KCT0005829
Recruiting
未知
Research on monitoring technique of pressure ulcer patients to develop wearable sensors for prevention of decubitus ulcer
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Yonsei University
- Enrollment
- 20
- Status
- Recruiting
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Patients with pressure ulcers in areas that are clinically vulnerable to pressure (tail bone, hip, scapula, heel, occipital region, etc.) and who are below grade II in EPUAP ulcer grading
- •2\) Those who are at risk of limited behavior due to one of the following predictors that may develop and worsen bedsores
- •\-70 years of age or older
- •\-Current smoking history
- •\-Low body mass index and malnutrition
- •\-History of bedsores
- •\-Dry and flaky skin
- •\-Underlying disease (degenerative neurological disease, cerebrovascular disease, cerebrospinal cord injury, cancer, diabetes, heart failure, etc.)
- •3\) A person who voluntarily agrees to this study and writes a consent form after IRB approval
- •4\) Those who can visit the hospital outpatient clinic (use a wheelchair) and follow\-up during the test period
Exclusion Criteria
- •1\) Patients with systemic conditions accompanied by instability of vital signs such as infection or organ failure
- •2\) Persons with findings accompanied by a local infection of the pressure sore
- •3\) Persons with skin diseases (atopic dermatitis, contact dermatitis, psoriasis, etc.) that may affect the examination findings
- •4\) A person who has not voluntarily agreed to this study after IRB approval and did not fill out a consent form
- •5\) Vulnerable test subjects (pregnant women, newborns, minors, persons in prison, military personnel, employees of the research director, etc.)
- •6\) Subjects who cannot read and understand the consent form (illiteracy, etc.)
Outcomes
Primary Outcomes
Not specified
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