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Caregiver training may stop bedsores in homebound patients

NCT ID NCT07313046

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 teaching caregivers how to prevent pressure ulcers (bedsores) can lower the risk for patients receiving home care. The training covered skin care, repositioning, and pressure relief methods. Researchers measured patients' risk levels before and after the training to see if it helped.

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

57 people

The number who actually took part.

Started

Jul 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

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: * Inclusion Criteria The study includes: * Patients registered with the Home Care Health Unit, * Volunteers willing to participate in the study, * Caregivers of patients classified as high or medium risk according to the Braden Risk Assessment Scale, * • Caring for a patient who is not cared for by different individuals, * Aged 18 years or older, * Able to speak Turkish, * Without speech or hearing problems, * Cognitive competence sufficient to understand and answer questions. Exclusion Criteria: * • Not registered with the Home Care Health Unit, * Whose patient is classified as low risk according to the Braden Risk Assessment Scale, * • Those with more than one caregiver, * Those who did not agree to participate in the study, * Those under the age of 18, * Those who did not speak Turkish, * Those with speech and hearing problems, * Caregivers who did not have the cognitive ability to understand and answer the questions were not included 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

  • Bartın University

    Bartın, Merkez, 74100, Turkey (Türkiye)

More trials for these conditions

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