NEO Rehab Program for Premature Infants at Risk for Cerebral Palsy
Primary Purpose
Cerebral Palsy, Prematurity, Early Intervention
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
NeoRehab Bundle
Routine care
Sponsored by
About this trial
This is an interventional treatment trial for Cerebral Palsy focused on measuring cerebral palsy, prematurity, early intervention, parent-driven, brain plasticity, motor outcome
Eligibility Criteria
Inclusion Criteria:
- GA at birth: ≤32 weeks gestation and/or birthweight ≤1500 grams
- Infants 7 days or older
- Ability of parents or identified designated surrogate (e.g. grandparent) to perform the interventions
- Abnormal writhing GMs defined by the presence of a poor repertoire pattern on 2 consecutive assessments or the presence of a cramped-synchronized pattern on any assessment
Exclusion Criteria:
- Clinically unstable (requiring high frequency mechanical ventilation, vasopressor support, need for continuous intravenous pain or sedation medication)
- If their parents do not speak English
- If parental participation is hindered (e.g. incarceration).
Sites / Locations
- University of Virginia
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Intervention
Routine care
Arm Description
Parent-driven intervention bundle of 6 evidence-based elements: vocal soothing, scent exchange, comforting touch, kangaroo care, infant massage and physical therapy
Routine care per unit guidelines
Outcomes
Primary Outcome Measures
Parental satisfaction of a parent-driven NeoRehab bundle in preterm infants at risk for cerebral palsy.
The following measure will be used to measure study parental satisfaction:
Weekly interviews with parental participants
Acceptability of a parent-driven NeoRehab bundle in preterm infants at risk for cerebral palsy.
The following measure will be used to measure study acceptability:
Recruitment rates
Retention rates of a parent-driven NeoRehab bundle in preterm infants at risk for cerebral palsy.
The following measure will be used to assess the retention rate of study participants:
- Rate of follow-up at the 3 month outpatient visit
Adherence rates to study protocol
Activity logs
Impact of the NeoRehab bundle on motor performance using the Test of Infant Motor Performance (TIMP)
Motor outcomes will be assessed at NICU discharge and at 3 months using the Test of Infant Motor Performance (TIMP). The lower the score the poorer the motor function.
Impact of the NeoRehab bundle on neurologic function as assessed by the Hammersmith Infant Neurological Examination (HINE).
Neurologic function will be assessed at NICU discharge and at 3 months postmenstrual age using the Hammersmith Infant Neurological Examination (HINE) instrument. The HINE is a 26 items scale that evaluates cranial nerve function, posture, quality and quantity of movements, muscle tone, and reflexes and reactions. Lower the score the poorer the motor function. The HINE has a sensitivity of 90% for prediction of motor outcome.
Impact of the NeoRehab bundle on infants' general movements.
The impact of the intervention on the infants' general movement will be assessed at NICU discharge and at 3 months postmenstrual age using the general movement assessment (GMA) tool. The GMA has been shown to reliably identify infants at high risk for CP and can be implemented shortly after birth making it an ideal screening tool for preterm infants. Cramped-synchronized writhing general movements followed by absent fidgety general movements is a movement pattern that has been shown to be highly specific of later development of cerebral palsy.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04330859
Brief Title
NEO Rehab Program for Premature Infants at Risk for Cerebral Palsy
Official Title
NEO Rehab Program for Premature Infants at Risk for Cerebral Palsy
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
May 25, 2019 (Actual)
Primary Completion Date
October 10, 2020 (Actual)
Study Completion Date
August 1, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Virginia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The goal of this project is to investigate the acceptability, feasibility and fidelity of an innovative NICU rehabilitation program that will include six multimodal, gestational age (GA) appropriate, parent-administered interventions (vocal soothing, scent exchange, comforting touch, kangaroo care, infant massage and physical therapy). Using the general movement assessment (GMA) instrument, the investigators will determine the effects of this program on short-term motor outcomes (general movements (GMs), cranial nerves, posture, movements, tone, and reflexes) in premature infants (≤32 week's gestation and/or ≤1500 grams birthweight) identified as at-risk for CP. The short-term motor outcomes will be measured using the GMA, the Test of Infant Motor Performance (TIMP) and the Hammersmith Infant Neurological Examination (HINE) instruments. This novel program will be applied during the neonatal intensive care unit (NICU) hospitalization when the brain is highly plastic and actively developing with the goal to mitigate severity of brain injury and its impact on development.
Detailed Description
The two following specific aims will be tested:
Aim 1: Enroll 60 preterm infants (<32 weeks' gestation and/or ≤1500 grams) with abnormal GMA into a pilot randomized control trial to evaluate the acceptability, feasibility (practicality) and fidelity (adherence, exposure and engagement) of a multimodal GA appropriate rehabilitation program during NICU hospitalization compared to standard of care. The investigators will evaluate:
Acceptability using recruitment, refusal, retention, and follow-up rates as well as weekly interviews with parental participants
Feasibility (practicality) using direct observations and weekly interviews with parental participants
Fidelity (adherence, exposure and engagement) using visitation data, activity logs, direct observations, and weekly interviews.
Aim 2: Examine the effect of a multimodal NICU-based rehabilitation program on short-term motor outcomes (general movements, cranial nerves, posture, movements, tone, and reflexes) of premature infants at risk for cerebral palsy (CP) at discharge from the NICU and at 3 months corrected age. The investigators hypothesize that this type of GA appropriate multimodal NICU-based rehabilitation program will positively impact short-term motor outcomes by normalizing general movements and improving TIMP and HINE scores.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy, Prematurity, Early Intervention, Family Centered Care
Keywords
cerebral palsy, prematurity, early intervention, parent-driven, brain plasticity, motor outcome
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
70 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Parent-driven intervention bundle of 6 evidence-based elements: vocal soothing, scent exchange, comforting touch, kangaroo care, infant massage and physical therapy
Arm Title
Routine care
Arm Type
Placebo Comparator
Arm Description
Routine care per unit guidelines
Intervention Type
Other
Intervention Name(s)
NeoRehab Bundle
Intervention Description
The NICU rehabilitation program includes six multimodal, GA appropriate, parent-administered interventions (vocal soothing, scent exchange, comforting touch, kangaroo care, infant massage and physical therapy)
Intervention Type
Other
Intervention Name(s)
Routine care
Intervention Description
Routine NICU care including talking, touching and holding the participant per unit guideline as well as physical therapy, occupational therapy, and speech therapy per unit guideline
Primary Outcome Measure Information:
Title
Parental satisfaction of a parent-driven NeoRehab bundle in preterm infants at risk for cerebral palsy.
Description
The following measure will be used to measure study parental satisfaction:
Weekly interviews with parental participants
Time Frame
2 years
Title
Acceptability of a parent-driven NeoRehab bundle in preterm infants at risk for cerebral palsy.
Description
The following measure will be used to measure study acceptability:
Recruitment rates
Time Frame
2 years
Title
Retention rates of a parent-driven NeoRehab bundle in preterm infants at risk for cerebral palsy.
Description
The following measure will be used to assess the retention rate of study participants:
- Rate of follow-up at the 3 month outpatient visit
Time Frame
2 years
Title
Adherence rates to study protocol
Description
Activity logs
Time Frame
2 years
Title
Impact of the NeoRehab bundle on motor performance using the Test of Infant Motor Performance (TIMP)
Description
Motor outcomes will be assessed at NICU discharge and at 3 months using the Test of Infant Motor Performance (TIMP). The lower the score the poorer the motor function.
Time Frame
2 years
Title
Impact of the NeoRehab bundle on neurologic function as assessed by the Hammersmith Infant Neurological Examination (HINE).
Description
Neurologic function will be assessed at NICU discharge and at 3 months postmenstrual age using the Hammersmith Infant Neurological Examination (HINE) instrument. The HINE is a 26 items scale that evaluates cranial nerve function, posture, quality and quantity of movements, muscle tone, and reflexes and reactions. Lower the score the poorer the motor function. The HINE has a sensitivity of 90% for prediction of motor outcome.
Time Frame
2 years
Title
Impact of the NeoRehab bundle on infants' general movements.
Description
The impact of the intervention on the infants' general movement will be assessed at NICU discharge and at 3 months postmenstrual age using the general movement assessment (GMA) tool. The GMA has been shown to reliably identify infants at high risk for CP and can be implemented shortly after birth making it an ideal screening tool for preterm infants. Cramped-synchronized writhing general movements followed by absent fidgety general movements is a movement pattern that has been shown to be highly specific of later development of cerebral palsy.
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
23 Weeks
Maximum Age & Unit of Time
32 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
GA at birth: ≤32 weeks gestation and/or birthweight ≤1500 grams
Infants 7 days or older
Ability of parents or identified designated surrogate (e.g. grandparent) to perform the interventions
Abnormal writhing GMs defined by the presence of a poor repertoire pattern on 2 consecutive assessments or the presence of a cramped-synchronized pattern on any assessment
Exclusion Criteria:
Clinically unstable (requiring high frequency mechanical ventilation, vasopressor support, need for continuous intravenous pain or sedation medication)
If their parents do not speak English
If parental participation is hindered (e.g. incarceration).
Facility Information:
Facility Name
University of Virginia
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35110644
Citation
Letzkus L, Conaway M, Miller-Davis C, Darring J, Keim-Malpass J, Zanelli S. A feasibility randomized controlled trial of a NICU rehabilitation program for very low birth weight infants. Sci Rep. 2022 Feb 2;12(1):1729. doi: 10.1038/s41598-022-05849-w.
Results Reference
result
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NEO Rehab Program for Premature Infants at Risk for Cerebral Palsy
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