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Sleep Organization in Premature Infants With Feeding Difficulties

Sleep Organization in Premature Infants With Feeding Difficulties

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01946308
Enrollment
25
Registered
2013-09-19
Start date
2011-09-30
Completion date
2012-07-31
Last updated
2020-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Premature Infant Sleep

Keywords

sleep, sleep efficiency, active sleep, quiet sleep, arousals, premature infant, conformational positioning, mattress, feeding difficulty, neonatal intensive care unit, sleep state, behavioral observation, stress behavior, self-regulatory behavior, surgery, gastrointestinal

Brief summary

Babies born too soon, premature babies, can have complications following birth because their systems are immature. Hospitals help prevent deformities and delays in motor development by using therapeutic positioning to provide containment as they would experience in the womb. They also often have trouble eating. They have discomfort, are irritable, refuse to eat and cry because their digestive system is immature. The neonatal intensive unit can create stress and disrupt their sleep. Going from active to deep sleep is essential for infant brain development, learning and memory formation. Their sleep states early in life predict their developmental outcome. The purpose is to determine whether a conformational positioning system, one that can mold to the baby and contain him or her, will allow more time asleep in premature infants with feeding problems compared to the standard crib mattress. We hypothesize that the number of total sleep time will be longer and the number of arousals out of sleep lower when they are sleeping on the conformational positioning system compared to the mattress.

Detailed description

Premature infants are at risk for complications due to the immaturity of motor, gastrointestinal, respiratory, cutaneous and behavioral systems. Therapeutic positioning is routinely used to provide containment, maintain a flexed position and prevent skeletal deformities and delays in motor development. Premature infants have feeding difficulties and frequently experience gastroesophageal reflux, discomfort, refusal to feed, irritability, and crying. The neonatal intensive care environment can create stress and disrupts sleep-wake cycles and self-regulatory behaviors. Cycling from active to deep sleep states is required for neurosensory processing, learning, memory formation and brain plasticity. Sleep and waking states for premature infants are predictive of neurodevelopmental outcomes. The purpose of the study is to determine whether the use of conformational positioning will be associated with greater total sleep time in premature infants with a history feeding difficulty compared to positioning on a mattress alone. We hypothesize that the number of arousals and total sleep time will be affected by the support surface. Specifically, the number of arousals will be lower and total sleep time will be greater for infants when they are on a conformational positioning (CP) device compared to when they are on the standard positioning system (mattress) (SP). The use of CP will reduce the number of arousals, increase the total sleep time, and bring about behavioral states that are conducive to regulation of attention, state and motor response relative to SP.

Interventions

OTHERConformational positioning system

The conformational positioning system will be compared to the standard infant crib mattress.

Sponsors

Children's Hospital Medical Center, Cincinnati
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
26 Weeks to 36 Weeks
Healthy volunteers
No

Inclusion criteria

* Gestational age of \< 37 weeks * Feeding difficulty due to prematurity or a medical condition * Not taking sedative medications for 24 hours before sleep study * Post-surgery * Sufficiently medically stable to undergo procedures

Exclusion criteria

* Gestational age equal to or greater than 37 weeks * Clinical apnea * Require mechanical ventilatory support * Received sedative medications 24 hours before sleep study * Brain injury or neurological condition that limits movement * Orthopedic conditions requiring fixed positioning * Arthrogryposis * Osteogenesis imperfecta * Medically unstable such that procedures cannot be tolerated

Design outcomes

Primary

MeasureTime frameDescription
Sleep organization defined as efficiency, active sleep time, quiet sleep time, number of arousals, measured by polysomnographyOvernight, 10.5 hour standard EEG sleep studyStandard polysomnography electrodes are applied to the subject in the evening and the subject is placed on either the standard mattress or the conformational positioning system (assigned at random) for the first 5 hours. The subject is then moved onto the second treatment for the remainder of the study. EEG measures are recorded continuously over the entire period. The EEG data are assessed by trained sleep study physicians and clinical staff.

Secondary

MeasureTime frameDescription
Sleep state by behavioral observationTwo 30-minute periods, one on each treatment, during the EEG sleep studyNurses trained in the techniques of premature infant behavioral state determination will observe the infant for two 30-minute periods while the EEG sleep study is being conducted. One nurse will observe when the subject is on the standard mattress and the other will observe when the subject is on the conformational positioning system. They will record specific behaviors observed in 2-minute intervals during the 30-minute period.

Other

MeasureTime frameDescription
Impact of prior surgery on sleep organizationOvernight, 10-hour sleep studyStandard polysomnography electrodes are applied to the subject in the evening and the subject is placed on either the standard mattress or the conformational positioning system (assigned at random) for the first 5 hours. The subject is then moved onto the second treatment for the remainder of the study. EEG measures are recorded continuously over the entire period. The EEG data are assessed by trained sleep study physicians and clinical staff. The sleep organization and behaviorally observed sleep state will be compared for the subjects grouped as having had surgery prior to the study or not having had surgery to ascertain the impact of surgery while controlling for the treatment effects.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026