The Impact of Anxiety/Depression on the Efficacy of Asthma Control Drugs and the Construction of a Predictive Model for the Risk of Acute Asthma Attacks

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age14+
SponsorXiangya Hospital of Central South University

About this trial

The goal of this clinical trial is to explore the impact of anxiety/depression on the efficacy of asthma controller medications and to develop a risk prediction model for asthma acute exacerbations in patients with asthma. It will also analyze the association between anxiety/depression severity and asthma severity. The main questions it aims to answer are:

Does anxiety/depression affect the therapeutic effect of asthma controller medications (e.g., asthma control level)? Can a reliable risk prediction model for asthma acute exacerbations be established based on anxiety/depression and other relevant factors? Researchers will conduct a prospective observational study to collect and analyze data from participants, without additional interventions beyond standard clinical care, to explore the above research questions.

Participants will:

Complete baseline assessments, including demographic information collection, medical history review, lung function tests, anxiety/depression evaluations (via GAD-7 and PHQ-9 scales), and provide biological samples (induced sputum, feces, blood) Undergo follow-up visits at 3, 6, 12, 18, and 24 months after baseline Report asthma symptoms, acute exacerbation events, and cooperate with required clinical checkups during follow-up

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of asthma according to the Global Initiative for Asthma (GINA) 2024 criteria.

Male or female patients aged 14 years or older.

Complete clinical data available.

Newly diagnosed asthma or stable asthma.

Disqualifiers

History of major lung diseases other than asthma, congestive heart failure, cor pulmonale, or recent cardiac or thoracic surgery.

Incomplete medical records.

Cognitive impairment or inability to complete psychological scale assessments.

Clinically diagnosed acute or chronic mental disorders, such as bipolar disorder or schizophrenia.

Trial population

The study population consists of asthma patients who meet all inclusion criteria of our research protocol. If a patient meets any of the exclusion criteria, they will not be included in the study scope.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • No intervention measures

    Other intervention

    No intervention measures

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Acute asthma attack

Number of acute asthma attacks in patients during follow-up period

Time frame
1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

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