A Comparison: High Intense Periodic vs. Every Week Therapy in Children With Cerebral Palsy (ACHIEVE) (ACHIEVE)
Primary Purpose
Cerebral Palsy
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Physical Therapy
Sponsored by
About this trial
This is an interventional treatment trial for Cerebral Palsy focused on measuring Cerebral Palsy, Motor Impairments
Eligibility Criteria
Inclusion Criteria:
- 2 to 8 years of age at initiation of treatment
- a diagnosis of motor delay or CP in GMFCS levels 1-V
- ability to tolerate a 2 hour therapy session based on parent report and evaluating therapists.
Exclusion Criteria:
- uncontrollable seizures or any co-morbid condition that prevents full participation during treatment sessions
- participation in another daily treatment program in the last 6 months
- auditory or visual conditions that prevent full participation during treatment sessions
- Progressive neurological disorder with no potential for improvement.
- Recent surgery where physical therapy is contraindicated.
Sites / Locations
- Nationwide Children's Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Usual weekly
High intensity periodic
Arm Description
Usual weekly physical therapy is 1 hours of therapy one day per week for 40 weeks.
High intensity periodic physical therapy is 2 hours of therapy 5 days a week for 2 weeks, followed by an 18 week break, followed by another bout of high intensity therapy for 2 hours of therapy every weekday for two 10-consecutive-weekdays, followed by another 18 week break from therapy.
Outcomes
Primary Outcome Measures
Change in Gross Motor Function Measure (GMFM)-88
GMFM evaluates change in gross motor function over time or with intervention in children
Secondary Outcome Measures
Change in Goal Attainment Scaling (GAS)
GAS creates patient, family, and clinical anchors as the external criterion for improvement by establishing activity or participation goals that reflect what an individual, family, and clinician consider meaningful or relevant.The GAS method allows for goals to be defined at different levels of mastery and assigned numerical values for score calculation, similar to a Likert scale. The scale will have 5 points representing different levels of mastery of the individual patient's goal. A score of -2 represents baseline, -1 less change than expected, 0 for the expected level of change, and +1 and +2 for achievement of more change than expected. To attempt to ensure ordinality, each level on the scale will be described and will reflect a single dimension of change that is measureable, achievable, and relevant
Change in Bayley Scales of Infant Development III
The Bayley Scales of Infant and Toddler Development-Third Edition is an individually administered test designed to assess developmental functioning of infants and toddlers. The Bayley-III assesses development in five areas: cognitive, language, motor, social-emotional, and adaptive behavior.
Change in Pediatric Evaluation and Disability Inventory (PEDI)
Administered as a parent survey. The PEDI is a descriptive measure of a child's current functional performance and can track changes over time. The PEDI measures both capability and performance of functional activities in three content domains: self-care, mobility, and social function.It can be used as a comprehensive clinical assessment of key functional capabilities and performance in children between the ages of six months and seven years.
Full Information
NCT ID
NCT02897024
First Posted
September 7, 2016
Last Updated
February 23, 2021
Sponsor
Ohio State University
Collaborators
Patient-Centered Outcomes Research Institute
1. Study Identification
Unique Protocol Identification Number
NCT02897024
Brief Title
A Comparison: High Intense Periodic vs. Every Week Therapy in Children With Cerebral Palsy (ACHIEVE)
Acronym
ACHIEVE
Official Title
A Comparison: High Intense Periodic vs. Every Week Therapy in Children With Cerebral Palsy (ACHIEVE)
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
September 2016 (Actual)
Primary Completion Date
December 2020 (Actual)
Study Completion Date
December 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University
Collaborators
Patient-Centered Outcomes Research Institute
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The ACHIEVE study is a comparison of the effectiveness of 2 intensities of physical therapy treatment for children with Cerebral Palsy in an outpatient physical therapy setting. High intensity periodic is 2 hours of focused and high intense treatment per weekday for 4 weeks. In comparison, usual weekly is considered standard of care; although both dosing models are used clinically for children with CP. Participants are assign to the treatment group at random. Participant who are unable to consent to randomization are allowed to chose a treatment group.
Detailed Description
The overall goal of this project is to compare the effectiveness of high intense periodic and usual weekly therapy in treating Cerebral Palsy (CP) in children 2-8 years of age for motor rehabilitation. In this prospective randomized controlled trial (RCT), 108 children ages 2 to 8 years of age with CP will be enrolled and assigned to one of 2 service delivery models: 1 hour per day, 1 x per week for 40 weeks (usual weekly); and 2 hours every weekday for two 10-consecutive-weekdays (total 4 weeks), for a repeated "periodic" bout (high intense periodic). Participants unable to consent to randomization are allowed to chose a treatment group. All patients enrolled in ACHIEVE will also have 1 hour per month of Physical Therapy Consultation (PTC) during the treatment period of 40 weeks (9 months). PTCs provide monthly motor skill monitoring, consultation, and home therapy program progression. Outcome evaluations will be performed by blinded evaluators at baseline (month 0, before treatment), month 9 for all patients to assess short term effects, and at months 12 and 18 for patients to assess long term effects. Parent surveys will be collected at 0, 4.5, and 9 months only (PC-2). Short-term and long-term effects will be analyzed to determine individual differences in children's response to intensity. A subset will be analyzed at 12 and 18 month.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
Keywords
Cerebral Palsy, Motor Impairments
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
108 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Usual weekly
Arm Type
Active Comparator
Arm Description
Usual weekly physical therapy is 1 hours of therapy one day per week for 40 weeks.
Arm Title
High intensity periodic
Arm Type
Experimental
Arm Description
High intensity periodic physical therapy is 2 hours of therapy 5 days a week for 2 weeks, followed by an 18 week break, followed by another bout of high intensity therapy for 2 hours of therapy every weekday for two 10-consecutive-weekdays, followed by another 18 week break from therapy.
Intervention Type
Other
Intervention Name(s)
Physical Therapy
Intervention Description
One-on-one physical therapy sessions (one therapist and one patient). Principles of motor learning used include repetition, task-specificity, active practice, generalization of skills, errors, structured practice, and developmentally appropriate feedback with sufficient time to practice.
Primary Outcome Measure Information:
Title
Change in Gross Motor Function Measure (GMFM)-88
Description
GMFM evaluates change in gross motor function over time or with intervention in children
Time Frame
Baseline (pre-treatment) and 9 months 12 months, and 18 months following initiation of treatment.
Secondary Outcome Measure Information:
Title
Change in Goal Attainment Scaling (GAS)
Description
GAS creates patient, family, and clinical anchors as the external criterion for improvement by establishing activity or participation goals that reflect what an individual, family, and clinician consider meaningful or relevant.The GAS method allows for goals to be defined at different levels of mastery and assigned numerical values for score calculation, similar to a Likert scale. The scale will have 5 points representing different levels of mastery of the individual patient's goal. A score of -2 represents baseline, -1 less change than expected, 0 for the expected level of change, and +1 and +2 for achievement of more change than expected. To attempt to ensure ordinality, each level on the scale will be described and will reflect a single dimension of change that is measureable, achievable, and relevant
Time Frame
Baseline (pre-treatment) and 9 months 12 months, and 18 months following initiation of treatment.
Title
Change in Bayley Scales of Infant Development III
Description
The Bayley Scales of Infant and Toddler Development-Third Edition is an individually administered test designed to assess developmental functioning of infants and toddlers. The Bayley-III assesses development in five areas: cognitive, language, motor, social-emotional, and adaptive behavior.
Time Frame
Baseline (pre-treatment) and 9 months 12 months, and 18 months following initiation of treatment.
Title
Change in Pediatric Evaluation and Disability Inventory (PEDI)
Description
Administered as a parent survey. The PEDI is a descriptive measure of a child's current functional performance and can track changes over time. The PEDI measures both capability and performance of functional activities in three content domains: self-care, mobility, and social function.It can be used as a comprehensive clinical assessment of key functional capabilities and performance in children between the ages of six months and seven years.
Time Frame
Baseline (pre-treatment) and 9 months 12 months, and 18 months following initiation of treatment.
Other Pre-specified Outcome Measures:
Title
Change in Pediatric Outcomes Questionnaire (PODCI)
Description
Parent survey to assess patients under the age of 19 years for overall health, pain, and ability to participate in normal daily activities, as well as more vigorous activities typically associated with young people. The target populations are children and adolescents ages 2-18 years with general health problems, specifically any problems related to bone and muscle conditions.
Time Frame
Collected at 0, 4.5 and 9 months (during the treatment period)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
2 to 8 years of age at initiation of treatment
a diagnosis of motor delay or CP in GMFCS levels 1-V
ability to tolerate a 2 hour therapy session based on parent report and evaluating therapists.
Exclusion Criteria:
uncontrollable seizures or any co-morbid condition that prevents full participation during treatment sessions
participation in another daily treatment program in the last 6 months
auditory or visual conditions that prevent full participation during treatment sessions
Progressive neurological disorder with no potential for improvement.
Recent surgery where physical therapy is contraindicated.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jill Heathcock, MPT, PhD
Organizational Affiliation
Ohio State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nationwide Children's Hospital
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43205
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
34529078
Citation
Scott KS, Barbosa GO, Pan J, Heathcock JC. Using the PODCI to Measure Motor Function and Parent Expectations in Children With Cerebral Palsy. Phys Ther. 2021 Dec 1;101(12):pzab215. doi: 10.1093/ptj/pzab215.
Results Reference
derived
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A Comparison: High Intense Periodic vs. Every Week Therapy in Children With Cerebral Palsy (ACHIEVE)
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