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Limited Market Release - MotionSense Clinical Use Evaluation

NCT05091918 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 101

Last updated 2024-07-10

Study results available
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Summary

Prospective evaluation of patient compliance and prescribed home exercise program using MotionSense wearable system during recovery from primary total knee arthroplasty.

Conditions

  • Knee Arthroplasty
  • Patient Engagement
  • Patient-Reported Outcome Measures (PROMs)

Interventions

DEVICE

MotionSense

MotionSense Wearable: Remote patient monitoring

Sponsors & Collaborators

  • Orthosensor, Inc.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
50 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-27
Primary Completion
2022-08-01
Completion
2022-08-01
FDA Device
Yes

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 NCT05091918 on ClinicalTrials.gov