Onderzoek naar gebruiksgemak van, voorkeur voor, en tevredenheid met twee verschillende inhalatoren bij patiënten met astma of COPD.
- Conditions
- asthmaastmaCOPDchronische bronchitislongemfyseem
- Registration Number
- NL-OMON21792
- Lead Sponsor
- Medisch Spectrum Twente, Enschede
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 110
Inclusion Criteria
1. Adult male or female patients aged > 40 with stable COPD or asthma;
2. Patients have to be naïve to the study inhalers, Accuhaler/Diskus and Elpenhaler for at least 1 year;
Exclusion Criteria
1. Patients currently participating in another randomised clinical trial;
2. Patients with body malformations or diseases affecting coordination and/or motor system;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percentage of patients doing at least 1 critical error using each device after reading the insert.
- Secondary Outcome Measures
Name Time Method 1. Percentage of patients doing at least 1 critical error using each device after the first instruction by the trainer;<br /><br>2. Number of instructions needed;<br /><br>3. Overall satisfaction with the device;<br /><br>4. The percentage of patients who prefer Accuhaler/Diskus.