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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04137835
Enrollment
60
Registered
2019-10-24
Start date
2021-06-01
Completion date
2025-12-01
Last updated
2024-10-04

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

Conditions

Osteoarthritis, Hip, Osteoarthritis, Knee, Osteoarthritis, Spine

Keywords

osteoarthritis

Brief summary

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

DEVICEShowmotion

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

Sponsors

University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
range of motion1 HOURmeasure, track, follow, compare the range of motion of anatomical articulations (such as shoulder and elbow for upper limb and hip and knee for lower limb) during movement, taking into account all clinical constraints related to easiness, quickness and portability.

Countries

United States

Contacts

Primary ContactCLAIRE COFER, BS
CLAIRE.COFER@CUANSCHUTZ.EDU303-724-1588

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026