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A Study on the Impact of Pharmacist-Led Tier-3 - Primary Care Collaborative Management on Inhalation Technique and Medication Adherence in COPD Patients: A Prospective, Multicenter, Randomized Controlled Trial

A Study on the Impact of Pharmacist-Led Tier-3 - Primary Care Collaborative Management on Inhalation Technique and Medication Adherence in COPD Patients: A Prospective, Multicenter, Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113028
Enrollment
Unknown
Registered
2025-11-24
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

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:A three-tiered hospital-community collaboration pharmacist intervention model based on risk stratification
Control group:Routine Management (Basic Inhalation Guidance + Outpatient Follow-up)

Sponsors

Drum Tower Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 40 years; 2. Meets the diagnostic criteria for COPD according to the "Chinese Guidelines for the Diagnosis and Treatment of Chronic Obstructive Pulmonary Disease (2021 Edition)" or the GOLD 2025 guidelines; 3. Condition is clinically stable (no acute exacerbations in the past 4 weeks); 4. Currently using at least one inhalation device for maintenance therapy (e.g., inhaled bronchodilators or inhaled corticosteroids); 5. At the start of the study, assessed to have improper inhaler use or insufficient medication adherence (e.g., incorrect inhalation technique identified at baseline examination, or poor adherence scale scores); 6. Possesses basic communication skills and can cooperate with questionnaires and follow-ups; 7. Voluntarily participates in the study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with severe comorbidities and an expected survival of less than 1 year (such as advanced malignant tumors, end-stage heart failure, etc.); 2. Patients with severe cognitive impairment or mental illness that prevents cooperation with the intervention; 3. Patients who have received systematic professional training on inhalation devices or pharmaceutical management guidance within the past year prior to the study (to avoid excessively high baseline levels being affected); 4. Other situations deemed unsuitable for inclusion in the study by the researchers.

Design outcomes

Primary

MeasureTime frame
Inhalation device usage accuracy rate;

Secondary

MeasureTime frame
Adverse Drug Reactions (ADRs) and Serious Adverse Events (SAEs);Test of Adherence to Inhalers;

Countries

China

Contacts

Public ContactQiuhui Wu

Nanjing University Medical School Affiliated Drum Tower Hospital

asdfghjklpoiu@2321.com+86 25 1234567

Outcome results

None listed

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