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ICU discharge screening may forecast mental and physical struggles

NCT ID NCT05690438

Knowledge-focused Sponsor: Region Stockholm 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether a quick screening when patients leave the intensive care unit (ICU) can predict if they will have psychological issues (like depression or anxiety) or new physical disabilities three months later. Researchers followed 773 adults who stayed in the ICU for at least 12 hours. They also examined how pain, resilience, and frailty affect recovery. The goal is to identify at-risk patients early so they can get the right support.

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.

Participants

773 people

The number who actually took part.

Started

Jan 2023

Finished

Apr 2025

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

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

Who is studied

General adult ICU population, all admitted patients will be consecutively screened for inclusion.

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: * Adult patients, ≥18 years old, with an ICU stay ≥12 hours, surviving to ICU discharge. Exclusion Criteria: * No home address * Dementia or other major cognitive dysfunction * Unsufficient knowledge of the Swedish language for answering follow-up questionnaires * Two or more limitations of treatment or moribund patient

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Conditions

The condition(s) this trial relates to.

anxiety disorder Depression Frailty Pain postintensive care syndrome

As listed by the trial registrant

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

Critical care

Contacts and locations

Locations

  • Capio S:t Göran's Hospital

    Stockholm, Sweden

  • Danderyd's Hospital

    Stockholm, Sweden

  • Karolinska University Hospital

    Stockholm, 113 45, Sweden

  • Södersjukhuset

    Stockholm, Sweden

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