[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"European University Cyprus\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":104},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,76],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100603255","omega-3-fatty-acids-in-muscle-function-and-health-100603255",false,"NCT07134140","Omega-3 Fatty Acids in Muscle Function and Health","Effects of Omega-3 Fatty Acid Supplementation on Muscle Performance, Neuromuscular Function, and Inflammation at Rest and Following Eccentric Exercise.","Inclusion Criteria:\n\n* Body Mass Index (BMI) within the normal range (18.5-25 kg\u002Fm²).\n* Healthy individuals without severe medical conditions (e.g., diabetes, coronary artery disease, hypertension, neuromuscular disorders).\n* No musculoskeletal injury in the lower limbs (e.g., bone fracture, tendon rupture, grade III muscle strain) within the last 6 months before enrollment.\n* Negative responses to all questions on the PAR-Q questionnaire indicating no contraindications to participating in exercise testing.\n* Mentally capable of providing informed consent.\n\nExclusion Criteria:\n\n* Use of any pharmaceutical medications (e.g., statins, aspirin, ibuprofen).\n* Use of dietary supplements (e.g., protein, vitamins) within the last 3 months before enrollment.\n* Participation in a structured training program involving more than three training sessions per week during the study period.\n* Following a special diet (e.g., intermittent fasting, ketogenic diet, vegetarian diet).\n* Allergy or intolerance to fish oil or olive oil.",true,"ALL","20 Years","45 Years",{"count":21,"type":22},32,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study aims to investigate the effects of omega-3 fatty acid supplementation on muscle performance, neuromuscular function, inflammation, and oxidative stress at rest and after eccentric exercise. The findings may provide insights into the role of omega-3 fatty acids in muscle function, physiology, and metabolism following muscle-damaging exercise. Additionally, the effects of omega-3 fatty acids on cardiovascular health will be investigated.",[28],"Healthy",[30,31,32],"omega-3","eccentric exercise","muscle function","NOT_YET_RECRUITING","2025-08-20",{"date":36,"type":37},"2025-08-21","ACTUAL",{"date":39,"type":22},"2025-09",{"date":41,"type":22},"2026-08",{"name":43,"class":44},"European University Cyprus","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":16,"sex":17,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":23,"phases":58,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":45},"100601960","assessing-the-validity-and-reliability-of-imu-systems-and-a-goniometer-in-cervical-motion-virgo-cm-100601960","NCT07117292","Assessing the Validity and Reliability of IMU Systems and a Goniometer in Cervical Motion (VIRGO-CM)","Assessing the Validity and Reliability of Two IMU Sensor Systems and a Goniometer in Multi-Planar Cervical Motion","VIRGO-CM","Inclusion Criteria:\n\n* Healthy adults aged 18 to 40 years\n* Able to understand and follow instructions\n* Provided informed consent\n\nExclusion Criteria:\n\n* History of cervical spine pathology, trauma, or surgery\n* Presence of neck pain, musculoskeletal, neurological, or vestibular disorders\n* Use of medications affecting sensorimotor function\n* Pregnancy\n* Any condition that may interfere with safe participation or data accuracy","18 Years","40 Years",{"count":57,"type":22},18,[25],"This study aims to evaluate how accurate and reliable two wearable sensor systems (inertial measurement units or IMUs) and a goniometer are in measuring cervical spine (neck) motion. Healthy adult volunteers will be asked to perform simple head movements in different directions while being assessed using the devices. The goal is to compare how closely these tools agree with each other and how consistently they record motion across repeated tests. This information will help determine whether the sensors are suitable for use in clinical settings to assess neck movement in future patient populations.",[61],"Cervical Spine Motion Assessment in Healthy Adults",[63,64,65,66,67],"Inertial Measurement Units (IMUs)","Cervical Spine","Wearable Sensors","Validity","Reliability","2025-08-04",{"date":70,"type":37},"2025-08-12",{"date":72,"type":22},"2025-08",{"date":74,"type":22},"2026-12",{"name":43,"class":44},{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":54,"maxAge":55,"enrollmentInfo":83,"targetDuration":4,"studyType":23,"phases":85,"briefSummary":86,"conditions":87,"keywords":90,"overallStatus":95,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":102,"locationsCount":103},"100571983","conservative-treatment-with-blood-flow-restriction-in-patients-with-total-acl-rupture-randomized-clinical-trial-100571983","NCT06727344","Conservative Treatment With Blood Flow Restriction in Patients With Total ACL Rupture. \"Randomized Clinical Trial\"","Comparison of Conservative Treatment With Blood Flow Restriction With Standard Management in Total ACL Rupture. \"Randomized Clinical Trial\"","Inclusion Criteria:\n\n* MRI-confirmed complete rupture of ACL. Ability to communicate and read fluently in Greek and be willing to keep their leg immobilised for the required period based on the study protocol.\n\nExclusion Criteria:\n\n* Heart disease, overweight, diabetes, pregnancy, thrombophilia, atrial fibrillation, heart failure, cancer, use of drugs that may increase blood clotting, use of hormones or contraceptives, any reason for not using BFR e.g., an open wound or serious skin problems and\u002For allergies to the cuff material.",{"count":84,"type":22},20,[25],"The goal of this randomised clinical trial is to evaluate the effects of exercise with blood flow restriction (BFR) in patients with a complete anterior cruciate ligament (ACL) rupture.\n\nThe main questions it aims to answer are:\n\n1. Does blood flow restriction adds any additional benefits to conservative treatment of the ACL?\n2. Does bracing promotes spontaneous healing to the ACL\n\nResearchers will compare bracing and BFR to bracing and sham BFR to see if the intervention provides any additional benefits to the conservative management of this injury.\n\nParticipants will:\n\n1. Use a knee brace for 6 weeks with adjustments according to protocol\n2. Follow and identical exercise plan with either BFR (intervention group) or BFR sham (control group)\n3. Follow a home based exercise program.",[88,89],"ACL","ACL - Anterior Cruciate Ligament Rupture",[91,92,93,94,88],"BFR","Blood Flow Restriction","Brace","ACL rupture","RECRUITING","2025-03-29",{"date":98,"type":37},"2025-04-03",{"date":100,"type":37},"2025-02-01",{"date":39,"type":22},{"name":43,"class":44},2,""]