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ICU study reveals: lying still too long raises bedsores risk

NCT ID NCT07355439

Knowledge-focused Sponsor: SEMA ŞAHİNER Source: ClinicalTrials.gov ↗

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 82 intensive care patients to see how the time they spend in one position affects their risk of developing pressure injuries (bedsores). Researchers checked skin changes like redness, bruising, and moisture, and used a standard risk scale. The goal was to find better ways to prevent these painful injuries in critically ill patients.

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

82 people

The number who actually took part.

Started

Jun 2024

Finished

Jun 2025

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

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: * \- If the patient is conscious, they must volunteer to participate in the study. * For unconscious patients, a first-degree relative (mother, father, spouse, child) must agree to participate in the study. * The patient's dependency level score on the Barthel Activities of Daily Living Index must be 90 or below (moderately dependent, severely dependent, completely dependent). * The patient must not have developed a pressure injury. * The patient must be meeting their daily calorie needs as determined by the nutrition team. * There must be no contraindications to turning the patient to any side. * Patients who are at low risk according to the pressure injury scale (15 points or above according to the Braden Risk Assessment Scale). * The patient must not have an acute neurological problem. * Patients with a GCS score above 7. Exclusion Criteria: * \- If the patient is conscious, they do not consent to participate in the study. * For unconscious patients, their first-degree relative does not consent to participate in the study. * Patients with a Barthel Activities of Daily Living Index score above 90 (mildly dependent, fully independent). * The patient has an existing pressure injury. * The patient is not meeting their daily calorie needs as determined by the nutrition team. * There is a contraindication to turning the patient to any side. * Patients with moderate to high risk according to the pressure injury scale (score below 15 according to the Braden Risk Assessment Scale). * The patient has an acute neurological problem. * Patients with a GCS score of 7 or below.

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Conditions

The condition(s) this trial relates to.

decubitus ulcer prevention target

As listed by the trial registrant

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

Pressure injury Risk assessment

Contacts and locations

Locations

  • Bartin University

    Bartın, 74100, Turkey (Türkiye)

More trials for these conditions

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