CClinicalTrials.gg
RecruitingNCT06488144ReAKTIVUpdated Jan 8, 2026

Rehabilitation for Arthritis of The Knee: mainTaining Improvement for Veterans

A Phase 3 interventional study of Health coach and Remote Incentive Program in Osteoarthritis, Knee, sponsored by VA Office of Research and Development. Recruiting at 5 sites in United States. Open to participants aged 40 Years to 90 Years. Per ClinicalTrials.gov, last updated 2026-01-08.

Sponsored by VA Office of Research and Development · Phase 3, Interventional, and Treatment

From the registry’s dates

  • Started Dec 2025; still recruiting 9 months later.
Phase
Phase 3
Study type
Interventional
Enrollment
254
Allocation
Randomized
Ages
40 Years to 90 Years
Sex
All
01

Study summary

The aims are to determine whether 1) an incentive based on behaviorally-enhanced gamification and social incentives and 2) health coaching can promote adherence to exercise and physical activity after physical therapy for osteoarthritis of the knee (KOA). The research design is a randomized clinical trial with factorial design

This randomized clinical trial of 254 patients using a factorial design will leverage a clinical trial platform developed through the University of Pennsylvania that allows for the remotely capture important patient-reported outcomes and other interaction through a participant's smart phone. The investigators will randomize participants to receive social incentives with gamification to promote adherence to prescribed exercises as well as maintenance of greater levels of physical activity and compare to controls that receive a Fitbit but no additional incentive. Participants may also be randomized to receive a health coach. The investigators will utilize mobile applications for smart phones and wearable activity trackers through the Way-to-Health platform and assess, in real time, the impact of the interventions on patient-reported function and pain (as measured by the Knee Osteoarthritis Outcome Score) as well as physical activity. Participants will be followed for 2 years, with a total of 5 in-person visits.

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. Importantly, while physical therapy is valuable for patients with KOA, lack of adherence to home exercises and low overall physical activity limit the durability of response. The current proposal aims to address two important knowledge gaps in the management of KOA in order to improve pain and function.

Read the detailed description

Knee osteoarthritis (KOA) is a high-priority problem among the aging population, and in particular, among Veterans. Few interventions have been shown effective in the long-term management of symptoms. Current guidelines for non-operative KOA management include strong recommendations for exercise delivered through standard physical therapy (PT) and the promotion of greater physical activity. Standard physical therapy (PT) interventions characterized by 6-8 week of supervised exercises (e.g., strengthening peri-articular tissues) and mobility training (e.g., improving biomechanics and movement patterns) are safe and effective at improving and facilitating mobility, activity participation, and overall quality of life. While PT is a recognized and necessary aspect of KOA care, its clinical benefits are often short-lived and begin to decline following PT due to poor long-term adherence - leading physicians to increasingly rely on the use of non-steroidal anti-inflammatories and opioids over time. The lack of effective strategies to sustain the clinical benefits achieved in PT for individuals with KOA remains a critical gap.

The investigators aim to study two interventions designed based on their ability to address 5 key theories for maintaining behaviors that are supported by the literature. Specifically, the proposed study will evaluate a remote and behaviorally-designed intervention in combination with health coaching to influence long-term behavioral change after standard-of-care PT. The behavioral intervention utilizes tools such as goal setting, gamification (the use of game design elements), loss aversion, monitoring, and social incentives, to 1) increase motivation, 2) improve self-monitoring and self-regulation, 3) provide psychological and physical resources, 4) influence the development of healthy long-term habits, and 5) a provide supportive environment with social support. The behavioral intervention will be studied combined with health coaching with a focus on the same goals but through motivational interviewing to address personal, environmental, and social barriers. The investigators aim to clearly quantify the value of each as well as their value when used in combination.

The investigators has already utilized concepts from behavioral economics (a scientific field aiming to understand how to motivate individuals) to develop remotely-applied interventions that incorporate the concepts of gamification, social incentives, and loss aversion to promote improvements in physical activity using an innovative web-based platform. The investigators SPiRE-funded pilot study "Marching On for Veterans with Osteoarthritis of the Knee" demonstrated excellent feasibility, rapid recruitment, improvements in reported symptoms, and high patient satisfaction. The multi-site study is actively enrolling Veterans and is ahead of schedule.

The investigators propose to fill important knowledge gaps in this area with a large, pragmatic clinical trial. In this study, the investigators will randomize in a factorial design to receive no intervention, the remote behavioral intervention, a remote health coach, or both, after being released from a standard PT intervention with proven efficacy in order to promote the maintenance of symptomatic gains observed during PT. To accomplish these aims, the investigators will utilize innovative mobile applications for smart phones through the Way-to-Health (WTH) platform and assess, in real time, the impact of the intervention on the primary outcome of patient-reported symptoms as measured by the Knee Osteoarthritis Outcome score. The investigators will also monitor adherence to specific knee-related exercises at home. Way to Health allows for the recording of outcomes in real time, as they occur, thereby avoiding information bias due to poor recall and participation bias. The investigative team includes investigators with experience conducting similar trials using this infrastructure as well as expertise in behavioral economics and motivational interviewing. The study also involves a centralized organizational structure in close collaboration with investigators across the country.

Aim 1: To determine if a personalized and remotely-applied behavioral intervention based on insights from behavioral economics can sustain the symptomatic gains following physical therapy for KOA. Hypothesis: A remotely-applied program will result in maintenance of higher KOOS scores after PT by promoting greater adherence, self-efficacy, habituation, and social support.

Aim 2: To determine if a remote health coach can sustain the symptomatic gains following physical therapy for KOA. Hypothesis: Those that are randomized to receive a health coach will maintain higher KOOS scores after PT.

Aim 3: To determine how the behavioral intervention and health coaching interventions interact with each other. Hypothesis: The effect of both interventions will be additive such that the greatest improvement in symptoms will occur among those that receive both interventions.

02

Conditions studied

  • Osteoarthritis, Knee

Keywords

  • physical therapy
  • health coach
  • behavioral intervention
03

In context

Osteoarthritis, Knee

3,302 studies on the registry are indexed under Osteoarthritis, Knee; 608 are open to participants now.

This study's planned enrollment of 254 is above the median of 70 across 2,731 interventional studies indexed under Osteoarthritis, Knee.

Browse Osteoarthritis, Knee studies →

Lead sponsor

VA Office of Research and Development is the lead sponsor of 1,733 studies on the registry; 396 are open to participants now.

Of its 206 completed or terminated interventional studies of FDA-regulated products, 180 (87%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Clinical diagnosis or chronic knee osteoarthritis.
  • Age between 40-90 years
  • Initiating physical therapy for KOA (has initial appointment within the next month or had first PT visit within the last 7 days)
  • To be randomized: PT feels that they are able to safely and reliably participate in ongoing exercise.
  • To be randomized: must have completed at least 4 virtual or in-person appointments with PT
  • To be randomized: must sync their Fitbit at least monthly.

Exclusion criteria

Exclusion Criteria:

  • Lack of a smart phone allowing interaction with the WTH platform
  • Inability to walk 2 blocks without assistance
  • Poorly controlled crystalline arthritis or other diagnosis of inflammatory arthritis.
  • Treating provider or LSI believes life-expectancy is \<1 year
  • Based on LSI or treating provider discretion: exclusions may occur for severe heart failure, unstable angina, end stage renal disease, severe chronic obstructive or other pulmonary disease, or other chronic illness felt to limit participants ability to participate in exercise or resulting in potential safety risk
  • Severe pain in a non-knee area limiting daily function
  • Non-English speakers or poor reading ability limiting ability to interact with text messages.
  • Pregnancy
  • Receiving physical therapy outside of the VA.
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Factorial assignment
Masking
None (open label)
Enrollment
254 participants (estimated)

Study arms

  • No intervention
    No Intervention

    Neither Intervention

  • Experimental
    Health Coaching, No Incentives

    Receives a Health Coach but no Incentive Program

    Behavioral: Health coach

  • Experimental
    No Health Coach, Receives Incentives

    Does not receive a health coach but does receive the incentive program.

    Behavioral: Remote Incentive Program

  • Experimental
    Health Coaching, Receives Incentives

    Receives both a health coach and the incentive program

    Behavioral: Health coach · Behavioral: Remote Incentive Program

Interventions

  • BehavioralHealth coach

    Health Coaching

  • BehavioralRemote Incentive Program

    Behavioral incentive program including gamification, social incentivization, and monitoring.

06

What researchers measure

Primary outcomes

  1. KOOS (Knee Osteoarthritis Outcome Score)

    The KOOS score is a validated and widely used measure of knee-related pain and physical functioning that has been validated in both knee injury and KOA populations. The KOOS measures symptoms and disability on five subscales: Pain, other Symptoms, Function in Activities of Daily Living, Function in Sports and Recreation, and Quality of Life (QOL). Range is from 0-100 for each subscale with lower scores suggesting worse patient experience.

    Time frame: all available measures between 6-18 months (time-averaged effect)

Secondary outcomes

  1. Average Daily Step Counts

    Change in average daily step counts (averaged over the prior month) throughout follow-up (time-averaged effect).

    Time frame: 0-18 Months

  2. Change in Self Efficacy for excercise

    Self-efficacy for exercise scale (change from baseline; time-averaged effect). Range 0-100 with higher scores representing more confidence in exercise.

    Time frame: 6-18 months

  3. Change in gait speed

    Change in walking speed over a 4 meter testing zone (time-averaged effect)

    Time frame: 6-18 months

  4. 30 second sit-to-stand

    Number of times a person can stand and sit within 30 seconds (time-averaged effect)

    Time frame: 6-18 months

  5. Patient Reported Outcomes Measurement Information System Pain Intensity

    Change from baseline in PROMIS Pain Intensity (time-averaged effect). Scale 0-100 (higher score indicates more pain).

    Time frame: 6-18 Months

07

Study locations

1 of 5 sites recruiting
  • Birmingham VA Medical Center, Birmingham, AL
    Birmingham, Alabama 35233-1927, United States
    Not yet recruiting
  • Omaha VA Nebraska-Western Iowa Health Care System, Omaha, NE
    Omaha, Nebraska 68105-1850, United States
    Not yet recruiting
  • VA Portland Health Care System, Portland, OR
    Portland, Oregon 97207-2964, United States
    Not yet recruiting
  • Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA
    Philadelphia, Pennsylvania 19104-4551, United States
    • Joshua F Baker, MD MSCE · Contact · Joshua.Baker@va.gov · (215) 823-5800
    • Joshua F. Baker, MD MSCE · Principal investigator
    Recruiting
  • VA Puget Sound Health Care System Seattle Division, Seattle, WA
    Seattle, Washington 98108-1532, United States
    Not yet recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06488144
Lead sponsor
VA Office of Research and Development
Responsible party
Sponsor
First posted
Jul 5, 2024
Start date
Dec 10, 2025
Primary completion
May 31, 2029 (estimated)
Completion
Jan 1, 2030 (estimated)
Last update
Jan 8, 2026

Study contacts

Joshua F Baker, MD MSCE
Contact
Joshua.Baker@va.gov
(215) 823-5800
Joshua F. Baker, MD MSCE
principal investigator · Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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