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Telemedicine in Early Childhood Constraint Therapy in Cerebral Palsy (APPLES-TELE)

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Emory University

Status

Enrolling

Conditions

Cerebral Palsy

Treatments

Other: APPLES-tele
Behavioral: Standard of Care
Behavioral: Parent-centered Approach (PCA) Support Intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04997109
STUDY00003197
2R01HD081120 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This study assesses two active treatments in different sequences and a standard of care group among infants with cerebral palsy.

Full description

Cerebral palsy (CP) is a disorder characterized by impairments of sensorimotor function resulting from neural insults in the perinatal period. Every year almost 10,000 children are born with CP in the US. CP incidence ranges from 2 to 3 per 1000 in North America, Australia, and Europe and is difficult to estimate in the developing world. Intervention strategies to promote function of children with CP must be adaptable to settings where resources or access may be limited, yet simultaneously integrate best clinical evidence and neuroscientific principles. Upper extremity (UE) impairments are present in a significant portion of children with CP, some with hemiplegia (~25% children with CP), and others with quadriplegia, in which one arm and hand may be more affected than the other (another ~25%). UE impairments in CP result from a combination of motor and sensory dysfunctions including a lack of high-quality motor experience, which combined with "noisy" (often faulty) sensory input, challenges the acquisition of new effective motor patterns.

Among the various approaches to improve UE function in infants with CP are constraint-induced movement therapy (the use of constraints on less affected limbs) and bimanual therapy (training of both extremities in coordination). Brief sessions of parent-delivered, infant-initiated, goal-directed, success-motivated and repetitive activity in enriched sensory environments can be effective, while respecting fundamental principles of infant development and home life. Parent administration of the intervention helps preserve the integrity of early parent-child relationships, critical to establishment of infants' sense of self, safety, and independence.

Finally, to take full advantage of neuroplasticity and maximize potential downstream developmental effects, it is essential to intervene as early as possible in children with CP. Promising new treatments such as transcranial magnetic stimulation, robotic-assisted movements and technology enhancements to movement feedback are in development. However, these interventions require substantial investments of highly-skilled therapists, technology, infrastructure and access to academic facilities. While the new interventions advance the cutting-edge of motor intervention development, on another leading edge, parent-delivered therapist-directed telehealth interventions are becoming more widespread, addressing a critical need for lower-resource interventions.

Healthcare systems resources are limited, and can be difficult to access due to geographic and socioeconomic obstacles. While telehealth therapy seems eminently practical, and a natural extension of current interventions for infants with CP, it faces its own scientific challenges. The same essential attributes of physical therapy that make it so effective in person can make it difficult to deliver via telehealth. Telehealth therapy in infants requires a level of parent engagement, knowledge and parenting skills that is sometimes lacking. Feasible telehealth interventions to improve function in infants with CP must also address the challenges faced by their parents in conducting the sessions through effective parenting supports.

In this study, infant participants with CP will be randomized to one of three treatment groups:

  1. The APPLES intervention via telehealth (APPLES-tele) followed by a parent-centered approach (PCA) intervention
  2. The PCA intervention followed by the APPLES-tele intervention
  3. The standard of care

Outcome measures will be standardized assessments of hand/arm function and validated parent-report measures of infant motor activity.

Enrollment

267 estimated patients

Sex

All

Ages

4 to 13 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 4 to 13 months, corrected age
  • Diagnosis of CP or classification of high-risk for CP as determined by published guidelines (>95% risk of later CP)
  • Hammersmith Infant Neurological Exam (HINE) arm asymmetry score of greater than or equal to 2 and/or neuroimaging consistent with perinatal involvement
  • Hand Assessment for Infants (HAI) difference between hands ≥2, with an observable and relative difference in quality or amount of movement between hands, as determined by HAI-certified study therapists and/or a unimanual Bayley score difference between hands >1
  • Parent/legal guardian is able to provide informed consent

Exclusion criteria

  • Congenital malformation of the brain or musculoskeletal system (MSK)
  • Receipt of botulinum toxin to the affected extremity within 3 months of study entry
  • Any prior long-term hard constraint programs

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

267 participants in 3 patient groups

APPLES-tele first, then PCA
Experimental group
Description:
Participants receiving the APPLES-tele intervention for 6 weeks followed by the PCA intervention for 6 weeks.
Treatment:
Behavioral: Parent-centered Approach (PCA) Support Intervention
Other: APPLES-tele
PCA first, then APPLES-tele
Experimental group
Description:
Participants receiving the PCA intervention for 6 weeks followed by the APPLES-tele intervention for 6 weeks.
Treatment:
Behavioral: Parent-centered Approach (PCA) Support Intervention
Other: APPLES-tele
Standard of Care Control Arm
Active Comparator group
Description:
Participants receiving the standard of care for 6 weeks.
Treatment:
Behavioral: Standard of Care

Trial contacts and locations

4

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Central trial contact

Nathalie Maitre, MD, PhD

Data sourced from clinicaltrials.gov

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