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Recruiting NCT04137835

Non-invasive Evaluation of Upper and Lower Body Function With Showmotion

No phase Interventional Osteoarthritis, Hip Osteoarthritis, Knee Osteoarthritis, Spine

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Showmotion.
Who it may be relevant to
Registry conditions: Osteoarthritis, Hip, Osteoarthritis, Knee, Osteoarthritis, Spine. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

It is very important to understand joint and body kinematics and muscles activity in clinical settings, which is relevant to identify issues related to the spine, the upper and lower limbs due to injury. In this study, the investigators will use an innovative platform, Showmotion to establish baseline of shoulder, hip, knee and spine kinematics and muscles activity from 60 healthy volunteers.

Detailed description

Upper and lower body functional evaluation is challenging and relevant to identify the issues related to injury. Current technique still stays at visual observation.

Showmotion™ (NCS Lab, Carpi, Italy) is an innovative platform that provides a comprehensive analysis to monitor motion patterns of the whole body using WISE sensors, proprietary wireless inertial and magnetic units (MIMU) developed by NCS Lab (Italy).

Using the data acquired from MIMU and validated protocols for upper and lower limbs, Showmotion is able to measure, objectify and store three dimensional kinematic variables highlighting underlying information and allowing an in-depth analysis of the movement in real time.

Compared to the classic motion analysis performed with cameras in special research laboratories, the Showmotion™ technology allows the user to analyze the movements of the subjects in any place, quickly, and without the need to a long process of data analysis.

Interventions

  • Device Showmotion
    Each healthy volunteers will wear sensors at the interested joint and do the measurement.

Primary outcome measures

  • range of motion [Time frame: 1 HOUR]

Eligibility criteria

Inclusion criteria

  • Healthy people (without musculoskeletal pathologies of the joint of interest)
  • Age > 18, <65
  • Volunteers given written informed consent
  • Ability to understand and execute instructions at all stages of the procedure

Exclusion criteria

  • Age > 65, < 18
  • Active infections
  • Surgery at joint of interest
  • BMI (Body Mass Index) >30 kg/m2
  • Pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Supportive care

Study locations

United States · 1 center
  • University of Colorado Anschutz Medical Campus — Aurora

Identifiers

NCT: NCT04137835 · 19-2272

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗