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Effect of a standard medication device demonstration system on patients’ skill scores in a Chinese pharmacy

Effect of a standard medication device demonstration system on patients’ skill scores in a Chinese pharmacy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043592
Enrollment
Unknown
Registered
2021-02-23
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-06-14

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

Conditions

asthma/COPD/diabetes

Interventions

turbuhaler-standard education:turbuhaler-standard education
discus-standard education:discus-standard education
Tiotropium-standard education:Tiotropium-standard education
turbuhaler-reading group:turbuhaler-reading
discus-reading group:discus-reading
Tiotropium-reading group:Tiotropium-reading
nasal-spray standard education:nasal-spray standard education
Semi-quantitative respiratory device standardization education group:Semi-quantitative respiratory device standardization education
Semi-quantitative respiratory device-reading group:Semi-quantitative respiratory device-reading
nasal-spray-reading group:nasal-spray-reading
insulin pen standard education group:insulin pen standard education
insulin pen-reading group:insulin pen-reading
Turbular-uneducated group:none
discus-uneducated:none
Tiotropium-uneducated:none
Semi-quantitative respiratory device uneducated group:none
nasal-spray uneducated group:none
insulin-pen uneducated group:none

Sponsors

the Second Affiliated Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged >18 years old; 2. Diagnosis of "allergic rhinitis" or "asthma" or "COPD" or "diabetes" and first use of "insulin pen" or "nasal spray" or "tiotropium bromide powder aerosol" or "discus" or "dubo" or "semi-quantitative inhalation device".

Exclusion criteria

Exclusion criteria: 1. Tumors; 2. Pregnant or lactating women; 3. Other disorders that affect memory or mood.

Design outcomes

Primary

MeasureTime frame
operation correctness;

Secondary

MeasureTime frame
edcuation duration;

Countries

China

Contacts

Public ContactHuang Yuwen

the Second Affiliated Hospital of Zhejiang University School of Medicine

1615693362@qq.com+86 13588809205

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026