[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"osteoporotic-fracture\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:osteoporotic-fracture":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100640591","post-osteoporotic-fracture-exercise-program-100640591",false,"NCT07595991","Post-osteoporotic Fracture Exercise Program","Community Osteoporosis Exercise Class for People Post Fracture","Inclusion Criteria:\n\n* Diagnosed with osteoporosis.\n* History of low trauma fracture within the past year\n* Cleared for physical activity using the get active questionnaire, 100 bpm resting heart rate or less, 160 mm Hg diastolic blood pressure or less\n* Able to understand and provide informed consent.\n* Residing within the study's geographic area (e.g., London, Ontario).\n\nExclusion Criteria:\n\n* Individuals who do not understand the English language\n* Medical conditions contraindicating participation in exercise (e.g., uncontrolled cardiovascular disease, severe respiratory illness).\n* Cognitive impairments that prevent informed consent or participation.\n* Recent major surgeries or medical events limiting physical activity.\n* Participation in conflicting clinical trials or rehabilitation programs.\n* Residents outside the designated study area.","ALL","18 Years",{"count":19,"type":20},100,"ESTIMATED","INTERVENTIONAL",[23],"NA","Those with osteoporosis often have weaker bones and this leads to higher chances of fractures. Therefore, the investigators want to evaluate the feasibility and safety of group exercise classes specifically designed for individuals with osteoporosis who had an osteoporotic fracture. By focusing on this high-risk population, the investigators want to see whether such exercise interventions can be an option for improving bone health, reducing the risk of future fractures, and enhancing physical function without compromising safety.",[26,27],"Osteoporosis","Osteoporotic Fracture",[26,29,30],"Exercise Intervention","Osteoporotic fracture","NOT_YET_RECRUITING","2026-05-12",{"date":34,"type":35},"2026-05-19","ACTUAL",{"date":37,"type":20},"2026-05",{"date":39,"type":20},"2028-02",{"name":41,"class":42},"Western University, Canada","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":55,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":43},"100630891","sacroplasty-for-sacral-insufficiency-fractures-100630891","NCT07493564","Sacroplasty for Sacral Insufficiency Fractures.","Sacroplasty for Sacral Insufficiency Fractures: a Randomised Controlled Trial.","SACRA","Inclusion Criteria:\n\n* Age 50 years or older\n* Low-energy sacral or posterior pelvic fracture confirmed on CT or MRI\n* Symptom duration ≤6 weeks with ongoing pain ≥48 hours\n* Suitable for sacroplasty under local anesthetic with optional sedation\n* Informed consent provided by participant or consultee agreement under the Mental Capacity Act 2005\n\nExclusion Criteria:\n\n* High-energy or unstable pelvic ring fracture requiring open fixation\n* Active infection or malignancy at fracture site\n* Uncorrectable coagulopathy or anatomy precluding safe sacroplasty\n* Life expectancy \\\u003C3 months\n* Participation in conflicting interventional trial\n* Previous sacroplasty\n* Patient not suitable for sacroplasty under local anesthetic with optional sedation","50 Years",{"count":54,"type":20},78,[23],"This study is designed to determine whether sacroplasty, a minimally invasive procedure to stabilize sacral fractures, improves quality of life and functional recovery in adults aged 50 years or older with sacral or posterior pelvic fragility fractures. These fractures are common in older adults and can cause prolonged pain, reduced mobility, and an increased rate of mortality and risk of complications such as pneumonia, blood clots and pressure sores. Standard treatment usually involves pain management, physiotherapy and mobilization but recovery can be slow.\n\nParticipants will be randomly assigned to receive either sacroplasty under local anaesthetic (with optional sedation) performed by interventional radiologists or standard non-surgical care including analgesia and physiotherapy. Follow-up assessments will take place at 6 weeks and 6 months to evaluate pain, mobility, healthcare use, safety and overall quality of life.\n\nThe goal of the study is to provide evidence on whether sacroplasty can accelerate recovery, reduce complications and improve independence and quality of life in older adults with these fractures.",[58,27],"Sacral Fracture",[60,61,62,63,64,65],"sacroplasty","Sacral insufficiency fracture","Pelvic fragility fracture","Minimally invasive","Pain management","Functional recovery","2026-03-23",{"date":68,"type":35},"2026-03-25",{"date":70,"type":20},"2027-01",{"date":72,"type":20},"2030-12",{"name":74,"class":75},"Hull University Teaching Hospitals NHS Trust","OTHER_GOV"]