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Effectiveness of Positioning in Preterm Neonates

Primary Purpose

Premature Baby 26 to 32 Weeks, Preterm Birth

Status
Enrolling by invitation
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
Positioning in flexion
Sponsored by
University of Patras
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Premature Baby 26 to 32 Weeks focused on measuring preterm, positioning, snuggle up, general movements

Eligibility Criteria

24 Weeks - 33 Weeks (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Νeonates of 32 weeks of gestation or less

Exclusion Criteria:

Νeonates

  • with congenital deformities or genetic anomalies
  • with neurological deficits detected at 1st week post-natal
  • of multiple birth (triplets and over) or breech deliveries

Sites / Locations

  • University of Patras

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Positioning in flexion

Control group

Arm Description

Intervention: Positioning of body in flexion and aligment towards midline with Snuggle up (Philips, USA)

No intervention

Outcomes

Primary Outcome Measures

Change from baseline General movements at 40 weeks
General Movements (GM's) of Prechtl using 5-minute video observations of each neonate for the assessment
Change from 40 weeks Denver II Developmental Screening Test at 4 months of corrected age
The purpose of the test is to identify young children with developmental problems

Secondary Outcome Measures

Change from baseline Beats per minute (heart rate ) at 40 weeks
The heart rate will be measured with a monitor connected to the neonate
Change from baseline Breaths per minute (respiratory rate) at 40 weeks
The respiratory rate will be measured with a monitor connected to the neonate
Change from baseline Weight at 40 weeks
Weight gained during the intervention period measured with the NICU scales
Days till full feeding
This information will be collected from each neonate's file
Days the neonate needed oxygen
This information will be collected from neonates file
Duration of stay in the NICU
This information will be collected from neonates file

Full Information

First Posted
January 19, 2020
Last Updated
May 10, 2023
Sponsor
University of Patras
Collaborators
University Hospital of Patras
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1. Study Identification

Unique Protocol Identification Number
NCT04251260
Brief Title
Effectiveness of Positioning in Preterm Neonates
Official Title
Effectiveness of Positioning on the Movement and Clinical Physiological Outcomes of Preterm Neonates
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
September 20, 2022 (Actual)
Primary Completion Date
November 30, 2024 (Anticipated)
Study Completion Date
December 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Patras
Collaborators
University Hospital of Patras

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Introduction: When babies are born prematurely, they are deprived of their usual space limits (uterus walls). This along with the action of gravity to which they are exposed after birth, makes the neonates have a low muscle tone, acquire a posture of extension, being more irritable and having difficulties with their alertness-sleep cycle. There are few studies that have assessed the effectiveness of positioning of premature neonates. However, none of these studies has focused on exploring the effects of positioning on the patterns of movement and gross motor function of the pre-term neonates. Aim: The aim of this study is to investigate the effects of positioning on the patterns of movement, gross motor development and physiological clinical outcomes of pre-term neonates. Methods: A sample of pre-term neonates of ≤ 32 weeks of gestation from the Neonatal Intensive Care Unit (NICU) of the General University Hospital of Patras will be randomly assigned to two groups. The intervention group will receive positioning with Snuggle up (Philips, USA), while the control group will receive usual care. Outcomes will be assessed with the general movements of Prechtl and the Denver II scale at baseline and at term-age of each neonate. Physiological outcomes will be also assessed such as heart rate, respiratory rate, weight gained from baseline to term-age, days to achieve full oral feeding, days on the ventilator, days on oxygen, and duration of stay in the NICU. Basic characteristics of the neonates will be obtained from their medical record, i.e. weeks of gestation at birth, gender, type of birth (normal or Caesarian), weight at birth, and Αpgar score and will be used to compare the 2 groups for similarities at the baseline of the trial.
Detailed Description
Study Protocol Introduction: The NICU provides a sensory overload through excessive handling, noisy environment, neglected cry, prolonged sleep state and social interactions of the newborns with the professionals. All these make difficult the internal organization of the preterm neonate (Pereira et al, 2013). Also, when babies are born prematurely, their muscles have not yet acquired the appropriate tone which is normally low compared to the muscle tone of full-term neonates. With the deprivation of their usual space limits (uterus walls) and the action of gravity to which the neonates are exposed after birth, the preterm neonates acquire a posture of extension, which is contrary to the flexion they usually adopt in the uterus. This extension position does not help the flexion of their limbs and makes the hand-mouth activities and meeting the middle line difficult. Further, the deprivation of the physical rhythms of the neonates' usual space creates insecurity, irritability, increased extensive motor activity and difficulties with respiration and alertness-sleep cycle (Toso et al, 2015; Zarem et al, 2013). There is a randomized controlled trial (RCT) that investigated the effectiveness of positioning on the general condition and ability to be fed of 100 neonates (≤ 32 weeks of gestation). This study compared a positioning using the Dandle Roo (DandleLion Medical) with traditional or other positioning (e.g. rolls of sheets, snuggle up) (Madlinger-Lewis et al, 2013). At term-age, a significant difference was found between the two groups, favoring the Dandle Roo positioning, in the movements symmetry as assessed with the NICU Network Neurobehavioral Scale (mean difference: 0.90, 95% confidence intervals: 0.05 to 1.75). No other significant differences were observed at rest of outcomes. Another RCT including 56 preterm neonates (27-32 weeks of gestation) explored the effects of positioning with the Snuggle up and Bendy Pumpers (Philips, USA) in comparison to traditional positioning (rolls of soft fabric). The results showed a significant difference between the two groups, favoring the intervention group, in respiratory rate, oxygen saturation, score of cardiovascular stability, and weight gain (p<0.5) (Sathish et al, 2017). However, none of these previous studies has investigated any differences in the patterns of movement of the pre-term neonates after a positioning intervention. For example, no study has assessed the gross motor function of the pre-term neonates using the general movements of Prechtl after a positioning intervention, although this assessment is considered important for the prognosis of the motor development and ability for independence of these children (Einspieler et al, 2016). No previous study has also assessed the effect of positioning in the long-term neuro-developmental progress of pre-term children with scales such as the Denver II scale, which scale is also important for the prognosis of the development of the neonate. Aim of the study: The current trial aims at exploring the effectiveness of positioning in a "flexion" position on the movement and clinical outcome of neonates (≤32 weeks of gestation), which group of neonates is a high-risk group. Methods: Inclusion criteria: neonates of 32 weeks of gestation or less. Exclusion criteria: neonates with congenital deformities, genetic anomalies, or neurological deficits detected at 1st week post-natal, neonates of multiple birth (triplets and over) or breech deliveries. Two groups of neonates will be randomly assigned using a concealed method (sealed envelopes) either to positioning (intervention group) or to usual care (control group). In order to maintain similar gestational ages throughout the two groups, participants will be stratified by gestational age (≤28 weeks and >28 weeks). Each stratum will have an independent randomization scheme. The intervention group will be positioned in flexion (lower limbs in flexion, hands in midline) with a positioning aid, the Snuggle up (Philips, USA). With positioning, the neonates bottom is tucked down in the snuggle up pocket, legs are aligned and gently flexed and hands are placed towards midline and near the face. The control group will not receive any positioning in flexion and the neonates will lie as usually. This study has been approved by the Research Committee of the General University General Hospital of Patra (decision: 246, date: 09/04/2019). Factors that may affect the neonates' condition should be controlled, and be similar to both groups of neonates. Such factors are light, noise, temperature of room (incubator), touching from nursing staff or others etc. The intervention group will receive positioning during day and night throughout the intervention period. Neonates may be removed from positioning when a nurse or mother needs to feed them, that is a period that will not last more than 1 hour/day. The principal investigator (TB) will demonstrate the positioning to the Neonatal Intensive Care Unit (NICU) nursing staff, and will check each week during the intervention period the positioning of the neonates as well as will reply to any questions of the staff. The physiological status (normal functioning) of the neonates will be checked regularly by the neonatologist in charge and the nurses of the NICU. Outcomes Assessments of the 2 groups (intervention and control group) will take place at baseline and again at term-age of each neonate. For assessment, the General Movements (GM's) of Prechtl (Einspieler et al, 2016) using 5-minute video observations of each neonate will be used. The GM's assessment is a non-invasive assessment and can be used from birth up to 5 months. In this study, the detailed GM's assessment will be conducted by two pediatric physiotherapists, independently. The two assessors have a long-lasting experience in assessing/treating small children and infants and will be blind to which group the neonates will be assigned. There is evidence that the GM's (total score) demonstrate high test-retest reliability with Intra-class Correlation Coefficients (ICCs) or Pearson coefficients exceeding 0.84 (Yeh et al, 2016), while there were lower correlation coefficients during the initial period of writhing movements (6-8 weeks post-natal). A significant amount of test-retest reliability was also found for each sub-category of the Detailed GM's assessment with ICCS exceeding 0.80, except for the assessment of "speed" (ICC: 0.51) (Yeh et al, 2016). Evidence of moderate to good intra-tester reliability has also been demonstrated (kappa coefficient: 0.44-0.63) (Bernhardt et al, 2011), and 97-100% agreement between raters for the GM's total score. Assessment will also be performed with the Denver II scale (at term-age and 4 months of corrected age). This scale has shown a significant amount of validity for assessing the neuro-developmental progress of babies and infants. The assessment with the Denver II scale will be performed by a neonatologist of the NICU, who will be blind to the neonates' assignment. The principal investigator will film all the videos at baseline and at post-intervention (at term-age for each neonate). Video recording will follow a typical method of observation of the GM's, and each video will have a 5-minute duration for a more reliable observation of the movement of each neonate. Video recording will take place at least 30 minutes after the neonate is fed and during periods in which the neonate is awake and is moving. Other parameters that will be examined at baseline and post-intervention are the heart rate, respiratory rate, weight gained from baseline to post-intervention, days to achieve full oral feeding, days on the ventilator, days on oxygen, and duration of stay in the NICU. Demographics and basic characteristics of the neonates will be recorded such as weeks of gestation at birth, gender, type of birth (normal or Caesarian), weight at birth, and Αpgar score to compare the 2 groups for similarities at the baseline of the trial. These data will be obtained from the neonates' medical record. Written information about the study will be provided to the neonates' parents and written consent will be asked from either the mother or father (or the guardian of the neonate) before the neonate enters the trial. Detailed information will be also provided to all the staff of the NICU involved in the study. A code number will be given to each neonate to maintain his/her anonymity, during data analysis and dissemination of results. Babies videos needed for assessment will not be accessible from internet or other sharing mediums. Video recording The neonate will lie on his/her back in the incubator, with no clothes and dressed only with a diaper. The surface of the incubator should be flat and of plain color (e.g. white) with no patterns etc. to avoid interference with accurate scoring in movement assessment. The neonate should be in a calm state, not irritated and not sleeping either. If the baby is crying and is unsettled it will be difficult to film, therefore, in this case the filming will be postponed and completed at an alternative time. It is best that the neonate cannot see the nurse or other person except for the person filming as this may attract the baby's attention. No dummies or toys should be used and no interaction with the neonate by talking or touching throughout the video recording period. A simple camera on a tripod (height 1.5 meters), will be placed next to the incubator and above the neonate at an angle so that the neonate can be seen in the frame (including his/her feet and hands). As afore-mentioned, 5-minute videos will be recorded twice (at the beginning and at term-age). Data analysis: Data will initially be presented using mean and standard deviation (descriptive data). For comparisons between the intervention and control group, the ANOVA and independent t-test will be used (SPSS). Differences will be considered statistically significant when p value is <0.5.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Premature Baby 26 to 32 Weeks, Preterm Birth
Keywords
preterm, positioning, snuggle up, general movements

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Only the principal investigator who is not an assessor will know the allocation of the neonates to the 2 groups. The assessors will be blind to the allocation of the neonates.
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Positioning in flexion
Arm Type
Experimental
Arm Description
Intervention: Positioning of body in flexion and aligment towards midline with Snuggle up (Philips, USA)
Arm Title
Control group
Arm Type
No Intervention
Arm Description
No intervention
Intervention Type
Other
Intervention Name(s)
Positioning in flexion
Intervention Description
The intervention group will be positioned in flexion (i.e. lower limbs in flexion, hand in midline) with an aid, the Snuggle up (Philips, USA). With positioning, the neonates bottom is tucked down in the snuggle up pocket, legs are aligned and gently flexed and hands towards midline and near the face. Positioning will be demonstrated to the nursing staff of the Neonatal Intensive Care Unit (NICU). The intervention group will receive positioning during day and night throughout the intervention period.
Primary Outcome Measure Information:
Title
Change from baseline General movements at 40 weeks
Description
General Movements (GM's) of Prechtl using 5-minute video observations of each neonate for the assessment
Time Frame
From baseline to 40 weeks
Title
Change from 40 weeks Denver II Developmental Screening Test at 4 months of corrected age
Description
The purpose of the test is to identify young children with developmental problems
Time Frame
From 40 weeks to 4 months of corrected age
Secondary Outcome Measure Information:
Title
Change from baseline Beats per minute (heart rate ) at 40 weeks
Description
The heart rate will be measured with a monitor connected to the neonate
Time Frame
From baseline to 40 weeks
Title
Change from baseline Breaths per minute (respiratory rate) at 40 weeks
Description
The respiratory rate will be measured with a monitor connected to the neonate
Time Frame
From baseline to 40 weeks
Title
Change from baseline Weight at 40 weeks
Description
Weight gained during the intervention period measured with the NICU scales
Time Frame
From baseline to 40 weeks
Title
Days till full feeding
Description
This information will be collected from each neonate's file
Time Frame
Up to 40 weeks
Title
Days the neonate needed oxygen
Description
This information will be collected from neonates file
Time Frame
Up to 40 weeks
Title
Duration of stay in the NICU
Description
This information will be collected from neonates file
Time Frame
Up to 40 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
24 Weeks
Maximum Age & Unit of Time
33 Weeks
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Νeonates of 33 weeks of gestation or less Exclusion Criteria: Νeonates with congenital deformities or genetic anomalies with neurological deficits detected at 1st week post-natal of multiple birth (triplets and over) or breech deliveries
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Theofani Bania
Organizational Affiliation
University of Patras, Greece
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Patras
City
Patra
ZIP/Postal Code
265 04
Country
Greece

12. IPD Sharing Statement

Citations:
PubMed Identifier
26676439
Citation
Toso BR, Viera CS, Valter JM, Delatore S, Barreto GM. Validation of newborn positioning protocol in Intensive Care Unit. Rev Bras Enferm. 2015 Nov-Dec;68(6):1147-53. doi: 10.1590/0034-7167.2015680621i. English, Portuguese.
Results Reference
background
PubMed Identifier
23477978
Citation
Zarem C, Crapnell T, Tiltges L, Madlinger L, Reynolds L, Lukas K, Pineda R. Neonatal nurses' and therapists' perceptions of positioning for preterm infants in the neonatal intensive care unit. Neonatal Netw. 2013 Mar-Apr;32(2):110-6. doi: 10.1891/0730-0832.32.2.110.
Results Reference
background
PubMed Identifier
21616611
Citation
Bernhardt I, Marbacher M, Hilfiker R, Radlinger L. Inter- and intra-observer agreement of Prechtl's method on the qualitative assessment of general movements in preterm, term and young infants. Early Hum Dev. 2011 Sep;87(9):633-9. doi: 10.1016/j.earlhumdev.2011.04.017. Epub 2011 May 26.
Results Reference
background
Citation
Sathish Y, Edward Lewis L, Angelitta Noronha J, George A, Snayak B, S Pai M, et al. Clinical Outcomes of Snuggle up Position Using Positioning Aids for Preterm (27-32 Weeks) Infants. Iranian Journal of Neonatology. 2017
Results Reference
background
PubMed Identifier
24626374
Citation
Pereira FL, Nogueira de Goes Fdos S, Fonseca LM, Scochi CG, Castral TC, Leite AM. [Handling of preterm infants in a neonatal intensive care unit]. Rev Esc Enferm USP. 2013 Dec;47(6):1272-8. doi: 10.1590/S0080-623420130000600003. Portuguese.
Results Reference
background
PubMed Identifier
24374602
Citation
Madlinger-Lewis L, Reynolds L, Zarem C, Crapnell T, Inder T, Pineda R. The effects of alternative positioning on preterm infants in the neonatal intensive care unit: a randomized clinical trial. Res Dev Disabil. 2014 Feb;35(2):490-7. doi: 10.1016/j.ridd.2013.11.019. Epub 2013 Dec 25. Erratum In: Res Dev Disabil. 2015 Jun-Jul;41-42:101-2.
Results Reference
background
PubMed Identifier
26365130
Citation
Einspieler C, Marschik PB, Pansy J, Scheuchenegger A, Krieber M, Yang H, Kornacka MK, Rowinska E, Soloveichick M, Bos AF. The general movement optimality score: a detailed assessment of general movements during preterm and term age. Dev Med Child Neurol. 2016 Apr;58(4):361-8. doi: 10.1111/dmcn.12923. Epub 2015 Sep 14.
Results Reference
background
PubMed Identifier
27313378
Citation
Yeh KK, Liu WY, Wong AM, Chung CY, Lien R, Chuang YF. Intra-observer reliability of Prechtl's method for the qualitative assessment of general movements in Taiwanese infants. J Phys Ther Sci. 2016 May;28(5):1588-94. doi: 10.1589/jpts.28.1588. Epub 2016 May 31.
Results Reference
background

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Effectiveness of Positioning in Preterm Neonates

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