NCT07774494

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

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Trial Health Score

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

Enrollment
144

participants targeted

Target at P75+ for not_applicable

Timeline
9mo left

Started Oct 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 19, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

October 15, 2026

Expected
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2027

15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2027

Last Updated

August 20, 2026

Status Verified

August 1, 2026

Enrollment Period

8 months

First QC Date

August 14, 2026

Last Update Submit

August 18, 2026

Conditions

Keywords

Artificial IntelligenceMothersPatient EducationReadiness for Hospital DischargeHealth Education

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

EXPERIMENTAL

Mothers 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.

Behavioral: AI-Assisted Written Discharge Education

AI-Assisted Video Discharge Education

EXPERIMENTAL

Mothers 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.

Behavioral: AI-Assisted Video Discharge Education

Routine Discharge Education

ACTIVE COMPARATOR

Mothers will receive the institution's routine discharge education before the posttest.

Behavioral: Routine Discharge Education

Interventions

A written discharge education booklet developed with support from ChatGPT based on standard discharge content and expert review.

AI-Assisted Written Discharge Education

A video discharge education intervention developed with support from Gemini Notebook and designed to cover the same learning objectives as the written material.

AI-Assisted Video Discharge Education

Standard discharge education routinely provided by the institution.

Routine Discharge Education

Eligibility Criteria

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

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)

Location

MeSH Terms

Conditions

BronchiolitisBronchitisHealth Education

Condition Hierarchy (Ancestors)

Respiratory Tract InfectionsInfectionsBronchial DiseasesRespiratory Tract DiseasesLung Diseases, ObstructiveLung DiseasesAdherence InterventionsMedication AdherencePatient CompliancePatient Acceptance of Health CareTreatment Adherence and ComplianceHealth BehaviorBehavior

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: Three-arm, parallel-group, pretest-posttest randomized controlled trial
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.

Locations