Study of the KinexConnect Telerehabilitation System (KCTRS)

Sponsor
Kinex Medical Company, LLC (Industry)
Overall Status
Active, not recruiting
CT.gov ID
NCT04191798
Collaborator
Health Factors Inc (Other)
60
1
2
41.9
1.4

Study Details

Study Description

Brief Summary

A randomized, single-blind study comparing telerehabilitation at home with continuous passive motion (CPM) and a tablet-based patient engagement application (KinexConnect) versus traditional outpatient physical therapy (PT) following total knee arthroplasty (TKA).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Telerehabilitation using the KinexConnect system for rehabilitation after TKA.
  • Behavioral: Traditional outpatient PT for rehabilitation after TKA.
N/A

Detailed Description

The Randomized Study of the KinexConnect Telerehabilitation System is a 1:1 randomized, single-blind, prospective cohort study to be conducted at one investigational site in the United States. The study compares at-home telerehabilitation system versus traditional outpatient PT following total knee arthroplasty (TKA). The telerehabilitation system involves a tablet-enabled patient engagement application, the KinexConnect App, to be used in conjunction with a continuous passive motion (CPM) machine.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
All TUG and RoM assessments will be performed by trained physician assistants who will remain blinded to allocation throughout the study
Primary Purpose:
Treatment
Official Title:
Randomized Study of the KinexConnect Telerehabilitation System Versus Outpatient Physical Therapy After Total Knee Arthroplasty
Actual Study Start Date :
Nov 1, 2019
Anticipated Primary Completion Date :
Oct 31, 2022
Anticipated Study Completion Date :
Apr 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: KinexConnect

Rehab at Home Patients

Behavioral: Telerehabilitation using the KinexConnect system for rehabilitation after TKA.
KinexConnect subjects are asked to Perform CPM therapy for 4 weeks. Perform a KCK home exercise program (HEP) for 6 weeks.

Active Comparator: Outpatient PT

In-person PT patients

Behavioral: Traditional outpatient PT for rehabilitation after TKA.
Control subjects are asked to undergo standard outpatient physical therapy (PT) with a licensed physical therapist plus supplemental home exercises as directed. Nominally patients are expected to have 3 PT sessions per week for 4 weeks.

Outcome Measures

Primary Outcome Measures

  1. Change in the Timed up and Go (TUG) Test score [3 months]

    The TUG score is the measurement of time for a person to rise from a standard armchair (seat height 46 cm), walk 3 meters, turn, walk back to the chair, and sit down as quickly as possible. The mean scores for patients in both arms are derived and compared against each other. Closer the trial arm mean is to the control arm mean, the better.

  2. Change in the Timed up and Go (TUG) Test score [1 year]

    The TUG score is the measurement of time for a person to rise from a standard armchair (seat height 46 cm), walk 3 meters, turn, walk back to the chair, and sit down as quickly as possible. The mean scores for patients in both arms are derived and compared against each other. Closer the trial arm mean is to the control arm mean, the better.

  3. Economic Benefit [3 months]

    Expenses associated with rehabilitation after surgery will be based on costs associated with CPM rental fees and outpatient physical therapy visits. Estimates will be applied wherever actual expense data is not available.

  4. Economic Benefit [1 year]

    Expenses associated with rehabilitation after surgery will be based on costs associated with CPM rental fees and outpatient physical therapy visits. Estimates will be applied wherever actual expense data is not available.

Secondary Outcome Measures

  1. Change in Active Range of Motion (ARoM) [3 months and 6 months]

    Active Range of Motion is the difference between the maximum Flexion and maximum Extension the patient is able to achieve with independent effort

  2. Change in Passive Range of Motion (PRoM) [3 months and 6 months]

    Passive Range of Motion is the difference between the maximum Flexion and maximum Extension the patient is able to achieve when bearable force is exerted by the clinician.

  3. Change in Pain as measured by the Verbal Descriptive Scale (VDS) [3 months and 1 year]

    This is a self reported outcome by the patient based on their expression of pain at a given time point when presented with the 7 verbal cues. The levels of pain reported vary from "No Pain" to "Most Intense Pain Imaginable". Higher the intensity of pain, worse the outcome

  4. Change in the Knee Osteoarthritis Outcome Score (KOOS) [3 months and 1 year]

    The KOOS is a standardized and validated patient outcome score that assess functional limitation in patient with knee osteoarthritis. The survey questionnaire is filled out in its entirety by the patient. The five patient-relevant subscales of KOOS are scored separately: Pain (nine items); Symptoms (seven items); ADL Function (17 items); Sport and Recreation Function (five items); Quality of Life (four items). A Likert scale is used and all items have five possible answer options scored from 0 (No Problems) to 4 (Extreme Problems) and each of the five scores is calculated as the sum of the items included. Scores are transformed to a 0-100 scale, with zero representing extreme knee problems and 100 representing no knee problems.

  5. Change in the New Knee Society Score (NKSS) - Patient Satisfaction and Expectation [3 months and 1 year]

    The patient satisfaction and patient expectation scores are calculated by having the relevant sections of the survey questionnaire is filled out in its entirety by the patient. Patient Satisfaction is scored 0 - 40 points and Patient Expectation is scored 0 -15 points. with Zero being the worst outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Planned for a primary unilateral TKA.

  2. At least 21 years of age.

  3. Capable of understanding the study requirements and giving written informed consent.

  4. Willing and able to comply with either therapy program.

  5. Has easy access to caregiver support.

Exclusion Criteria:
  1. Active range-of-motion (ARoM) < 80 degrees in target knee.

  2. Unable to read and write in English.

  3. Lack of email capability to receive recovery trend information.

  4. Previous knee intervention in target knee.

  5. Previous knee joint infection in either knee.

  6. Received a revision TKA (opposite knee).

  7. Planned for bilateral TKA.

  8. Self-reported pregnancy.

  9. Reason for arthroplasty being for the treatment of fracture, infection or malignancy.

  10. Other physical or mental impairments or medical conditions that may affect ability to complete therapy as prescribed.

  11. Unwilling to participate.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Des Moines Orthopedic Surgeons Des Moines Iowa United States 50266

Sponsors and Collaborators

  • Kinex Medical Company, LLC
  • Health Factors Inc

Investigators

  • Principal Investigator: Barron Bremner, DO, Des Moines Orthopedic Suregons

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Kinex Medical Company, LLC
ClinicalTrials.gov Identifier:
NCT04191798
Other Study ID Numbers:
  • KC-07
First Posted:
Dec 10, 2019
Last Update Posted:
Jun 22, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Kinex Medical Company, LLC
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 22, 2022