Knee Arthroplasty Rehabilitation Outcomes Study

Not Applicable

Completed

• Conditions: Total Knee Arthroplasty; Rehabilitation

• Registration Number: NCT02426190
• Lead Sponsor: MedStar National Rehabilitation Network

Brief Summary

The objective of the KAROS study is to compare rehabilitation outcomes between 3 proposed protocols and a current standard of care protocol for the purpose of identifying better practice for outpatient rehabilitation among patients with single total knee replacement. The 3 advanced protocols involve use of an anti-gravity treadmill and/or the patterned electrical neuromuscular stimulation (PENS). Both medical modalities have been cleared by the FDA to be used in medical rehabilitation, including total knee replacement.

Detailed Description

Not available

Study Timeline

• Study Start: 2014-10
• Study First Submitted: 2015-04-08
• Study First Submitted QC: 2015-04-21
• Study First Posted: 2015-04-24
• Primary Completion: 2017-12
• Study Completion: 2017-12-31
• Status Verified: 2019-04
• Last Update Submitted: 2019-04-12
• Last Update Posted: 2019-04-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 386

Inclusion Criteria

• Patients who undergo an elective single total knee arthroplasty and initiate their outpatient rehabilitation therapy within 3 weeks after surgery.
• Patients who are 40 years old or older.
• Patients who weight less than 320 lb to accommodate the weight limit to use the anti-gravity treadmill.

Exclusion Criteria

• Patients who had any lower extremity joint replacement less than 1 year prior the current total knee replacement.
• Patients who are pregnant or may be pregnant.
• Patients who have a medical history of neurologic disorders.
• Patients who have received more than 2 weeks of other formats of rehabilitation prior their outpatient rehabilitation program.
• Patients who received any cancer treatment in the past year prior the current surgery.
• Patients who have uncontrolled cardiovascular hypertension.
• Patients who have cardiac demand pacemakers and/or implanted defibrillators.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
AM-PAC (Activity Measure for Post Acute Care) Basic Mobility score: Baseline	Baseline	The primary outcome measure is the AM-PAC Basic Mobility score. AM-PAC is a patient-reported instrument to measure functional level in 3 domains: basic mobility, daily activity, and applied cognition. For the purpose of the study, only the basic mobility domain was measured. Using item-response theory, the AM-PAC program selects the most representative questions from its extensive item bank to ask when measuring a patient's functional level. This study used the AM-PAC basic mobility paper short form designed for outpatient settings. The short-form consists of 18 questions and produces a raw score (18 to 72) transformed into a score ranging from 29.41 to 80.30 based on item-degree of difficulty. Higher transformed scores denote higher functional mobility: 34 - 51.9 = limited indoor mobility; 52 - 65.9 = enhanced indoor mobility; 66 and above = outdoor mobility.
AM-PAC (Activity Measure for Post Acute Care) Basic Mobility score: Discharge from outpatient rehabilitation	Discharge from outpatient rehabilitation (on average 2 months from baseline)	The primary outcome measure is the AM-PAC Basic Mobility score upon discharge from outpatient therapy. AM-PAC is a patient-reported instrument to measure functional level in 3 domains: basic mobility, daily activity, and applied cognition. For the purpose of the study, only the basic mobility domain was measured. Using item-response theory, the AM-PAC program selects the most representative questions from its extensive item bank to ask when measuring a patient's functional level. This study used the AM-PAC basic mobility paper short form designed for outpatient settings. The short-form consists of 18 questions and produces a raw score (18 to 72) transformed into a score ranging from 29.41 to 80.30 based on item-degree of difficulty. Higher transformed scores denote higher functional mobility: 34 - 51.9 = limited indoor mobility; 52 - 65.9 = enhanced indoor mobility; 66 and above = outdoor mobility.

Trial Locations

Locations (1)

MedStar National Rehabilitation Network; 🇺🇸 Washington, District of Columbia, United States