THE I-PASS COMMUNICATION METHOD ON NURSE PERCEPTION OF HANDOVER QUALITY
THE EFFECTIVENESS OF THE I-PASS COMMUNICATION METHOD ON NURSE PERCEPTION OF HANDOVER QUALITY IN THE INPATIENT WARD OF WELAS ASIH HOSPITAL, WEST JAVA PROVINCE
1 other identifier
interventional
46
1 country
1
Brief Summary
The goal of this non-clinical study is to determine whether the I-PASS communication method influences the improvement of handover quality among nurses. The main questions it aims to answer are: What are the perceptions of handover quality prior to implementing the I-PASS method? What are the perceptions of handover quality after using the I-PASS method? How do nurse characteristics (gender, age, education, employment status, length of service, and clinical nurse level) affect the improvement of handover quality perceptions when using the I-PASS method? What is the implementation retention of the I-PASS communication method? Is there a significant effect of the I-PASS communication method on nurses' perceptions of handover quality? Participants will: Participate in training sessions regarding the I-PASS communication method. Implement the I-PASS method during handover processes for two weeks. Complete questionnaires to assess handover quality.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 15, 2026
CompletedFirst Submitted
Initial submission to the registry
April 25, 2026
CompletedFirst Posted
Study publicly available on registry
May 1, 2026
CompletedMay 1, 2026
March 1, 2026
14 days
April 25, 2026
April 25, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Handover Quality
Handover quality measure by the handover evaluation scale instrument
two weeks
Study Arms (2)
Training I-PASS handoff bundle
EXPERIMENTALPartisipant in experimental arms will receive I-PASS handoff bundle into daily nursing process for 2 weeks
SBAR
NO INTERVENTIONThe control group continues to utilize the hospital's existing standard operating procedure, the SBAR (Situation, Background, Assessment, Recommendation) method, observed two weeks not training I-PASS handoff bundle
Interventions
The intervention proceeds of Training I-PASS handoff bundle in three phases: preparation, training, and evaluation. First, eligible nurses are recruited, provided with informed consent, and grouped by shifts. After a baseline assessment, participants undergo two 90-minute training sessions over two weeks. Next, the I-PASS method is implemented for 14 days, with compliance monitored through direct shift-based observations and checklists. Handover quality is measured via the Handover Evaluation Scale (HES) at three intervals: pre-test (baseline), mid-point (week two), and post-test (week three). Continuous researcher monitoring ensures protocol fidelity throughout the process.
Eligibility Criteria
You may qualify if:
- General practitioner nurses who working in the internal ward
- General practitioner nurses with a minimum of 6 months of the clinical experience
You may not qualify if:
- Clinical nurse manager / leader who did not provide nursing care (e.g Head nurse)
- Nurses on leave
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Welas Asih General Hospital West Java Province
Bandung, West Java, 40191, Indonesia
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Agnes Stephania Penu, BSN, MSc, RN
Faculty of Nursing, Universitas Padjadjaran
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Miss
Study Record Dates
First Submitted
April 25, 2026
First Posted
May 1, 2026
Study Start
April 1, 2026
Primary Completion
April 15, 2026
Study Completion
April 15, 2026
Last Updated
May 1, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
This research considers ethical values such as autonomy, confidentiality, beneficence, non- maleficence and justice