[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"activity-motor\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:activity-motor":35},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,55,84,116,137,153,184],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100640820","phase-1-hormones-outcomes-and-pain-pathways-in-exercise-study-100640820",false,"NCT07579182","Hormones, Outcomes, and Pain Pathways in Exercise Study","Mechanical and Non-mechanical Contributions to Chronic Neck, Shoulder, Arm, and Back Pain in Full-busted Women","HOPE","Inclusion Criteria:\n\n1. Able to provide informed consent\n2. Age of 18 to 60 years\n3. Assigned female sex at birth\n4. Right-handed by self-declaration\n5. Willing to participate in one online testing session and up to four in-person testing sessions\n6. Bra band size between 32-40\"\n7. International Physical Activity Questionnaire - Short Form (IPAQ-SF) score of 2 or higher\n8. An answer of \"NO\" to any item of the general health questions of the PARQ+\n9. No history of surgery to the: back, neck, or shoulders or joint replacement\n10. No history of implanted pacemakers or other stimulation devices\n11. No history of spinal cord injury (SCI)\n\nExclusion Criteria:\n\n1. Inability to provide informed consent\n2. Age 17 years old or younger or 61 years or older\n3. Assigned male sex at birth\n4. Left-handed by self-declaration\n5. Not willing to participate in one online testing session and up to four in-person testing sessions\n6. Bra band size greater than 40\" or less than 32\"\n7. IPAQ-SF score of 1 or lower\n8. An answer of \"YES\" to any item of the general health questions of the PARQ+\n9. History of limb amputation (upper or lower extremity)\n10. Presence of open pressure sores on the upper or lower extremities\n11. Currently pregnant or lactating\u002Fbreastfeeding\n12. History of surgery to the: back, neck, or shoulders or joint replacement\n13. History of breast cancer and\u002For mastectomy\n14. History of implanted pacemakers or other stimulation devices\n15. History of spinal cord injury (SCI)\n16. History of joint disease including osteoarthritis and\u002For Rheumatoid Arthritis\n17. History of the following neurological diseases: Cerebrovascular accident (CVA, stroke), Alzheimer's Disease (AD), Dementia (of any form), Huntington's Disease, Traumatic Brain Injury (TBI), Spinal cord injury (SCI), Multiple Sclerosis (MS), Parkinson's Disease (PD), Polio, Paraproteinaemic Demyelinating Neuropathy (PDN) and\u002For Monoclonal Gammopathy of Undetermined Significance (MGUS), Myasthenia Gravis, Muscular Dystrophy, Guillain-Barré Syndrome, Scoliosis, Charcot-Marie-Tooth Disorder or other hereditary neuropathies\n\nAdditional Inclusion Criteria for Intervention Group:\n\na. Self-declared breast size of D-I cup (US sizes: D, E, F, G, H)\n\nAdditional Inclusion Criteria for the Control Group:\n\na. Self-declared breast size of A-C cup (US sizes: AA, A, B, C)",true,"FEMALE","18 Years","60 Years",{"count":22,"type":23},140,"ESTIMATED","INTERVENTIONAL",[26],"PHASE1","The goal of the proposed project is to evaluate a mechanical intervention (sports bras designed specifically for full busted women) to alleviate neck, shoulder, arm, and back pain in full-busted women and investigate the contribution of non-mechanical pathways associated with this type of pain in women. Specifically, the investigators will investigate how sex-hormones, inflammation, and remapping of specific regions of the brain contribute to the manifestation of neck, shoulder, arm, and back pain in full-busted women across the lifespan.",[29,30,31,32,33,34,35,36,37,38,39,40,41],"Breast Pain","Mastalgia","Back Pain","Back Pain, Low","Neck Pain","Chest Pain","Activity, Motor","Healthy Aging","Weight, Body","Inflammation","Gonadal Steroid Hormones","Neuronal Plasticity","Neuromuscular Manifestations","RECRUITING","2026-05-28",{"date":45,"type":46},"2026-06-02","ACTUAL",{"date":48,"type":46},"2026-05-17",{"date":50,"type":23},"2029-09",{"name":52,"class":53},"University of Houston","OTHER",1,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":4,"eligibilityCriteria":61,"healthyVolunteers":17,"sex":62,"minAge":63,"maxAge":64,"enrollmentInfo":65,"targetDuration":4,"studyType":24,"phases":67,"briefSummary":69,"conditions":70,"keywords":73,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":54},"100553682","efficacy-trial-of-healthy-together-juntos-100553682","NCT06489262","Efficacy Trial of Healthy Together (\"Juntos\")","Efficacy Trial of Healthy Together \"Juntos\": A Family-based Digital Lifestyle Intervention for Hispanic Adolescents and Their Parents","Inclusion Criteria:\n\nAdolescent\n\n1. Lives with participating biological parent or legal guardian;\n2. Self-identifies as Hispanic;\n3. Is between the ages of 12-15years old;\n4. Has access to a smartphone;\n5. Does not meet recommendations for physical activity as determined by a validated 2-item screener;\n6. Does not meet recommendations for daily fruit and vegetable intake (proxy for diet quality) as determined by a validated 2-item screener;\n7. Exceeds recommendations for screen time (proxy for sedentary behavior) as determined by a validated 6-item screener\n\nParent\n\n1. Is the biological parent or legal guardian of and lives with the adolescent;\n2. Self-identifies as Hispanic;\n3. Has access to a smartphone;\n\nExclusion Criteria:\n\nAdolescent\n\n1. Has BMI \\\u003C5th (underweight) or ≥95th percentile (obesity);\n2. Has a parent-reported chronic medical condition (e.g., type 2 diabetes) that requires more intensive intervention;\n3. Has parent-reported responses on a physical activity readiness questionnaire (PAR-Q) that indicates a serious health issue, and a physician does not approve participation;\n4. Has a parent-reported cognitive or developmental delay (e.g., Down Syndrome) that may interfere with understanding program materials.\n\nParent\n\n1. Provides PAR-Q responses that indicate a serious health issue and a physician does not approve participation;\n2. Reports family plans to move out of South Florida during the study follow-up period","ALL","12 Years","15 Years",{"count":66,"type":23},750,[68],"NA","The purpose of this study is to assess the efficacy of a family-based digital (web and mobile phone-based) program known as Healthy Together (\"Juntos\") in preventing increases in body mass index and improving moderate-to-vigorous physical activity, diet quality, and percentage body fat among Hispanic adolescents.",[71,35,72],"Obesity","Diet, Healthy",[74],"Hispanic, family, digital health, obesity prevention, physical activity, nutrition","2026-03-19",{"date":77,"type":46},"2026-03-23",{"date":79,"type":46},"2025-02-28",{"date":81,"type":23},"2029-05-31",{"name":83,"class":53},"University of Miami",{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":4,"eligibilityCriteria":90,"healthyVolunteers":11,"sex":18,"minAge":91,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":24,"phases":94,"briefSummary":95,"conditions":96,"keywords":100,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":54},"100494730","with-love-grandma-con-cario-abuelita-pilot-study-100494730","NCT05721976","With Love, Grandma (\"Con Cariño, Abuelita\") Pilot Study","Pilot Study of a Multigenerational Digital Lifestyle Intervention for Hispanic Female Cancer Survivors and Their Families","Cancer Survivor Inclusion Criteria:\n\n* Grandmother\n* Self-identifies as Hispanic\n* Diagnosis of breast cancer (stages I-III), endometrial or ovarian cancer (stages I-II)\n* Completed active treatment (i.e., surgery, chemotherapy, and\u002For radiation)\n* Body Mass Index (BMI) ≥ 25 (overweight range)\n* Engages in \\\u003C150 minutes\u002Fweek of moderate physical activity\n* English or Spanish speaking\n* Owns a mobile device with internet access (e.g., smartphone, tablet)\n* Lives in South Florida\n\nDaughter of Cancer Survivor Inclusion Criteria:\n\n* Adult daughter of the identified cancer survivor (21 years of age or older)\n* Has at least 1 living child ages ≤16 years old\n* Body Mass Index (BMI) ≥ 25 (overweight range) OR engages in \\\u003C150 minutes\u002Fweek of moderate physical activity\n* English or Spanish speaking\n* Owns a mobile device with internet access (e.g., smartphone, tablet)\n* Lives in South Florida\n\nDaughter of Cancer Survivor Exclusion Criteria:\n\n* Has been diagnosed with distant metastatic cancer\n* Has not completed active treatment (i.e., surgery, chemotherapy, and\u002For radiation)\n* Has uncontrolled schizophrenia or bipolar disorder\n* Has a preexisting medical condition that precludes unsupervised physical activity (e.g., severe orthopedic conditions,wheelchair bound).\n\nCancer Survivor Exclusion Criteria:\n\n* Has uncontrolled schizophrenia or bipolar disorder\n* Has a preexisting medical condition that precludes unsupervised physical activity (e.g., severe orthopedic conditions, wheelchair bound)","21 Years",{"count":93,"type":23},60,[68],"The purpose of this study is to assess the feasibility, acceptability, and preliminary effects of a digital (web and mobile-phone-based) program to improve lifestyle behaviors (physical activity, dietary intake) among Hispanic female cancer survivors and adult daughters.",[97,98,99,71,35,72],"Cancer, Breast","Cancer, Uterus","Cancer, Ovary",[101,102,103,104,105,106],"Hispanic","family","digital health","cancer survivorship","physical activity","nutrition","2026-02-24",{"date":109,"type":46},"2026-02-25",{"date":111,"type":46},"2023-02-22",{"date":113,"type":23},"2026-12-31",{"name":115,"class":53},"University of Miami Sylvester Comprehensive Cancer Center",{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":4,"eligibilityCriteria":122,"healthyVolunteers":17,"sex":62,"minAge":123,"maxAge":124,"enrollmentInfo":125,"targetDuration":4,"studyType":24,"phases":127,"briefSummary":128,"conditions":129,"keywords":4,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":134,"leadSponsor":136,"locationsCount":54},"100622069","power-training-progression-methods-100622069","NCT07378826","Power Training Progression Methods","Comparison of Power Training Progression Methods in Older Independently Living Adults.","Inclusion Criteria:\n\n* 50 - 90 years of age.\n* Be able to walk 50m without any sort of assistance device.\n* Be able to understand and communicate in English to properly conduct the training and testing processes.\n\nExclusion Criteria:\n\n* Uncontrolled cardiovascular or neuromuscular disease that prevent participation in a training program.\n* Any systemic inflammatory or autoimmune conditions such as rheumatoid arthritis, or other serious concomitant medical illness.\n* Unresolved injury or surgery to the upper or lower limbs that prevents weight training.\n* \\- Montreal Cognitive Assessment (MoCA) score below 18","50 Years","90 Years",{"count":126,"type":23},45,[68],"This study will investigate the impact of two unique progression models for power training in a sample of healthy older adults. The objective is to identify the most practical methodology for implementing power training, which is considered a critical marker of functional capacity in older populations.",[35],"2026-01-30",{"date":132,"type":46},"2026-02-02",{"date":130,"type":46},{"date":135,"type":23},"2027-05-30",{"name":83,"class":53},{"id":138,"slug":139,"hasResults":11,"nctId":140,"briefTitle":141,"officialTitle":142,"acronym":4,"eligibilityCriteria":143,"healthyVolunteers":11,"sex":62,"minAge":123,"maxAge":144,"enrollmentInfo":145,"targetDuration":4,"studyType":24,"phases":146,"briefSummary":147,"conditions":148,"keywords":4,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":149,"startDateStruct":150,"completionDateStruct":151,"leadSponsor":152,"locationsCount":54},"100622068","low-versus-high-load-training-and-parkinsons-disease-100622068","NCT07378813","Low Versus High Load Training and Parkinson's Disease","Comparison of Changes in Neuromuscular and Functional Performance Due to Resistance Training With Low-Load or High-Load in Persons With Parkinson's Disease.","Inclusion Criteria:\n\n* Parkinson's Disease Hoehn \\& Yahr Stages 1-3\n* Able to walk 50m unassisted\n* Able to understand and communicate in English\n* A Montreal Cognitive Assessment (MoCA) score above 18\n\nExclusion Criteria:\n\n* Uncontrolled cardiovascular or other neuromuscular disease that prevent participation in a training program\n* Any systemic inflammatory or autoimmune conditions such as rheumatoid arthritis, or other serious concomitant medical illness\n* Unresolved injury or surgery to the upper or lower limbs that prevents weight training.","85 Years",{"count":93,"type":23},[68],"This study will compare the effects of high-load resistance training to low-load resistance training, on measures of muscle strength and power and tests of daily performance in older adults with Parkinson's disease.",[35],{"date":132,"type":46},{"date":130,"type":46},{"date":135,"type":23},{"name":83,"class":53},{"id":154,"slug":155,"hasResults":11,"nctId":156,"briefTitle":157,"officialTitle":158,"acronym":159,"eligibilityCriteria":160,"healthyVolunteers":17,"sex":62,"minAge":19,"maxAge":161,"enrollmentInfo":162,"targetDuration":4,"studyType":24,"phases":164,"briefSummary":165,"conditions":166,"keywords":169,"overallStatus":174,"whyStopped":4,"lastUpdateSubmitDate":175,"lastUpdatePostDateStruct":176,"startDateStruct":178,"completionDateStruct":180,"leadSponsor":182,"locationsCount":4},"100600090","comparison-of-the-effects-of-aerobic-anaerobic-exercises-on-hormonal-and-immune-biomarkers-100600090","NCT07092969","Comparison of the Effects of Aerobic-Anaerobic Exercises on Hormonal and Immune Biomarkers","Comparison of the Effects of Aerobic and Anaerobic Exercises on Hormonal and Immune Biomarkers Measured by Blood and Saliva in Young Individuals","Biomarkers","Inclusion Criteria:\n\n* Being a university student,\n* Being between the ages of 18 and 25.\n\nExclusion Criteria:\n\n* Having orthopedic problems that prevent exercise,\n* Having cognitive or mental health problems that prevent participation in exercise,\n* Having chronic systemic diseases such as cardiac, pulmonary, or nephrological.","25 Years",{"count":163,"type":23},90,[68],"This study aims to compare the effects of aerobic and anaerobic exercise on hormonal, immunological, and metabolic biomarkers in young individuals using blood and saliva samples. It will also assess participants' physical activity levels, depression levels, and general lifestyle habits to explore their relationship with biomarker profiles. Biomarkers such as testosterone, progesterone, cortisol, IgA, alpha-amylase, insulin, lactate, and various inflammatory cytokines will be measured using ELISA. The study seeks to evaluate the physiological and psychosocial effects of different types of exercise in a holistic manner.",[35,159,167,168],"Exercise","Immunity",[170,171,172,173],"Exercise physiology","Aerobic and anaerobic exercis","Hormonal and immunological responses","Physical activity","NOT_YET_RECRUITING","2025-07-28",{"date":177,"type":46},"2025-07-30",{"date":179,"type":23},"2025-09-15",{"date":181,"type":23},"2026-09-15",{"name":183,"class":53},"Sakarya Applied Sciences University",{"id":185,"slug":186,"hasResults":11,"nctId":187,"briefTitle":188,"officialTitle":189,"acronym":190,"eligibilityCriteria":191,"healthyVolunteers":17,"sex":62,"minAge":192,"maxAge":63,"enrollmentInfo":193,"targetDuration":4,"studyType":24,"phases":195,"briefSummary":196,"conditions":197,"keywords":4,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":199,"lastUpdatePostDateStruct":200,"startDateStruct":202,"completionDateStruct":204,"leadSponsor":206,"locationsCount":54},"100550549","reference-values-for-the-muscle-power-sprint-test-100550549","NCT06448520","Reference Values for the Muscle Power Sprint Test","Reference Values for the Muscle Power Sprint Test in Children Aged 5-12 Years","Ref MPST","Inclusion Criteria:\n\n* Age 5-12 years\n* Attending primary education at one of the participating schools or attending participating after-school childcare centers.\n\nExclusion Criteria:\n\n* Contra-indication for maximal exercise due to cardiac or respiratory morbidities\n* Injuries limiting maximal exercise capacity\n* Known with motor function impairment which may hamper maximal exercise (e.g. neurologic comorbidities)","5 Years",{"count":194,"type":23},480,[68],"The goal of this prospective, cross-sectional study is to develop updated reference values for the Muscle Power Sprint Test (MPST) in children aged 5-12 years.\n\nThe main question it aims to answer is:\n\n• What are reference ('normal') values for the MPST in children aged 5-12 years?\n\nParticipants will be asked to perform six short sprints of fifteen meters each, with a ten-second rest between each effort.",[198,35],"Development, Child","2025-02-24",{"date":201,"type":46},"2025-02-25",{"date":203,"type":46},"2024-12-01",{"date":205,"type":23},"2025-09",{"name":207,"class":53},"Erasmus Medical Center"]