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Can a Nurse's guidance ease the trauma of ICU for families?

NCT ID NCT07603219

Symptom relief Sponsor: Medical University of Gdansk 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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This pilot study will test a nurse-led educational program for caregivers of ICU patients. The program includes an informational brochure and one-on-one teaching to help families understand what to expect. Researchers will enroll 20 adult caregivers to see if the program is feasible and acceptable, and whether it might reduce anxiety and depression.

What this could mean

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

Active substance
Nurse-led educational intervention (informational brochure and in-person teaching)
What this could lead to
If it works, this could lead to a simple, low-cost way to reduce stress and improve satisfaction for families of ICU patients.
What could go wrong
This is a very small pilot study (20 people) testing only feasibility, not effectiveness. The intervention may not reduce distress or may not be practical in busy ICUs.

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 20 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Sep 2027

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

Accepted

You do not need to have the condition being studied to take part.

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: Patients: * Age \>18 years * ICU stay \> 24h Caregivers: * Age \>18 years * consent to participate in the study * meeting the definition of a caregiver * able to complete questionnaires Exclusion Criteria: Patients: * Age \< 18 years * Discharged/Deceased form ICU \< 24h Caregivers: * Age \< 18 years * without cognitive impairment * no consent to participate in the study * No able to complete questionnaires

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As listed by the trial registrant

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

Caregiver Icu patients

How to take part

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  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  2. 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.

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