[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"aromatase-inhibitors\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:aromatase-inhibitors":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,50],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100618669","impact-of-pilates-exercises-on-bone-mineral-density-in-breast-cancer-survivors-receiving-hormonal-therapy-100618669",false,"NCT07334626","Impact of Pilates Exercises on Bone Mineral Density in Breast Cancer Survivors Receiving Hormonal Therapy","PilatesBCS2026","Inclusion Criteria:\n\n1. Female breast cancer survivors aged 40-60 years.\n2. Histologically confirmed stage I-III breast cancer.\n3. Currently receiving hormonal therapy (aromatase inhibitors) for at least 3 months.\n4. At risk of osteoporosis or with low bone mineral density (BMD) defined by T-score ≤ -1.0 at lumbar spine or hip.\n5. Medically cleared for exercise, specifically low-to-moderate intensity Pilates.\n6. Able to attend supervised exercise sessions three times per week for 12 weeks.\n7. Willing and able to provide written informed consent.\n\nExclusion Criteria:\n\n1. Metastatic (stage IV) or recurrent breast cancer.\n2. History of osteoporotic fractures in the past 12 months.\n3. Severe cardiovascular, respiratory, or musculoskeletal conditions that contraindicate exercise.\n4. Uncontrolled hypertension, diabetes, or thyroid disorders.\n5. Current use of corticosteroids.\n6. Active bone metabolic disease other than osteoporosis (e.g., Paget's disease, osteomalacia).\n7. Severe cognitive impairment or psychiatric illness preventing adherence to exercise or supplementation.\n8. Known allergy or intolerance to calcium or vitamin D supplementation.\n9. Participation in another clinical trial with structured exercise or bone-targeted intervention within the last 3 months.","FEMALE","40 Years","60 Years",{"count":20,"type":21},60,"ESTIMATED","INTERVENTIONAL",[24],"NA","Breast cancer survivors receiving endocrine (hormonal) therapy (aromatase inhibitors) are at high risk for cancer treatment-induced bone loss and osteoporosis due to estrogen depletion.",[27,28,29,30,31],"Breast Cancer","Breast Cancer Survivors","Aromatase Inhibitors","Osteoporosis or Osteopenia","Pilates Exercise",[33,34,35,36],"pilates exercises","breast cancer survivors","bone mineral denisty","aromatase inhibitors","RECRUITING","2026-01-14",{"date":40,"type":41},"2026-01-15","ACTUAL",{"date":43,"type":41},"2026-01-01",{"date":45,"type":21},"2026-09-30",{"name":47,"class":48},"Benha University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":58,"minAge":4,"maxAge":4,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":61,"briefSummary":62,"conditions":63,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":49},"100565497","ai-based-skeleton-recognition-system-for-rehabilitation-exercise-in-breast-cancer-survivors-a-randomized-controlled-trial-100565497","NCT06642948","AI-based Skeleton Recognition System for Rehabilitation Exercise in Breast Cancer Survivors: A Randomized Controlled Trial","Evaluating the Efficacy of Structured Exercise Interventions in Alleviating Aromatase Inhibitor-Induced Arthralgia in Breast Cancer Survivors: A Randomized Controlled Trial","AiRE-MS","Inclusion Criteria:\n\n* 1\\. Pathologically confirmed hormone receptor-positive breast cancer (stage I, II, III).\n\n  2\\. Initiation of treatment with aromatase inhibitors (e.g., anastrozole, letrozole, exemestane).\n\n  3\\. Postmenopausal women, including those with surgically induced menopause. 4. Clear consciousness, no cognitive or communication impairments, and able to comply with the intervention.\n\n  5\\. Informed consent obtained, with voluntary participation in the study. 6. Bone and joint symptoms with a Brief Pain Inventory (BPI) score of ≥3, or presence of at least one of the following risk factors: elevated bone turnover markers, reduced vitamin D levels, increased inflammatory cytokines, elevated C-reactive protein, or elevated rheumatoid factor.\n\n  7\\. Not participating in any physical therapy or exercise-based interventions that may interfere with this study.\n\nExclusion Criteria:\n\n\\- 1. Recurrence of breast cancer or distant metastasis. 2. Presence of other malignancies. 3. Diagnosed rheumatoid arthritis, bone and joint trauma, or other severe bone and joint diseases.\n\n4\\. Bone mineral density T-score \\\u003C-2.5. 5. Presence of absolute contraindications to exercise.","ALL",{"count":60,"type":21},80,[24],"This study aims to develop and evaluate an artificial intelligence (AI)-based skeletal recognition system designed to support real-time, interactive rehabilitation exercise (RE programs. The goal is to mitigate musculoskeletal symptoms associated with endocrine therapy in breast cancer survivors.Endocrine therapy remains a cornerstone in the treatment of hormone receptor-positive breast cancer, typically extending over 5 to 10 years. While the therapeutic benefits of endocrine therapy are well established, agents such as aromatase inhibitors frequently induce musculoskeletal symptoms (MS), including joint pain, stiffness (particularly morning stiffness), carpal tunnel syndrome, tenosynovitis, myalgia, and muscle weakness. These symptoms, which may be continuous or intermittent, can affect both central (spine, hips, shoulders) and peripheral joints (elbows, wrists, knees, feet), severely compromising patients' quality of life (QoL). Although physical exercise has been demonstrated to alleviate these symptoms, adherence to adequate exercise regimens remains suboptimal among patients. Furthermore, there is no consensus on the optimal type, duration, or intensity of exercise interventions, and standardized protocols are lacking. Recognizing exercise as a long-term behavior, we are developing a home-based, AI-assisted rehabilitation program tailored to the specific needs of patients undergoing endocrine therapy.",[64,27,65,29],"Musculoskeletal Symptoms","Endocrine Therapy","2024-10-14",{"date":68,"type":41},"2024-10-15",{"date":70,"type":21},"2024-10-20",{"date":72,"type":21},"2025-01-01",{"name":74,"class":48},"Fudan University"]