|

The Effect of Smart Ring Assisted Physiotherapeutic Intervention After TKR

RECRUITINGN/ASponsored by Coxa, Hospital for Joint Replacement
Actively Recruiting
PhaseN/A
SponsorCoxa, Hospital for Joint Replacement
Started2022-11-02
Est. completion2026-12
Eligibility
Age18 Years – 70 Years
Healthy vol.Accepted

Summary

The goal of this randomized controlled trial is to learn about the effect of a wearable activity tracker assisted physiotherapeutic intervention on the risk of poor patient reported outcome after a primary total knee replacement. The main question it aims to answer is whether a wearable activity tracker assisted physiotherapeutic intervention and remote monitoring may help to decrease the number of the poor patient reported post-operative outcome 12 months after a primary total knee replacement. Participants will receive standard postoperative care which includes physiotherapy appointments 4 weeks and 3 months after the surgery and they will use smart rings (Oura ring) 3 months postoperatively. Patients will be remotely monitored to follow their recovery from total knee replacement surgery: the study group physiotherapists will follow the patients' activity and sleep and if necessary, make a contact with patient if there seems to low activity indicating difficulties with recovering from the surgery. Researchers will compare the intervention group to a group of participants who will receive only standard postoperative care with physiotherapy appointments 4 weeks and 3 months, to see if the use of the Oura ring may decrease the number of participants with poor patient reported post-operative outcome after total knee replacement.

Eligibility

Age: 18 Years – 70 YearsHealthy volunteers accepted
Inclusion Criteria:

* Patients undergoing primary TKA for primary osteoarthritis.
* Patients able to consent and willing to comply with the study protocol.
* Patients aged 18 to 70 years
* Patients is able to use a smartphone and a smart ring.

Exclusion Criteria:

* Patients unwilling to provide informed consent
* \>15 degrees varus or valgus, or \> 15 degrees fixed flexion deformity
* Physical, emotional, or neurological conditions that would compromise the patient, e.g., poor compliance with postoperative rehabilitation and follow-up (e.g., drug or alcohol abuse, serious mental illness, general neurological conditions, such as Parkinson, MS, etc.)
* Patients unable to attend the study physiotherapy appointments at the outpatient clinic.
* Patients unable to wear Oura ring (example in case of OA or rheumatoid arthritis in the finger joints).
* Patients with cardiac arrhythmia.

Conditions2

ArthritisOsteo Arthritis Knee

Browse More Trials

Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.