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Effect of Clinical Pharmacist-Led Fine-Grained Pharmaceutical Care on Inhalation Technique, Medication Adherence, and Clinical Outcomes in Patients with Chronic Obstructive Pulmonary Disease: A Prospective Cohort Study

Effect of a Pharmacist-Led Inhaler Management Program on Technique and Adherence in COPD: A Prospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114050
Enrollment
Unknown
Registered
2025-12-05
Start date
2025-12-08
Completion date
Unknown
Last updated
2025-12-08

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:The intervention comprised two core components delivered by clinical pharmacists: (1) Evidence-based prescription optimization: Pharmacists provided prescribing physicians with GOLD
Control Group:The control group received usual pharmaceutical care provided by outpatient pharmacists.

Sponsors

Fengdu County People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. A clinical diagnosis of Chronic Obstructive Pulmonary Disease (COPD), established in accordance with both the 2025 Global Initiative for Chronic Obstructive Lung Disease (GOLD) report and the 2021 Chinese Thoracic Society guidelines. 2. Age 60–80 years, with a clinically documented COPD duration exceeding one month and verified issues with inhaler selection or technique. 3. Possession of adequate literacy and cognitive ability to provide written informed consent, successfully complete all components of the 6-month educational intervention, and participate in scheduled follow-up evaluations. 4. Physical ability, as confirmed by baseline assessment, to handle and operate inhaler devices independently.

Exclusion criteria

Exclusion criteria: 1. Impaired consciousness, or significant cognitive, linguistic, or communicative deficits that would invalidate informed consent or preclude meaningful participation. 2. Severe visual, auditory, or motor impairments that would substantially interfere with performing study-specific procedures. 3.Demonstrated inability or unwillingness to commit to and comply with the complete 6-month structured training and follow-up protocol. 4.Presence of multiple uncontrolled systemic comorbidities, active malignancy (except localized non-melanoma skin cancer), or clinically significant dysfunction of major organ systems. 5. Concurrent active respiratory pathologies that could interfere with pulmonary function test interpretation or confound COPD assessment. 6.Documented history of non-adherence to medical care, anticipated poor protocol compliance, or explicit refusal to participate in the pharmacist-led intervention. 7.Active or inadequately controlled psychiatric disorders that, in the investigator’s judgment, could compromise decision-making capacity, adherence, or safety.

Design outcomes

Primary

MeasureTime frame
The primary outcome was the rate of improper inhaler use, including technique errors and inappropriate device selection.;

Secondary

MeasureTime frame
Medication adherence, as assessed by the Morisky Medication Adherence Scale (MMAS), with scores ranging from 0 to 8.;The mean CAT score;Number of moderate-to-severe acute exacerbations during the study period.;Lung function status;

Countries

China

Contacts

Public ContactHuabo Wei

Fengdu County People's Hospital

weihuabojack@sina.com+86 159 7897 3031

Outcome results

None listed

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