Viewing Study NCT04924205



Ignite Creation Date: 2024-05-06 @ 4:16 PM
Last Modification Date: 2024-10-26 @ 2:06 PM
Study NCT ID: NCT04924205
Status: RECRUITING
Last Update Posted: 2023-06-06
First Post: 2021-06-07

Brief Title: A Comparison Of Primary TKA Rehabilitation Using A Smart Orthotic Versus Outpatient Physical Therapy
Sponsor: Nicolas Noiseux MD FRCSC
Organization: University of Iowa

Study Overview

Official Title: A Prospective Comparison Of Primary Total Knee Arthroplasty Rehabilitation Using A Smart Orthotic Versus Outpatient Physical Therapy
Status: RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This will be a prospective randomized noninferiority clinical trial comparing rehabilitation methods post-total knee arthroplasty TKA Population of interest is adult hipknee clinic patients over age 18 who are indicated for unilateral primary total knee arthroplasty All TKA patients are prescribed physical therapy PT for rehabilitation post-operatively The investigators will compare this current treatment with a new validated wearable smart knee brace FM2 Knee Brace that can be used for rehabilitation post-TKA Following enrollment in the study the investigators will match and randomize participants into two cohorts outpatient PT versus FM2 Knee Brace Outpatient PT group will be prescribed routine six-week course of outpatient PT no pool exercises remainder at therapists discretion to start as soon as possible upon discharge The FM2 Knee Brace group will complete device set up at pre-op visit and will be prescribed 3-4 exercises to complete at their discretion over six weeks The investigators will collect measurements of knee flexion extension total arc of motion at pre-op visit and at 6-week 3-month and 1-year post-op visits The investigators will also plan to record additional PROs therapy compliance and complication rates The investigators will compare the two groups to test whether the new FM2 Knee Brace is noninferior to regular PT when recovering from TKA and if the new technology could be an alternative to outpatient PT
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None