Efficacy of an Evidence-based Telehealth Intervention in Modifying Health Behavior
Running, not enrolling · Not applicable
Conditions studied: Post-traumatic Osteoarthritis, Knee Sprain, Knee Injuries
In brief
The overall objective of this study is to evaluate the efficacy of the mare telehealth intervention platform and the intervention on patients' readiness to manage osteoarthritis and patient reported outcomes. To accomplish the stated objectives the investigators will conduct a randomized controlled trial. The independent variable will be group (Intervention vs. Control) and the dependent variables will be patient reported knee status (SA1) and readiness to manage arthritis measures (SA2a), as well as activity level (SA2b). We will also compare knowledge about post-traumatic osteoarthritis (PTOA) between groups prior to and following the intervention (SA3).
Key facts
- Study ID
- NCT07187024
- Run by
- Keller Army Community Hospital
- People needed
- 65
- Starts
- 2020-07-24
- Expected to finish
- 2026-09-01
- Last updated by the study team
- 2025-09-22
Who can join
Age: 18 and older, up to 54. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Current or former United States Military Academy (USMA) cadet or active duty service member who has had at least one Anterior Cruciate Ligament (ACL) surgery
You may not qualify if…
- Do not have access to a personal mobile device (tablet or smart phone)
- Are less than 6 months post-surgery
- Known deployment within the next 12 months that would remove them from connectivity with a telehealth application for more than 3 months
- Have not been cleared for full unrestricted return to activity/duty post ACL reconstruction
Where it is running
- Keller Army Community Hospital — West Point, New York, United States
Full record on ClinicalTrials.gov
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