Research on Disease Control and Mental Health Status of Adolescent Asthma Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Eligible participants will complete a battery of assessment questionnaires.
- Who it may be relevant to
- Registry conditions: Asthma (Diagnosis), Adolescent - Emotional Problem. Basic parameters: 12 years — 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
Background: Currently in China, adolescent asthma care is characterized by both undertreatment and overtreatment. Patients in this age group may exhibit negative emotions toward disease treatment and long-term control. Insufficient disease knowledge, irregular lifestyle habits, and negative attitudes toward the disease can all reduce medication adherence, affect disease control outcomes, and thereby increase the risk of severe chronic respiratory conditions and disease burden in adulthood. Objectives: To assess disease control status in adolescent asthma patients, evaluate the psychological well-being of patients and their family members, and understand patients' self-management skills and readiness for transition to adulthood. Procedures: Eligible participants will complete a series of assessment questionnaires through the Youran Huxi mobile application, including questionnaires on asthma control, physical activity, psychological health, self-management behaviors, and transition readiness. The study period is 12 months; the baseline assessment involves one-time completion of written questionnaires with no interim follow-up visits. The study does not intervene in clinical diagnosis or treatment decisions.
Interventions
- Other Eligible participants will complete a battery of assessment questionnaires
Data on demographic characteristics, asthma control status, anxiety and depression symptoms, self-management self-efficacy, and transition readiness were collected via standardized questionnaires
Primary outcome measures
- anxiety state [Time frame: From the diagnosis of asthma to the end of this survey at 12month]
- depression state [Time frame: From the diagnosis of asthma to the end of this survey at 12month]
Secondary outcome measures (2)
- disease control level [Time frame: From the 4 weeks prior to enrollment to the end of this survey at 12month]
- Adolescent readiness for the transition period of asthma [Time frame: From the diagnosis of asthma to the end of this survey at 12month]
Eligibility criteria
Inclusion criteria
- Meet the asthma diagnostic criteria of GINA 2025
- Age 12 to 18 years old
- The parents and the child patient agreed and filled out the questionnaire completely.
Exclusion criteria
- Children with other respiratory diseases such as bronchiectasis, bronchiolitis, cystic fibrosis and pneumonia
- Combined with chronic diseases of other systems
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07412119 · Adolescent Asthma 001