CClinicalTrials.gg
Status unknownNCT02649803Updated Aug 15, 2016

Pediatric Asthma Control Under Community Management Model in China

An interventional study of asthma APP in Asthma, sponsored by Shanghai Children's Medical Center. Status unknown at 1 site in China. Open to participants aged 1 Month to 18 Years. Per ClinicalTrials.gov, last updated 2016-08-15.

Sponsored by Shanghai Children's Medical Center · Not applicable, Interventional, and Health services research

The sponsor has not verified this record recently (last verified Aug 2016), so the status shown — last known as Enrolling by invitation — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
800
Allocation
Not applicable
Ages
1 Month to 18 Years
Sex
All
01

Study summary

The purpose of this study is to learn the pediatric asthma control status under community management model. To learn the differences of pediatric asthma control status when subjects assigned to community hospitals or Shanghai Childrens Medical Centre. To learn the treatment adherence and the frequency of asthma attack under community management model.

Read the detailed description

Subjects diagnosed as pediatric asthma at Shanghai Children's Medical Center will be consecutively screened and eligible patients will be recruited. For each enrolled patient, basic information as well as baseline medical condition will be collected by the investigators. Asthma medicine will be prescribed by the investigator according to patient's asthma severity and control status. The subject will be assigned to the nearest community hospital or Shanghai Children's Medical Center, whichever is nearer to the subject's home, for their future onsite visits. The patient's caregiver will be instructed to install the study-specified application program (APP) at their smart phone and learn how to use this APP.

During the study, patients will receive 12 months standard treatment, prescribed by the investigators according to "Guideline for the diagnosis and optimal management of asthma in children".

The patients' caregiver will be prompted to fill out an asthma control questionnaire and asthma control test via their smart phone APP every month.

Patients will be requested to visit prearranged community hospitals at month 1, 3, 6, 9 and arrange their last visit back to Shanghai Children's Medical Center at month 12. During each onsite visit, asthma-related information will be collected by the investigators.

Meanwhile, subjects will receive PEF (>5 years old) and FENO tests for evaluation of lung function and inflammation level. After comprehensive assessment of the patient's symptom control, risk factors, occurrence of exacerbations, and practical issues (cost, ability to use the device, and adherence), the investigator will make the decision on whether stepping up or stepping down asthma treatment.

This study ends up without follow-up.

02

Conditions studied

  • Asthma

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Keywords

  • pediatric
  • asthma control
  • community
03

In context

Asthma

3,921 studies on the registry are indexed under Asthma; 507 are open to participants now.

This study's planned enrollment of 800 is above the median of 83 across 2,752 interventional studies indexed under Asthma.

Browse Asthma studies →

Lead sponsor

Shanghai Children's Medical Center is the lead sponsor of 37 studies on the registry; 14 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Month to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Out-patient, female or male, aged less than 18 years old
  2. Diagnosed as asthma according to "Guideline for the diagnosis and optimal management of asthma in children"
  3. Consent should be obtained by subjects' guardian
  4. The subjects or subjects' caregiver must have a smart phone at their disposal

Exclusion criteria

Exclusion Criteria:

  1. Presenting with differential diagnosis of asthma such as congenital heart disease, gastro-oesophageal reflux, bronchopulmonary dysplasis, bronchiolitis obliterans, etc.
  2. Allergy to any inhaler cortical steroid
  3. Subject with other diseases that may interfere the study results judged by the investigators.
  4. Participation in any analogous clinical study within 3 months
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
800 participants (estimated)

Study arms

  • Other
    community hospital

    During the study, subjects who diagnosed as asthma according to "Guideline for the diagnosis and optimal management of asthma in children" will be assigned to the nearest community hospital or Shanghai Children's Medical Center, and receive 12 months standard treatment, prescribed by the investigators according to "Guideline for the diagnosis and optimal management of asthma in children". The patient's caregiver will be instructed to install asthma APP at their smart phone to follow up.

    Behavioral: asthma APP

Interventions

  • Behavioralasthma APP

    Subjects diagnosed as pediatric asthma at Shanghai Children's Medical Center will be consecutively screened and eligible patients will be recruited (enrolment visit, V1). The subject will be assigned to the nearest community hospital or Shanghai Children's Medical Center, whichever is nearer to the subject's home, for their future onsite visits (V2-V5). The patient's caregiver will be instructed to install the asthma APP at their smart phone and learn how to use this APP.

    Also known as: study-specified asthma application program

06

What researchers measure

Primary outcomes

  1. asthma control questionnaire

    The patients' caregiver will be prompted to fill out an asthma control questionnaire via their smart phone APP every month. This questionnaire contains questions regarding renewal of prescription, adherence, control status, asthma attack and health economic information.

    Time frame: 1 year

Secondary outcomes

  1. asthma control test

    caregiver will also be asked to fill out an asthma control test (for patients 12 years or older) , childhood asthma control test (for patients aged 5-12) , or GINA assessment of asthma control in children 5 years and younger.

    Time frame: 1 year

Other outcomes

  1. FENO tests

    Subjects will receive FENO(Fractional exhaled nitric oxide, parts per billion, ppb) tests for evaluation of lung inflammation level.

    Time frame: 1 year

  2. PEF (>5 years old)

    Subjects(older than 5 years) will receive PEF (Peak expiratory flow, L/min) tests for evaluation of lung function.

    Time frame: 1 year

07

Study locations

1 site
  • Shanghai children's medical center
    Shanghai, Shanghai 200127, China
08

References and documents

Publications

  • Zhang J, Zhao L, Zhao D, Chen Z, Li S, Zhang H, Zhang L, Yuan S, Tang M, Wu Y, Zhong W, Xu J, Zhao LX, Liu SY, Hong J, Yin Y. Reliability and validity of the Chinese version of the Test for Respiratory and Asthma Control in Kids (TRACK) in preschool children with asthma: a prospective validation study. BMJ Open. 2019 Aug 26;9(8):e025378. doi: 10.1136/bmjopen-2018-025378. Erratum In: BMJ Open. 2019 Sep 13;9(9):e025378corr1. doi: 10.1136/bmjopen-2018-025378corr1. PubMed 31455696 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 15, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02649803
Lead sponsor
Shanghai Children's Medical Center
Responsible party
Sponsor
First posted
Jan 7, 2016
Start date
Mar 2016
Primary completion
Jan 2018 (estimated)
Completion
Jun 2019 (estimated)
Last update
Aug 15, 2016

Study contacts

Yong Yin, PhD
principal investigator · Shanghai Children's Medical Center

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2016. You cannot join it, but the record below documents what was studied.

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