Skip to content

Therapy adherence, errors in inhalation technique and usability of real-time feedback with the RS01X* in COPD patients: a pilot study

Therapy adherence, errors in inhalation technique and usability of real-time feedback with the RS01X* in COPD patients: a pilot study - RS01X* in COPD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON57743
Enrollment
10
Registered
2024-02-15
Start date
2024-02-26
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

COPD

Interventions

The patients continue their usual care (e.g., scheduled visits to their pulmonologists) during the study. They receive feedback on their inhalation errors and therapy adherence.

Sponsors

Medisch Spectrum Twente
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients: - A clinical diagnosis of COPD - >= 40 years of age - Using the RS01/Breezhaler - Able to understand and read the Dutch language - In possession of a smart mobile device and WiFi at home Health care providers: Pulmonary physician or Pulmonary nurse

Exclusion criteria

Exclusion criteria: Patients: - Participation in another clinical trial involving eHealth - Presence of disease, impairing use of an inhaler (e.g., Parkinson*s disease, rheumatism)

Design outcomes

Primary

MeasureTime frame
The main study endpoints are: 1) the weekly therapy adherence to the medication taken once daily with the RS01X*, 2) the type and 3) number of errors in inhalation technique during the four weeks patients will use the RS01X* at home, and 4) the type and 5) number of errors made at the start and the end of the study during the observation of the inhalation technique.

Secondary

MeasureTime frame
Secondary endpoints are: 1) the usability of the application for patients, 2) the ease of linking the RS01X* with the application and 3) the usability of the HCP portal.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Aug 9, 2026