Cranial Cup Use for the Prevention of Positional Head Shape Deformity in the NICU

Not Applicable

Terminated

Interventions: Device: Cranial cup device and Moldable positioner
Device: Moldable positioner device

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:

There are several inclusion criteria for participation in the study:

1. Infants born at \>/= 22 weeks gestation

2. Infant that are \</= 7 days of age

3. Infants that receive medical clearance from their healthcare team

4. Infants that have an estimated minimum NICU length of stay = / \> 14 days from the time of enrollment

Infants were stratified by study site and weight at enrollment (\< 1000 grams versus = / \> 1000 grams).

Recruitment & Eligibility

Inclusion Criteria

Infants born at >/= 22 weeks gestation
Infant that are </= 7 days of age
Infants that receive medical clearance from their healthcare team
Infants that have an estimated minimum NICU length of stay = / > 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

Arm && Interventions

Group	Intervention	Description
Cranial cup device and Moldable positioner device	Cranial cup device and Moldable positioner	The cranial cup for 12/24 hours and the moldable positioner device was used for positioning infants the remainder of the 24 hours
Moldable positioner device	Moldable positioner device	Moldable positioner device was used for positioning infants for 24/24 hours
Cranial cup device and Moldable positioner device	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

Primary Outcome Measures

Name	Time	Method
Cranial Abnormalities Were Measured at Hospital Discharge	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 Outcome Measures

Name	Time	Method
Incidence of Cardiorespiratory	daily up to 120 days	daily log of cardiorespiratory events (apnea, bradycardia, oxygen desaturation) collected on a daily positioning log at the infant's bedside