NCT07761234

Brief Summary

This study aims to evaluate the effectiveness of an app-based delirium in-service education program for intensive care unit (ICU) nurses, specifically examining its impact on their knowledge, learning self-efficacy, and clinical reasoning.The primary research questions are as follows:

  1. 1.Does the app intervention implemented at different time points enhance ICU nurses' knowledge of delirium?
  2. 2.Does the app intervention implemented at different time points enhance ICU nurses' learning self-efficacy?
  3. 3.Does the app intervention implemented at different time points improve ICU nurses' clinical reasoning skills?

Trial Health

87
On Track

Trial Health Score

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

Enrollment
102

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2026

Shorter than P25 for not_applicable

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

February 9, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

July 26, 2026

Completed
17 days until next milestone

First Posted

Study publicly available on registry

August 12, 2026

Completed
Last Updated

August 12, 2026

Status Verified

August 1, 2026

Enrollment Period

2 months

First QC Date

July 26, 2026

Last Update Submit

August 7, 2026

Conditions

Keywords

ApplicationDelirium In-service EducationLearning Self-efficacyClinical ReasoningSystem Usability

Outcome Measures

Primary Outcomes (3)

  • Delirium cognitive

    adopted the "Cognitive Care for Delirium Assessment among Nursing Staff in Intensive Care Units" questionnaire by Hou et al. (2024). The original questionnaire had 15 questions. To balance statistical indicators with "content validity" in clinical practice, 6 questions were ultimately retained after screening based on difficulty and discrimination. Each question's answer was scored as correct (1 point) or incorrect (0 points), and the scores were summed to form an individual's total score, reflecting the subject's knowledge level. The maximum score was 6 points, with higher scores indicating more accurate knowledge about delirium.

    Evaluations were conducted at three time points: baseline (T0), immediately post-intervention (T1), and four weeks post-intervention (T2).

  • Learning self-efficacy

    Using the "Delirium Care Self-Efficacy Scale" by Chang et al. (2023), scores ranged from 13 to 65. The higher the score, the higher the self-efficacy in delirium care learning.

    Evaluations were conducted at three time points: baseline (T0), immediately post-intervention (T1), and four weeks post-intervention (T2).

  • clinical reasoning

    The Clinical Reasoning Tendency Scale for Nursing Students (Huang et al., 2018) was used. It consists of 16 items with a total score ranging from 16 to 80 points. Higher scores indicate better clinical reasoning ability among nurses.

    Evaluations were conducted at three time points: baseline (T0), immediately post-intervention (T1), and four weeks post-intervention (T2).

Study Arms (2)

Application Intervention(APP)

EXPERIMENTAL

receiving an APP intervention constructed on the Notion platform and integrated with gamified learning via Kahoot

Other: Application Intervention

traditional classroom lectures

NO INTERVENTION

receiving traditional classroom lectures

Interventions

receiving an APP intervention constructed on the Notion platform and integrated with gamified learning via Kahoot)

Application Intervention(APP)

Eligibility Criteria

Age20 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Registered Nurses (RNs) with a valid nursing license.
  • Currently employed in an adult medical or surgical intensive care unit (ICU), having passed the probationary period, and with at least six months of clinical work experience.
  • Willing to participate in this study.

You may not qualify if:

  • Those who are unable to complete the full study procedure due to leave of absence without pay, maternity leave, or long-term sick/extended leave.
  • Unit nurse managers (Head Nurses).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

No. 1, Yida Rd., Jiaosu Li, Yanchao Dist.

Kaohsiung City, Taiwan (r.o.c.), 82445, Taiwan

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
FACTORIAL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Nurse Practitioner in Emergency and Critical Care

Study Record Dates

First Submitted

July 26, 2026

First Posted

August 12, 2026

Study Start

February 9, 2026

Primary Completion

March 31, 2026

Study Completion

March 31, 2026

Last Updated

August 12, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

In accordance with the principle of confidentiality, all participant data will be kept strictly confidential.

Locations