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Tele-Rehab after ventilator: a new way to boost recovery?

NCT ID NCT06343545

Knowledge-focused Sponsor: Hospital Israelita Albert Einstein Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This completed study tested whether a telemedicine-based program could improve quality of life for adults who needed a breathing machine (ventilator) due to acute respiratory failure. The program included rehabilitation strategies during the ICU stay, hospital ward, and for two months after leaving the hospital. Researchers measured quality of life 90 days after discharge in 1,916 participants.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
telemedicine-based rehabilitation program
What this could lead to
If successful, this could show that a structured telemedicine program improves quality of life and recovery for patients after a serious respiratory illness requiring a ventilator.
What could go wrong
This is a completed trial, but results are not yet published. The intervention is complex and may not be easy to implement widely, and benefits may vary by patient.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

1,916 people

The number who actually took part.

Started

Jun 2024

Finished

Sep 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Aged ≥18 years 2. 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. 3. Need for invasive mechanical ventilation. Exclusion Criteria: 1. Severe underlying disease with a life expectancy of less than 3 months; 2. Absence of a responsible family member for cases of patients with communication difficulties (aphasia, severe cognitive impairment, non-native speakers of Portuguese); 3. Absence of telephone contact; 4. Participants already included in the study; 5. Unavailability to carry out telephone follow-ups.

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Conditions

The condition(s) this trial relates to.

acute respiratory failure COVID-19

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Acute respiratory failure

Contacts and locations

Locations

  • Centro De Pesquisa Em Medicina Tropical - CEPEM

    Porto Velho, Rondônia, Brazil

  • Fundação de Medicina Tropical Dr. Heitor Vieira Dourado

    Manaus, Amazonas, Brazil

  • Hospital Estadual Dirceu Arcoverde

    Parnaíba, Piauí, Brazil

  • Hospital Estadual de Doenças Tropicais Dr. Anuar Auad

    Goiânia, Goiás, Brazil

  • Hospital Geral de Roraima - HGR

    Boa Vista, Roraima, Brazil

  • Hospital Geral de Vitória da Conquista

    Vitória da Conquista, Estado de Bahia, Brazil

  • Hospital Geral e Maternidade Tereza Ramos

    Lages, Santa Catarina, Brazil

  • Hospital Municipal Aparecida de Goiania - HMAP

    Aparecida de Goiânia, Goiás, Brazil

  • Hospital Municipal Pedro I

    Campina Grande, Paraíba, Brazil

  • Hospital Municipal Ronaldo Gazolla

    Rio de Janeiro, Brazil

  • Hospital Municipal de Salvador

    Salvador, Estado de Bahia, Brazil

  • Hospital Regional Norte - HRN

    Sobral, Ceará, Brazil

  • Hospital Regional de Augustinópolis

    Augustinópolis, Tocantins, Brazil

  • Hospital Regional de Samambaia

    Brasília, Federal District, Brazil

  • Hospital São Sebastião Martir

    Venâncio Aires, Rio Grande do Sul, Brazil

  • Hospital Universitário - Universidade Estadual de Londrina

    Londrina, Paraná, Brazil

  • Hospital de Emergência Dr. Daniel Houly

    Arapiraca, Alagoas, Brazil

  • Hospital de Messejana Dr. Carlos Alberto Studart Gomes (HM)

    Fortaleza, Ceará, Brazil

  • Instituto de Medicina Integral "Prof. Fernando Figueira" - IMIP

    Recife, Pernambuco, Brazil

  • Santa Casa de Misericórdia de Belo Horizonte

    Belo Horizonte, Minas Gerais, Brazil

More trials for these conditions

Other studies related to the condition(s) this trial covers.