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NCT07412119
Research on Disease Control and Mental Health Status of Adolescent Asthma Patients
trial testing Eligible participants will complete a battery of assessment questionnaires in Asthma (Diagnosis) in 460 participants. Not yet recruiting.
1 October 2027
Quick facts
| Lead sponsor | Beijing Children's Hospital |
|---|---|
| Status | Not yet recruiting |
| Study type | OBSERVATIONAL |
| Enrollment | 460 |
| Start date | 1 April 2026 |
| Primary completion | 1 October 2027 |
| Estimated completion | 1 December 2027 |
Drugs / interventions tested
- Eligible participants will complete a battery of assessment questionnaires
Conditions studied
- Asthma (Diagnosis) — all drugs for Asthma (Diagnosis) →
- Adolescent - Emotional Problem — all drugs for Adolescent - Emotional Problem →
Sponsor
Beijing Children's Hospital
Who can join
Adults 12 to 18, any sex, with Asthma (Diagnosis) or Adolescent - Emotional Problem. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07412119
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Beijing Children's Hospital trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07412119 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Beijing Children's Hospital
- Last refreshed: 17 February 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07412119.
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