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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04561232
Other study ID # 19-016773
Secondary ID 1R01HD098364-01A
Status Recruiting
Phase N/A
First received
Last updated
Start date December 15, 2020
Est. completion date March 1, 2026

Study information

Verified date January 2024
Source Children's Hospital of Philadelphia
Contact Laura Prosser, PhD
Phone 215-590-2495
Email prosserl@chop.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this project is to characterize the evolution of locomotor learning over the first 18 months of life in infants at high risk for cerebral palsy (CP). To characterize how locomotor skill is learned (or not learned) during this critical period, the investigators will combine established protocols using robust, unbiased robotic and sensor technology to longitudinally study infant movement across three consecutive stages during the development of impaired human motor control - early spontaneous movement, prone locomotion (crawling), and upright locomotion (walking).


Description:

Early spontaneous leg movements will be measured monthly from 1-4 months of age. Infants who remain at high risk for CP by month 4 as measured by the General Movements Assessment and the Test of Infant Motor Performance (TIMP) at 4 months of age will continue to locomotor training phases. Prone locomotor training using the Self-Initiated Prone Progression Crawler (SIPPC) will be delivered from 5-9 months of age. Upright locomotor training with dynamic weight support (DWS) will be delivered from 9-18 months of age. Repeated assessments of locomotor skill, movement quality, training characteristics, and variables that may mediate locomotor learning will be collected at time points from 1 month to 18 months of post-term age. Investigators will examine the relationships between motor error and locomotor skill acquisition over time, anticipating that experiencing and correcting movement errors is critical to skill acquisition in infants at risk for CP; the contribution of other training characteristics (movement time, movement variability, and postural control) to locomotor learning; and how learning is mediated by neurobehavioral factors outside of training. Investigators will develop comprehensive models of training predictors and mediators for prone and upright locomotor learning.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date March 1, 2026
Est. primary completion date March 1, 2026
Accepts healthy volunteers No
Gender All
Age group N/A to 6 Weeks
Eligibility Inclusion Criteria: - less than 6 weeks of age (corrected for prematurity, if applicable) - have a history of an early brain injury associated with high risk for cerebral palsy including periventricular leukomalacia, hypoxic-ischemic encephalopathy, intraventricular hemorrhage, hydrocephalus, stroke, neonatal seizures, or intracranial cystic lesion - family is able to commit to study visits Exclusion Criteria: * known genetic condition unrelated to cerebral palsy (CP) or congenital abnormalities Infants with fidgety movements on the General Movements Assessments (GMA) at 3 months of age or a score greater than -0.5sd below the mean on the Test of Infant Motor Performance at 4 months of age will not progress in the study because these infants are unlikely to have CP.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Prone and Upright Locomotor Training
During the movement observation phase, infants will wear a wireless movement sensor at each ankle for two days. Research staff will show the caregivers how to place the sensors in the morning and charge them overnight. The training protocol for the prone training will consist of: 1) Warm-up. 2) Assisted movement of the arms and legs. 3) Calibration of the infant's arm and leg positions. 4) Self-initiated mobility for up to five minutes. For upright training, the environment will be arranged to encourage active motor exploration and variability in walking activities.The therapist will assist the child as needed to encourage upright locomotor activities, but only the minimum amount needed to perform the task. Weight assistance will be gradually reduced as postural control and coordination improve.

Locations

Country Name City State
United States Children's Hospital of Philadelphia Philadelphia Pennsylvania

Sponsors (4)

Lead Sponsor Collaborator
Children's Hospital of Philadelphia Children's Hospital Los Angeles, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), University of Oklahoma

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Cognition The cognition age equivalent obtained from the Bayley Scales of Infant and Toddler Development- Fourth Edition (BSID-IV). This value describes what age the child is currently similar to in their cognitive performance, and all values are reported in months of age. The range of values on the scale 0-42 months of age. A higher number value means a greater cognitive ability. Up to 18 months
Other Motivation to Move Scale The Motivation to Move Scale is scored from video data of infant behavior during treatment sessions. Children are classified on a scale of 1 to 5 with higher scoring indicating increased motivation to move. Up to 18 months
Primary Gross Motor Function Measure-66 The Gross Motor Function Measure-66 (GMFM-66) is a Rasch-analyzed measure of gross motor function designed for children with cerebral palsy (CP). Computation of the GMFM-66 score involves statistical weighting of the raw item scores for difficulty. Scores range from 0 to 100 with higher scores indicating more functional ability. Up to 18 months
Primary Movement Observation Coding System The Movement Observation Coding System will use video coding to assess postural control, arm and leg movements, and goal directed movement. Up to 18 months
Secondary Early spontaneous movement Wearable sensor data will be analyzed to describe leg movements produced across in the natural environment. Up to 4 months
Secondary Error rate - prone Error during prone locomotor training will measured using the Self-Initiated Prone Progression Crawler (SIPPC). Up to 18 months
Secondary Error rate - upright Error during upright locomotor training will measured using the dynamic weight support (DWS) technology. Up to 18 months
Secondary Movement index Movement index is the percent of time moving during each therapy session which will be recorded by sensors. Up to 18 months
Secondary Postural control Postural control will be measured from video coding of therapy sessions. Up to 18 months
Secondary Movement variability - prone Movement variability during prone locomotor training will be measured using the Self-Initiated Prone Progression Crawler (SIPPC). Up to 18 months
Secondary Movement variability - upright Movement variability during upright locomotor training will be measured by video coding. Up to 18 months
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