Pilot study to test usability of wearable biosensor in elderly with non-specific complaints
Completed
- Conditions
- elderly with non-specific complaints
- Registration Number
- NL-OMON20672
- Lead Sponsor
- Philips Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
Group 1: Optimal triage in the pre-hospital setting
•Age ≥ 65 years;
Exclusion Criteria
Group 1: Optimal triage in the pre-hospital setting
•Patients with positive anamnesis and/or medical examination for specific complaints;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the successful usage of the wearable biosensor with the smartphone app (i.e. patient feedback, caregiver feedback, raw device data, technical operational data),
- Secondary Outcome Measures
Name Time Method The frailty index