Skip to content

Validation of the Accuracy and Validity of the Childhood Asthma Model for Clinical Decision Support (CAMCDS)

Validation of the Accuracy and Validity of the Childhood Asthma Model for Clinical Decision Support (CAMCDS)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100045283
Enrollment
Unknown
Registered
2021-04-10
Start date
2021-06-01
Completion date
Unknown
Last updated
2021-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric asthma

Interventions

Gold Standard:According to the diagnostic criteria of asthma in the 2016 guidelines for the diagnosis and treatment of bronchial asthma in children, the children were clinically diagnosed as asthma. R
Index test:Childhood&#32
model&#32
for&#32
clinical&#32

Sponsors

Children's hospital of Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 14 Years

Inclusion criteria

Inclusion criteria: 1.Age =4 years old; 2.3 Relevant chief complaints of asthma-like symptoms such as repeated wheezing, coughing, shortness of breath, chest tightness, etc. within a month; 3.Guardians or children with decision-making ability (>10 years old) sign informed consent; 4.Children diagnosed or suspected of having asthma: According to the medical history of the past six months, those who meet one of the following criteria are diagnosed as asthma: (1)Anti-inflammatory treatment (such as inhalation of corticosteroids and/or anti-leukotriene drugs) for 4-8 weeks, increased forced expiratory volume per second (FEV1)>= 12%; (2)The rate of change of peak expiratory flow (continuous monitoring for 2 weeks) >= 13%. Suspected asthma: Participants were diagnosed with asthma without a lung function test before entering school.

Exclusion criteria

Exclusion criteria: 1.Children or caregivers of children have problems in expression, understanding, reading or writing; 2.Any other participants who are not suitable to participate in the project judged by investigators of this study, such as participants who cant be able to cooperate with pulmonary function test.

Design outcomes

Primary

MeasureTime frame
Accuracy;

Countries

China

Contacts

Public ContactLu Min

Children's hospital of Shanghai

lumin61@aliyun.com+86 13801939303

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026