Co-Bedding as a Comfort Measure for Twins Undergoing Painful Procedures (CComforT)
Neonatal Procedural Pain Response
About this trial
This is an interventional treatment trial for Neonatal Procedural Pain Response focused on measuring Co-bedding, Procedural pain, Twin, Comfort, RCT
Eligibility Criteria
Inclusion Criteria:
All medically stable twin infants admitted to the NICU who are:
- Free from infection; and
- Breathing room air or receiving oxygen via nasal prongs.
- Twins may be receiving feeds via gavage tubes, IV therapy via peripheral or central line, and may be experiencing periods of apnea.
Exclusion Criteria:
- Weigh less than 1000 grams;
- Receiving ventilator support;
- Have chest tubes or umbilical catheter in situ;
- Have major congenital anomalies or chromosomal aberrations; OR
- If only one of the twins require overhead phototherapy.
Sites / Locations
- IWK Health Centre
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Co-bedding
Standard care
Twin infants will be placed together in a Incubator or crib lying side-by-side. Twins will be diaper clad and nested together in boundaries consistent with neonatal care practices. All infants will have cardio-respiratory monitoring while co-bedding. Infants in the co-bedding group be co-bedded for no less than 24 hours prior to heelstick to allow for stabilization following transfer. The heelstick being studied will occur no greater than 10 days following initiation of co-bedding. Duration of co-bedding will be recorded and controlled for in the analysis if necessary. Monitoring and video-tape recording will take approximately 20-30 minutes per participant - a baseline period (5-10 minutes prior to heel stick), warming (3 minutes), heel stick (2-5 minutes), and recovery phase (approximately 10 minutes).
For infants who are randomized to receive standard care, the twin pair will remain in separate incubators as per current NICU policy. The infant will be nested in boundaries consistent with neonatal care practices. The heelstick may occur at any time following randomization (within 10 days) to maintain consistency between groups.