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Pediatric Guideline Adherence and Outcomes- Argentina

Primary Purpose

TBI (Traumatic Brain Injury)

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
PEGASUS Program for Care
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for TBI (Traumatic Brain Injury) focused on measuring guideline adherence, implementation fidelity

Eligibility Criteria

undefined - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Mechanism or head CT consistent with TBI
  • <18 years old
  • GCS (Glasgow Coma Scale) score ≤8 at any point during hospital admission

Exclusion Criteria:

- none

Sites / Locations

  • Hospital el CruceRecruiting
  • Hospital Sor LudovicaRecruiting
  • Hospital Interzonal Especializado Materno InfantilRecruiting
  • Hospital Municipal del Nino de San JustoRecruiting
  • Hospital de Ninos Eva PeronRecruiting
  • Hospital Materno Infantil Dr. Hector QuintanaRecruiting
  • Hospital Regional ReconquistaRecruiting
  • Hopital Victor J. VilelaRecruiting
  • Hospital del Nino JesusRecruiting
  • Hospital de La Santisima TrinidadRecruiting
  • Hospital Humberto NottiRecruiting
  • Hospital Publico Materno InfantilRecruiting
  • Hospital AlassiaRecruiting
  • Centro Provincial de Salud Infantil Eva PeronRecruiting
  • Hospital Carlos Van BurenRecruiting
  • Hospital de Trauma Manuel GiagniRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

No Intervention

Arm Label

Baseline

PEGASUS Program (Intervention)

Usual Care (Control)

Arm Description

All sites will collect usual care data from 9 months to 21 months.

This arm (half of the sites) will receive the PEGASUS program (intervention) from 21 months to 57 months.

This arm (half of the sites) will maintain usual care. They will receive the opportunity for the PEGASUS program training (intervention) at the end of study data collection (57 months) period.

Outcomes

Primary Outcome Measures

TBI guideline adherence
The main outcome will be measured as the sum of indicators to which care was adhered by the number of relevant adherence indicators for a given patient during ICU stay.

Secondary Outcome Measures

Clinical Pathway Adoption
This outcome will be measured as yes/no for each eligible patient at intervention centers.
Discharge Survival
We will examine the number of survivors between intervention and control centers (descriptive and not powered for this outcome).
GOSE-Peds. Pediatric Version of the Glasgow Outcome Scale-Extended
We will examine participants' Pediatrics Glasgow Outcome Scale-Extended (GOSE-Peds). GOS-E PEDS Score: 8-Death 7- Vegetative State (VS) 6- Lower Severe Disability (Lower SD) 5- Upper Severe Disability (Upper SD) 4- Lowe Moderate Disability (Lower MD) 3- Upper Moderate Disability (Upper MD) 2- Lower Good Recovery (Lower GR) 1-Upper Good Recovery (Upper GR) -Higher scores represent an increasing level of disability.
Mortality
We will examine participants' mortality at 3 months post discharge
DIBQ (Determinants of Implementation Behaviors Scale)
This questionnaire measures the constructs found in the TDF (Theoretical Domain Framework). We will use the short version with 41 items.
Value added processes assessed by Organizational Questionnaire for Participant Hospitals
We will ask participant sites to answer a Hospital, Unit and Medical Staff Information, Quality of Care, Medication and Culture of Safety questionnaire developed by Monica S. Vavilala, Bryan Weiner and Silvia Lujan for this study.
Changes in patient outcomes from time in - to time out- of the system based on manipulations of KPIs
We will examine the behavior of TBI care processes. We will evaluate the effect of interventions on key guideline indicators, adherence to Guidelines, and GOSE-Peds (described in out come 4). Inputs from parameter estimates from the regression models (Aim 1) and inputs from VSMs (Aim 2) will be used to develop computer simulation models using commercially available discrete event modeling and simulation software (e.g., SIMIO®, Simio LLC, Sewickley, PA). Parameter estimates from the regression models will then be used to model the distribution of the 15 indicators from the Pediatric Guidelines that are already integrated in the process flow. This provides a way to observe changes in patient outcomes from time-in to time-out of the system based on manipulations of KPIs. Each KPI will be initially "weighted" based on the parameter estimates obtained from the regression models.

Full Information

First Posted
January 7, 2019
Last Updated
December 8, 2021
Sponsor
University of Washington
Collaborators
Children's National Research Institute, Centro de Informática e Investigación Clínica (CIIC), Washington State University, National Institute of Neurological Disorders and Stroke (NINDS)
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1. Study Identification

Unique Protocol Identification Number
NCT03896789
Brief Title
Pediatric Guideline Adherence and Outcomes- Argentina
Official Title
Implementation Fidelity and Benefits of the Critical Care Pediatric Guideline Adherence and Outcomes Program in Traumatic Brain Injury
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
September 30, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Children's National Research Institute, Centro de Informática e Investigación Clínica (CIIC), Washington State University, National Institute of Neurological Disorders and Stroke (NINDS)

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
Pediatric traumatic brain injury (TBI) is the leading killer of children worldwide but effective treatments for TBI are limited. Although evidenced-based pediatric TBI guidelines exist, adherence to these guidelines is low,leading us to develop a new Pediatric Guideline Adherence and Outcomes (PEGASUS) program to increase TBI guideline adherence. We propose to test the PEGASUS program's ability to improve TBI guideline adherence and outcomes.
Detailed Description
Specific Aim 1: Determine the relationship between PEGASUS program implementation and TBI guideline adherence (Aim 1a), and assess system, provider, patient, implementation and guideline factors associated with TBI guideline adherence (Aim 1b). Hypothesis: Centers that receive the PEGASUS program have higher TBI guideline adherence (main outcome), as well as better discharge survival and 3-month Glasgow Outcome Scale-Extended (GOSE) score (secondary outcomes) than centers who receive usual care. Specific Aim 2: Create a value stream map (VSM) to identify value-added processes of care associated with TBI guideline adherence. Hypothesis: ICU activity flows of TBI care during the first 72 hours will reveal value-added as well as non-value-added processes in severe TBI care. PEGASUS program implementation will result in more value-added TBI care processes and better TBI guideline adherence. Specific Aim 3: Use computer simulation to develop and disseminate a real-world best practices blueprint for TBI guideline adherence. Hypothesis: This model will identify the impact of the PEGASUS program on key performance indicators (KPIs), outcomes (Aim 1), and process activities (Aim 2). Iterative computer simulations will then demonstrate the relationship among PEGASUS program components and how relative changes in these components impact the magnitude, direction and choice of operations downstream in TBI care and patient outcomes to inform development of a blueprint for wide dissemination of best-practice guidelines.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
TBI (Traumatic Brain Injury)
Keywords
guideline adherence, implementation fidelity

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Parallel cluster RCT following a baseline data collection period when all sites are in the 'control/usual care state'.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
540 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Baseline
Arm Type
No Intervention
Arm Description
All sites will collect usual care data from 9 months to 21 months.
Arm Title
PEGASUS Program (Intervention)
Arm Type
Experimental
Arm Description
This arm (half of the sites) will receive the PEGASUS program (intervention) from 21 months to 57 months.
Arm Title
Usual Care (Control)
Arm Type
No Intervention
Arm Description
This arm (half of the sites) will maintain usual care. They will receive the opportunity for the PEGASUS program training (intervention) at the end of study data collection (57 months) period.
Intervention Type
Other
Intervention Name(s)
PEGASUS Program for Care
Intervention Description
This is in essence a checklist of pediatric guidelines to follow for participants who meet inclusion criteria. Site staff will receive training in how to implement this pathway into their usual care.
Primary Outcome Measure Information:
Title
TBI guideline adherence
Description
The main outcome will be measured as the sum of indicators to which care was adhered by the number of relevant adherence indicators for a given patient during ICU stay.
Time Frame
ICU Stay, approximately up to 2 weeks
Secondary Outcome Measure Information:
Title
Clinical Pathway Adoption
Description
This outcome will be measured as yes/no for each eligible patient at intervention centers.
Time Frame
within 24 hours of patient admission
Title
Discharge Survival
Description
We will examine the number of survivors between intervention and control centers (descriptive and not powered for this outcome).
Time Frame
At Hospital Discharge, approximately up to 5 weeks
Title
GOSE-Peds. Pediatric Version of the Glasgow Outcome Scale-Extended
Description
We will examine participants' Pediatrics Glasgow Outcome Scale-Extended (GOSE-Peds). GOS-E PEDS Score: 8-Death 7- Vegetative State (VS) 6- Lower Severe Disability (Lower SD) 5- Upper Severe Disability (Upper SD) 4- Lowe Moderate Disability (Lower MD) 3- Upper Moderate Disability (Upper MD) 2- Lower Good Recovery (Lower GR) 1-Upper Good Recovery (Upper GR) -Higher scores represent an increasing level of disability.
Time Frame
3 months post discharge
Title
Mortality
Description
We will examine participants' mortality at 3 months post discharge
Time Frame
3 months post discharge
Title
DIBQ (Determinants of Implementation Behaviors Scale)
Description
This questionnaire measures the constructs found in the TDF (Theoretical Domain Framework). We will use the short version with 41 items.
Time Frame
Baseline, and quarterly during year 1 after randomization; then once annually through study completion, approximately 3 years, for intervention sites.
Title
Value added processes assessed by Organizational Questionnaire for Participant Hospitals
Description
We will ask participant sites to answer a Hospital, Unit and Medical Staff Information, Quality of Care, Medication and Culture of Safety questionnaire developed by Monica S. Vavilala, Bryan Weiner and Silvia Lujan for this study.
Time Frame
Baseline and annually through study completion, approximately 3 years
Title
Changes in patient outcomes from time in - to time out- of the system based on manipulations of KPIs
Description
We will examine the behavior of TBI care processes. We will evaluate the effect of interventions on key guideline indicators, adherence to Guidelines, and GOSE-Peds (described in out come 4). Inputs from parameter estimates from the regression models (Aim 1) and inputs from VSMs (Aim 2) will be used to develop computer simulation models using commercially available discrete event modeling and simulation software (e.g., SIMIO®, Simio LLC, Sewickley, PA). Parameter estimates from the regression models will then be used to model the distribution of the 15 indicators from the Pediatric Guidelines that are already integrated in the process flow. This provides a way to observe changes in patient outcomes from time-in to time-out of the system based on manipulations of KPIs. Each KPI will be initially "weighted" based on the parameter estimates obtained from the regression models.
Time Frame
during ICU care, approximately up to 2 weeks

10. Eligibility

Sex
All
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Mechanism or head CT consistent with TBI <18 years old GCS (Glasgow Coma Scale) score ≤8 at any point during hospital admission Exclusion Criteria: - none
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Julia Velonjara, MPH
Phone
2067449430
Email
julialv@uw.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Monica Vavilala, MD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital el Cruce
City
Florencio Varela
State/Province
Buenos Aires
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karina Cinquegrani
Facility Name
Hospital Sor Ludovica
City
La Plata
State/Province
Buenos Aires
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pablo Castellani
Facility Name
Hospital Interzonal Especializado Materno Infantil
City
Mar Del Plata
State/Province
Buenos Aires
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Paula Medici
Facility Name
Hospital Municipal del Nino de San Justo
City
San Justo
State/Province
Buenos Aires
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matias Penazzi
Facility Name
Hospital de Ninos Eva Peron
City
San Fernando Del Valle De Catamarca
State/Province
Catamarca
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Graciela Romero
Facility Name
Hospital Materno Infantil Dr. Hector Quintana
City
San Salvador De Jujuy
State/Province
Jujuy
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Silvina Avalos
Facility Name
Hospital Regional Reconquista
City
Reconquista
State/Province
Santa Fe
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alejandro Mansur
Facility Name
Hopital Victor J. Vilela
City
Rosario
State/Province
Santa Fe
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ariel Segado
Facility Name
Hospital del Nino Jesus
City
San Miguel De Tucumán
State/Province
Tucuman
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gladys Correa
Facility Name
Hospital de La Santisima Trinidad
City
Cordoba
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carlos Davila
Facility Name
Hospital Humberto Notti
City
Mendoza
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marta Mosciaro
Facility Name
Hospital Publico Materno Infantil
City
Salta
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sandra Elizabeth Chuchuy
Facility Name
Hospital Alassia
City
Santa Fe
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mariela Alassia
Facility Name
Centro Provincial de Salud Infantil Eva Peron
City
Santiago Del Estero
Country
Argentina
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabriela Lopez Cruz
Facility Name
Hospital Carlos Van Buren
City
Valparaíso
Country
Chile
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adriana Diettes
Facility Name
Hospital de Trauma Manuel Giagni
City
Asuncion
Country
Paraguay
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Natalia Gomez Arriola

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified data will be shared with Co-Investigators
IPD Sharing Time Frame
Monthly as available

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Pediatric Guideline Adherence and Outcomes- Argentina

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