Investigation and Analysis of the NIS Protection Level and Influencing Factors of Clinical Nurses

NCT06733779 | Completed

• 1 other identifier: K2023-192
• Study Type: observational
• Target: 17,164
• Locations: 1 country
• Sites: 1

Brief Summary

To investigate and analyze differences in the incidence of needle stick injuries and the influencing factors among clinical nurses in different economic regions. The online questionnaire survey was conducted by stratified and network sampling methods. A total of 17,164 questionnaires were collected, which included demographic characteristics of nurses; knowledge, beliefs, and behaviors related to needle injury protection of nurses; hospital management, training, and assessment of "needle injury" protocols. Additionally, the knowledge, beliefs, and behaviors of nurses in needle stick injuries were compared according to the economic region, and the correlation between influencing factors was analyzed.

Conditions

Needle Injury

Outcome Measures

Primary Outcomes (1)

• differences in the incidence of needle stick injuries and the influencing factors among clinical nurses in different economic regions.

  to analyze the incidence rate in different regions and ralated influencing factors.

  up to 12 weeks.

Study Arms (3)

Eastern region Western region

Located in eastern region of China

Other: observation

Centrel region

Located in the central region of China

Other: observation

Western region

Located in western region of China

Other: observation

Interventions

observation OTHER

cross-sectional study

Centrel region; Eastern region Western region; Western region

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Age Groups: Adult (18-64)
• Sampling Method: Non-Probability Sample

Study Population

in-service and on-the-job clinical nurses working in tertiary hospitals

You may qualify if:

• \- cetificated nurse; voluntarily cooperated with the investigators;

You may not qualify if:

• \- nursing students,; nursing managers; individuals taking maternity leave due to pregnancy or childbirth; refusal to participate in the survey, questionnaire completion time not meeting the minimum requirement; reverse entry selections; incomplete responses.

Sponsors & Collaborators

• First Affiliated Hospital of Chongqing Medical University: lead

Study Sites (1)

the First Affiliated Hospital of Chongqing Medical University

Chongqing, Chongqing Municipality, China

Location

MeSH Terms

Interventions

Observation

Intervention Hierarchy (Ancestors)

Methods; Investigative Techniques

Study Officials

• Ying Shen, M.D

  First Affiliated Hospital of Chongqing Medical University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: CASE ONLY
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: associate-professor

Study Record Dates

• First Submitted: December 7, 2024
• First Posted: December 13, 2024
• Study Start: November 9, 2022
• Primary Completion: February 16, 2023
• Study Completion: August 1, 2023
• Last Updated: December 13, 2024

Record last verified: 2024-12

Locations

CN (1)