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- Klinische proef NCT07613242
Multimodal Assisted Diagnosis for Pediatric Respiratory Diseases Using Questionnaires, Cough Sounds, and Breath Sounds
A Prospective Observational Study of Multimodal Assisted Diagnosis for Pediatric Respiratory Diseases Using Symptom Questionnaires, Cough Sounds, and Breath Sounds
Studie Overzicht
Toestand
Interventie / Behandeling
Gedetailleerde beschrijving
Studietype
Inschrijving (Geschat)
Contacten en locaties
Studiecontact
- Naam: Yong Yin
- Telefoonnummer: +83015 86-021-38626161
- E-mail: yinyong9999@163.com
Studie Locaties
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Shanghai Municipality
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Shanghai, Shanghai Municipality, China, 200127
- Shanghai Children's Medical Center
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Contact:
- Yong Yin
- Telefoonnummer: +83015 86-021-38626161
- E-mail: yinyong9999@163.com
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
- Volwassen
Accepteert gezonde vrijwilligers
Bemonsteringsmethode
Studie Bevolking
Beschrijving
Inclusion Criteria:
Children aged 28 days to 18 years, regardless of sex, will be eligible for inclusion. The disease group will include children presenting to the outpatient department, emergency department, or inpatient wards of Shanghai Children's Medical Center with cough, wheezing, fever with respiratory symptoms, nasal congestion, rhinorrhea, sore throat, or other respiratory complaints. Participants should be able to complete the symptom questionnaire, cough sound recording, and breath sound recording, and their guardians must provide informed consent and allow review of relevant medical history and diagnostic information. The healthy control group will include children recruited from routine health examinations or children without respiratory complaints, with no acute respiratory symptoms within the past 4 weeks, no known history of chronic respiratory diseases, no obvious respiratory abnormalities on health assessment or research team review, the ability to complete relevant data collection, and guardian informed consent.
Exclusion Criteria:
Participants will be excluded if they have severe cardiopulmonary malformations, long-term tracheostomy or mechanical ventilation, severe neuromuscular disorders, severe immunodeficiency, or other conditions that may substantially alter cough sound characteristics or affect the clinical presentation of respiratory diseases. Children whose primary diagnosis at the current visit is a non-respiratory disease and who are not suitable for this study will also be excluded. Participants who are unable to complete the symptom questionnaire, or whose cough sound or breath sound recordings remain of insufficient quality after repeated attempts, will not be included or will be excluded from the corresponding modality-specific analysis. Participants with only one unavailable modality may be included in analyses based on the completed modalities but will be excluded from analyses requiring the missing modality. Healthy controls will be excluded from the main control analysis if recent respiratory symptoms, a history of chronic respiratory disease, or other conditions that may affect acoustic features are identified.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
Cohorten en interventies
Groep / Cohort |
Interventie / Behandeling |
|---|---|
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Children with respiratory complaints
Children aged 28 days to 18 years presenting with cough, wheezing, fever with respiratory symptoms, nasal congestion, rhinorrhea, sore throat, or other respiratory complaints.
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Participants will complete a structured symptom questionnaire, cough sound recording using a smartphone application, and breath sound recording using an electronic stethoscope.
These data will be used to develop and evaluate a multimodal assisted diagnostic model and will not guide real-time clinical decision-making.
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Healthy controls
Children aged 28 days to 18 years recruited from routine health examinations or without respiratory complaints, with no acute respiratory symptoms within the past 4 weeks and no known chronic respiratory disease.
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Participants will complete a structured symptom questionnaire, cough sound recording using a smartphone application, and breath sound recording using an electronic stethoscope.
These data will be used to develop and evaluate a multimodal assisted diagnostic model and will not guide real-time clinical decision-making.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Area under the receiver operating characteristic curve of the multimodal assisted diagnostic model
Tijdsspanne: Through study completion, an average of 1 year
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The area under the receiver operating characteristic curve will be used to evaluate the diagnostic performance of the multimodal assisted diagnostic model integrating symptom questionnaire, cough sound, and breath sound data.
The model will be assessed against the final clinical research label for distinguishing children with respiratory diseases from healthy controls and for identifying major pediatric respiratory disease categories.
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Through study completion, an average of 1 year
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Area under the precision-recall curve of the multimodal assisted diagnostic model
Tijdsspanne: Through study completion, an average of 1 year
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The area under the precision-recall curve will be used to evaluate the diagnostic performance of the multimodal assisted diagnostic model, particularly in settings with imbalanced disease categories.
The model will be assessed against the final clinical research label.
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Through study completion, an average of 1 year
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Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
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Sensitivity of the multimodal assisted diagnostic model
Tijdsspanne: Through study completion, an average of 1 year
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Through study completion, an average of 1 year
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Specificity of the multimodal assisted diagnostic model
Tijdsspanne: Through study completion, an average of 1 year
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Through study completion, an average of 1 year
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Positive predictive value of the multimodal assisted diagnostic model
Tijdsspanne: Through study completion, an average of 1 year
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Through study completion, an average of 1 year
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Negative predictive value of the multimodal assisted diagnostic model
Tijdsspanne: Through study completion, an average of 1 year
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Through study completion, an average of 1 year
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F1 score of the multimodal assisted diagnostic model
Tijdsspanne: Through study completion, an average of 1 year
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Through study completion, an average of 1 year
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Accuracy of the multimodal assisted diagnostic model
Tijdsspanne: Through study completion, an average of 1 year
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Through study completion, an average of 1 year
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Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: Yong Yin, Shanghai Children's Medical Center
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Pathologische processen
- Ziekten van het immuunsysteem
- Luchtweginfecties
- Infecties
- Ziekten van de luchtwegen
- Longziekten
- Bronchiale ziekten
- Longziekten, obstructief
- Ademhalingsovergevoeligheid
- Overgevoeligheid, Onmiddellijk
- Overgevoeligheid
- Longontsteking
- Pathologische aandoeningen, tekenen en symptomen
- Door de gemeenschap verworven infecties
- Astma
- Ziekte
- Gemeenschap verworven pneumonie
Andere studie-ID-nummers
- SCMCIRB-YJ20260516
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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