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Telemedicine in ICUs: 22,000-Patient trial tests if virtual rounds cut hospital stays

NCT ID NCT05960994

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 package of telemedicine services — including daily rounds by a specialist, a team of nurses and therapists, and a focus on safety — could reduce how long patients stay in the intensive care unit (ICU). Researchers enrolled 22,000 patients from public and philanthropic hospitals across Brazil. The goal was to see if these virtual tools improve care and shorten ICU stays.

What this could mean

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

Active substance
telemedicine intervention package (daily specialist rounds, multidisciplinary team care, and quality/safety management)
What this could lead to
If successful, this could show that telemedicine tools can improve ICU efficiency and patient outcomes in resource-limited settings.
What could go wrong
This is a completed trial, but results are not yet published. The interventions are complex and may not be easily replicated in other hospitals.

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

22,000 people

The number who actually took part.

Started

Jan 2024

Finished

May 2026

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 for Intensive care units: * Intensive care units from public or philanthropic hospitals. * ICUs with a minimum of 7 and a maximum of 20 beds. * Intensive care units with physician and nurses available 24 hours a day and physiotherapist available at least ≥ 18 hours a day. Exclusion Criteria for Intensive care units: * Intensive care units with structured multidisciplinary round more than three times a week conducted by an intensive care physician (certified), documented in the medical record, with a fixed duration (\>5 min / patient), using some supporting tool (checklist or standard form), goal oriented, based on established protocols, including all the patients admitted to the ICU. * Intensive care units already doing audit and feedback with specific planning. * Dedicated coronary care units/cardiac intensive care units or other specialized units (cardiac surgery, neurological, burned patients). * Step-down units or semi-intensive cardiac care unit. * Intensive care units without availability of substitute renal therapy. * ICU coordinator specialist in intensive care medicine and management training (MBA in Health Management or equivalent). Inclusion Criteria for patients: * Adult patients (≥ 18 years old). Exclusion Criteria for patients: * Admission for other reasons than medical (e.g., judicial cause, legal reasons, safety reasons). * Previously included in the TELESCOPE II trial (for the primary outcome analysis).

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Einstein Hospital Israelita

    São Paulo, São Paulo, 05651-901, Brazil

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