NCT07561762

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
46

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2026

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
14 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 15, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 15, 2026

Completed
10 days until next milestone

First Submitted

Initial submission to the registry

April 25, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 1, 2026

Completed
Last Updated

May 1, 2026

Status Verified

March 1, 2026

Enrollment Period

14 days

First QC Date

April 25, 2026

Last Update Submit

April 25, 2026

Conditions

Keywords

I-PASSCommunicationHandover QualityPatient SafetyNurse

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

EXPERIMENTAL

Partisipant in experimental arms will receive I-PASS handoff bundle into daily nursing process for 2 weeks

Other: Training I-PASS handoff bundle

SBAR

NO INTERVENTION

The 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.

Training I-PASS handoff bundle

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Communication

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Agnes Stephania Penu, BSN, MSc, RN

    Faculty of Nursing, Universitas Padjadjaran

    PRINCIPAL INVESTIGATOR

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

Locations