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Patient-Specific Predictions for Post-Knee Replacement Satisfaction (SensorRCT Trial)

N/A
Waitlist Available
Led By Brent Lanting
Research Sponsored by Lawson Health Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up pre-operation and 1-year post-operation
Awards & highlights
No Placebo-Only Group

Summary

This trial is testing whether patients who are told what to expect after a total knee replacement will be more satisfied with the surgery. The hypothesis is that they will be, which could lead to decreased costs from patients who are dissatisfied with the surgery.

Who is the study for?
This trial is for patients with osteoarthritis who are scheduled for a primary total knee replacement. It's not suitable for those getting both knees replaced at once, individuals who can't read, write or speak English, or have conditions affecting their walk or previous knee surgeries.
What is being tested?
The study tests if knowing the predicted outcome of knee surgery improves patient satisfaction. One group will receive standard pre-op info while the other will also get predictions on their post-surgery function based on a sensor test and machine learning.
What are the potential side effects?
Since this trial focuses on information delivery rather than medication or invasive procedures, there are no direct side effects related to drugs or surgical interventions being studied.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre-operation and 1-year post-operation
This trial's timeline: 3 weeks for screening, Varies for treatment, and pre-operation and 1-year post-operation for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Patient Satisfaction
Secondary study objectives
Cost Effectiveness
Other study objectives
EuroQuol 5D (EQ-5D)
Global Rating of Change Scale (GROC)
Knee Injury and Osteoarthritis Outcome Score (KOOS)
+4 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: Standard Care GroupExperimental Treatment1 Intervention
Standard Pre-Operative Total Knee Arthroplasty Information
Group II: Outcome Prediction GroupExperimental Treatment2 Interventions
Patient-Specific Prediction of Functional Outcome and Standard Pre-Operative Total Knee Arthroplasty Information

Find a Location

Who is running the clinical trial?

Lawson Health Research InstituteLead Sponsor
681 Previous Clinical Trials
431,300 Total Patients Enrolled
Brent LantingPrincipal InvestigatorLawson Health Science Centre
2 Previous Clinical Trials
159 Total Patients Enrolled

Media Library

Outcome Prediction Group Clinical Trial Eligibility Overview. Trial Name: NCT04775719 — N/A
Patient Satisfaction Research Study Groups: Outcome Prediction Group, Standard Care Group
Patient Satisfaction Clinical Trial 2023: Outcome Prediction Group Highlights & Side Effects. Trial Name: NCT04775719 — N/A
Outcome Prediction Group 2023 Treatment Timeline for Medical Study. Trial Name: NCT04775719 — N/A
~1 spots leftby Feb 2025
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