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Study identifier: NCT05599776 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

The Effect of Smart Ring Assisted Physiotherapeutic Intervention After TKR

Condition: Osteo Arthritis Knee  ·  Sponsor: Coxa, Hospital for Joint Replacement

PhaseNA
Planned participants338
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Aleksi Reito, MD, PhD  ·  +358444729631  ·  aleksi.reito@pshp.fi

Elisa Leinonen, RN  ·  +358331178030  ·  elisa.leinonen@coxa.fi

Always discuss trial participation with your own doctor first.

Locations (1)

Coxa Hospital for Joint ReplacementTampere, Pirkanmaa, FinlandRecruiting

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Source record: clinicaltrials.gov/study/NCT05599776