search
Back to results

Cardboard Cot in Neonatal Thermoregulation: A Randomized Cross Over Trial (CCot)

Primary Purpose

Infant, Premature, Hypothermia, Newborn

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cardboard Cot Care
Incubator Care
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Infant, Premature focused on measuring Neonate, Premature, Hypothermia, Cardboard, Cot

Eligibility Criteria

1 Minute - 5 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Estimated gestational age < 36 6/7 weeks
  • Hospitalized in the NICU at University Teaching Hospital in Zambia
  • Requiring incubator/radiant warmer for at least 1 week

Exclusion Criteria:

  • Abdominal wall defect or myelomeningocele
  • Major congenital anomalies
  • Blistering skin disorder
  • Suspected Sepsis
  • Requiring ongoing respiratory support

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    Cardboard Cot Care

    Incubator Care

    Arm Description

    Stable infant will be nursed in a cardboard cot, lined with reflective film for 24 hour period of time. Infant's axillary temperature will be taken at 1 hour after randomization, at 6 hours after randomization, and 24 hours after randomization. After 24 hours, infant will be swapped to the other arm (Incubator Care), and back for a total of 2 24-hour periods in each arm.

    Stable infant will be nursed in an incubator for 24 hour period of time. Infant's axillary temperature will be taken at 1 hour after randomization, at 6 hours after randomization, and 24 hours after randomization. After 24 hours, infant will be swapped to the other arm (Cardboard Cot Care), and back for a total of 2 24-hour periods in each arm.

    Outcomes

    Primary Outcome Measures

    Moderate (32.-35.9° C) or Severe (<32.0° C) hypothermia per Axillary Temperature
    Temperature taken via axilla for 1 minute duration
    Moderate (32.0-35.9° C) or Severe (<32.0° C) hypothermia per Axillary Temperature
    Temperature taken via axilla for 1 minute duration
    Moderate (32.-35.9° C) or Severe (<32.0°C) hypothermia per Axillary Temperature
    Temperature taken via axilla for 1 minute duration

    Secondary Outcome Measures

    Normothermia (Axillary temperature 36.0 - 38.0° C)
    Temperature taken via axilla for 1 minute duration
    Hypothermia (Axillary temperature < 36.0° C)
    Temperature taken via axilla for 1 minute duration
    Mean Axillary Temperature in each device
    Average of all axillary temperatures taken per device
    Rate of Moderate hypothermia (32.0-35.9° C) after placement in warming device
    Temperature taken via axilla for 1 minute duration
    Rate of Moderate hypothermia (32.0-35.9°C) after placement in warming device
    Temperature taken via axilla for 1 minute duration
    Rate of Moderate hypothermia (32.0-35.9° C) after placement in warming device
    Temperature taken via axilla for 1 minute duration
    Rate of Severe hypothermia (<32.0° C) after placement in warming device
    Temperature taken via axilla for 1 minute duration
    Rate of Severe hypothermia (<32.0° C) after placement in warming device
    Temperature taken via axilla for 1 minute duration
    Rate of Severe hypothermia (<32.0° C) after placement in warming device
    Temperature taken via axilla for 1 minute duration
    Rate of Hyperthermia (>38.0°C) after placement in warming device
    Temperature taken via axilla for 1 minute duration

    Full Information

    First Posted
    November 14, 2017
    Last Updated
    October 22, 2021
    Sponsor
    University of Alabama at Birmingham
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT03344978
    Brief Title
    Cardboard Cot in Neonatal Thermoregulation: A Randomized Cross Over Trial
    Acronym
    CCot
    Official Title
    Cardboard Cot in Neonatal Thermoregulation: A Randomized Cross Over Trial in Prevention of Moderate or Severe Hypothermia in Preterm Infants Requiring at Least 1 Week of Incubator
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2021
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Unable to recruit participants
    Study Start Date
    June 11, 2019 (Actual)
    Primary Completion Date
    September 27, 2021 (Actual)
    Study Completion Date
    September 27, 2021 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Alabama at Birmingham

    4. Oversight

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

    5. Study Description

    Brief Summary
    This study will determine whether the efficacy of Mylar-lined cardboard cots is equivalent to traditional incubators in their ability to prevent hypothermia (axillary temperature < 36° C) in preterm neonates <36 6/7 weeks gestational age in a randomized cross-over designed trial. Infants will be randomized to receive care in the cardboard cot or incubator and then cross over to the other device for 24 hour periods, rotating for a total of 96 hours total trial time.
    Detailed Description
    The aim of the trial is to determine whether a corrugated cardboard cot will assist in maintaining infant axillary temperatures comparing it to the temperatures of the same infant being nursed in low heat incubators. The study will be done in the context of standard medical care, including the WHO thermoregulation protocol (warm delivery rooms, immediate drying after birth, early and exclusive breastfeeding, postponement of bathing and weighing, and appropriate bundling). The cardboard cot is approximately 24 inches long to accommodate the length of the infant and about 12 inches wide to accommodate term infants, even beyond the first months after birth. The cots are fully lined with a reflective metallized film sheet of Mylar. The cot will be covered with a cardboard piece also lined in reflective film up to about the infant's shoulders so that the infant's face is visible. Attached to the lid is a 5 inch cardboard flap lined with reflective film which folds down into the body of the cot to reduce heat loss. Infants ≤ 36 6/7 weeks gestation will be randomized to receive care in a cardboard cot or an incubator. Infants will begin care in one device and after 24 hours will cross over to the other device for another 24 hours. The process will be repeated once more for a total of 96 hours of study duration. The infants will be normothermic and stable when they are enrolled in the trial. Axillary temperatures will be measured at 1 hr, 6 hours and 24 hours after being placed in the cost or incubator. Infants with observed hypothermia (<36° C) will have measures taken to increase temperature (i.e. adding blankets, hat).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Infant, Premature, Hypothermia, Newborn
    Keywords
    Neonate, Premature, Hypothermia, Cardboard, Cot

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Model Description
    Randomized crossover. Participant will be randomly assigned initially to care in one of two devices for 24 hours, then crossed over to other device for 24 hours. This will be repeated once more for a total of 96 hours study time. Patterns may be A-B-A-B or B-A-B-A.
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Cardboard Cot Care
    Arm Type
    Active Comparator
    Arm Description
    Stable infant will be nursed in a cardboard cot, lined with reflective film for 24 hour period of time. Infant's axillary temperature will be taken at 1 hour after randomization, at 6 hours after randomization, and 24 hours after randomization. After 24 hours, infant will be swapped to the other arm (Incubator Care), and back for a total of 2 24-hour periods in each arm.
    Arm Title
    Incubator Care
    Arm Type
    Placebo Comparator
    Arm Description
    Stable infant will be nursed in an incubator for 24 hour period of time. Infant's axillary temperature will be taken at 1 hour after randomization, at 6 hours after randomization, and 24 hours after randomization. After 24 hours, infant will be swapped to the other arm (Cardboard Cot Care), and back for a total of 2 24-hour periods in each arm.
    Intervention Type
    Other
    Intervention Name(s)
    Cardboard Cot Care
    Other Intervention Name(s)
    CCot
    Intervention Description
    Infant maintained in reflective film-lined cot for a period of 24 hours. Axillary temperatures will be taken at 1 hour, 6 hours, and 24 hours after randomization. If temperatures found < 36° C. at any time, an additional blanket and hat will be added to infant to improve temperature. Infant may be moved to incubator or radiant warmer. All other care will be standard of care at University Teaching Hospital, including warm delivery rooms, immediate drying, postponed bathing and weighing, early and exclusive breastfeeding, and Kangaroo Mother Care as continuously as possible.
    Intervention Type
    Other
    Intervention Name(s)
    Incubator Care
    Intervention Description
    Infant maintained in standard incubator for a period of 24 hours. Axillary temperatures will be taken at 1 hour, 6 hours, and 24 hours after randomization. If temperatures found < 36° C. at any time, an additional blanket and hat will be added to infant to improve temperature. All other care will be standard of care at University Teaching Hospital, including warm delivery rooms, immediate drying, postponed bathing and weighing, early and exclusive breastfeeding, and Kangaroo Mother Care as continuously as possible.
    Primary Outcome Measure Information:
    Title
    Moderate (32.-35.9° C) or Severe (<32.0° C) hypothermia per Axillary Temperature
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    1 hour after placement in warming device
    Title
    Moderate (32.0-35.9° C) or Severe (<32.0° C) hypothermia per Axillary Temperature
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    6 hours after placement in warming device
    Title
    Moderate (32.-35.9° C) or Severe (<32.0°C) hypothermia per Axillary Temperature
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    24 hours after placement in warming device
    Secondary Outcome Measure Information:
    Title
    Normothermia (Axillary temperature 36.0 - 38.0° C)
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    1-96 hours after beginning of study
    Title
    Hypothermia (Axillary temperature < 36.0° C)
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    1-96 hours after beginning of study
    Title
    Mean Axillary Temperature in each device
    Description
    Average of all axillary temperatures taken per device
    Time Frame
    4 months
    Title
    Rate of Moderate hypothermia (32.0-35.9° C) after placement in warming device
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    1 hour after placement in warming device
    Title
    Rate of Moderate hypothermia (32.0-35.9°C) after placement in warming device
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    6 hours after placement in warming device
    Title
    Rate of Moderate hypothermia (32.0-35.9° C) after placement in warming device
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    24 hours after placement in warming device
    Title
    Rate of Severe hypothermia (<32.0° C) after placement in warming device
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    1 hour after placemnt in warming device
    Title
    Rate of Severe hypothermia (<32.0° C) after placement in warming device
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    6 hours after placement in warming device
    Title
    Rate of Severe hypothermia (<32.0° C) after placement in warming device
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    24 hours after placement in warming device
    Title
    Rate of Hyperthermia (>38.0°C) after placement in warming device
    Description
    Temperature taken via axilla for 1 minute duration
    Time Frame
    4 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    1 Minute
    Maximum Age & Unit of Time
    5 Days
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Estimated gestational age < 36 6/7 weeks Hospitalized in the NICU at University Teaching Hospital in Zambia Requiring incubator/radiant warmer for at least 1 week Exclusion Criteria: Abdominal wall defect or myelomeningocele Major congenital anomalies Blistering skin disorder Suspected Sepsis Requiring ongoing respiratory support
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Colm P Travers, MB BCh BAO
    Organizational Affiliation
    University of Alabama at Birmingham
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Cardboard Cot in Neonatal Thermoregulation: A Randomized Cross Over Trial

    We'll reach out to this number within 24 hrs