Knee Arthroplasty Clinical Trial
Official title:
COmmunity Based Rehabilitation After Knee Arthroplasty (CORKA): A Prospective Two Arm Individually Randomised Controlled Trial
Background The CORKA study was developed in response to a commissioned call by the National Institute for Health Research (NIHR) Health Technology Assessment (HTA) programme for research into a functional home based rehabilitation programme for patients who may be at risk of poor outcome after knee arthroplasty. Design The CORKA trial is a prospective individually randomised controlled trial with blinded outcome assessment at baseline, 6 and 12 months. The study will also include a qualitative and a health economic analysis. Participants will be randomised to one of two arms, 'home-based rehabilitation' or 'Usual Care'. Those in the usual care arm will receive a minimum of 1 and a maximum of 6 sessions of physiotherapy as delivered locally, e.g. class, one to one, etc. Those in the intervention arm will receive 7 sessions of a functional rehabilitation programme over a 12 week timescale. The intervention will be delivered using physiotherapists and physiotherapy assistants in the participants' home. Participants will be followed up at 6 months and 12 months
n/a
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT05279092 -
Yale Steroid Enhanced Versus Exparel Nerveblock TKA RCT Study
|
Phase 2 | |
| Completed |
NCT02581683 -
Magnesium Sulfate in Adductor Canal Blocks
|
Phase 4 | |
| Completed |
NCT02413996 -
Effects of Virtual Reality Rehabilitation in Patients With Total Knee Arthroplasty
|
N/A | |
| Completed |
NCT01191593 -
The Efficacy of Adductor-Canal-Blockade on Pain and Morphine Consumption After Revision Knee Arthroplasty
|
Phase 4 | |
| Completed |
NCT01140815 -
Functional Performance of the Journey Deuce Bicompartmental Versus the Genesis II Total Knee System
|
Phase 4 | |
| Completed |
NCT03847324 -
Physiotherapy and Therapeutic Education on Patients With Pain Catastrophism Scheduled for a Total Knee Arthroplasty
|
N/A | |
| Active, not recruiting |
NCT06096727 -
The Energize! Study for Adults With Knee Replacement
|
N/A | |
| Active, not recruiting |
NCT01705886 -
Clinical and Economic Comparison of Robot Assisted Versus Manual Knee Replacement
|
||
| Terminated |
NCT01705366 -
Clinical Outcomes of Knee Replacement
|
||
| Recruiting |
NCT01225484 -
Perioperative Analgesia After Knee Arthroplasty
|
Phase 4 | |
| Completed |
NCT00367289 -
CT for Diagnosis of Implant Stability in Revision Arthroplasty
|
N/A | |
| Withdrawn |
NCT03421938 -
Effect of Downhill-uphill Walking Exercises on Functional Level and Muscle Strength in Patients With Knee Arthroplasty.
|
N/A | |
| Active, not recruiting |
NCT04467970 -
Unicompartmental Knee Arthroplasty vs High Tibial Osteotomy.
|
N/A | |
| Not yet recruiting |
NCT06130813 -
Increased Perioperative Communication Program in Knee Arthroplasty
|
N/A | |
| Recruiting |
NCT06293144 -
the 95% Effective Dose of Ciprofol for Adjunctive Sedation Undergoing Knee Arthroplasty in Elderly People
|
Early Phase 1 | |
| Active, not recruiting |
NCT04679857 -
Substitution of the PCL in TKA With UC or PS Design
|
N/A | |
| Completed |
NCT06293131 -
Median Effective Dose of Ciprofol-Assisted Sedation for Elderly Patients Undergoing Knee Arthroplasty
|
Early Phase 1 | |
| Completed |
NCT05091918 -
Limited Market Release - MotionSense Clinical Use Evaluation
|
N/A | |
| Recruiting |
NCT02934802 -
Non-Interventional Consecutive and Prospective Study of e.Motion® PS Pro Prosthesis in the Total Knee Artroplasty
|
||
| Active, not recruiting |
NCT02791477 -
Functional Results With Attune Fixed Bearing Posterior Stabilized Knee Arthroplasty (A-16)
|
N/A |