Feasibility study: introcution of warables in hip fracture patients (75+)

Not Applicable

Completed

• Conditions: hip fracture; 10017322

• Registration Number: NL-OMON26551
• Lead Sponsor: Reinier de Graaf ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 68

Inclusion Criteria

- Patients who are admitted due to a hip fracture \ - 75 years and older

Exclusion Criteria

- Patients who refuse to wear the wearable or whose medical and nursing team object to the course of events - Patients at others wards but the GTU - Patients who are unable or unwilling to grant permission in the deferred consent setting - No more than 8 patients in parallel can be accommodated in the study

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>There are 3 end points: 1) The percentage of the entire population of hip fracture patients (75+) enrolled in the study (&gt; 70%); 2) Patient satisfaction with the wearable (= 70%); 3) Successful logistics process that is tested by storing the wearable data per included patient (&gt; 80%).</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>none</p><br>