The Adding Value of Parents to Nursing Care in the Control of FiO2
Primary Purpose
Premature Birth of Newborn
Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Standard procedure
Experimental procedure
Sponsored by
About this trial
This is an interventional other trial for Premature Birth of Newborn
Eligibility Criteria
Inclusion Criteria:
- Related to child
- Preterm neonates less than 32 weeks or less than 1500 g hospitalized in the Neonatal Intensive Care Unit at Hospital 12 de Octubre.
- Receiving supplemental oxygen ≤0.4 administered by CPAP or conventional nasal cannula or high flow or children with BiPAP (flow generator with double level pressure)
- Minimum age 7 days old.
- Related to the mother:
- Absence of health problems that allows her to perform the task.
- Availability to frequently visit her baby with the father or with a companion, at least for 20 hours, not consecutive.
- Understanding of the study and the Spanish language by the mother and father or companion.
- Signed informed consent.
Exclusion Criteria:
- Evidence of pneumothorax or pneumomediastinum.
- Non-compliance with study protocol.
- Requiring treatment with vasoactive drugs.
Sites / Locations
- Hospital Universitario 12 de OctubreRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Control by nursing.
Control by parents.
Arm Description
FiO2 adjusted manually by nursing staff. Intervention: Other. Standard procedure
FiO2 adjusted manually by parents. Intervention. Other. Experimental procedure
Outcomes
Primary Outcome Measures
Children maintained within the saturation ranges in each group
Percentage of time the child is kept within the ranges of saturation in each group
Secondary Outcome Measures
Full Information
NCT ID
NCT02306317
First Posted
December 1, 2014
Last Updated
March 14, 2018
Sponsor
Carmen Rosa Pallas
Collaborators
Hospital Universitario 12 de Octubre
1. Study Identification
Unique Protocol Identification Number
NCT02306317
Brief Title
The Adding Value of Parents to Nursing Care in the Control of FiO2
Official Title
Changing the Paradigm for Improving Neonatal Care: Clinical Study on Optimal Oxygen-saturation Time and the Adding Value of Parents to Nursing Care in the Control of Fi02
Study Type
Interventional
2. Study Status
Record Verification Date
March 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 2014 (Actual)
Primary Completion Date
June 2018 (Anticipated)
Study Completion Date
June 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Carmen Rosa Pallas
Collaborators
Hospital Universitario 12 de Octubre
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to determine whether saturation control by parents in children younger than 32 weeks or under 1500 g versus conventional care performed by nursing increases the time in which these patients remain at optimal saturation range. If the hypothesis of this study is confirmed premature infants could prevent episodes of hypoxia-hyperoxia and also give more relevance to the role of parents in caring for their children admitted in a neonatal intensive care unit.
Detailed Description
Both episodes of hyperoxia and hypoxemia in preterm infants increase morbidity and mortality. Nowadays the adjustment of FiO2 is manually controlled, which means it depends on the staff, needing multiple adjustments throughout the day.
The investigators's hypothesis is that the FiO2 control by parents, improve the percentage of time in range of optimum saturation at least 10% compared to control by nurses.
The aim of this study is to compare the proportion of time with oxygen saturation (SpO2) within the assigned target range, in the preterm infants whose parents modify the fraction of inspired oxygen (FiO2) versus the nursing staff modifying group.
This is a randomized controlled clinical study in the neonatal intensive care unit at Hospital 12 de Octubre. Patients will be randomized in two groups, Experimental Group: parents controlling the saturation ranges, they will manually adjust FiO2 versus the Control Group: controlled by nursing staff (standard procedure). Saturations will be registered and adjustments of FiO2 will be filmed for nonconsecutive 20-hours periods. Twenty-three patients will be enrolled in each group.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Premature Birth of Newborn
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
46 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control by nursing.
Arm Type
Active Comparator
Arm Description
FiO2 adjusted manually by nursing staff. Intervention: Other. Standard procedure
Arm Title
Control by parents.
Arm Type
Experimental
Arm Description
FiO2 adjusted manually by parents. Intervention. Other. Experimental procedure
Intervention Type
Other
Intervention Name(s)
Standard procedure
Intervention Description
FiO2 manually controlled by nursing
Intervention Type
Other
Intervention Name(s)
Experimental procedure
Intervention Description
FiO2 manually controlled by parents, after training.
Primary Outcome Measure Information:
Title
Children maintained within the saturation ranges in each group
Description
Percentage of time the child is kept within the ranges of saturation in each group
Time Frame
20-40 hours as maximum
10. Eligibility
Sex
All
Minimum Age & Unit of Time
7 Days
Maximum Age & Unit of Time
9 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Related to child
Preterm neonates less than 32 weeks or less than 1500 g hospitalized in the Neonatal Intensive Care Unit at Hospital 12 de Octubre.
Receiving supplemental oxygen ≤0.4 administered by CPAP or conventional nasal cannula or high flow or children with BiPAP (flow generator with double level pressure)
Minimum age 7 days old.
Related to the mother:
Absence of health problems that allows her to perform the task.
Availability to frequently visit her baby with the father or with a companion, at least for 20 hours, not consecutive.
Understanding of the study and the Spanish language by the mother and father or companion.
Signed informed consent.
Exclusion Criteria:
Evidence of pneumothorax or pneumomediastinum.
Non-compliance with study protocol.
Requiring treatment with vasoactive drugs.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carmen R. Pallás Alonso, Dra.
Phone
34 913908272
Email
carmenrosa.pallas@salud.madrid.org
First Name & Middle Initial & Last Name or Official Title & Degree
M. Dolores Martín Pelegrina, Dra.
Phone
34 913908272
Email
mariadolores.martinp@salud.madrid.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carmen R. Pallás Alonso, Dra.
Organizational Affiliation
Hospital Universitario 12 de Octubre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario 12 de Octubre
City
Madrid
ZIP/Postal Code
28041
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carmen R. Pallás Alonso, Dra
Phone
34 913908272
First Name & Middle Initial & Last Name & Degree
M. Dolores Martín Pelegrina, Dra.
Phone
34 913908272
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
29676033
Citation
Martin-Pelegrina MD, Lorenzo-Rodriguez A, Lora-Pablos D, Munoz-Amat B, Morales-Betancourt C, Pallas-Alonso CR. FiO2 control by parents of preterm infants admitted to a neonatal intensive care unit: A pilot study. Acta Paediatr. 2018 Aug;107(8):1471-1472. doi: 10.1111/apa.14364. Epub 2018 May 11. No abstract available.
Results Reference
derived
Learn more about this trial
The Adding Value of Parents to Nursing Care in the Control of FiO2
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