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Simple QR code video may ease ICU family anxiety

NCT ID NCT07660705

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 22, 2026 · Updated 2 times

Summary

This study tests whether giving family members of ICU patients a QR code that links to an educational video can improve their understanding of the ICU and reduce their anxiety. Participants are randomly assigned to receive either standard verbal information or the same information plus access to the video. Researchers measure knowledge, anxiety, and satisfaction at the start, within 24 hours, and again 72 hours later.

What this could mean

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

Active substance
QR Code-Based Digital Educational Video
What this could lead to
If it works, this could offer a simple, low-cost way to help families cope with the stress of having a loved one in the ICU.
What could go wrong
This is a small, single-center study, so results may not apply broadly. The video may not reduce anxiety more than standard verbal information.

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

150 people

The number who actually took part.

Started

Jun 2026

Finished

Jul 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

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: * Age 18 years or older * First-degree family member of a patient admitted to the intensive care unit * Able to read and understand Turkish * Able to use a smartphone * Able to access QR code-based educational materials * Willing to participate and provide written informed consent Exclusion Criteria: * History of a diagnosed psychiatric disorder * Current use of anxiolytic or antidepressant medication * Visual or hearing impairment preventing participation in video-based education * First-degree family member who is an active healthcare professional involved in patient care * Inability to complete study questionnaires or follow-up assessments * Refusal to participate in the study

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Elazığ Fethi Sekin City Hospital

    Elâzığ, Merkez, 23100, Turkey (Türkiye)

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