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Rehabilitation after hip fractures in elderly

COMplex Fracture Orthopedic Rehabilitation - Real-time visual biofeedback on weight bearing versus standard training methods in the treatment of proximal femur fractures in elderly: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28693
Enrollment
186
Registered
2017-10-31
Start date
2017-03-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Proximal femur fracture

Interventions

Participants in the intervention group receive, in addition to the standard institutional protocol, real-time, visual feedback about weight bearing during the 30-meter walk. The physical therapist has

Sponsors

UMC Utrecht
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. The participants rehabilitate from a proximal femur fracture following low energy trauma (e.g. fall from standing position). 2. The participants have a prescribed unrestricted weight bearing after (surgical) treatment of their fracture. 3. The participants have an expected clinical rehabilitation duration of ≥2 weeks. 4. The participants are ≥60 years. 5. The participants have a bodyweight ≤120 kilogram.

Exclusion criteria

Exclusion criteria: 1. People with cognitive impairment, defined as a score <18 on the Mini-Mental State Examination. 2. People who are readmitted to the hospital within two weeks after study participation, for example for infectious complications. 3. People with co-morbidities that affected gait significantly prior to the proximal femur fracture.

Design outcomes

Primary

MeasureTime frame
The primary outcome measures are the SensiStep parameters maximum peak load (in %bodyweight) and step duration (in seconds), which will be correlated with the discharge date from the rehabilitation center. It will be investigated if higher maximum peak loads and shorter step durations correlate with the end of rehabilitation (i.e. discharge date).

Secondary

MeasureTime frame
Secondary outcomes include other spatio-temporal gait parameters and validated clinical tests, including the Elderly Mobility Scale (EMS), the Functional Ambulation Categories (FAC) and the Visual Analogue Scale (VAS). Spatio-temporal gait parameters measured by the SensiStep will be correlated to the mobility scores (e.g. EMS, FAC and VAS).

Contacts

Public ContactM. Raaben

Department of Surgery, UMC Utrecht, Suite G04.228

M.Raaben-2@umcutrecht.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)