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Evaluating an Intelligent Module for Pressure Injury Nursing Management (IM-PINM)

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Xiamen Humanity Hospital

Status

Completed

Conditions

Pressure Injury

Study type

Observational

Funder types

Other

Identifiers

NCT07208747
HAXM-MEC-20250815-069-01

Details and patient eligibility

About

This is a study conducted in a hospital to evaluate whether applying an intelligent information technology can help nurses better prevent and manage bedsores (also known as pressure injuries) in hospitalized patients. Bedsores are a serious skin problem for patients who are bedridden for long periods. The researchers will compare the situation before and after using the intelligent program to see if it has an impact on the occurrence and outcomes of pressure injuries. We invite eligible hospitalized patients to participate. Participants' nursing data will be anonymously recorded and analyzed to evaluate the effectiveness of this intelligent program.

Full description

Background:Pressure injuries are common nursing complications in clinical practice, and their occurrence can reduce patients' quality of life, affect rehabilitation, and increase medical costs. This project aims to utilize information technology to build a comprehensive and intelligent pressure injury care management platform, providing scientific evidence for clinical decision-making and supporting standardized management of pressure injuries and improvement in nursing quality.

Objective:To construct an intelligent module for the pressure injury nursing management system and to explore its application effects in pressure injury management.

Methods:Based on the hospital nursing information system, an intelligent module was constructed to achieve functions such as intelligent decision-making for pressure injury risk assessment, intelligent staging judgment, visual online assessment and review, outcome tracking,and home care linkage, as well as monitoring quality control indicators.

Enrollment

75,263 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Length of stay ≥ 2 hours after admission

Exclusion criteria

  • 1: Terminal condition (expected survival time < 48 hours) 2: Refusal to participate in data collection

Trial design

75,263 participants in 2 patient groups

Exposed Cohort
Description:
The nursing staff routinely used the intelligent pressure-injury management module as part of standard care throughout 2024.
Routine Care Cohort
Description:
The nursing staff provided routine pressure-injury care without the use of the intelligent module throughout 2023.

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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