- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica 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
Panoramica dello studio
Stato
Intervento / Trattamento
Descrizione dettagliata
Tipo di studio
Iscrizione (Stimato)
Contatti e Sedi
Contatto studio
- Nome: Yong Yin
- Numero di telefono: +83015 86-021-38626161
- Email: yinyong9999@163.com
Luoghi di studio
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Cina, 200127
- Shanghai Children's Medical Center
-
Contatto:
- Yong Yin
- Numero di telefono: +83015 86-021-38626161
- Email: yinyong9999@163.com
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
Accetta volontari sani
Metodo di campionamento
Popolazione di studio
Descrizione
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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Coorti e interventi
Gruppo / Coorte |
Intervento / Trattamento |
|---|---|
|
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.
|
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.
|
|
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.
|
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.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Area under the receiver operating characteristic curve of the multimodal assisted diagnostic model
Lasso di tempo: Through study completion, an average of 1 year
|
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.
|
Through study completion, an average of 1 year
|
|
Area under the precision-recall curve of the multimodal assisted diagnostic model
Lasso di tempo: Through study completion, an average of 1 year
|
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.
|
Through study completion, an average of 1 year
|
Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Sensitivity of the multimodal assisted diagnostic model
Lasso di tempo: Through study completion, an average of 1 year
|
Through study completion, an average of 1 year
|
|
Specificity of the multimodal assisted diagnostic model
Lasso di tempo: Through study completion, an average of 1 year
|
Through study completion, an average of 1 year
|
|
Positive predictive value of the multimodal assisted diagnostic model
Lasso di tempo: Through study completion, an average of 1 year
|
Through study completion, an average of 1 year
|
|
Negative predictive value of the multimodal assisted diagnostic model
Lasso di tempo: Through study completion, an average of 1 year
|
Through study completion, an average of 1 year
|
|
F1 score of the multimodal assisted diagnostic model
Lasso di tempo: Through study completion, an average of 1 year
|
Through study completion, an average of 1 year
|
|
Accuracy of the multimodal assisted diagnostic model
Lasso di tempo: Through study completion, an average of 1 year
|
Through study completion, an average of 1 year
|
Collaboratori e investigatori
Investigatori
- Investigatore principale: Yong Yin, Shanghai Children's Medical Center
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Processi patologici
- Malattie del sistema immunitario
- Infezioni delle vie respiratorie
- Infezioni
- Malattie delle vie respiratorie
- Malattie polmonari
- Malattie bronchiali
- Malattie polmonari, ostruttive
- Ipersensibilità respiratoria
- Ipersensibilità, immediata
- Ipersensibilità
- Polmonite
- Condizioni patologiche, segni e sintomi
- Infezioni acquisite in comunità
- Asma
- Patologia
- Polmonite acquisita in comunità
Altri numeri di identificazione dello studio
- SCMCIRB-YJ20260516
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Multimodal respiratory data collection
-
Acorai ABCompletatoArresto cardiacoStati Uniti, Svezia, Regno Unito, Canada, Danimarca, Belgio
-
The Hong Kong Polytechnic UniversityLogistics and Supply Chain MultiTech R&D Centre, Hong KongReclutamentoSoggetti maschi e femmine saniHong Kong
-
Memorial Sloan Kettering Cancer CenterCompletatoCancro alla prostataStati Uniti