REVIVe: Frailty, Rehabilitation, and Outcomes in Critically Ill Adult and Pediatric Survivors of COVID-19 or Acute Respiratory Infection

Status: Recruiting
Location: See all (28) locations...
Study Type: Observational
SUMMARY

Background: Many adults and some children with COVID-19 or acute respiratory infection become critically ill and need advanced life support in the Intensive Care Unit (ICU). Frailty is a medical condition of reduced function and health. Adults with frailty have a lower chance of surviving critical illness. The investigators are still learning about critically ill adults with COVID-19 or acute respiratory infection, and do not have much information on how frailty affects outcomes in critically ill children, with or without COVID-19 or acute respiratory infection. Rehabilitation can help survivors of COVID-19 or acute respiratory infection by improving strength and improve quality of life (QOL).

Objectives: The main goal of this research study is to see if patients with frailty have a lower chance of surviving COVID-19 or acute respiratory infection critical illness and more health problems after survival than patients without frailty. The investigators will also study the types of rehabilitation received by patients with COVID-19 or acute respiratory infection.

Methods: The investigators will include adults and children with COVID-19 or acute respiratory infection who are admitted to the ICUs that participate in the study. The investigators will gather data about each patient, including before and during their illness. Outcomes: The investigators will collect level of frailty, function, and types of therapy, or rehabilitation received by patients. In adults, the investigators are most interested in learning if frailty influences mortality, or death. In children, the investigators are most interested in whether children with COVID-19 or acute respiratory infection critical illness are more likely to develop frailty. The investigators will also study post-hospital discharge location in survivors (e.g., home, rehabilitation). Relevance: The COVID-19 pandemic is a global public health crisis. It is critical to understand how COVID-19 and other acute respiratory infection critical illness affects groups of people who are at higher risk, and the impact on outcomes that are important to patients, like functioning and QOL. The results will help policy makers plan post-hospital services for survivors, help healthcare workers understand the importance of rehabilitation practice for patients with COVID-19 or acute respiratory infection, and help researchers develop treatments to improve QOL after COVID-19 or acute respiratory infection.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Adult and pediatric survivors of COVID-19 or acute respiratory infection admitted to participating intensive care units (ICUs) and PICUs. The investigators define children as less than, and adults as greater than or equal to, 18 years old, respectively. The investigators will include adults and pediatrics with a confirmed diagnosis of COVID-19, pediatric patients with MIS-C, and adults and pediatrics with suspected or proven acute respiratory infection with onset within 14 days of ICU/PICU admission and requiring invasive mechanical ventilation, non-invasive ventilation, or high flow oxygen therapy.

Locations
Other Locations
Canada
Brantford General Hospital
RECRUITING
Brantford
Alberta Children's Hospital
ACTIVE_NOT_RECRUITING
Calgary
University of Alberta
RECRUITING
Edmonton
Izaak Walton Killam Hospital for Children
RECRUITING
Halifax
QEII Health Sciences Centre
RECRUITING
Halifax
Hamilton General Hospital
RECRUITING
Hamilton
Juravinski Hospital
RECRUITING
Hamilton
McMaster Children's Hospital
ACTIVE_NOT_RECRUITING
Hamilton
St. Joseph's Healthcare Intensive Care Unit
RECRUITING
Hamilton
Kingston Health Sciences Centre
RECRUITING
Kingston
Hôpital Hôtel-Dieu de Lévis
RECRUITING
Lévis
London Health Sciences Centre
ACTIVE_NOT_RECRUITING
London
Centre hospitalier de l'Université de Montréal
RECRUITING
Montreal
Hôpital du Sacré-Cœur de Montréal
RECRUITING
Montreal
Montreal Children's Hospital
ACTIVE_NOT_RECRUITING
Montreal
The Centre hospitalier universitaire Sainte-Justine
NOT_YET_RECRUITING
Montreal
Royal Columbian Hospital
NOT_YET_RECRUITING
New Westminster
Children's Hospital of Eastern Ontario
ACTIVE_NOT_RECRUITING
Ottawa
The Ottawa Hospital
RECRUITING
Ottawa
Institut Universitaire de Cardiologie et de Pneumologie de Québec
RECRUITING
Québec
Saskatchewan Health Authority
RECRUITING
Regina
Hôpital Fleurimont - Sherbrooke
RECRUITING
Sherbrooke
Sturgeon Community Hopsital
NOT_YET_RECRUITING
St. Albert
Niagara Health System
RECRUITING
St. Catharines
St. Michael's Hospital
RECRUITING
Toronto
Sunnybrook Hospital
RECRUITING
Toronto
The Hospital for Sick Children
ACTIVE_NOT_RECRUITING
Toronto
Children's Hospital of Winnipeg
ACTIVE_NOT_RECRUITING
Winnipeg
Contact Information
Primary
Geoff Strong, PT, MS
revive@mcmaster.ca
905-522-1155
Time Frame
Start Date: 2022-08-24
Estimated Completion Date: 2025-10-01
Participants
Target number of participants: 900
Treatments
Adults
Adult survivors of COVID-19 or acute respiratory infection admitted to participating ICUs. Adults are defined as greater than or equal to, 18 years old. We will include adults with a confirmed diagnosis of COVID-19 or those with suspected or proven acute respiratory infection with onset within 14 days of ICU admission and requiring invasive mechanical ventilation, non-invasive ventilation, or high-flow oxygen therapy.
Pediatrics
Pediatric survivors of COVID-19, MIS-C, or acute respiratory infection admitted to participating pediatric intensive care units (PICUs). The investigators define children as less than 18 years old. We will include pediatric patients with COVID-19, those with multi-system inflammatory syndrome in children (MIS-C), and those with suspected or proven acute respiratory infection with onset within 14 days of ICU admission and requiring invasive mechanical ventilation, non-invasive ventilation, or high-flow oxygen therapy.
Related Therapeutic Areas
Sponsors
Collaborators: Canadian Institutes of Health Research (CIHR), Canadian Critical Care Trials Group
Leads: McMaster University

This content was sourced from clinicaltrials.gov