Actively Recruiting
Feasibility of Integrating Local Vibration Into Rehabilitation of Elderly Patients After Hip Fracture
Led by Hospices Civils de Lyon · Updated on 2026-02-09
25
Participants Needed
1
Research Sites
56 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Fractures of the upper end of the femur in elderly patients are the 2nd most common fracture. A fracture leads to a syndrome of psychomotor maladjustment, encouraged by pain and aggravated by hospitalisation. In 2014, 50,000 women and 16,000 men suffered this type of fracture every year. The consequences are serious, with a one-year mortality rate of 20 to 24% and an institutionalisation rate of 25%. In 2015, the direct cost of hip fracture in France was estimated at around €1 billion. In line with the recommendations of the National Institute for Health and Care Excellence (NICE) and the results of meta-analyses, it is recommended that, in the absence of surgical or medical contraindications, patients should be assessed within 24 hours of hip fracture surgery, with a view to initiating early mobilisation and multidisciplinary rehabilitation. It has been shown in healthy subjects that prolonged application of localised vibrations optimises nerve capacity, leading to an increase in maximum voluntary force. For population of frail elderly post-operative patients, this localised vibration technique could accelerate and improve functional recovery, particularly in terms of muscle strength, joint mobility and pain. A reduction in muscle loss is hoped for, with benefits in terms of tolerance compared with neurostimulation. As part of the implementation of the above-mentioned recommendations, the investigators wish to assess the quality of the integration of this technique, already in use in the department on an ad hoc basis, into the organisation of the department and of the patient's care pathway as a complement to the rehabilitation protocols, by identifying the obstacles and facilitating factors. The study will also provide the first estimates of the effect on muscle recovery. The investigator hypothesise that this local vibration protocol can be integrated into the rehabilitation department's work schedule and into the patient's care pathway, and that it will be acceptable to both the patient and the nursing staff.
CONDITIONS
Official Title
Feasibility of Integrating Local Vibration Into Rehabilitation of Elderly Patients After Hip Fracture
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 75 or over who have undergone surgery for a fracture of the upper end of the femur
- Hospitalised in the SMR department no later than 14 days after their operation
- Resource Iso Group greater than or equal to 3 on the Aggir scale
- Patient capable of consenting who has signed a consent form or, if unable to consent, has a trusted person, family member, or close relative who has signed consent within 2 days
- For patients under guardianship, guardian's consent is required; for those under curatorship, patient signs consent in presence of curator within 2 days
- Affiliated to a social security scheme
You will not qualify if you...
- Persons deprived of their liberty by a judicial or administrative decision
- Individuals with severe psycho-behavioral disorders such as major psychiatric or neurocognitive disorders
- Persons admitted to a health or social establishment for non-research purposes
- Contraindications to electrical stimulation including having active devices such as pacemakers, defibrillators, insulin pumps, neurostimulators
- Patients with phlebitis or risk of thrombosis
- Epileptic patients
- Patients with fragile skin or open wounds on the lower limbs
- Participants in another interventional study with an exclusion period still in progress at pre-inclusion
AI-Screening
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Trial Site Locations
Total: 1 location
1
HOPITAL PIERRE GARRAUD - Service de MEDECINE GERIATRIQUE
Lyon, France, 69005
Actively Recruiting
Research Team
A
Alexandre MENDIBIL, MD
CONTACT
S
Stéphanie TRIPOZ DIT MASSON
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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