Using infrared thermal cameras to prevent pressure wounds
Prevention of Pressure Wound Development With Infrared Thermal Camera
This study is testing if using infrared cameras can help spot early signs of pressure wounds in patients at high risk while they're in intensive care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 31 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Abant Izzet Baysal University Academic / other |
| Locations | 1 site (Bolu, Merkez) |
| Trial ID | NCT06219954 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the effectiveness of infrared thermography in preventing pressure wounds in patients admitted to intensive care. By comparing skin temperature in pressure-prone areas using traditional methods and infrared cameras, the researchers hope to detect early signs of pressure injuries before they become visible. The study focuses on patients with a Braden score of less than 18, indicating a higher risk for pressure ulcers. The findings could provide valuable insights into improving patient care and reducing the incidence of pressure wounds.
Who should consider this trial
Good fit: Ideal candidates for this study are patients aged 18 and over, receiving treatment in intensive care, and with a Braden score of less than 18.
Not a fit: Patients with existing skin damage, full-thickness pressure sores, or a Braden score over 18 may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce the incidence of pressure wounds in at-risk patients, improving their overall health outcomes.
How similar studies have performed: While the use of infrared thermography in this context is innovative, similar studies have shown promise in early detection of pressure injuries.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients receiving treatment in intensive care * Patients aged 18 and over * Patients with Braden score less than 18 points * Patients who are not transferred from another intensive care unit * Patients who can tolerate supine, prone and right/left lateral position changes and turns Exclusion Criteria: * Patients with previous acute or chronic skin damage or burns in the observation area * Patients with Braden score over 18 points * Patients with full-thickness pressure sores * Patients with protective dressings on the skin or undergoing hot and cold therapy that may affect the skin
Where this trial is running
Bolu, Merkez
- İzzet Baysal Devlet Hastanesi — Bolu, Merkez, Turkey (Recruiting)
Study contacts
- Study coordinator: Arzu İlçe
- Email: ilce_a@ibu.edu.tr
- Phone: +90 374 253 45 20
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.