Skip to content

The Effectiveness of Two Nursing Programs on the Surgery-related Pressure Injury

The Effectiveness of Two Nursing Programs on the Surgery-Related Pressure Injury in Surgery Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06316726
Enrollment
461
Registered
2024-03-18
Start date
2021-12-15
Completion date
2023-08-31
Last updated
2024-03-18

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

Conditions

Pressure Injury, Surgery

Keywords

surgery-related pressure injury, incidence, grade, sites, time

Brief summary

Introduction: This study was to compare the differences in the incidence, grade, and time of surgery-related pressure injuries between the two interventions; and describe the locations of surgery-related pressure injuries between the two interventions. Methods: This study adopted a true experimental research design with a convenience sampling method from the operating rooms of a teaching hospital in a northern region. The experimental group was randomly assigned by block to receive intervention A (full bed silicone mattress plus other measures), and the control group received intervention B (full bed silicone mattress plus usual care). Measurements include basic personal attributes, risk factors, grade, time, and location of occurrence related to surgery-related pressure injuries.

Interventions

COMBINATION_PRODUCTfull bed silicone mattress plus other measures

full bed silicone mattress plus put silicone pads on the head and shoulders, cotton rolls wraps bony prominence (elbows and heels), petrissage every two hours on shoulders to fingers and lower legs to heels, change location of ankle pads, use round gel full of air sit pad, a pillow on the knees

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

The experimental group was randomly assigned by block to receive intervention A (full bed silicone mattress plus other measures), and the control group received intervention B (full bed silicone mattress plus usual care).

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 20 and more years old * Over 4 hours lying flat on the operating table (eg., orthognathic surgery, microtia reconstruction surgery, etc.) * Those who are conscious clearly and can communicate in Mandarin and Taiwanese * Those with agree to participate in this study

Exclusion criteria

* Those whose skin is red, swollen, hot, painful, redness, rash, purple spots, bruising, scaly skin, damaged, etc. * Refuse to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
the occurrence of surgery-related pressure injuriesbaseline, pre-surgery; every two hours during the surgery till ten hours; and post-surgery to the 2nd day after surgerylincidence, grade, site, and time of surgery-related pressure injuries

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026