Study Measuring the Effects of Patient Data for Total Hip and Total Knee Arthroplasty Patients Using an APP Based Sensor for Home Exercise Performance Before and After Operation (ORTHOPATH)

Aesculap

Status: Withdrawn

Conditions: Arthroplasty, Replacement, Hip; Clinical Outcome; Arthroplasty, Replacement, Knee; Patient Satisfaction; Treatment Cost

Treatments: Device: Control; Device: OrthoPath

Study type: Observational

Funder types: Industry

Identifiers

NCT05182320

AAG-O-H-2108

Details and patient eligibility

About

Multicenter, Prospective, Randomized, Comparative Study Measuring the Effects on Clinical Outcomes, Patient Satisfaction, Costs and Benefits of Combined Pre-, Intra- and Postoperative Patient Data for THA and TKA Patients Using an APP Based Sensor for Home Exercise Performance Before and After Operation

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Primary, unilateral total knee and hip replacement patients
• Participant is min. 18 years of age
• Participant is able and willing to provide written informed consent
• Participant with ability to work with smart devices
• Participant having its own device (Apple iPhone or iPad with latest iOS version or Android tablet or smart phone min. Android version 6) and are able to handle the app and/or sensor

Exclusion criteria

• Pregnancy
• Participant has mental in capabilities - unable to give informed consent
• Participants who are unwilling or mentally and/or physically unable to adhere to study procedures
• Participant is having orthopaedic co-morbidities such as: previous HTO at indexed joint or prior UKA
• Flexion contracture > 15°
• Varus/valgus deformity > 10°
• Participant is having dementia or other cognitive impairment

Trial design

0 participants in 2 patient groups

OrthoPath

Treatment:

Device: OrthoPath

Control

Treatment:

Device: Control