Simple QR code video may ease ICU family anxiety
NCT ID NCT07660705
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
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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
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150 people
The number who actually took part.
- Started
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Jun 2026
- Finished
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Jul 2026
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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
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Elazığ Fethi Sekin City Hospital
Elâzığ, Merkez, 23100, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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