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

Not Applicable

Completed

• Conditions: Pressure Injury; Surgery
• Interventions: Combination Product: full bed silicone mattress plus other measures

• Registration Number: NCT06316726
• Lead Sponsor: Chang Gung Memorial Hospital

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.

Detailed Description

Not available

Study Timeline

• Status Verified: 2021-05
• Study Start: 2021-12-15
• Primary Completion: 2023-08-31
• Study Completion: 2023-08-31
• Study First Submitted: 2024-02-29
• Study First Submitted QC: 2024-03-15
• Last Update Submitted: 2024-03-15
• Study First Posted: 2024-03-18
• Last Update Posted: 2024-03-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 461

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
intervention A	full bed silicone mattress plus other measures	full bed silicone mattress plus other measures

Primary Outcome Measures

Name	Time	Method
the occurrence of surgery-related pressure injuries	baseline, pre-surgery; every two hours during the surgery till ten hours; and post-surgery to the 2nd day after surgeryl	incidence, grade, site, and time of surgery-related pressure injuries

Trial Locations

Locations (1)

Taoyuan Chang Gung Memorial Hospital; 🇨🇳 Taoyuan, Taiwan