS.My child has seizures and is taking medication for them.
Research Study Groups:
This trial has the following groups:- Group 1: Sham Conditioning
- Group 2: Remote Ischemic Conditioning (RIC)
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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