[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Boise State University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":80},{"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":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":4},"100647272","motor-imagery-and-turning-practice-to-improve-mobility-pilot-trial-100647272",false,"NCT07705360","Motor Imagery and Turning Practice to Improve Mobility: Pilot Trial","Motor Imagery and Turning Practice to Improve Mobility: MI-TURN Pilot Trial","MI-TURN","Inclusion Criteria:\n\n* Age 65 years or older.\n* Self-report difficulty with turning, balance, or walking-related mobility tasks.\n* Self-report increased fall risk, including a history of falls, fall-related injury, multiple falls within the previous year, or fear of falling due to balance or walking concerns.\n* Report some difficulty with walking-related activities, such as turning, walking longer distances, climbing stairs, or completing household activities.\n* Willingness to be randomized to either study group and complete all study procedures.\n* Living independently in the community and able to travel to the research site.\n* Ability to perform motor imagery, defined by a qualifying score on the Motor Imagery Questionnaire - Revised Second Version.\n* Access to an internet-connected computer capable of playing videos with sound in a quiet environment.\n* Ability to provide informed consent.\n\nExclusion Criteria:\n\n* Diagnosis or symptoms of a neurological disorder or central nervous system injury, including Alzheimer's disease, Parkinson's disease, multiple sclerosis, or stroke.\n* Contraindications to transcranial magnetic stimulation (TMS) or non-invasive brain stimulation procedures.\n* Use of medications known to substantially affect central nervous system function.\n* Severe arthritis or musculoskeletal impairment that would limit safe participation in mobility training.\n* Severe obesity (body mass index greater than 35 kg\u002Fm²).\n* Significant cardiovascular, pulmonary, renal, or other uncontrolled medical conditions that may limit safe participation.\n* Myocardial infarction or major cardiac surgery within the previous year.\n* Cancer treatment within the previous year, excluding nonmelanoma skin cancer or cancers with excellent prognosis.\n* Uncontrolled hypertension at rest (systolic blood pressure \\>180 mmHg and\u002For diastolic blood pressure \\>100 mmHg).\n* Bone fracture or joint replacement within the previous 6 months.\n* Current participation in physical therapy or cardiopulmonary rehabilitation targeting lower extremity function.\n* Current enrollment in another clinical trial that may interfere with study participation or outcomes.\n* Inability to communicate effectively with study personnel or inability to understand English-language study procedures.\n* Plans to relocate from the area during the study period.\n* Any additional safety or compliance concerns identified by the investigative team.",true,"FEMALE","65 Years",{"count":21,"type":22},30,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to evaluate whether combining in-person turning practice with home-based Motor Imagery Therapy (MIT) is feasible and may improve mobility in community-dwelling older adults aged 65 years and older who report balance or turning-related mobility concerns. MIT involves mentally practicing movements and watching movement demonstrations without physically performing the movement.\n\nThe main questions this study aims to answer are whether it is feasible for older adults to complete a combined in-person and home-based turning and motor imagery program based on attendance, retention, and activity monitor use; whether adding MIT to a turning intervention improves turning performance more than a comparison program focused on stress management education; whether MIT increases daily physical activity, increases walking intensity, and reduces sedentary time in daily life; and whether measures of brain function related to movement control predict how much participants improve following the intervention.\n\nResearchers will compare a locomotor turning intervention combined with MIT (Loco+MIT) to a locomotor turning intervention combined with stress management education (Loco+SME) to determine whether MIT leads to greater improvements in mobility and daily activity.\n\nParticipants will attend five laboratory visits that include mobility testing, brain stimulation assessments, and physical activity assessments. Participants will also complete six weeks of in-person turning practice sessions held twice per week and home-based sessions three times per week consisting of either motor imagery training or stress management education. In addition, participants will wear a physical activity monitor during daily life to measure movement and sedentary behavior and will complete follow-up assessments after the intervention to evaluate changes in mobility and activity over time.",[28,29],"Mobility Impairment","Community Dwelling Older Adults",[31,32,33,34,35,36,37],"Motor Imagery","Locomotor Training","Mobility","Older Adults","Transcranial Magnetic Stimulation","Turning Performance","Physical Activity","NOT_YET_RECRUITING","2026-07-14",{"date":41,"type":42},"2026-07-15","ACTUAL",{"date":44,"type":22},"2026-08-01",{"date":46,"type":22},"2029-01-31",{"name":48,"class":49},"Boise State University","OTHER",{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":17,"sex":57,"minAge":58,"maxAge":4,"enrollmentInfo":59,"targetDuration":4,"studyType":23,"phases":61,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":79},"100584346","stress-management-for-college-students-100584346","NCT06888141","Stress Management for College Students","Virtual Intervention Targeting Distress in College Students: A Pilot Study","Inclusion Criteria:\n\n* 18 years of age or older\n* college student\n\nExclusion Criteria:\n\n* Younger than 18 years of age","ALL","18 Years",{"count":60,"type":22},500,[25],"The goal of this clinical trial is to learn if a virtual task can reduce distress in college students. The main questions it aims to answer are:\n\n1. Will those who complete the virtual task have less distress?\n2. Will men and women both benefit equally from the virtual task?\n\nResearchers will compare the virtual task to a control task (another virtual task that we expect will not impact distress) to see if distress differs.\n\nParticipants will spend 20 minutes engaging in the virtual task (or the control task) on 3 different days all within one week. They will complete a survey about their well-being before starting the first virtual task and again \\~6 weeks afterward.",[64],"Distress, Emotional",[66,67,68,69],"virtual intervention","men\u002Fmale","college students","emotional distress","RECRUITING","2025-03-14",{"date":73,"type":42},"2025-03-21",{"date":75,"type":42},"2025-02-18",{"date":77,"type":22},"2026-02-18",{"name":48,"class":49},1,""]