Usability of the Smart Hallway System in Clinical Setting

Sponsor
University Rehabilitation Institute, Republic of Slovenia
Study ID
NCT06645054
Status
Recruiting
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Conditions

  • Amputation
  • Gait Disorders, Neurologic

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Standard rehabilitation — BEHAVIORAL
    The patients will receive standard rehabilitation that comprises assessment performed by a multidisciplinary team (physical-and-rehabilitation-medicine specialist physician, physiotherapist, occupational therapist, psychologist, social worker, prosthetics-and-orthotics engineer).
  • Lower-limb prosthesis — DEVICE
    The patients from the LLL group will be fitted with an appropriate lower-limb prosthesis.
  • Lower-limb orthosis — DEVICE
    The patients from the LLO group will be fitted with an appropriate lower-limb orthosis.

Study Details

The aim of the study is to examine suitability of data and processed reports acquired from the Smart Hallway system for clinical settings in terms of user acceptability and accuracy for use in clinical practice.

Key Dates

First listed
Oct 16, 2024
Start date
Mar 24, 2024
Status verified
Jun 2026
Primary completion
Sep 30, 2026
Completion
Sep 30, 2026

Study Design

Enrollment
100 participants (estimated)

Arms

  • Arm: LLL
    Rehabilitation patients with lower limb loss
  • Arm: LLO
    Rehabilitation patients fitted with a lower limb orthosis

Primary Outcome Measure

Smart Hallway [ Time Frame: Upon admission to rehabilitation ]

Central Contacts

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