Cranial Cup Use for the Prevention of Positional Head Shape Deformity in the NICU
Trial Snapshot
- Phase
- Not Applicable
- Status
- Terminated
- Sponsor
- Boston Children's Hospital
- Enrollment
- 88
- Locations
- 1
- Primary Endpoint
- Cranial Abnormalities Were Measured at Hospital Discharge
Study Overview
Brief Summary
Many hospitalized infants can develop a flattening of the back or sides of their head. This condition develops gradually when an infant's head rests on a firm or semi-firm surface for a prolonged period of time. Premature infants are more likely to have a positional head shape deformity because they may spend longer periods of time in a crib. Infants participating in this study will be randomly assigned to either standard treatment, which is a moldable positioner device, or to a cranial cup device and moldable positioner for positioning. The purpose of this prospective single-blinded randomized clinical trial will be to evaluate the effectiveness of the cranial cup in preventing positional head shape deformity in the NICU patient population.
Detailed Description
The primary outcome for this study will be cranial index and cranial symmetry measured at hospital discharge; the secondary outcome measure is the incidence of oxygen desaturation events (apnea, bradycardia and oxygen desaturation).
The pilot study was undertaken to evaluate if the cranial cup can be successfully incorporated into the NICU patient care regime, the pilot study included 5 infants.
The main trial enrollment was estimated to be 160 infants from 4 centers. Upon enrollment infants will be randomized to one of two study groups
- Cranial cup and moldable positioner
- Moldable positioner
Inclusion criteria:
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- — to 10 Days (Child)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •1. Infants born at \>/= 22 weeks gestation
- •2. Infant that are \ 14 days from the time of enrollment
Exclusion Criteria
- •Infants that require only prone positioning to maintain airway patency (such as those with Pierre Robin Syndrome/Sequence) will not be eligible to participate; this is because infants must be able to lie supine for at least part of the day to use the cranial cup
- •Infants requiring medical devices such as a continuous ventricular drain, subgaleal shunt, or intravenous catheters (unless placement of the IV is temporary) prevent proper positioning using the cranial cup
- •Infants with a craniofacial anomaly, cervical anomaly, or critical airway infants
- •Infants with Cutis Aplasia or significant skin breakdown to the scalp, because the cranial cup may worsen a preexisting condition
- •Infants with a prenatal diagnosis of craniosynostosis
- •Infants deemed not suitable for participation by the attending neonatologist
- •Infants that are to be transferred to a non-participating hospital within 14 days of enrollment as this timeframe may not be adequate to show a difference in head shapes
Arms & Interventions
Cranial cup device and Moldable positioner device
The cranial cup for 12/24 hours and the moldable positioner device was used for positioning infants the remainder of the 24 hours
Intervention: Cranial cup device and Moldable positioner (Device)
Cranial cup device and Moldable positioner device
The cranial cup for 12/24 hours and the moldable positioner device was used for positioning infants the remainder of the 24 hours
Intervention: Moldable positioner device (Device)
Moldable positioner device
Moldable positioner device was used for positioning infants for 24/24 hours
Intervention: Moldable positioner device (Device)
Outcomes
Primary Outcomes
Cranial Abnormalities Were Measured at Hospital Discharge
Time Frame: up to 120 days
Cranial abnormality measurements were obtained at hospital discharge by orthotists blinded to the study group assignment. Cranial abnormalities include both cranial index measures and cranial symmetry measures. Cranial index (normal measurement between 73%-85%) was obtained dividing the head width (M-L) by length (A-P) then multiplying it by 100%. Cranial symmetry (normal measurement of\<8mm) was obtained by calculating the difference in the right and left anterior-posterior measures.
Secondary Outcomes
- Incidence of Cardiorespiratory(daily up to 120 days)
Investigators
Michele DeGrazia
Director Nursing Research, NICU
Boston Children's Hospital