An Analysis of the Current Status and Influencing Factors in Nurse Practitioners' and Nurses' Use of Point-of-Care Ultrasound (POCUS)

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20+
SponsorNational Taiwan University Hospital

About this trial

This study targets clinical nurses and nurse practitioners in Taiwan, with an anticipated sample size of approximately 1,000 participants. A cross-sectional survey design will be employed, using an electronic questionnaire to collect data on healthcare professionals' knowledge of point-of-care ultrasound (POCUS), its clinical scope and frequency of use, attitudes toward its clinical application, and experiences with related education and training.

Upon completion of data collection, descriptive statistics will be used to present the current status of POCUS utilization. Additionally, differences in knowledge, attitudes, and usage patterns across participants with varying background characteristics will be compared to identify factors associated with the clinical implementation of POCUS.

Eligibility criteria

Qualifiers

Aged ≥20 years and able to read and understand Traditional Chinese.

Self-reported current clinical practice in Taiwan as a licensed registered nurse (RN) or nurse practitioner (NP).

Currently engaged in clinical work involving direct patient care, including but not limited to emergency departments, intensive care units, medical and surgical wards, operating rooms, anesthesia-related units, dialysis units, obstetrics and pediatrics, and outpatient settings.

Have read the electronic study information sheet and voluntarily provided informed consent by selecting "I agree to participate in this study" before completing the questionnaire.

Disqualifiers

Not currently involved in direct patient care, or primarily engaged in administrative, managerial, educational, or research administrative roles (e.g., nursing supervisors, education and training administrative staff).

Incomplete or inconsistent responses to key background information, rendering classification impossible.

Trial design

Treatments tested in this trial

  • No intervention

Treatment groups

1,000 Participants
are divided into 1 treatment group