Effect of AI-Assisted Discharge Education on Parents of Children With Bronchitis/Bronchiolitis
The Effect of AI-Supported Discharge Education on Mothers' Knowledge Levels, Anxiety, and Readiness for Discharge: A Randomized Controlled Experimental Study
1 other identifier
interventional
144
1 country
1
Brief Summary
This randomized controlled trial aims to evaluate the effects of artificial intelligence-assisted discharge education on mothers of children hospitalized with bronchitis/bronchiolitis. A total of 162 mothers will be randomly assigned to one of three groups: AI-assisted written discharge education, AI-assisted video discharge education, or routine discharge education. The primary outcome will be mothers' knowledge of home care after discharge. Secondary outcomes will include anxiety, readiness for hospital discharge, and satisfaction with discharge education. The study hypothesizes that AI-assisted written and video discharge education will improve mothers' knowledge and readiness for discharge, reduce anxiety, and increase satisfaction compared with routine discharge education.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Oct 2026
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
August 14, 2026
CompletedFirst Posted
Study publicly available on registry
August 19, 2026
CompletedStudy Start
First participant enrolled
October 15, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
June 15, 2027
Study Completion
Last participant's last visit for all outcomes
June 30, 2027
August 20, 2026
August 1, 2026
8 months
August 14, 2026
August 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Maternal Knowledge Score Regarding Home Care After Discharge
Maternal knowledge will be assessed using a 10-item true/false knowledge test developed according to the content of the discharge education. Each correct answer is scored as 1 and each incorrect answer as 0, yielding a total score ranging from 0 to 10. Higher scores indicate greater knowledge.
Baseline before randomization and at hospital discharge, during the same hospitalization.
Secondary Outcomes (3)
Change in Readiness for Hospital Discharge
Baseline before randomization and at hospital discharge, during the same hospitalization
Change in Maternal Anxiety Level
Baseline before randomization and at hospital discharge, during the same hospitalization.
Maternal Satisfaction With Discharge Education
At hospital discharge, during the same hospitalization.
Study Arms (3)
AI-Assisted Written Discharge Education
EXPERIMENTALMothers will receive AI-assisted written discharge education on home care after discharge for children with bronchitis/bronchiolitis. After completion of the posttest, routine discharge education will be provided before hospital discharge.
AI-Assisted Video Discharge Education
EXPERIMENTALMothers will receive AI-assisted video discharge education covering the same learning objectives as the written education. After completion of the posttest, routine discharge education will be provided before hospital discharge.
Routine Discharge Education
ACTIVE COMPARATORMothers will receive the institution's routine discharge education before the posttest.
Interventions
A written discharge education booklet developed with support from ChatGPT based on standard discharge content and expert review.
A video discharge education intervention developed with support from Gemini Notebook and designed to cover the same learning objectives as the written material.
Standard discharge education routinely provided by the institution.
Eligibility Criteria
You may qualify if:
- Mother of a child hospitalized with a diagnosis of bronchitis/bronchiolitis
- Child hospitalized for at least 3 days
- Willing to participate and provide informed consent
- Able to read and understand Turkish and communicate sufficiently to complete the study forms
- Owns a smartphone
You may not qualify if:
- Unable to read/view the educational materials or complete the study forms
- Child requiring intensive care, experiencing severe clinical deterioration, or having a condition preventing completion of the study
- Child with an additional chronic disease or special care needs
- Mother who is a healthcare professional
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Osmaniye Training and Research Hospital
Osmaniye, Osmaniye, 80000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Profesor
Study Record Dates
First Submitted
August 14, 2026
First Posted
August 19, 2026
Study Start (Estimated)
October 15, 2026
Primary Completion (Estimated)
June 15, 2027
Study Completion (Estimated)
June 30, 2027
Last Updated
August 20, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be publicly shared due to participant confidentiality and data protection considerations.