RESilience in Hip frActure Patients measured with the Eforto(R) measurement & monitoring system

Completed

• Conditions: geriatrische syndromen; veroudering; ageing; geriatric syndromes; hip fracture

• Registration Number: NL-OMON49900
• Lead Sponsor: Ziekenhuisgroep Twente

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 22 July 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 110

Inclusion Criteria

At ZGT,110 patients admitted to the Geriatric Fracture Center will be
recruited. Inclusion criteria are: 70+ years, being surgically treated for a
hip fracture, being admitted to the geriatrics geriatric fracture center for at
least 48 hours, cognitively able to provide informed consent.

Exclusion Criteria

Being judged by their treating physician as unable to participate.
Being identified as a patient with palliative treatment regimen at the time of
inclusion.
Being physically unable to perform the hand grip measurements.
Severe cognitive impairment.
Unable to communicate sufficiently in Dutch.
Deafness.
A pathological or periprosthetic fracture.
A total hip replacement.
Contact isolation.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>Primary exposure:<br /><br>• muscle fatiguability combined with self-perceived fatigue, measured daily<br /><br>using the eforto® system.<br /><br><br /><br>Primary outcomes:<br /><br>• delayed length of stay due to a complication</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary outcome measures of recovery:<br /><br>• ADL functionality<br /><br>• Mobility<br /><br>• Mortality<br /><br>• Wellbeing<br /><br>• Complications<br /><br>• Readmissions<br /><br>• Discharge destination<br /><br>• Frailty</p><br>