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Can a sensor device boost brain and body recovery after hip fracture?

NCT ID NCT07392515

Symptom relief Sponsor: C.O.T. Cure Ortopediche Traumatologiche S.p.A. Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study is testing whether adding a sensor-based device to standard physical therapy can improve both thinking and movement in frail older adults recovering from hip fracture surgery. Thirty participants aged 65-89 will use the device for part of their rehab. The goal is to see if this tech-enhanced approach leads to better cognitive and motor outcomes than conventional therapy alone.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
sensor-based rehabilitation device
What this could lead to
If successful, this approach could offer a more effective way to help elderly patients recover both movement and thinking after a hip fracture.
What could go wrong
This is a small, early-stage study with only 30 participants, so results may not apply broadly. The device is an add-on, not a replacement for standard care.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2026

Expected to finish

Jul 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

65 to 89 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age between 65 and 89 years * Patients who have undergone one of the following surgical treatments specifically for proximal femur fracture including Total hip arthroplasty (total hip replacement), Partial hip arthroplasty (hemiarthroplasty), Intramedullary nailing * Time since surgery not exceeding 15 days * Clinical stability * Patients admitted to the rehabilitation wards of the centers involved in the study and therefore eligible for rehabilitative therapy. Exclusion Criteria: * Age \> 90 years * Age \< 65 years * Refusal to sign the informed consent form * Behavioral or cognitive disorders limiting compliance with the rehabilitative treatment * Presence of mechanical instability of the implanted surgical device * Clinical instability (e.g., sepsis, severe anemia, cardiorespiratory failure) or pre-existing comorbidities affecting ambulation (neurological diseases or chronic pre-existing disabilities) * Concomitant presence of other fractures that prevent the possibility of carrying out a rehabilitative treatment * Severe visual impairments not correctable with lenses that prevent the patient from performing the treatment using digital tools * Pre-existing motor disability prior to the femur fracture due to other systemic diseases (e.g., advanced-stage neurodegenerative diseases, severe heart failure) * Conditions contraindicating the use of sensors (pacemaker, epilepsy, skin lesions, open wounds, and severe allergies in areas of contact with the devices).

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Conditions

The condition(s) this trial relates to.

bone fracture Femoral Fractures hip fracture

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Fracture femur Hip arthroplasty replacement Total hip arthroplasty (THA)

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • COT - Cure Ortopediche Traumatologiche

    RECRUITING

    Messina, Italy, 98124, Italy

  • Fondazione Don Carlo Gnocchi - Centro Santa Maria della Provvidenza

    NOT_YET_RECRUITING

    Roma, Italy, 00166, Italy

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