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A medical research facing patients with COPD

Impacts of multifaced pharmaceutical intervention on prognosis of patients with chronic obstructive pulmonary disease —— A cluster RCT based on Cough and Wheeze pharmaceutical Clinic

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086943
Enrollment
Unknown
Registered
2024-07-15
Start date
2024-08-01
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Chronic obstructive pulmonary disease

Interventions

Intervention group:This study was based on the IMB model to construct a multi-faced pharmaceutical intervention based on digital means
control group:Usual pharmaceutical care

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Be 18 years of age or older; 2.Clinically diagnosed with chronic obstructive pulmonary disease (COPD) diagnosed by a physician with a severity of grade 2 to 4 according to the GOLD pulmonary function class, and an estimated FEV1<80% after inhalation of bronchodilators (previous pulmonary function test reports can be accepted as the basis for screening); 3.Patients who have been used inhalant incorrectly in practice; 4.Voluntarily participate in this clinical study and sign a written informed consent form;

Exclusion criteria

Exclusion criteria: 1.Unable to obtain informed consent from patients or family members; 2.During pregnancy; 3.Patients with terminal disease, malignant tumor, pulmonary tuberculosis, cardiopulmonary failure, etc., and patients unable to cooperate with the pulmonary function test due to disease status; 4.According to the doctor's judgment, there are cognitive and mental impairments, severe visual, auditory, and communication impairments, as well as other situations that affect the use of inhalers; 5.Difficulty in movement, limited mobility, or other reasons, it is expected that long-term follow-up cannot be completed; 6.Participation in other pharmaceutical intervention studies; 7.Other situations where the pharmacist determines that the research subject is unable to comply with the trial plan;

Design outcomes

Primary

MeasureTime frame
St George' s Respiratory Questionnaire, SGRQ;Medical cost;

Secondary

MeasureTime frame
Pulmonary function indicators;Annual incidence of acute exacerbation of chronic obstructive pulmonary disease;Test of Adherence to Inhalers, TAI;European Quality of Life-5 Dimensions-5 Level Version Scale;Pharmaceutical Service Questionnaire;

Countries

China

Contacts

Public ContactLihong Liu

China-Japan Friendship Hospital

hongllh@126.com+86 10 85231788

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026