Peer-Learning Versus Physician-Led POCUS Training for Nurse Practitioners in Integrative Volume Status Assessment
Feasibility of a Peer-Learning Ultrasound Program to Enhance Nurse Practitioners' Competence in Integrative Volume Status Assessment
연구 개요
상태
상세 설명
This quasi-experimental study aims to compare two instructional models-physician-led versus peer NP-led POCUS training-and their effects on learners' outcomes and clinical skill performance.
Methods:
Sixty NPs, either in practice or under training, will be recruited and non-randomly assigned to either the experimental group (peer-led instruction) or the control group (physician-led instruction), based on their course availability, simulating real-world clinical education allocation:
- Experimental group: Hands-on training led by NPs who have completed a structured POCUS curriculum and passed both teaching and practical assessments.
- Control group: Hands-on training delivered by specialist physicians.
To ensure the quality and standardization of instructional delivery and operational procedures, two groups of nurse practitioners received the training program in separate cohorts. The educational intervention was structured into two phases: the first phase consisted of a two-hour online course covering fundamental ultrasound theory, relevant anatomical structures, and key points in clinical application; the second phase was a four-hour in-person hands-on workshop focusing on clinical scanning techniques and image interpretation skills. The instructional content encompassed five core structures: (1) inferior vena cava (IVC) assessment, (2) pleural effusion detection, (3) ascites identification, (4) hydronephrosis evaluation, and (5) bladder volume estimation and urinary retention interpretation.
Participants completed a pre-test prior to the training, a first post-test immediately after the course, and a second post-test three months later. The assessment tools included: (1) a POCUS knowledge questionnaire, (2) a self-confidence scale, (3) an image interpretation assessment, and (4) an Objective Structured Clinical Examination (OSCE).
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Chiang-Yi Chen, master
- 전화번호: +886928124530
- 이메일: a865292@gmail.com
연구 장소
-
-
Taipei
-
Taipei, Taipei, 대만, 100
- National Taiwan University Hospital
-
연락하다:
- Chiang-Yi Chen, master
- 전화번호: 0928124530
- 이메일: a865292@gmail.com
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
Participants aged 18 years or older. Licensed nurse practitioners or nurse practitioner trainees currently enrolled in an accredited nurse practitioner training program.
Able to understand the study procedures and provide written informed consent. Able to participate in the complete training program and study assessments, including baseline, post-training, and 1-month follow-up assessments.
No prior formal POCUS training, or only limited basic exposure without systematic training experience.
Exclusion Criteria:
Participants who have previously completed a formal point-of-care ultrasound training program.
Participants who are unable to complete the full training program or study assessment procedures.
-
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 지지 요법
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Nurse Practitioner-Led Peer Teaching Group
Participants in this arm will receive a structured POCUS training program delivered by trained nurse practitioner instructors.
The intervention includes a 2-hour online course covering basic ultrasound principles, relevant anatomy, and clinical applications, followed by a 4-hour hands-on practice session focused on integrative volume status assessment, including IVC, pleural effusion, ascites, hydronephrosis, and bladder assessment.
|
Participants will receive a structured point-of-care ultrasound training program delivered by trained nurse practitioner instructors.
The program includes a 2-hour online lecture and a 4-hour hands-on practice session.
Training focuses on integrative volume status assessment, including ultrasound evaluation of the inferior vena cava, pleural effusion, ascites, hydronephrosis, and bladder volume or urinary retention.
|
|
활성 비교기: Experimental
Participants in this group will receive the same structured POCUS training program delivered by trained physician instructors.
The program includes a 2-hour online lecture and a 4-hour hands-on practice session focused on integrative volume status assessment, including inferior vena cava, pleural effusion, ascites, hydronephrosis, and bladder assessment.
|
Participants will receive a structured point-of-care ultrasound training program delivered by trained nurse practitioner instructors.
The program includes a 2-hour online lecture and a 4-hour hands-on practice session.
Training focuses on integrative volume status assessment, including ultrasound evaluation of the inferior vena cava, pleural effusion, ascites, hydronephrosis, and bladder volume or urinary retention.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Change in POCUS Clinical Performance Score
기간: Baseline, immediately after the training program, and 1 month after the training program
|
POCUS clinical performance will be assessed using an Objective Structured Clinical Examination (OSCE).
Participants will be evaluated on ultrasound probe positioning, image acquisition, anatomical identification, clinical interpretation, and integration of findings for volume status assessment, including inferior vena cava, pleural effusion, ascites, hydronephrosis, and bladder assessment.
Higher scores indicate better clinical performance.
|
Baseline, immediately after the training program, and 1 month after the training program
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Change in POCUS Knowledge Score
기간: Baseline, immediately after the training program, and 1 month after the training program
|
POCUS knowledge will be assessed using a structured 10-item questionnaire covering basic ultrasound principles, organ identification, and clinical applications.
Higher scores indicate better POCUS knowledge.
|
Baseline, immediately after the training program, and 1 month after the training program
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
- 202507102RINE
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .