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Telemedicine-Based Constraint Therapy for Cerebral Palsy (APPLES-TELE Trial)
N/A
Recruiting
Led By Nathalie Maitre, MD, PhD
Research Sponsored by Emory University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Diagnosis of CP or classification of high-risk for CP as determined by published guidelines (>95% risk of later CP)
Aged 4 to 13 months, corrected age
Must not have
Congenital malformation of the brain or musculoskeletal system (MSK)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, week 6 (after the first intervention), week 12 (after the second intervention)
Awards & highlights
No Placebo-Only Group
Summary
This trial tests two therapies for infants with cerebral palsy: one delivered via telehealth and one focused on parent-led activities at home. Both aim to improve hand and arm function by involving parents in consistent exercises.
Who is the study for?
This trial is for infants aged 4 to 13 months at risk of or diagnosed with cerebral palsy, who have been patients in certain clinics. They must show arm movement differences and haven't had long-term constraint programs, brain or musculoskeletal malformations, or recent botulinum toxin treatments.
What is being tested?
The study compares two active treatments: APPLES-tele and PCA Support Intervention against standard care. Infants will receive these interventions in different sequences to see which is more effective for early childhood development.
What are the potential side effects?
As this trial involves non-pharmaceutical interventions focused on therapy and support, traditional side effects like those from medication are not applicable. However, there may be fatigue or frustration during the exercises.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am diagnosed with or at high risk for cerebral palsy.
Select...
My child is between 4 to 13 months old, considering their corrected age.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I was born with a brain or musculoskeletal system malformation.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, week 6 (after the first intervention), week 12 (after the second intervention)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, week 6 (after the first intervention), week 12 (after the second intervention)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Bayley Scales of Infant and Toddler Development (Bayley-3) More Affected Arm Motor Function Score
Change in Parenting Styles and Dimensions Questionnaire (PSDQ) Authoritative Scale Score
Secondary study objectives
Change in Bayley Scales of Infant and Toddler Development (Bayley-3) Global Fine Motor Function Score
Change in Hand Assessment in Infants (HAI) Score
Change in Infant Motor Activity Log (IMAL) How Often Score
+2 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: PCA first, then APPLES-teleExperimental Treatment3 Interventions
Participants receiving the PCA intervention for 6 weeks followed by the APPLES-tele intervention for 6 weeks.
Group II: APPLES-tele first, then PCAExperimental Treatment3 Interventions
Participants receiving the APPLES-tele intervention for 6 weeks followed by the PCA intervention for 6 weeks.
Group III: Standard of Care Control ArmActive Control1 Intervention
Participants receiving the standard of care for 6 weeks.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Standard of Care
2017
Completed Phase 4
~4420
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) include physical and occupational therapy, botulinum toxin injections, and oral antispasticity medications. Physical and occupational therapy aim to improve motor function and daily living skills through targeted exercises and activities that enhance strength, coordination, and flexibility.
Botulinum toxin injections temporarily reduce spasticity by blocking nerve signals to the muscles, which helps in delaying muscle shortening and improving range of motion. Oral antispasticity medications, such as baclofen and benzodiazepines, work by relaxing muscles and reducing muscle stiffness.
These treatments are crucial for CP patients as they help manage spasticity, improve functional abilities, and enhance overall quality of life.
Case for gait analysis as part of the management of incomplete spinal cord injury.
Case for gait analysis as part of the management of incomplete spinal cord injury.
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Who is running the clinical trial?
Emory UniversityLead Sponsor
1,697 Previous Clinical Trials
2,603,646 Total Patients Enrolled
2 Trials studying Cerebral Palsy
86 Patients Enrolled for Cerebral Palsy
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)NIH
2,051 Previous Clinical Trials
2,731,277 Total Patients Enrolled
33 Trials studying Cerebral Palsy
8,645 Patients Enrolled for Cerebral Palsy
Nathalie Maitre, MD, PhDPrincipal InvestigatorEmory University
1 Previous Clinical Trials
92 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am diagnosed with or at high risk for cerebral palsy.I am a patient at a NICU, Early Developmental, or stroke clinic.I was born with a brain or musculoskeletal system malformation.I have not received botulinum toxin in my affected limb in the last 3 months.My child is between 4 to 13 months old, considering their corrected age.
Research Study Groups:
This trial has the following groups:- Group 1: APPLES-tele first, then PCA
- Group 2: PCA first, then APPLES-tele
- Group 3: Standard of Care Control Arm
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
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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