Adding Value in Knee Arthroplasty Post-total Knee Replacement (TKR) Care Navigator Trial (AViKA)
Primary Purpose
Osteoarthritis, Degenerative Joint Disease
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Care Navigator
Standard Post-Operative TKA Care
Sponsored by
About this trial
This is an interventional treatment trial for Osteoarthritis focused on measuring Osteoarthritis, Total Knee Replacement, total Knee Arthroplasty, Post operative recovery, TKA, Post-operative recovery TKR, Care Navigator
Eligibility Criteria
Inclusion Criteria:
- Scheduled to undergo primary TKA at Brigham & Women's Hospital
- Osteoarthritis is the principal underlying diagnosis
- Age >=40 at the projected date of TKA
- English-speaking
Exclusion Criteria:
- Osteoarthritis is not the principal underlying diagnosis (e.g. inflammatory arthritis)
- Dementia
- Psychological issues that preclude participation, as identified by participating surgeons
- Non-English speaker
- Diagnosis other than Osteoarthritis or secondary Osteoarthritis
- Age < 40 at the projected date of TKA
- Lives in a nursing home
- Implantation of Unicompartamental Knee Arthroscopy or Interpositional Arthroplasty
- Bilateral TKA in same admission (simultaneous)or planned bilateral within 6 months
Sites / Locations
- Brigham & Women's Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Care Navigator Intervention Group
Usual Care Group
Arm Description
Subjects randomized to the Care Navigator Intervention group will receive up to 10 telephone calls from a care navigator for 5 months post-operatively
Subjects in the Usual Care group receive the current standard post-operative TKA care
Outcomes
Primary Outcome Measures
Change in WOMAC Physical Function
The change in functional status will be measured using the WOMAC Physical Function scale at Baseline and 6 months
Secondary Outcome Measures
Satisfaction
Percentage of patients in each study arm who reported being very satisfied with the results of TKA
Range of Motion
Percentage of participants able to bend knee at least 120 degrees
Full Information
NCT ID
NCT01540851
First Posted
February 21, 2012
Last Updated
January 16, 2018
Sponsor
Brigham and Women's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01540851
Brief Title
Adding Value in Knee Arthroplasty Post-total Knee Replacement (TKR) Care Navigator Trial
Acronym
AViKA
Official Title
Adding Value in Knee Arthroplasty Post TKR Care Navigator Trial
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
July 24, 2011 (Actual)
Primary Completion Date
May 10, 2014 (Actual)
Study Completion Date
May 10, 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The objectives of this research are to:
Conduct a proof of concept randomized controlled trial with up to 300 patients undergoing primary total knee replacement (TKA) at Brigham and Women's Hospital (BWH). The trial will compare a "Care Navigator" post-discharge intervention versus "Usual Care" post discharge management of patients undergoing TKA. The intervention will focus on the challenging process of transitions from the acute care hospital to inpatient or outpatient rehabilitation, and from inpatient rehabilitation to home.
The principal goals of the trial are:
To establish whether "Care Navigator" intervention improves functional outcomes as compared with the "Usual Care" treatment six months after TKA surgery.
To establish whether "Care Navigator" intervention is cost effective six months after TKA surgery.
The investigators hypothesize that:
Incorporating the Care Navigator role into the "Usual Care" treatment will increase TKA patients' rate of adherence to the rehabilitation protocol and improve functional outcomes.
Addition of a Care Navigator is cost-effective.
Detailed Description
The "Post-TKA Care Navigator" proof of concept intervention will be implemented as a randomized controlled trial. The investigators aim to identify and enroll a cohort of up to 300 subjects who have decided to undergo total knee replacement (TKA) at BWH. Subjects will be patients of the five orthopedic surgeons at Brigham and Women's Hospital who perform the most TKAs: Drs. Wright, Brick, Ready, Martin and Thornhill. Subjects will be followed from about two weeks prior to the operation to six months after discharge.
The investigators will assign patients into two groups, at random: 1) receiving current standard of post-operative care and 2) adding "Post-TKA Care Navigator". The role of the Care Navigator will be to follow up with patients via frequent telephone conversations, ranging from weekly during the first month to bi-weekly for the next 6 weeks to monthly by the 14th week post op. subjects assigned to the care navigator will receive up to 10 telephone calls over a period of 5 months. The goal of the Care Navigator would be to ensure or encourage compliance with physical therapy, triage patient concerns, questions and complaints, and identify those patients that require a call from a clinician to address a problem in the recovery process. For those issues that can be resolved easily at home the navigator would suggest strategies. The value of the post-TKA Care Navigator will be assessed by comparing functional status, satisfaction with surgery, utilization of health care, adherence to physical therapy, range of knee motion and intervention costs across the two randomized groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Degenerative Joint Disease
Keywords
Osteoarthritis, Total Knee Replacement, total Knee Arthroplasty, Post operative recovery, TKA, Post-operative recovery TKR, Care Navigator
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
308 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Care Navigator Intervention Group
Arm Type
Active Comparator
Arm Description
Subjects randomized to the Care Navigator Intervention group will receive up to 10 telephone calls from a care navigator for 5 months post-operatively
Arm Title
Usual Care Group
Arm Type
Active Comparator
Arm Description
Subjects in the Usual Care group receive the current standard post-operative TKA care
Intervention Type
Behavioral
Intervention Name(s)
Care Navigator
Intervention Description
Subjects assigned to the Care Navigator intervention group will receive 10 calls from a care navigator after discharge from the hospital for 5 months after their total knee replacement.
Intervention Type
Other
Intervention Name(s)
Standard Post-Operative TKA Care
Intervention Description
Subjects assigned to the Standard Post-Operative TKA Care group will receive the current standard of care for post-operative care
Primary Outcome Measure Information:
Title
Change in WOMAC Physical Function
Description
The change in functional status will be measured using the WOMAC Physical Function scale at Baseline and 6 months
Time Frame
Change in functional status from baseline to 6 months
Secondary Outcome Measure Information:
Title
Satisfaction
Description
Percentage of patients in each study arm who reported being very satisfied with the results of TKA
Time Frame
Measured at 6 months post TKA
Title
Range of Motion
Description
Percentage of participants able to bend knee at least 120 degrees
Time Frame
6 months after TKA
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Scheduled to undergo primary TKA at Brigham & Women's Hospital
Osteoarthritis is the principal underlying diagnosis
Age >=40 at the projected date of TKA
English-speaking
Exclusion Criteria:
Osteoarthritis is not the principal underlying diagnosis (e.g. inflammatory arthritis)
Dementia
Psychological issues that preclude participation, as identified by participating surgeons
Non-English speaker
Diagnosis other than Osteoarthritis or secondary Osteoarthritis
Age < 40 at the projected date of TKA
Lives in a nursing home
Implantation of Unicompartamental Knee Arthroscopy or Interpositional Arthroplasty
Bilateral TKA in same admission (simultaneous)or planned bilateral within 6 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elena Losina, PhD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham & Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
24119081
Citation
Losina E, Collins JE, Daigle ME, Donnell-Fink LA, Prokopetz JJ, Strnad D, Lerner V, Rome BN, Ghazinouri R, Skoniecki DJ, Katz JN, Wright J. The AViKA (Adding Value in Knee Arthroplasty) postoperative care navigation trial: rationale and design features. BMC Musculoskelet Disord. 2013 Oct 12;14:290. doi: 10.1186/1471-2474-14-290.
Results Reference
background
PubMed Identifier
26714179
Citation
Losina E, Collins JE, Wright J, Daigle ME, Donnell-Fink LA, Strnad D, Usiskin IM, Yang HY, Lerner V, Katz JN. Postoperative Care Navigation for Total Knee Arthroplasty Patients: A Randomized Controlled Trial. Arthritis Care Res (Hoboken). 2016 Sep;68(9):1252-9. doi: 10.1002/acr.22829. Epub 2016 Jul 28.
Results Reference
result
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Adding Value in Knee Arthroplasty Post-total Knee Replacement (TKR) Care Navigator Trial
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