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Wearable Technology in Shoulder Range of Motion

NCT03195751 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2017-10-06

No results posted yet for this study

Summary

The scope of the research is to determine if a motion-based software development kit may substitute for a manual goniometer. If so, this opens up the possibility of remote telemonitoring of upper extremities patients.

Conditions

  • Normal Upper Extremity

Interventions

DEVICE

Software development kit measurements

This proprietary SDK (FocusMotion) processes user motions recorded by the hardware (accelerometer, gyroscope, magnometer). As data is collected, the software development kit (SDK) classifies the motion as repetitive or non-repetitive, and repetitive motions are further analyzed. As the user completes a movement, the SDK tracks the number of repetitions performed, technique, and rest time. The SDK can provide real-time feedback to the user regarding their form by comparing the movement to a template of an ideal motion for that particular action. The SDK is compatible with any operating system, phone, or wearable device, providing seamless integration with pre-existing technologies.

DEVICE

Manual Goniometer Measurements

A manual goniometer was used to measure the range of motion of the shoulder.

Sponsors & Collaborators

  • The Cleveland Clinic

    lead OTHER

Principal Investigators

  • Joseph P Iannotti, MD PhD · The Cleveland Clinic

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-09-13
Primary Completion
2017-09-23
Completion
2017-09-23

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03195751 on ClinicalTrials.gov