Other Preterm Infants Clinical Trial
Official title:
Cognitive Processing in Preterm Infants and NICU Music Therapy
Several positive physiological and behavioural outcomes have been observed in preterm infants
exposed to music therapy during their stay at Neonatal Intensive Care Units (NICU). There is
ample evidence in the literature showing that brief exposure to music can lead to superior
performance on a host of cognitive tasks in laboratory settings in children, adolescent and
adults. However, till date no study has examined the cognitive benefits of NICU music therapy
in preterm infants. Further habituation tests have been employed to examine cognitive
functioning in infants in laboratory setting but the same test have not been employed as a
measure to examine early cognitive functioning in preterm infants.
This project will be carried out to examine the benefits of NICU music therapy on the
cognitive functioning of preterm infants born at 27- 33 weeks of gestational age. A
randomized controlled research design will be employed to compare cognitive functioning
between the treatment and control group at 18 - 24 months of corrected gestational age. The
treatment group will be exposed to music therapy during their stay in NICU and the controlled
group will be exposed to all standardized care available at our institution except music
therapy. Habituation tests will be used to examine cognitive functioning of the preterm
infants in groups at 18 - 24 months of gestational age.
Following previous research, our hypothesis is that infants in the experimental group will display significantly more positive scores on a collection of physiological and behavioural measurements. The stimuli used at each age will be targeted to the infants' developmental level. Bayley Scales of Infant Development will also be administered at 18 - 24 months as part of high risk infant follow up. These data will be included in the analysis for outcome measurement. While seated in a high-chair or their parent's lap, infants will be habituated to a series of images of a particular shape (e.g., a triangle), while their looking time to each stimulus is measured. Each image during habituation will be a unique token of the category (i.e., all different triangles). Habituation will be individually determined, and defined as cumulative looking across three successive trials that is 50% than cumulative looking across the first three trials. Following habituation, infants will be shown a novel token of the habituation shape (e.g., a new triangle) and a novel shape (e.g., a square), in counterbalanced order. If infants recognize the category change, they should look longer at novel category compared to the novel token. For each test, two dependent measures will be sampled: rate of habituation and amount of dishabituation to the novel category. Mixed ANOVA and paired t-tests will be used to analyze the data. As preterm infants have been shown to be delayed on these kinds of tasks, we hypothesize that the experimental group will habituate to each category faster, and/or display stronger dishabituation scores compared to the preterm. We will also use multiple regression analyses to examine relations between the NICU physiological and behavioural measures and the cognitive measures. We hypothesize that infants who most strongly benefited from their therapies in the NICU will display the most advanced cognitive abilities. An intention-to-treat- analysis will be performed for cognitive measures as well. The cognitive assessment at 2 and 4 months that were to be carried out at the Developmental Lab at University of Regina is now canceled due to feasibility concerns. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02231801 -
Monitoring of Vital Signs During Skin-to-skin Holding by Mothers of Their Preterm Babies
|
N/A | |
Completed |
NCT01450436 -
Impact of Preterm Body Composition at Discharge on 2 Years Neurological Development (ASQ Evaluation)
|
||
Completed |
NCT02268968 -
Use of Topical Lidocaine to Reduce Pain in Preterm Infants Receiving Nasal CPAP Continuous Positive Airway Pressure
|
Phase 1 | |
Completed |
NCT02073071 -
Effects of Infant Formula on the Growth and Tolerance in Preterm/Low Birth Weight Infants
|
N/A | |
Withdrawn |
NCT02224859 -
Invictus Medical, Medical Cranial Support Device (CSD) is a Device Safety Study in Infants at Risk of Head Ulcers.
|
N/A | |
Completed |
NCT01944956 -
Swallowing Sound in Preterm Infant Evaluation of Feeding Maturation
|
N/A | |
Terminated |
NCT02040909 -
Optimizing Propofol Dosing for (Preterm) Newborn Infants That Need Endotracheal Intubation
|
Phase 1 | |
Not yet recruiting |
NCT01772927 -
Clinical Tolerance of Numeta 13%
|
N/A | |
Completed |
NCT00233324 -
Surfactant Positive Airway Pressure and Pulse Oximetry Trial
|
Phase 3 | |
Completed |
NCT02192996 -
Probiotic Supplementation to Improve the GUT Microbiota of Very Low Birth Weight Preterm, a Pilot Study
|
Phase 0 | |
Completed |
NCT02404623 -
The Effect of Vitamin D Administration to Premature Infants on Vitamin D Status and Respiratory Morbidity
|
N/A |