An interventional study of AI-Assisted Written Discharge Education and AI-Assisted Video Discharge Education in Bronchiolitis and Bronchitis, sponsored by Osmaniye Korkut Ata University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to female participants, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-20.
Sponsored by Osmaniye Korkut Ata University · Not applicable, Interventional, and Health services research
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.
This is a three-arm, parallel-group, pretest-posttest randomized controlled trial. Mothers who meet the eligibility criteria will be randomized in a 1:1:1 ratio after baseline assessments. The written education group will receive AI-assisted written discharge education, the video education group will receive AI-assisted video discharge education covering the same learning objectives, and the control group will receive routine discharge education.
Knowledge, anxiety, and readiness for hospital discharge will be assessed at baseline and before discharge. Satisfaction with discharge education will be assessed after the intervention. In the two experimental groups, routine discharge education will be provided after completion of the posttest and before hospital discharge.
289 studies on the registry are indexed under Bronchiolitis; 51 are open to participants now.
This study's planned enrollment of 144 is above the median of 100 across 195 interventional studies indexed under Bronchiolitis.
Browse Bronchiolitis studies →Osmaniye Korkut Ata University is the lead sponsor of 35 studies on the registry; 7 are open to participants now.
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Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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
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
Mothers will receive the institution's routine discharge education before the posttest.
Behavioral: Routine Discharge Education
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.
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.
Time frame: Baseline before randomization and at hospital discharge, during the same hospitalization.
Change in Readiness for Hospital Discharge
Readiness for hospital discharge will be assessed using the 26-item Pediatric Readiness for Hospital Discharge Scale (Ped-RHDS). Higher scores indicate greater readiness for hospital discharge.
Time frame: Baseline before randomization and at hospital discharge, during the same hospitalization
Change in Maternal Anxiety Level
Maternal anxiety will be assessed using a Visual Analog Scale (VAS) ranging from 0 to 10, where 0 indicates no anxiety and 10 indicates the highest level of anxiety. Higher scores indicate greater anxiety.
Time frame: Baseline before randomization and at hospital discharge, during the same hospitalization.
Maternal Satisfaction With Discharge Education
Satisfaction with discharge education will be assessed using a Visual Analog Scale (VAS) ranging from 0 to 10, with higher scores indicating greater satisfaction with the discharge education.
Time frame: At hospital discharge, during the same hospitalization.
Plan to share: No — Individual participant data will not be publicly shared due to participant confidentiality and data protection considerations.
No publications or documents are linked to this record.
Start is estimated for Oct 2026; primary completion for Jun 2027, 8 months later.
Of 54 non-industry interventional studies with no phase under Bronchiolitis, half reached primary completion within 22 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 35. This study's planned 8 months is below that.
Counting every sponsor, half of 57 studies reached it within 22 months; a quarter within 11 and three quarters within 35.
How these figures are worked out, and which studies are left out of them.
This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.
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Osmaniye Korkut Ata University