[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Keller Army Community Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":75},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100542361","dynamic-muscular-electrical-stimulation-following-anterior-cruciate-ligament-reconstruction-in-military-academy-cadets-100542361",false,"NCT06341868","Dynamic Muscular Electrical Stimulation Following Anterior Cruciate Ligament Reconstruction in Military Academy Cadets","Dynamic Gait-Synchronous Neuromuscular Electrical Stimulation Following Anterior Cruciate Ligament Reconstruction","Inclusion Criteria:\n\n1. United States Military Academy cadet between ages of 17-27 years\n2. Undergoing a Primary ACL Reconstruction, or Revision ACL Reconstruction\n\nExclusion Criteria:\n\n1. Concomitant or prior high tibial osteotomy (HTO)\n2. Concomitant or prior cartilage restoration procedure\n3. Concomitant ligamentous reconstruction (lateral collateral ligament; posterior cruciate ligament; medial collateral ligament)\n4. Contraindications to using the KneeStim device\n\n   \\- Use of pacemaker, defibrillators, or other implanted electronic devices, as this may cause electric shock, burns, electrical interference, or death Unstable angina or decompensated heart failure Epilepsy or history of seizure disorder Pregnancy or planning to become pregnant (Self reported) Critical ischemia of lower limbs Moderate to severe dementia Altered sensation at the knee such that the user cannot feel a pinprick Undiagnosed pain syndromes\n5. Any meniscus tear precluding weight bearing for 6 weeks.","ALL","17 Years","27 Years",{"count":20,"type":21},60,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to examine the effects of 12 weeks of post-operative use of a novel wearable electrical stimulation knee sleeve device (KneeStim) on post-operative biomechanical function (gait). Participants will be United States Military Academy cadets aged 17-27 years. The main questions it aims to answer are:\n\n* Examine the effects of KneeStim wear on cadets' post-operative gait\n* Examine changes in site-specific skeletal muscle mass\n* Examine the changes in patient-reported outcomes\n* Assess time to return to full duty\n* Compare Bioelectrical Impedance Analysis (BIA) measurements to Magnetic Resonance Imaging (MRI) measurements (total thigh volume)\n* Determine the concurrent criterion validity of the KneeStim device compared to gold- standard metrics (3D Motion Capture)\n\nParticipants will undergo body composition analysis, MRI, strength testing, standard of care rehabilitation, gait analysis, and complete surveys. Participants will wear the KneeStim during their standard of care rehabilitation visits for the first 5 weeks post-operative, and throughout daily tasks from 6-12 weeks.\n\nResearchers will compare a control group (standard of care + KneeStim controlled low intensity) to an experimental group (standard of care + KneeStim flexible intensity) to assess the aims previously mentioned..",[27],"Anterior Cruciate Ligament Injuries",[29,30,31,32],"knee","Anterior Cruciate Ligament","Gait","Neuromuscular electric stimulation","RECRUITING","2025-12-30",{"date":36,"type":37},"2026-01-02","ACTUAL",{"date":39,"type":37},"2024-09-19",{"date":41,"type":21},"2026-09",{"name":43,"class":44},"Keller Army Community Hospital","FED",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":16,"minAge":17,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":45},"100592075","examining-the-most-effective-method-to-reduce-running-ground-contact-time-100592075","NCT06988709","Examining the Most Effective Method to Reduce Running Ground Contact Time","Inclusion Criteria:\n\n* Military Service Member or USMA cadet between the ages of 17-60\n* Run at least 2 miles three times per week for the past 3 months\n* Able to run for at least 15 continuous minutes at a self-selected speed\n* Fluent in the English language to read and provide informed consent and follow study instructions\n\nExclusion Criteria:\n\n* Lower extremity or low back pain in the previous 3 months\n* Lower extremity or low back surgery in the previous 6 months\n* Self-reported pregnancy or given birth within the last 6 months\n* Currently on a profile that restricts or limits running",true,"60 Years",{"count":55,"type":21},30,[24],"The purpose of our study is to establish the most effective running retraining technique to decrease ground contact time. This will be investigated by applying three running retraining conditions and assessing the change in ground contact time and other biomechanical variables between the runner's baseline running and each retraining technique.",[59],"Healthy Runners",[61,62,63,64,65,66],"running","ground","gait","retraining","contact","time","2025-12-05",{"date":69,"type":37},"2025-12-12",{"date":71,"type":37},"2025-05-01",{"date":73,"type":21},"2026-12-01",{"name":43,"class":44},""]