Improving rehabilitation for veterans after knee surgery
Official title: Improving Rehabilitation for Veterans After Total Knee Arthroplasty Using Individualized Recovery Trajectories
Run by VA Office of Research and Development · NCT05288803 · Data updated 2026-11-12
This study is testing a new tool to help veterans recover better after knee surgery by personalizing their rehabilitation based on their individual needs and goals.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 40 Years to 90 Years |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | VA Office of Research and Development Federal |
| Locations | 2 sites (Aurora, Colorado and 1 other locations) |
| Status | Recruiting |
| Started | April 1, 2022 |
| Main results expected | March 31, 2027 |
| Study ends | June 30, 2027 |
| Registry record updated | October 8, 2026 |
| Trial ID | NCT05288803 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are veterans who have undergone total knee arthroplasty and are seeking outpatient rehabilitation within three weeks post-surgery.
✕Probably not a fit
Patients who received postoperative rehabilitation in home health or skilled nursing facilities, or those aged under 40 or over 90, may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study examines a new clinical decision support tool designed to enhance rehabilitation for veterans recovering from total knee arthroplasty (TKA). The tool aims to personalize rehabilitation treatments based on individual patient needs, goals, and preferences, rather than applying a one-size-fits-all approach. By analyzing recovery data from similar historical patients, the tool predicts recovery trajectories, allowing clinicians to allocate resources more effectively and identify veterans at risk for suboptimal outcomes. This approach seeks to improve functional recovery while reducing the number of physical therapy visits required post-surgery.
Why it matters
Potential benefit: If successful, this tool could lead to more efficient and effective rehabilitation for veterans, improving their recovery outcomes after knee surgery.
How similar studies have gone: Other studies have shown promise in using personalized rehabilitation approaches, but this specific clinical decision support tool is a novel application in the context of TKA rehabilitation.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: -Veterans who have undergone total knee arthroplasty who present for outpatient rehabilitation treatment at the participating clinics within three weeks of surgery Exclusion Criteria: \- postoperative rehabilitation treatment received in the home health or skilled nursing
Where it's running
-
Rocky Mountain Regional VA Medical Center, Aurora, CO
Aurora, Colorado, United States Recruiting -
VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
Pittsburgh, Pennsylvania, United States Recruiting
Study contacts
- Principal investigator: Jennifer E. Stevens-Lapsley, PhD — Rocky Mountain Regional VA Medical Center, Aurora, CO
- Study coordinator: Jennifer E Stevens-Lapsley, PhD
- Email: Jennifer.Stevens-Lapsley@va.gov
- Phone: (303) 949-9304
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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This study tests whether rivaroxaban, apixaban, or LMWH work differently to support blood flow in the legs after total knee replacement in adults.
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Cryotherapy to Cut Opioid Use After Knee Replacement
This trial tests whether compressive cryotherapy with a Game Ready device can lower opioid use and improve recovery after total knee replacement in adults 60–80.
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This study tests whether older adults (65 or older, 70 per description) who have same-day discharge after hip or knee replacement show changes in cognitive test performance from before surgery to the first day after surgery.
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Preoperative Genicular Nerve Block for Knee Replacement
This study tests whether giving a genicular nerve block before knee replacement can reduce pain after surgery and lower opioid use.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.