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ICU staff training aims to cut Post-ICU syndrome in half

NCT ID NCT07542613

Knowledge-focused Sponsor: Carola Giménez-Esparza Vich Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether a structured training program for ICU staff can reduce post-intensive care syndrome (PICS)—physical, thinking, or emotional problems that can last months after a serious illness. About 900 adults who stay in the ICU for at least 48 hours will be followed for a year. Researchers will compare usual care before and after the training to see if it helps patients recover better.

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

About 900 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2026

Expected to finish

Jan 2028

An estimate. End dates often move.

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. Adults aged 18 years or older 2. Patients who stay in the intensive care unit (ICU) for at least 48 hours 3. Written informed consent provided by the patient, or by a legal representative or family member if the patient is unable to decide Exclusion Criteria: 1. Patients with a decision to limit life-sustaining treatments (for example, not starting or stopping treatments such as mechanical ventilation, vasoactive drugs, dialysis, or resuscitation) 2. Patients expected to be discharged from the ICU within the next 24 hours 3. Patients who are unable to attend follow-up visits after hospital discharge (for example, due to relocation, language barriers, transfer to or from another hospital, or inability to attend clinic visits) 4. Patients with a life expectancy of less than 3 months 5. Patients with severe cognitive impairment or severe mental illness before ICU admission that would make assessments difficult 6. Patients with severe brain injury or severe neurological diseases that prevent proper evaluation of physical or cognitive function

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Conditions

The condition(s) this trial relates to.

Critical Illness postintensive care syndrome

As listed by the trial registrant

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

Critical illness Post-intensive care syndrome (PICS)

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Vega Baja University Hospital

    RECRUITING

    Orihuela, Alicante, 03314, Spain

  • Vega Baja University Hospital

    NOT_YET_RECRUITING

    Murcia, Murcia, 30005, Spain

More trials for these conditions

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