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A Pragmatic Trial to Determine the Benefit of Behaviorally Enhanced Exercise Incentives and Corticosteroid Injections in Osteoarthritis of the Knee Marching On for Veterans With Osteoarthritis of the Knee (MOVE-OK)

Primary Purpose

Osteoarthritis of the Knee

Status
Recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Social Incentives and Gamification to Promote Exercise
Corticosteroid Injection given in A-B order
No Social Incentive applied
Procedure: Corticosteroid Injection given in B-A order
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis of the Knee focused on measuring corticosteroid injection, physical activity, pain, disability, behavioral incentives, Osteoarthritis, Osteoarthritis, Knee, Arthritis, Joint Diseases, Musculoskeletal Diseases, Rheumatic Diseases

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Veterans in VA Rheumatology or Orthopedic clinics
  • Chronic knee osteoarthritis
  • Indication for joint injection
  • Previous joint injections for palliation
  • Patient expresses interest in increasing their physical activity
  • Patient is able to walk 1/2 mile per day

Exclusion Criteria:

  • Intra-articular hardware or other contraindication to joint injection
  • Lack of smart phone
  • Acute exacerbation of osteoarthritis or knee pain
  • Comorbid condition that precludes safe exercise

Sites / Locations

  • Washington DC VA Medical Center, Washington, DCRecruiting
  • Omaha VA Nebraska-Western Iowa Health Care System, Omaha, NERecruiting
  • Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PARecruiting
  • VA Puget Sound Health Care System Seattle Division, Seattle, WARecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

Arm Label

Social Incentives and Gamification, Corticosteroid AB

No Incentive, Corticosteroid AB

Social Incentives and Gamification, Corticosteroid BA

No Incentive, Corticosteroid BA

Arm Description

Participants will receive a support person and be able to interact with a web-based platform to progress through levels based on their achievement of step goals. The participants will receive injections in A-B order (corticosteroids, then lidocaine only)

Participants will only receive reminders to sync their activity monitor. The participants will receive injections in A-B order (corticosteroids, then lidocaine only)

Participants will receive a support person and be able to interact with a web-based platform to progress through levels based on their achievement of step goals. The participants will receive injections in B-A order (lidocaine only, then corticosteroids)

Participants will only receive reminders to sync their activity monitor. The participants will receive injections in B-A order (lidocaine only, then corticosteroids)

Outcomes

Primary Outcome Measures

Percent change from baseline in weekly average steps per day
Steps measured by a wearable activity monitor
Change in Knee Injury and Osteoarthritis Outcome Score (KOOS)
KOOS assessed by survey at 2 week intervals. KOOS scores range from 0 to 100 with 0 representing worse knee problems and 100 representing no knee problems.

Secondary Outcome Measures

Change in PROMIS pain intensity score
Assessed by survey at 2 week intervals. Scores range from 3-15 and are converted to T-Scores. A high score represents greater pain.
Change in PROMIS Fatigue
Assessed by survey at 4 week intervals

Full Information

First Posted
August 26, 2021
Last Updated
May 25, 2023
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT05035810
Brief Title
A Pragmatic Trial to Determine the Benefit of Behaviorally Enhanced Exercise Incentives and Corticosteroid Injections in Osteoarthritis of the Knee Marching On for Veterans With Osteoarthritis of the Knee
Acronym
MOVE-OK
Official Title
A Pragmatic Trial to Determine the Benefit of Behaviorally Enhanced Exercise Incentives and Corticosteroid Injections in Osteoarthritis of the Knee
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 14, 2022 (Actual)
Primary Completion Date
November 30, 2024 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Knee osteoarthritis (KOA) is one of the most common and disabling conditions among Veterans. Management of KOA is challenging as there are few effective treatments other than joint replacement. Importantly, low levels of physical activity in patients with knee problems might worsen pain and disability. This study aims to determine the feasibility of using methods to change behavior that use social incentives and promote physical activity through playing games and interacting with a web-based platform. The study will also evaluate an important and widely used treatment, namely corticosteroid injections. Participants will be randomized into one of 4 arms and will receive a different combination of social incentives and injections. The study will evaluate which approach is most effective at promoting physical activity and reducing pain and disability.
Detailed Description
Knee osteoarthritis (KOA) is one of the most prevalent and disabling conditions among Veterans and accounts for high morbidity and high costs for the VA. Management of KOA is challenging as there are few consistently effective treatments other than joint replacement. Importantly, chronic reductions in physical activity in patients with KOA may worsen pain, physical function, and exacerbate the metabolic consequences of obesity. Moreover, the greater mortality observed in symptomatic knee OA populations is likely mediated through its effect on physical activity. The current proposal aims to derive preliminary data to support a large pragmatic trial testing the impact of interventions geared towards improving physical activity and function in KOA patients. Promoting physical activity has been shown to be helpful in reducing pain and improving function in KOA and other groups. However, promoting behavioral change in the arthritis population is a significant challenge. The group has shown that social incentives [and gamification] derived from concepts from the field of behavioral economics to promote behavioral change and increase physical activity can be both practical and effective in other settings. The investigators' group is studying incentives in patients with inflammatory arthritis with the goal of addressing fatigue, pain, and deficits in physical function. The incentivization of physical activity using this approach represents a novel intervention for the managing symptoms of KOA and to improving overall health. Analgesic therapies can help KOA patients participate in exercise therapy. However, whether corticosteroid injections, a commonly used medical therapy for KOA pain, has a positive impact of physical activity is unknown and is an additional important question addressed by the current proposal. Despite widespread use, definitive data demonstrating a consistent benefit of corticosteroids are lacking. A large randomized trial recently tested the effects of repeated corticosteroids injections every 3 months for a period of 2 years on patient reported pain as well as progression of disease measured by magnetic resonance imaging (MRI). This study demonstrated no improvement in pain compared to saline injections. In addition, a small but statistically significant decline in cartilage thickness on MRI was observed, raising a concern for side effects. These recent data might suggest that corticosteroid injections result in more harm than good, and may discourage providers from performing this intervention. However, there are critical weaknesses to this study. Pain and function were only assessed at 3-month intervals, while previous trials have suggested that peak benefit is expected at 4-8 weeks. Moreover, the clinical and biologic significance decrease in cartilage thickness is unclear. The investigators propose to fill these important knowledge gaps with an innovative and efficient pragmatic clinical trial with a factorial and crossover design. A large and definitive practical trial would lead to better understanding of the clinical effectiveness of these interventions, the meaningfulness of their combined impact, and the subgroups that are most likely to derive benefit. This clinical trial will leverage unique resources available through the Penn Center for Innovation to better capture important patient-reported outcomes in real-time through a web-based platform. The study will also test the feasibility of a crossover and factorial design to improve efficiency and reduce confounding. Each patient will receive each intervention (saline, corticosteroids) in random order over 1 year. A factorial design will be employed and will randomize participants to receive social incentives with gamification to promote increases in their physical activity. To accomplish these aims, the investigators will utilize innovative mobile applications for smart phones and wearable activity trackers through the Way-to-Health platform and assess, in real time, the impact of the intervention on patient-reported function and pain as well as physical activity. The technology will allow for the recording of outcomes as they occur, between clinic visits, thereby avoiding information bias due to poor recall. It will also provide real-time assessment of symptoms, providing granular assessments of response over time. Aim 1: To determine whether an incentive based on behaviorally-enhanced gamification can improve physical activity among patients with KOA and reduce self-reported pain and disability. The intervention will result in sustained improvements in average daily step counts over 10 months. Aim 2: To determine if corticosteroid injections can reduce pain and disability in patients with KOA when compared to lidocaine only. Participants will report improvements in self-reported pain and disability, and improvements in quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis of the Knee
Keywords
corticosteroid injection, physical activity, pain, disability, behavioral incentives, Osteoarthritis, Osteoarthritis, Knee, Arthritis, Joint Diseases, Musculoskeletal Diseases, Rheumatic Diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Model Description
Participants are randomized with a software application to receive social incentives to promote physical activity. They will also be randomized to receive corticosteroid injections in a crossover design.
Masking
ParticipantInvestigator
Masking Description
It is not possible to blind participants to the social incentives they will receive. For the injection aspect of the study, both the investigator and participant will be unaware of the injection being given and the syringe will be covered to obscure the view of the patient.
Allocation
Randomized
Enrollment
240 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Social Incentives and Gamification, Corticosteroid AB
Arm Type
Experimental
Arm Description
Participants will receive a support person and be able to interact with a web-based platform to progress through levels based on their achievement of step goals. The participants will receive injections in A-B order (corticosteroids, then lidocaine only)
Arm Title
No Incentive, Corticosteroid AB
Arm Type
Active Comparator
Arm Description
Participants will only receive reminders to sync their activity monitor. The participants will receive injections in A-B order (corticosteroids, then lidocaine only)
Arm Title
Social Incentives and Gamification, Corticosteroid BA
Arm Type
Experimental
Arm Description
Participants will receive a support person and be able to interact with a web-based platform to progress through levels based on their achievement of step goals. The participants will receive injections in B-A order (lidocaine only, then corticosteroids)
Arm Title
No Incentive, Corticosteroid BA
Arm Type
Active Comparator
Arm Description
Participants will only receive reminders to sync their activity monitor. The participants will receive injections in B-A order (lidocaine only, then corticosteroids)
Intervention Type
Behavioral
Intervention Name(s)
Social Incentives and Gamification to Promote Exercise
Intervention Description
The intervention will provide social incentives and gamification to promote physical activity.
Intervention Type
Drug
Intervention Name(s)
Corticosteroid Injection given in A-B order
Intervention Description
The study will compare corticosteroid injections with lidocaine to lidocaine only in a crossover design. These participants will receive the medication in A-B order.
Intervention Type
Behavioral
Intervention Name(s)
No Social Incentive applied
Intervention Description
No social incentive will be applied
Intervention Type
Drug
Intervention Name(s)
Procedure: Corticosteroid Injection given in B-A order
Intervention Description
The study will compare corticosteroid injections with lidocaine to lidocaine only in a crossover design. These participants will receive the medication in B-A order.
Primary Outcome Measure Information:
Title
Percent change from baseline in weekly average steps per day
Description
Steps measured by a wearable activity monitor
Time Frame
Measured weekly over 10 months (for exercise intervention)
Title
Change in Knee Injury and Osteoarthritis Outcome Score (KOOS)
Description
KOOS assessed by survey at 2 week intervals. KOOS scores range from 0 to 100 with 0 representing worse knee problems and 100 representing no knee problems.
Time Frame
Measured bi-weekly over 3 months (for injection intervention)
Secondary Outcome Measure Information:
Title
Change in PROMIS pain intensity score
Description
Assessed by survey at 2 week intervals. Scores range from 3-15 and are converted to T-Scores. A high score represents greater pain.
Time Frame
Measured bi-weekly over 3-10 months
Title
Change in PROMIS Fatigue
Description
Assessed by survey at 4 week intervals
Time Frame
Measured every 4 weeks over 3-10 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Veterans in VA Rheumatology or Orthopedic clinics Chronic knee osteoarthritis Indication for joint injection Previous joint injections for palliation Patient expresses interest in increasing their physical activity Patient is able to walk 1/2 mile per day Exclusion Criteria: Intra-articular hardware or other contraindication to joint injection Lack of smart phone Acute exacerbation of osteoarthritis or knee pain Comorbid condition that precludes safe exercise
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joshua F Baker, MD MSCE
Phone
(215) 823-5800
Email
Joshua.Baker@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
William T Leach, MA BS
Phone
(215) 823-4630
Ext
204630
Email
William.Leach@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joshua F. Baker, MD MSCE
Organizational Affiliation
Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington DC VA Medical Center, Washington, DC
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20422
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mercedes Quinones, MD
Phone
202-745-8000
Email
Mercedes.Quinones@va.gov
Facility Name
Omaha VA Nebraska-Western Iowa Health Care System, Omaha, NE
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68105-1873
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bryant England, MD
Phone
402-888-6728
Email
Bryant.England@va.gov
First Name & Middle Initial & Last Name & Degree
Bridget Kramer
Email
bridget.kramer@unmc.edu
Facility Name
Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104-4551
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joshua F Baker, MD MSCE
Phone
215-823-5800
Email
Joshua.Baker@va.gov
First Name & Middle Initial & Last Name & Degree
Joshua F. Baker, MD MSCE
Facility Name
VA Puget Sound Health Care System Seattle Division, Seattle, WA
City
Seattle
State/Province
Washington
ZIP/Postal Code
98108
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katherine D Wyshan, MD
Phone
206-764-2251
Email
Katherine.Wysham@va.gov

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data sets will be available through a formal request process through the PI and co-investigators. Data will not be shared without the approval of CVCVAMC IRB. When shared, data will be de-identified and anonymized.
Citations:
PubMed Identifier
35897080
Citation
Leach W, Doherty C, Olave M, England BR, Wysham K, Kerr G, Quinones M, Ogdie A, White D, Neogi T, Scanzello CR, Baker JF. Protocol for a multi-center randomized controlled trial to evaluate the benefits of exercise incentives and corticosteroid injections in osteoarthritis of the knee (MOVE-OK). Trials. 2022 Jul 27;23(1):604. doi: 10.1186/s13063-022-06529-w.
Results Reference
derived

Learn more about this trial

A Pragmatic Trial to Determine the Benefit of Behaviorally Enhanced Exercise Incentives and Corticosteroid Injections in Osteoarthritis of the Knee Marching On for Veterans With Osteoarthritis of the Knee

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