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The GROWNDUP Study of Late Preterm Births (GROWNDUP)

Primary Purpose

Preterm Birth

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Specialized LPTB clinic
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Preterm Birth focused on measuring Late preterm infant, Complications, Hospital readmissions, Follow-up, Pilot study

Eligibility Criteria

undefined - 1 Month (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

- singleton or twins born at 34 and 0 days to 36 weeks and 6 days gestational age. Infants admitted to the Level 2 Nursery or newborn nursery at McMaster Children's Hospital or St. Joseph's Healthcare Hamilton or Level 3 Nursery (NICU) at McMaster Children's Hospital will be included.

Exclusion Criteria:

  • triplets and infants with major cardiac anomalies, metabolic disorders, significant gastrointestinal anomalies, intrauterine growth restriction, potential genetic syndromes, neurologic anomalies or severe sepsis/meningitis and LPTB requiring mechanical ventilation (post-delivery room resuscitation with prolonged CPAP or intubation) will be excluded.
  • mothers who have a history of substance use at any time during pregnancy or alcohol use after confirmation of pregnancy
  • participants must be able to understand English and speak English as this pilot does not currently have the financial support to sponsor interpreters.

Sites / Locations

  • St. Joseph's Hospital
  • McMaster Children's Hospital & McMaster University

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Current management of LPTB

Specialized LPTB Clinic

Arm Description

The current pragmatic, but non-systematic, pattern of management of LPTB infants. Growth measurements, feeding histories/methods, illness history including emergent visits to clinicians, walk-in clinics and emergency departments and breast-feeding support clinics, and basic developmental milestones (as itemized in the Rourke Developmental screening tool) will be recorded by families and primary health care providers as itemized in the Memory Book at the assessments made at the discretion of the health care providers.

Additional 6 specialized LPTB follow-up clinic visits attended by pediatricians and neonatologists. Detailed findings from physical examination, feeding histories/methods, illness history including emergent visits to clinicians, walk-in clinics and emergency departments and breast-feeding support clinics, basic developmental milestones (as itemized in the Rourke Developmental screening tool) and physician recommendations will be recorded at each appointment. These will be compared to those obtained from families and primary health care providers as itemized in the Memory Book.

Outcomes

Primary Outcome Measures

Recruitment Rate
Recruitment Rate during first six months of pilot. Reported as the percentage of subjects recruited from those eligible to participate.

Secondary Outcome Measures

Infant Weight Gain
Weight Gain reported in grams.

Full Information

First Posted
December 3, 2012
Last Updated
April 7, 2015
Sponsor
McMaster University
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1. Study Identification

Unique Protocol Identification Number
NCT01747603
Brief Title
The GROWNDUP Study of Late Preterm Births
Acronym
GROWNDUP
Official Title
The GROWNDUP Study: Pilot to Assess the Feasibility of an RCT for Promoting Growth, Nutrition and Development Through a Specialized Late Preterm Clinic
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Unknown status
Study Start Date
May 2013 (undefined)
Primary Completion Date
August 2015 (Anticipated)
Study Completion Date
August 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This pilot study will examine the feasibility of conducting a large randomized clinical trial (RCT) to examine the role of a novel, specialized follow-up clinic in preventing complications among late preterm infants (LPTB), born between 34 and 36 weeks gestational age. 1) Study Process: Success will be achieved if 80% of a target population of 100 subjects is met within the first 6 months of recruitment being initiated. 2) Study Resources: Success will be achieved if 80% of follow up appointments are scheduled in a timely manner and if specialized LPTB physicians in the intervention complete assessments 75% of the time in the allocated time frame and 3) Scientific: 95% data completeness on data collection forms will be identified as success A specialized LPTB follow-up clinic is innovative as no studies have evaluated such a programme and standardized follow-up and guidelines for the care of LPTB infants after discharge from hospital do not exist. Until recently, the incorrect assumption has been that these infants are healthy and have limited risks compared to term infants. The study's main question, in addition to assessing the feasibility of this pilot, is: "Do differences exist in short-tem clinical and developmental outcomes among LPTB infants enrolled in an RCT who are randomized to a specialized LPTB follow-up programme when compared to infants randomized to current pragmatic management?" A RCT will provide evidence for the development of guidelines for the follow-up of LPTB infants in the first 6 months of life to reduce complications, readmissions and developmental problems. The results of this study can be generalized to tertiary care and community hospitals and the general population.
Detailed Description
Late preterm births comprise 70-75% of all preterm births in Ontario and 5.8% of all births in the province. These infants are at significant risk for complications but no guidelines or follow-up programmes exist for decreasing the short and long-term complications associated with LPTB. This project will lay the groundwork for gathering the research evidence to support: An RCT that will study if a specialized LPTB clinic is effective in reducing short-term medical and developmental complications and hospital readmissions, Development of a sustainable long-term follow-up programme supported by evidence, Development of a database to track long-term complications, with the goal of identifying potential risk factors earlier in late preterm infants, Creation and dissemination of Evidence-Based Guidelines, research results for frontline health care providers (GPs, Midwives, etc.), community hospitals and Local Health Integration Networks, Creation and dissemination of Parent Educational Resources for discharge of LPTB infants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Birth
Keywords
Late preterm infant, Complications, Hospital readmissions, Follow-up, Pilot study

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Current management of LPTB
Arm Type
No Intervention
Arm Description
The current pragmatic, but non-systematic, pattern of management of LPTB infants. Growth measurements, feeding histories/methods, illness history including emergent visits to clinicians, walk-in clinics and emergency departments and breast-feeding support clinics, and basic developmental milestones (as itemized in the Rourke Developmental screening tool) will be recorded by families and primary health care providers as itemized in the Memory Book at the assessments made at the discretion of the health care providers.
Arm Title
Specialized LPTB Clinic
Arm Type
Experimental
Arm Description
Additional 6 specialized LPTB follow-up clinic visits attended by pediatricians and neonatologists. Detailed findings from physical examination, feeding histories/methods, illness history including emergent visits to clinicians, walk-in clinics and emergency departments and breast-feeding support clinics, basic developmental milestones (as itemized in the Rourke Developmental screening tool) and physician recommendations will be recorded at each appointment. These will be compared to those obtained from families and primary health care providers as itemized in the Memory Book.
Intervention Type
Other
Intervention Name(s)
Specialized LPTB clinic
Intervention Description
50% of enrolled infants will be randomized to the specialized LPTB follow-up clinic.
Primary Outcome Measure Information:
Title
Recruitment Rate
Description
Recruitment Rate during first six months of pilot. Reported as the percentage of subjects recruited from those eligible to participate.
Time Frame
14 months
Secondary Outcome Measure Information:
Title
Infant Weight Gain
Description
Weight Gain reported in grams.
Time Frame
14 months
Other Pre-specified Outcome Measures:
Title
Hospital Readmission
Description
The rates of hospital readmission will be determined for the first six months of life.
Time Frame
14 months

10. Eligibility

Sex
All
Maximum Age & Unit of Time
1 Month
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: - singleton or twins born at 34 and 0 days to 36 weeks and 6 days gestational age. Infants admitted to the Level 2 Nursery or newborn nursery at McMaster Children's Hospital or St. Joseph's Healthcare Hamilton or Level 3 Nursery (NICU) at McMaster Children's Hospital will be included. Exclusion Criteria: triplets and infants with major cardiac anomalies, metabolic disorders, significant gastrointestinal anomalies, intrauterine growth restriction, potential genetic syndromes, neurologic anomalies or severe sepsis/meningitis and LPTB requiring mechanical ventilation (post-delivery room resuscitation with prolonged CPAP or intubation) will be excluded. mothers who have a history of substance use at any time during pregnancy or alcohol use after confirmation of pregnancy participants must be able to understand English and speak English as this pilot does not currently have the financial support to sponsor interpreters.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lucy Giglia, MD FRCP(C) MSc
Organizational Affiliation
McMaster Children's Hospital & St. Joseph's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Joseph's Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 4A6
Country
Canada
Facility Name
McMaster Children's Hospital & McMaster University
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8S 4K1
Country
Canada

12. IPD Sharing Statement

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The GROWNDUP Study of Late Preterm Births

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