- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne 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
Przegląd badań
Status
Interwencja / Leczenie
Szczegółowy opis
Typ studiów
Zapisy (Szacowany)
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Yong Yin
- Numer telefonu: +83015 86-021-38626161
- E-mail: yinyong9999@163.com
Lokalizacje studiów
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Chiny, 200127
- Shanghai Children's Medical Center
-
Kontakt:
- Yong Yin
- Numer telefonu: +83015 86-021-38626161
- E-mail: yinyong9999@163.com
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dziecko
- Dorosły
Akceptuje zdrowych ochotników
Metoda próbkowania
Badana populacja
Opis
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.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
Kohorty i interwencje
Grupa / Kohorta |
Interwencja / Leczenie |
|---|---|
|
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.
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Area under the receiver operating characteristic curve of the multimodal assisted diagnostic model
Ramy czasowe: 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
Ramy czasowe: 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
|
Miary wyników drugorzędnych
Miara wyniku |
Ramy czasowe |
|---|---|
|
Sensitivity of the multimodal assisted diagnostic model
Ramy czasowe: Through study completion, an average of 1 year
|
Through study completion, an average of 1 year
|
|
Specificity of the multimodal assisted diagnostic model
Ramy czasowe: 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
Ramy czasowe: 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
Ramy czasowe: Through study completion, an average of 1 year
|
Through study completion, an average of 1 year
|
|
F1 score of the multimodal assisted diagnostic model
Ramy czasowe: Through study completion, an average of 1 year
|
Through study completion, an average of 1 year
|
|
Accuracy of the multimodal assisted diagnostic model
Ramy czasowe: Through study completion, an average of 1 year
|
Through study completion, an average of 1 year
|
Współpracownicy i badacze
Śledczy
- Główny śledczy: Yong Yin, Shanghai Children's Medical Center
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
- Procesy patologiczne
- Choroby układu odpornościowego
- Infekcje dróg oddechowych
- Infekcje
- Choroby Układu Oddechowego
- Choroby płuc
- Choroby oskrzeli
- Choroby płuc, obturacyjne
- Nadwrażliwość oddechowa
- Nadwrażliwość, natychmiastowa
- Nadwrażliwość
- Zapalenie płuc
- Stany patologiczne, oznaki i objawy
- Zakażenia pozaszpitalne
- Astma
- Choroba
- Pozaszpitalne zapalenie płuc
Inne numery identyfikacyjne badania
- SCMCIRB-YJ20260516
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .
Badania kliniczne na Multimodal respiratory data collection
-
Occlutech International ABJeszcze nie rekrutacjaSerce jednokomorowe | Wrodzona anomalia | Fenestracja | Niewydolność krążenia typu FontanStany Zjednoczone
-
Memorial Sloan Kettering Cancer CenterZakończonyRak prostatyStany Zjednoczone