Standard of Care
BehavioralStandard of Care provided by enrolling hospitals
NCT Number: NCT06343545
To evaluate, through a randomized clinical trial in groups/clusters (stepped wedge), the impact of specific bundles for disability prevention and early rehabilitation, focused on 3 domains (ICU, ward and post-discharge), on health-related quality of life and other long- and short-term outcomes, 90 days after hospital discharge, in critically ill patients affected by hypoxemic acute respiratory failure.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Hospital de Emergência Dr. Daniel Houly, Arapiraca, Alagoas, Brazil
Acute respiratory failure requiring invasive mechanical ventilation is associated with significant mortality rates. Furthermore, survivors often develop new physical, mental, and cognitive disabilities, as well as worsening clinical conditions, which can significantly impair their health-related quality of life. COVID-19 remains a notable cause of acute respiratory failure and long-term disabilities,6 with the added potential to cause persistent symptoms regardless of the infection's initial severity. Although the incidence of SARS-CoV-2-related respiratory failure has declined with the widespread adoption of vaccination, it persists as an endemic cause of pneumonia, particularly among patients with significant comorbidities, and is often part of the differential diagnosis in severe cases of acute hypoxemic respiratory failure. While bundles of interventions including analgesia optimization, sedation minimization, early mobilization, and delirium prevention, as well as screening for individuals at risk of new disabilities for early rehabilitation have been recommended to prevent disabilities in critical care patients, no large randomized clinical trial has yet demonstrated a significant impact on long-term health-related quality of life. Additionally, the burden of disability following critical illness is often associated with patients' inability to attend clinic-based follow-up, and telemedicine may serve as a tool to reduce healthcare inequalities. Accordingly, the primary objective of this cluster stepped-wedge randomized clinical trial is to assess the impact of a multicomponent telemedicine-based intervention on the health-related quality of life of patients with acute hypoxemic respiratory failure requiring invasive mechanical ventilation, evaluated 90 days after hospital discharge.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Standard of Care provided by enrolling hospitals
The study intervention is an evidence-based, multicomponent program focused on disability prevention and rehabilitation strategies, implemented during the patient's ICU stay, continued through ward admission, and extending up to two months post-hospital discharge.
Time frame: 90 days after hospital discharge
Health-related quality of life assessed by the Brazilian version of the 5-dimension, 3-level EuroQol scale (EQ-5D-3L)
Time frame: From study enrollment (ICU admission) to 90 days after hospital discharge
All cause mortality
Time frame: From study enrollment (ICU admission) to 90 days after hospital discharge
Days alive and free of hospital (not hospitalized)
Time frame: 30 days after hospital discharge
New hospitalization
Time frame: 90 days after hospital discharge
Return to work or usual activities (work, study)
Time frame: 90 days after hospital discharge
Anxiety and depression measured according to Hospital Anxiety and Depression Scale
Time frame: 90 days after hospital discharge
Incidence of new disabilities for instrumental activities of daily living assessed by the Lawton & Brody scale
Time frame: 90 days after hospital discharge
Prevalence of moderate, severe, or total physical disability assessed by the modified Barthel Index
Time frame: 90 days after hospital discharge
Ordinal scale from using World Health Organization
Time frame: 90 days after hospital discharge
Prevalence of cognitive impairment assessed by the Telephone Interview for Cognitive Status
Hospital Israelita Albert Einstein
Other
Evaluation of an Integrated Multicomponent Telemedicine-Based Intervention on Health-Related Quality of Life in Adults With Acute Respiratory Failure Requiring Mechanical Ventilation (Tele-Rehab MV Trial)
Acronym: Tele-Rehab MV
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05143372
Acute Respiratory Failure, COVID-19
Astana, Kazakhstan
View Trial DetailsNCT05334654
Acute Respiratory Failure, Anticoagulants
Catanzaro, Italy
View Trial DetailsNCT04601090
Acute Respiratory Distress Syndrome, Acute Respiratory Failure
Oslo, Norway
View Trial DetailsNCT04791241
Acute Respiratory Failure, COVID-19
Annecy, France
View Trial Details