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Research on monitoring technique of pressure ulcer patients to develop wearable sensors for prevention of decubitus ulcer

Research on monitoring technique of pressure ulcer patients to develop wearable sensors for prevention of decubitus ulcer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0005829
Enrollment
20
Registered
2021-01-27
Start date
2021-01-14
Completion date
Unknown
Last updated
2021-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Yonsei University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion 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 5) Men and women who are 19 years of age or older who can provide a legally valid consent form

Exclusion criteria

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.)

Design outcomes

Primary

MeasureTime frame
Measurement values ??of skin temperature, color, and erythema degree measured through thermal imaging camera, 3D camera, and Mexameter

Secondary

MeasureTime frame
Measurement value of skin elasticity measured by cutometer

Countries

Korea, Republic of

Contacts

Public ContactJu Hee Lee

Yonsei University Health System, Severance Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026