Trials / Completed
CompletedNCT04729920
Home Use of Mechanical Insufflation/Exsufflation Devices in Neuromuscular Diseases
Predictors of Home Use of Mechanical Insufflation/Exsufflation Devices in Neuromuscular Patients: a Cross-sectional Study
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 43 (actual)
- Sponsor
- Centre Hospitalier Universitaire Vaudois · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
With this cross-sectional study of adult subjects with neuromuscular disease in the French-speaking part of Switzerland, we aim to explore MI-E adherence using self-report questionnaires and device data in order to identify the factors that influence the pattern of MI-E use and satisfaction with the treatment. Determining potential barriers to regular long-term home use of MI-E could help in identifying the patients who would benefit most from this therapy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Mechanical insufflation/exsufflation device (MI-E) | download of device (MI-E) data and self-reported satisfaction with the device |
Timeline
- Start date
- 2019-09-15
- Primary completion
- 2020-05-01
- Completion
- 2020-05-01
- First posted
- 2021-01-29
- Last updated
- 2021-02-03
Locations
1 site across 1 country: Switzerland
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04729920. Inclusion in this directory is not an endorsement.