Development of a remote, patient-centric, clinical trial model using digital healthcare technology
Recruiting
- Conditions
- ALSAmyotrofic Lateral Sclerosis10029317
- Registration Number
- NL-OMON53924
- Lead Sponsor
- niversitair Medisch Centrum Utrecht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
1. Diagnosis with ALS according to the Gold Coast criteria
2. ENCALS risk profile ranging between -6 and -2
3. 18 years or older
4. Able to provide informed consent
Exclusion Criteria
Fulfilling the criteria for respiratory insufficiency (non-invasive ventilation
use >22 hours per day for 10 consecutive days or having a tracheostomy)
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Patient adherence defined as the number of completed measurements divided by<br /><br>the total number of assessments. Adherence will be assessed per parameter. </p><br>
- Secondary Outcome Measures
Name Time Method