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Study identifier: NCT05288803 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Improving Rehabilitation for Veterans After Total Knee Arthroplasty Using Individualized Recovery Trajectories

Condition: Total Knee Arthroplasty  ·  Sponsor: VA Office of Research and Development

PhaseN/A
Planned participants200
Who can joinAll sexes, 40 Years to 90 Years
Healthy volunteersNo

About this study

This study will examine the impact of a new clinical decision support tool for rehabilitation after total knee arthroplasty (TKA). Typically, TKA rehabilitation is generic with most patients receiving the same dosage and contents of rehabilitation despite notable diversity among patients who undergo TKA. The investigators clinical support decision tool is designed to help physical therapists tailor rehabilitation treatments and dosages to the individual needs, goals, and preferences of Veterans recovering from TKA. This study has the potential to improve Veterans' functional recovery after TKA, while simultaneously reducing the average number of physical therapy visits Veterans attend after surgery by tailoring rehabilitation dosage based upon need. This will ensure the Veterans Health Administration (VHA) has the resources and capacity to provide adequate rehabilitation to every Veteran seeking TKA in the VHA system. Additionally, if successful, this clinical decision support tool could be used to improve outcomes and access for additional patient populations in the future.

This description comes directly from the study's public registry record.

Talk to the study team

Jennifer E Stevens-Lapsley, PhD  ·  (303) 949-9304  ·  Jennifer.Stevens-Lapsley@va.gov

Amy L Peters  ·  (720) 261-9774  ·  Amy.Peters3@va.gov

Always discuss trial participation with your own doctor first.

Locations (2)

Rocky Mountain Regional VA Medical Center, Aurora, COAurora, Colorado, United StatesRecruiting
VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PAPittsburgh, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05288803