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

Primary Purpose

Cerebral Palsy

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
APPLES-tele
Parent-centered Approach (PCA) Support Intervention
Standard of Care
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cerebral Palsy

Eligibility Criteria

4 Months - 13 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Aged 4 to 13 months, corrected age
  • Patient at a participating neonatal intensive care unit (NICU) Early Developmental Clinic, outpatient physical and occupational therapy clinic and stroke clinic
  • 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 ≥3 as determined by HAI-certified study therapists
  • 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

Sites / Locations

  • Emory UniversityRecruiting
  • Kennedy Krieger InstituteRecruiting
  • Children's Hospital of PhiladelphiaRecruiting
  • The University of UtahRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

APPLES-tele first, then PCA

PCA first, then APPLES-tele

Standard of Care Control Arm

Arm Description

Participants receiving the APPLES-tele intervention for 6 weeks followed by the PCA intervention for 6 weeks.

Participants receiving the PCA intervention for 6 weeks followed by the APPLES-tele intervention for 6 weeks.

Participants receiving the standard of care for 6 weeks.

Outcomes

Primary Outcome Measures

Change in Bayley Scales of Infant and Toddler Development (Bayley-3) More Affected Arm Motor Function Score
The Bayley-3 instrument is a norm-referenced test assessing developmental delays in early childhood. The fine motor function of the more affected upper extremity is assessed using the 54 unimanual items of the Bayley-3 instrument. Responses are provided on a 3-point scale where 0 = the skill is not present, 1 = the skill is emerging, and 2 = the skill is mastered. Total unimanual fine motor raw scores for the more affected arm range from 0 to 108 where higher scores indicate greater fine motor function.
Change in Parenting Styles and Dimensions Questionnaire (PSDQ) Authoritative Scale Score
The Authoritative Parenting Style scale of the Parenting Styles and Dimensions Questionnaire (PSDQ) - short version, includes 15 items that are rated on a 5-point scale where 1 = never and 5 = always. The raw score ranges from 15 to 75 and higher scores indicate a more expression of the authoritative parenting style.

Secondary Outcome Measures

Change in Infant Motor Activity Log (IMAL) How Often Score
Parent perception of hand performance is assessed with the IMAL. The IMAL includes 20 items asking caregivers how often and how well the infant uses their less preferred hand. Responses are given on a 5-point Likert scale where 0 = not used and 5 = normal use. Raw scores on how often the infant uses their less preferred hand range from 0 to 100, with higher scores indicating more normal hand usage.
Change in Hand Assessment in Infants (HAI) Score
The HAI is an assessment evaluating quality and frequency of hand abilities in infants 3 to 12 months corrected age using a semi-structured 12-15 min videotaped play session that is scored by a certified therapist. There are 12 unimanual and 5 bimanual items, each is scored on a 3-point rating scale, of 0, 1, or 2 points. Each hand receives a raw score based upon performance on the unimanual items. The raw score for the more affected hand will be reported as a continuous variable. Total raw scores for the unimanual items range from 0 to 24 and higher scores indicate greater ability.
Change in Bayley Scales of Infant and Toddler Development (Bayley-3) Global Fine Motor Function Score
The Bayley-3 instrument is a norm-referenced test assessing developmental delays in early childhood. The fine motor function scale of the Bayley-3 instrument includes 66 items, and responses are provided on a 3-point scale where 0 = the skill is not present, 1 = the skill is emerging, and 2 = the skill is mastered. Total fine motor raw scores range from 0 to 132 where higher scores indicate greater fine motor function.
Change in Welch Emotional Connection Screen (WECS) Score
The WECS assesses parent-infant connection by examining four emotional connection dimensions of behavior: attraction, vocal communication, facial communication, and sensitivity. Items are rated on a 3-point scale where 1 = low and 3 = high. A WECS Mother (WECS-M) score is created by summing the four items for maternal connection while the four items for infant connection create a WECS Infant (WECS-I) score. Total WECS-M or WECS-I scores range from 4 to 12 where higher scores indicate greater connection.
Change in Maternal Confidence Questionnaire (MCQ) Score
The MCQ assesses parent knowledge and confidence in caring for and understanding their infant. The MCQ has 14 items which are scored on a 5-point scale where 1 = never and 5 = a great deal. Scores are reversed for some items and total scores range from 14 to 70. Higher scores indicate greater maternal confidence.

Full Information

First Posted
August 4, 2021
Last Updated
August 29, 2023
Sponsor
Emory University
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT04997109
Brief Title
Telemedicine in Early Childhood Constraint Therapy in Cerebral Palsy
Acronym
APPLES-TELE
Official Title
Telemedicine in Early Childhood Constraint Therapy in Cerebral Palsy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 23, 2022 (Actual)
Primary Completion Date
August 31, 2026 (Anticipated)
Study Completion Date
February 28, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study assesses two active treatments in different sequences and a standard of care group among infants with cerebral palsy.
Detailed 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: The APPLES intervention via telehealth (APPLES-tele) followed by a parent-centered approach (PCA) intervention The PCA intervention followed by the APPLES-tele intervention The standard of care Outcome measures will be standardized assessments of hand/arm function and validated parent-report measures of infant motor activity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Two active treatments will be administered in different sequences, and will be compared with a standard of care study arm.
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
267 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
APPLES-tele first, then PCA
Arm Type
Experimental
Arm Description
Participants receiving the APPLES-tele intervention for 6 weeks followed by the PCA intervention for 6 weeks.
Arm Title
PCA first, then APPLES-tele
Arm Type
Experimental
Arm Description
Participants receiving the PCA intervention for 6 weeks followed by the APPLES-tele intervention for 6 weeks.
Arm Title
Standard of Care Control Arm
Arm Type
Active Comparator
Arm Description
Participants receiving the standard of care for 6 weeks.
Intervention Type
Other
Intervention Name(s)
APPLES-tele
Other Intervention Name(s)
C-Mitt
Intervention Description
The APPLES-tele intervention is 5 weekly telehealth sessions of therapist-demonstrated tasks, delivered over a 6 week period. Infant participants wear a soft-constraint harness (C-Mitt) on their less affected arm for 6 hours per day, while their parent encourages them to use their more affected arm to complete play-based activities as instructed by the study therapist. As the infant experiences success, heavier objects are provided. During times when the C-Mitt is not worn, parents engage therapist-demonstrated bimanual play of increasing difficulty.
Intervention Type
Behavioral
Intervention Name(s)
Parent-centered Approach (PCA) Support Intervention
Intervention Description
The PCA support intervention is 5 weekly telehealth sessions delivered over a 6 week period. The PCA curriculum includes 5 basic principles of positive parenting from Triple P: ensuring a safe engaging environment, creating a positive learning environment, using assertive discipline, having reasonable expectations, and looking after yourself as a parent. All of these elements, when taught to parents in an individualized manner, can help promote responsivity, structure and expectations that are tailored to their child's condition and developmental stage. In addition, a curriculum of CP-specific knowledge will address the challenges unique to parents of children with CP, such as understanding principles of infant learning of new movements, challenges and solutions for self-directed activity in infants with CP.
Intervention Type
Behavioral
Intervention Name(s)
Standard of Care
Intervention Description
Participants will receive the usual care from being followed in high-risk infant follow-up (HRIF) programs in the Early Detection and Intervention (EDI) Network.
Primary Outcome Measure Information:
Title
Change in Bayley Scales of Infant and Toddler Development (Bayley-3) More Affected Arm Motor Function Score
Description
The Bayley-3 instrument is a norm-referenced test assessing developmental delays in early childhood. The fine motor function of the more affected upper extremity is assessed using the 54 unimanual items of the Bayley-3 instrument. Responses are provided on a 3-point scale where 0 = the skill is not present, 1 = the skill is emerging, and 2 = the skill is mastered. Total unimanual fine motor raw scores for the more affected arm range from 0 to 108 where higher scores indicate greater fine motor function.
Time Frame
Baseline, Week 6 (after the first intervention), Week 12 (after the second intervention)
Title
Change in Parenting Styles and Dimensions Questionnaire (PSDQ) Authoritative Scale Score
Description
The Authoritative Parenting Style scale of the Parenting Styles and Dimensions Questionnaire (PSDQ) - short version, includes 15 items that are rated on a 5-point scale where 1 = never and 5 = always. The raw score ranges from 15 to 75 and higher scores indicate a more expression of the authoritative parenting style.
Time Frame
Baseline, Week 6 (after the first intervention), Week 12 (after the second intervention)
Secondary Outcome Measure Information:
Title
Change in Infant Motor Activity Log (IMAL) How Often Score
Description
Parent perception of hand performance is assessed with the IMAL. The IMAL includes 20 items asking caregivers how often and how well the infant uses their less preferred hand. Responses are given on a 5-point Likert scale where 0 = not used and 5 = normal use. Raw scores on how often the infant uses their less preferred hand range from 0 to 100, with higher scores indicating more normal hand usage.
Time Frame
Baseline, Week 6 (after the first intervention), Week 12 (after the second intervention)
Title
Change in Hand Assessment in Infants (HAI) Score
Description
The HAI is an assessment evaluating quality and frequency of hand abilities in infants 3 to 12 months corrected age using a semi-structured 12-15 min videotaped play session that is scored by a certified therapist. There are 12 unimanual and 5 bimanual items, each is scored on a 3-point rating scale, of 0, 1, or 2 points. Each hand receives a raw score based upon performance on the unimanual items. The raw score for the more affected hand will be reported as a continuous variable. Total raw scores for the unimanual items range from 0 to 24 and higher scores indicate greater ability.
Time Frame
Baseline, Week 6 (after the first intervention)
Title
Change in Bayley Scales of Infant and Toddler Development (Bayley-3) Global Fine Motor Function Score
Description
The Bayley-3 instrument is a norm-referenced test assessing developmental delays in early childhood. The fine motor function scale of the Bayley-3 instrument includes 66 items, and responses are provided on a 3-point scale where 0 = the skill is not present, 1 = the skill is emerging, and 2 = the skill is mastered. Total fine motor raw scores range from 0 to 132 where higher scores indicate greater fine motor function.
Time Frame
Baseline, Week 6 (after the first intervention)
Title
Change in Welch Emotional Connection Screen (WECS) Score
Description
The WECS assesses parent-infant connection by examining four emotional connection dimensions of behavior: attraction, vocal communication, facial communication, and sensitivity. Items are rated on a 3-point scale where 1 = low and 3 = high. A WECS Mother (WECS-M) score is created by summing the four items for maternal connection while the four items for infant connection create a WECS Infant (WECS-I) score. Total WECS-M or WECS-I scores range from 4 to 12 where higher scores indicate greater connection.
Time Frame
Baseline, Week 6 (after the first intervention)
Title
Change in Maternal Confidence Questionnaire (MCQ) Score
Description
The MCQ assesses parent knowledge and confidence in caring for and understanding their infant. The MCQ has 14 items which are scored on a 5-point scale where 1 = never and 5 = a great deal. Scores are reversed for some items and total scores range from 14 to 70. Higher scores indicate greater maternal confidence.
Time Frame
Baseline, Week 6 (after the first intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Months
Maximum Age & Unit of Time
13 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 4 to 13 months, corrected age Patient at a participating neonatal intensive care unit (NICU) Early Developmental Clinic, outpatient physical and occupational therapy clinic and stroke clinic 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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nathalie Maitre, MD, PhD
Phone
(678) 476-5332
Email
nathalie.linda.maitre@emory.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nathalie Maitre, MD, PhD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nathalie Maitre, MD, PhD
Phone
678-476-5332
Email
Nathalie.linda.maitre@emory.edu
First Name & Middle Initial & Last Name & Degree
Nathalie Maitre, MD, PhD
Facility Name
Kennedy Krieger Institute
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21205
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vera Joanna Burton, MD, PhD
Email
BurtonJ@kennedykrieger.org
First Name & Middle Initial & Last Name & Degree
Vera Joanna Burton, MD, PhD
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Andrea F Duncan, MD, MS
Email
duncana@chop.edu
First Name & Middle Initial & Last Name & Degree
Andrea F Duncan, MD, MS
Facility Name
The University of Utah
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84112
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Betsy Ostrander, MD
Email
Betsy.ostrander@hsc.utah.edu
First Name & Middle Initial & Last Name & Degree
Betsy Ostrander, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Telemedicine in Early Childhood Constraint Therapy in Cerebral Palsy

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