Limited Market Release - MotionSense Clinical Use Evaluation (FS5)

OrthoSensor

Status: Completed

Conditions: Knee Arthroplasty; Patient-Reported Outcome Measures (PROMs); Patient Engagement

Treatments: Device: MotionSense

Study type: Interventional

Funder types: Industry

Identifiers

NCT05091918

Orthosensor

Details and patient eligibility

About

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

Full description

During the proposed study, the MotionSense wearable system will be used by patients undergoing total knee arthroplasty (TKA) surgery leading up to and after their surgery. The patients will be using the system to monitor their recovery during daily activities, log daily pain scores and patient reported outcomes while also supporting their prescribed home exercise program. Each patient will thereby participate in outpatient physiotherapy in line with their current standard of care, while the physiotherapist will leverage the opportunities of the presented platform to give the patient personalized reminders for their patient-specific home exercise program. The surgeon / research nurse will additionally be able to monitor the patients recovery remotely as the sensor / app data is shared to the OrthoLogIQ platform.

Enrollment: 101 patients

Sex: All

Ages: 50 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Planned for unilateral total knee surgery in the coming 4 weeks
• Age 50 to 80
• Owns a smart phone

Exclusion criteria

• BMI exceeding 35
• Severe skin conditions

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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101 participants in 1 patient group

MotionSense Wearable

Other group

Description:

Using MotionSense from pre-op to 90 days post-op during the recovery after primary TKA

Treatment:

Device: MotionSense