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Completed

NCT Number: NCT06343545

The Tele-Rehab MV Cluster Stepped-Wedge Randomized Clinical Trial

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital de Emergência Dr. Daniel Houly, Arapiraca, Alagoas, Brazil

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged ≥18 years
  • Admission to the ICU with hypoxemic acute respiratory failure in whom SARS-CoV-2 infection is part of the differential diagnosis will be enrolled. This does not imply that COVID-19 is the primary suspected cause, but rather that it is considered at least a possible (though not necessarily probable) diagnosis at the time of ICU admission.
  • Need for invasive mechanical ventilation.

Exclusion criteria

  • Severe underlying disease with a life expectancy of less than 3 months;
  • Absence of a responsible family member for cases of patients with communication difficulties (aphasia, severe cognitive impairment, non-native speakers of Portuguese);
  • Absence of telephone contact;
  • Participants already included in the study;
  • Unavailability to carry out telephone follow-ups.

Treatment and study plan

Standard of Care

Behavioral

Standard of Care provided by enrolling hospitals

Disability Prevention and Rehabilitation

Behavioral

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.

Primary outcomes

  1. Quality of life

    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)

Secondary outcomes

  1. Mortality

    Time frame: From study enrollment (ICU admission) to 90 days after hospital discharge

    All cause mortality

  2. Days alive and free of hospital

    Time frame: From study enrollment (ICU admission) to 90 days after hospital discharge

    Days alive and free of hospital (not hospitalized)

  3. Rehospitalization

    Time frame: 30 days after hospital discharge

    New hospitalization

  4. Return to work

    Time frame: 90 days after hospital discharge

    Return to work or usual activities (work, study)

  5. Anxiety and Depression

    Time frame: 90 days after hospital discharge

    Anxiety and depression measured according to Hospital Anxiety and Depression Scale

  6. New disability in instrumental activities of daily living

    Time frame: 90 days after hospital discharge

    Incidence of new disabilities for instrumental activities of daily living assessed by the Lawton & Brody scale

  7. Physical dependence

    Time frame: 90 days after hospital discharge

    Prevalence of moderate, severe, or total physical disability assessed by the modified Barthel Index

  8. Clinical Status

    Time frame: 90 days after hospital discharge

    Ordinal scale from using World Health Organization

  9. Cognitive impairment

    Time frame: 90 days after hospital discharge

    Prevalence of cognitive impairment assessed by the Telephone Interview for Cognitive Status

Sponsors and collaborators

Lead sponsor

Hospital Israelita Albert Einstein

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Apr 2, 2024
Registry last updated
Feb 23, 2026

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.

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