Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12617000805370
Ethics application status
Approved
Date submitted
26/05/2017
Date registered
1/06/2017
Date last updated
27/06/2019
Date data sharing statement initially provided
27/06/2019
Date results provided
27/06/2019
Type of registration
Prospectively registered

Titles & IDs
Public title
Portable neonatal sleep spaces to support optimal breastfeeding, close care and safe sleep in postnatal wards: a pilot
Scientific title
Enabling Safe and Close Care in Postnatal Environments: a pilot trial of portable neonatal sleep spaces to support optimal breastfeeding, close care and safe sleep
Secondary ID [1] 292077 0
None
Universal Trial Number (UTN)
U1111-1196-8694
Trial acronym
The ESCCaPE Pilot Trial
Linked study record
n/a

Health condition
Health condition(s) or problem(s) studied:
Safe infant sleeping 303459 0
breastfeeding 303462 0
maternal-infant attachment 303463 0
Condition category
Condition code
Reproductive Health and Childbirth 302869 302869 0 0
Breast feeding
Reproductive Health and Childbirth 302870 302870 0 0
Childbirth and postnatal care

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
On arrival to the postnatal unit, participants (mothers of well, term newborns meeting eligibility criteria) will be randomised to one of three options: ‘The First Days Pepi-Pod (inbed cosleeper and postnatal version of the Pepi-Pod)’, ‘The MaBim Neonatal Cot’ (side-car cot) or a standard bedside cot. An allocation to a cot is intended for the duration of hospitalisation.

ARM 1: The First Days Pod is a plastic container equipped with appropriate bedding designed to provide a zone of physical protection around baby as they sleep in an adult bed with a parent/adult caregiver in the postnatal environment. Participants will be shown the Video Clip titled ‘Safe, Sleep, Little One’ (CFOC Ltd, 2016) by the midwife once orientated to the postnatal ward. Participants allocated to the First Days Pepi-Pod will also be asked by the midwife to view the Picture Demonstration (CFOC Ltd, 2016) and the First Days Pod Safety Briefing and have their questions answered. Allocation to the First Days Pod is intended for the duration of hospitalisation.

ARM 2: The MaBim Neonatal Cot is a side car cot that converts to a three sided cot that is positioned adjacent to the adult postnatal bed to allow contact while on a separate sleep surface. All participants will be shown the Video Clip titled ‘Safe, Sleep, Little One’ (CFOC Ltd, 2016) by the midwife once orientated to the postnatal ward. Participants allocated to the MaBim neonatal crib will be shown the MaBim Product Brochure and the MaBim Safety Briefing by the midwife and have their questions answered. Allocation to the MaBim cot is intended for the duration of hospitalisation.

CONTROL: a standard hospital cot. All participants will be shown the Video Clip titled ‘Safe, Sleep, Little One’ (CFOC Ltd, 2016) by the midwife once orientated to the postnatal ward. Participants randomised to the control group (usual cot care) will receive standard care instructions including Hospital Cot Safety Briefing provided by the midwife and have their questions answered.

Intervention code [1] 298191 0
Treatment: Devices
Intervention code [2] 298220 0
Behaviour
Comparator / control treatment
The Control treatment is a standard hospital perspex cot.
Control group
Active

Outcomes
Primary outcome [1] 302260 0
Maternal acceptability of infant sleep spaces; assessed by Questionnaire (author developed)
Timepoint [1] 302260 0
Prior to discharge if hospital birth ?within 1-3 days post birth for vaginal deliveries and within 3-5 days post birth for caesarean deliveries)
Primary outcome [2] 302261 0
Staff perspectives of protocol feasibility in postnatal environment; assessed by Questionnaire (author developed)
Timepoint [2] 302261 0
at 16-20 weeks post study commencement
Secondary outcome [1] 335311 0
Maternal satisfaction with care; assessed by Maternal Satisfaction Questionnaire (ICHOM Pregnancy and Childbirth standard set (ICHOM, 2016)
Timepoint [1] 335311 0
Prior to discharge if hospital birth ?within 1-3 days post birth for vaginal deliveries and within 3-5 days post birth for caesarean deliveries)
Secondary outcome [2] 335409 0
Provision of culturally appropriate care/personal options and choice assessed by Demographic Questionnaire (author developed)
Timepoint [2] 335409 0
Prior to discharge if hospital birth ?within 1-3 days post birth for vaginal deliveries and within 3-5 days post birth for caesarean deliveries)
Secondary outcome [3] 335410 0
Breastfeeding method assessed by Breastfeeding Success Variable (ICHOM 2016)
Timepoint [3] 335410 0
Prior to discharge if hospital birth ?within 1-3 days post birth for vaginal deliveries and within 3-5 days post birth for caesarean deliveries); at infant age 6-8 weeks; at infant age 4 months
Secondary outcome [4] 335411 0
Breastfeeding Self-Efficacy assessed by Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF) (Dennis 2003)
Timepoint [4] 335411 0
Prior to discharge if hospital birth ?within 1-3 days post birth for vaginal deliveries and within 3-5 days post birth for caesarean deliveries); at infant age 6-8 weeks; at infant age 4 months
Secondary outcome [5] 335412 0
Maternal-Infant Attachment assessed by Mother-to-Infant Bonding Scale (MIBS) (Taylor et al 2005, ICHOM 2016)
Timepoint [5] 335412 0
Prior to discharge if hospital birth ?within 1-3 days post birth for vaginal deliveries and within 3-5 days post birth for caesarean deliveries); at infant age 6-8 weeks; at infant age 4 months
Secondary outcome [6] 335413 0
Maternal awareness of Safe Sleeping recommendations assessed by Maternal Safe Sleep Awareness Questionnaire (Schluter and Young 2002)
Timepoint [6] 335413 0
Prior to discharge if hospital birth ?within 1-3 days post birth for vaginal deliveries and within 3-5 days post birth for caesarean deliveries); at infant age 6-8 weeks; at infant age 4 months
Secondary outcome [7] 335414 0
Postnatal Incidence of shared sleeping assessed by Infant Sleep Observation Audit
Timepoint [7] 335414 0
Prior to discharge if hospital birth ?within 1-3 days post birth for vaginal deliveries and within 3-5 days post birth for caesarean deliveries)
Secondary outcome [8] 335415 0
Maternal reported shared sleeping assessed by Maternal Safe Sleep Awareness Questionnaire
Timepoint [8] 335415 0
Prior to discharge if hospital birth ?within 1-3 days post birth for vaginal deliveries and within 3-5 days post birth for caesarean deliveries); at infant age 6-8 weeks; at infant age 4 months
Secondary outcome [9] 335416 0
Maternal length of stay assessed by Maternal Chart Audit of admission and discharge dates
Timepoint [9] 335416 0
at Discharge from postnatal unit
Secondary outcome [10] 335417 0
Pre Intervention Staff Awareness of Safe Sleep Recommendations assessed by Staff Safe Sleep Questionnaire and Chart Audit (Young and Schluter 2002, Young et al 2008)
Timepoint [10] 335417 0
at 4 weeks prior to study commencement
Secondary outcome [11] 335418 0
Post Intervention Staff Awareness of Safe Sleep Recommendations assessed by Staff Safe Sleep Questionnaire and Chart Audit (Young and Schluter 2002, Young et al 2008)
Timepoint [11] 335418 0
at 16-20 weeks post study commencement
Secondary outcome [12] 335419 0
Staff acceptability of infant sleep spaces; assessed by Questionnaire (author developed)
Timepoint [12] 335419 0
at 16-20 weeks post study commencement
Secondary outcome [13] 335420 0
Postnatal adverse events assessed through PRIME system (records baby falls, adverse events from maternal beds or chairs)
Timepoint [13] 335420 0
At discharge if hospital birth ?within 1-3 days post birth for vaginal deliveries and within 3-5 days post birth for caesarean deliveries)

Eligibility
Key inclusion criteria
Maternal participants
- greater than or equal to 36 weeks of gestation at time of consent
- Attending the SCUH for antenatal care
- Intending to be admitted to the postnatal ward at the SCUH after the birth
- English speaking
- Intending to breastfeed
- Singleton pregnancy
- BMI less than 40
- greater than or equal to 15 years of age
- Ability to read and understand English
Minimum age
15 Years
Maximum age
No limit
Sex
Females
Can healthy volunteers participate?
Yes
Key exclusion criteria
- less than 36 weeks of gestation at time of consent
- Maternal condition which significantly interferes with breastfeeding
- Intending to feed infant with artificial formula
- Maternal BMI greater than or equal to 40
- less than 15 years of age
- Multiple pregnancy
- Newborn admitted to SCN or NICU immediately after birth
- Neonate requiring phototherapy with or without CPAP
- Inability to read and understand English

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Sealed opaque envelopes - for randomisation process by staff to Treatment groups: First Day Pod, MaBim Cot, Standard Cot
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a randomisation table created by
computer software (i.e. computerised sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis
A target sample of 180 maternal participants and their babies will be recruited (approximately 60 in each group) in this Pilot Study to allow an attrition rate of 50% during the 4 month follow-up period in order to achieve a final sample of 90 participants (with 30 mother-infant pairs in each group). The primary aim of this pilot is to gather observational data relating to the feasibility and acceptability of the Safe Sleep Enabler options and to test the non-blinded, randomised control trial protocol intended for a larger study.
Based on an estimated 30-40 eligible births per week at this regional hospital, and taking into account conservative participation rates of 40% and attrition post enrolment (50%), in addition to average length of hospital stay (approx. 1-3 days for vaginal deliveries, 3-5 days for delivery by caesarean section), it is anticipated that a maximum recruitment period of 5-6 months will be required to achieve the target sample of 180 eligible mothers and their babies with complete datasets.
The estimated staff population is approximately 80 nurses and midwives; it is anticipated that a target sample size of approximately 65-70 staff (approx. 80% response rate) will be achieved based on previous study participation with this cohort. Power calculations have not been conducted as the population is fixed by the maternity unit setting, and the primary aim of the pilot was to determine feasibility of the protocol and staff acceptance and use of a novel safe sleep enabler in this environment.
Audits of maternal charts and infant sleep observations prior to pilot RCT have been included to provide important baseline relating to current safe sleep practices in this setting. The sample size of 90-100 infant sleep observations and matched maternal chart audits will be adequate to provide a snapshot of current practice; to compare with data collected in previous studies in similar settings (Young et al., 2010); is feasible to collect within a relatively short period of time using in-kind time and resources available to the investigating research team; and provides the SCUH with valuable data to meet state guideline recommendations relating to current monitoring of safe sleep practices (Queensland Health, 2013).
Data analysis
Pilot Data collection and analyses will include maternal and infant demographics; breastfeeding outcomes (at discharge, 6-8 weeks and 4 months); length of stay; maternal-infant attachment; maternal satisfaction and perceptions relating to enabler use; staff time to recruit and educate families, perceptions relating to intervention impact and adverse events; and maternal and staff awareness of safe sleep recommendations (self reported and observed).
Maternal Data: Analysis of maternal data will be conducted using the principles of intention to treat. All participants who were enrolled and randomly allocated to treatment will be included and analysed in the groups to which they were randomised. A further analysis will be based on actual use, consistent with a recent published study using Wahakura (Baddock et al., 2017) which performed analyses based on intention to treat and actual use.
Statistical analyses will be performed to report the prevalence and proportions of variables surveyed. Questionnaire results will be entered into a purpose-built Microsoft Excel database for data cleaning and preparation for statistical analysis. A 10% random selection (approximately 9-10 questionnaires from each of the maternal records, staff survey and audits) will be double entered to assess data-entry accuracy and intra-rater reliability. Consistency checks will be performed on all variables to ensure that only valid responses will form the basis of the ensuing analysis.
Quantitative data will be analysed using descriptive techniques such as frequency and percentage and measures of central tendency and distribution (for example, mean and standard deviation or median and IQR). Normality of data will be assessed. Group comparisons to comparing equivalency of control and interventions will be conducted with Chi-squared test for categorical measures and analysis of variance or Kruskal-Wallis test for continuous measures as appropriate assessing for normality and equality of variances.
Staff Survey Data: Should continuous data be distributed symmetrically, then means and standard deviation (SD) will be reported. Medians, inter-quartile ranges (IQR), frequencies and percentages will be used to report the central tendency, spread and empirical distributions of categorical and non-symmetric continuous variables elicited at each survey. All bivariate comparisons of categorical frequencies will be undertaken using Fisher's exact test, log-linear and logistic models, while McNemar’s test and Agresti's test of symmetry will be used to detect differences between participants' responses at any two survey points (pretest vs post-test). Continuous data will be analysed using Student's t-test, Student's paired t-test, ANOVA or using their nonparametric equivalents (should the data exhibit non-normality).
Audit data: All qualitative data will be coded prior to data entry. Frequency data will be reported and analysed using standard categorical techniques (accounting for the matched nature of the data between mother and baby). Univariate linear modelling will be conducted for dependent variables that will include infant sleep position, infant placement in the cot, placement and securement of bedding; and presence of particular objects in the cot, e.g. Infant quilts, toys, cot bumpers.
All statistical comparisons will be analysed using the SAS or SPSS statistical software package (IBM Corp 2013). A value of p=0.05 will be used to define statistical significance for primary outcomes as they are independent of each other. We recognize that there are a large number of secondary outcomes and will report uncorrected p values with a nominal level of significance of 0.05.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
1/08/2017
Actual
5/03/2018
Date of last participant enrolment
Anticipated
28/02/2018
Actual
10/08/2018
Date of last data collection
Anticipated
26/06/2018
Actual
5/12/2018
Sample size
Target
160
Accrual to date
Final
94
Recruitment in Australia
Recruitment state(s)
QLD
Recruitment hospital [1] 8177 0
Sunshine Coast University Hospital - Birtinya
Recruitment postcode(s) [1] 16238 0
4575 - Birtinya

Funding & Sponsors
Funding source category [1] 296589 0
Charities/Societies/Foundations
Name [1] 296589 0
Wishlist Sunshine Coast Health Foundation
Country [1] 296589 0
Australia
Primary sponsor type
Hospital
Name
Sunshine Coast University Hospital
Address
Sunshine Coast University Hospital
16 Innovation Parkway
Birtanya QLD 4575
Country
Australia
Secondary sponsor category [1] 295541 0
University
Name [1] 295541 0
University of the Sunshine Coast
Address [1] 295541 0
University of the Sunshine Coast
Sippy Downs Drive
Sippy Downs
QLD 4556
Country [1] 295541 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 297810 0
Royal Brisbane and Women's Human Research Ethics Committee
Ethics committee address [1] 297810 0
Ethics committee country [1] 297810 0
Australia
Date submitted for ethics approval [1] 297810 0
09/05/2017
Approval date [1] 297810 0
17/05/2017
Ethics approval number [1] 297810 0
HREC/17/QRBW/162
Ethics committee name [2] 303711 0
University of the Sunshine Coast Human Research Ethics Committee
Ethics committee address [2] 303711 0
Ethics committee country [2] 303711 0
Australia
Date submitted for ethics approval [2] 303711 0
10/07/2017
Approval date [2] 303711 0
21/08/2017
Ethics approval number [2] 303711 0
A17991

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes
Attachments [1] 1738 1738 0 0
/AnzctrAttachments/373027-ESCCaPE_Protocol_CLEAN_V1.1_20170505.pdf (Protocol)
Attachments [2] 1739 1739 0 0
/AnzctrAttachments/373027-17-162 signed approval 17May17.pdf (Ethics approval)
Attachments [3] 1758 1758 0 0
/AnzctrAttachments/373027-ESCCaPE_SSD_PISCF_MASTER_CLEAN_V1.1_20170503.doc
Attachments [4] 1759 1759 0 0
/AnzctrAttachments/373027-ESCCaPE_StaffQuestionnaire_PIS_MASTER_CLEAN_V1.1_20170503.doc

Contacts
Principal investigator
Name 75166 0
Prof Jeanine Young
Address 75166 0
School of Nursing, Midwifery and Paramedicine,
University of the Sunshine Coast
Sippy Downs Drive
Sippy Downs QLD 4556
Country 75166 0
Australia
Phone 75166 0
+61754565898
Fax 75166 0
+61754565940
Email 75166 0
[email protected]
Contact person for public queries
Name 75167 0
Jeanine Young
Address 75167 0
School of Nursing, Midwifery and Paramedicine,
University of the Sunshine Coast
Sippy Downs Drive
Sippy Downs QLD 4556
Country 75167 0
Australia
Phone 75167 0
+61754565898
Fax 75167 0
+61754565940
Email 75167 0
[email protected]
Contact person for scientific queries
Name 75168 0
Jeanine Young
Address 75168 0
School of Nursing, Midwifery and Paramedicine,
University of the Sunshine Coast
Sippy Downs Drive
Sippy Downs QLD 4556
Country 75168 0
Australia
Phone 75168 0
+61754565898
Fax 75168 0
+61754565940
Email 75168 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
Data relating to the use of novel sleep spaces in postnatal units:
De-identified qualitative data - maternal responses
De-identified survey data - maternal responses (breastfeeding, maternal-infant attachment)
De-identified survey data - Health professionals - knowledge, attitudes relating to safe sleeping recommendations
When will data be available (start and end dates)?
Start Date: 14 December 2018 (when data collection closed on last participant)
End Date: No end date determined
Available to whom?
Researchers - upon request
Available for what types of analyses?
Systematic reviews/Meta-analyses of health professional knowledge and attitudes relating to safe sleep recommendations
Systematic reviews/meta-analyses relating to outcomes associated with portable infant sleep spaces
How or where can data be obtained?
USC Research Bank


What supporting documents are/will be available?

Doc. No.TypeCitationLinkEmailOther DetailsAttachment
2211Study protocol    373027-(Uploaded-29-05-2019-16-19-55)-Study-related document.pdf
2212Informed consent form    373027-(Uploaded-29-05-2019-16-19-55)-Study-related document.docx



Results publications and other study-related documents

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No documents have been uploaded by study researchers.

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