[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Nanjing Mingzhou Rehabilitation Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":105},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,41,62,85],{"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":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100637151","mindfulness-with-dual-task-training-in-post-stroke-mild-cognitive-impairment-100637151",false,"NCT07603102","Mindfulness With Dual-Task Training in Post-Stroke Mild Cognitive Impairment","Mindfulness Combined With Dual-Task Training for Post-Stroke Mild Cognitive Impairment: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Diagnosis of stroke confirmed by computed tomography (CT) or magnetic resonance imaging (MRI).\n* Time since stroke onset ≥3 months and medically stable.\n* Presence of mild cognitive impairment after stroke, defined by a Montreal - - Montreal Cognitive Assessment (MoCA) score \\\u003C 26.\n* Mini-Mental State Examination (MMSE) score ≥ 24.\n* Ability to walk independently with or without an assistive device for at least 10 meters.\n* Stable medication regimen for at least 4 weeks prior to enrollment.\n* Ability to understand study instructions and provide written informed consent.\n\nExclusion Criteria:\n\n* Severe aphasia, visual impairment, hearing impairment, or communication disorders that interfere with assessment or training participation.\n* Severe depression or other major psychiatric disorders.\n* Other neurological diseases affecting cognition or movement (e.g., Parkinson's disease, multiple sclerosis, traumatic brain injury).\n* Severe musculoskeletal, cardiovascular, or systemic diseases that contraindicate exercise participation.\n* Participation in other structured cognitive or rehabilitation intervention programs within the past 3 months.\n* Unstable medical condition or recurrent stroke during the study period.\n* Inability to safely complete the training protocol as determined by the study investigators.","ALL","55 Years",{"count":19,"type":20},60,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study aims to investigate whether a combined intervention of mindfulness and dual-task training can improve cognitive function and physical performance in individuals with mild cognitive impairment after stroke.",[26,27],"Stroke","Mild Cognitive Impairment (MCI)","RECRUITING","2026-05-16",{"date":31,"type":32},"2026-05-22","ACTUAL",{"date":34,"type":32},"2026-05-01",{"date":36,"type":20},"2026-11",{"name":38,"class":39},"Nanjing Mingzhou Rehabilitation Hospital","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":51,"briefSummary":52,"conditions":53,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":57,"completionDateStruct":59,"leadSponsor":61,"locationsCount":40},"100638146","isokinetic-training-with-blood-flow-restriction-for-patellofemoral-pain-syndrome-100638146","NCT07600827","Isokinetic Training With Blood Flow Restriction for Patellofemoral Pain Syndrome","Effects of Isokinetic Training Combined With Blood Flow Restriction in Patellofemoral Pain Syndrome","Inclusion Criteria:\n\n* Participants aged 18 to 40 years.\n* Clinical diagnosis of patellofemoral pain syndrome (PFPS).\n* Presence of anterior or retropatellar knee pain for at least 3 months.\n* Pain provoked by at least two activities that increase patellofemoral joint load, including squatting, stair climbing, running, jumping, prolonged sitting, or kneeling.\n* Average knee pain intensity of ≥3 on a 10-point visual analog scale (VAS) during aggravating activities.\n* Ability to participate in exercise training and attend scheduled intervention sessions.\n* Willingness to provide written informed consent.\n\nExclusion Criteria:\n\n* History of knee surgery or significant trauma to the lower extremity within the previous 12 months.\n* Clinical evidence of other knee disorders, including ligament injury, meniscal injury, patellar instability, osteoarthritis, or tendinopathy.\n* Presence of neurological, cardiovascular, or systemic musculoskeletal disorders that may affect lower limb function or exercise participation.\n* Current participation in other structured lower extremity rehabilitation or strength training programs.\n* Contraindications to blood flow restriction training, including uncontrolled hypertension, vascular disease, thromboembolic disorders, or clotting abnormalities.\n* Use of pain-relieving injections or surgical interventions for knee pain within the previous 6 months.\n* Pregnancy.\n* Inability to complete the assessment or intervention procedures.","18 Years","40 Years",{"count":19,"type":20},[23],"This randomized controlled trial aims to investigate the effects of isokinetic training combined with blood flow restriction (BFR) in individuals with patellofemoral pain syndrome (PFPS).",[54],"Patellofemoral Pain Syndrome","2026-05-15",{"date":31,"type":32},{"date":58,"type":32},"2026-02-25",{"date":60,"type":20},"2026-06",{"name":38,"class":39},{"id":63,"slug":64,"hasResults":11,"nctId":65,"briefTitle":66,"officialTitle":67,"acronym":4,"eligibilityCriteria":68,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":69,"enrollmentInfo":70,"targetDuration":4,"studyType":21,"phases":72,"briefSummary":73,"conditions":74,"keywords":4,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":40},"100587619","mindfulness-enhanced-dual-task-training-in-pd-mci-100587619","NCT06930742","Mindfulness-Enhanced Dual-Task Training in PD-MCI","Mindfulness-Enhanced Cognitive-Motor Dual-Task Training Using Balance and Isokinetic Systems for Parkinson's Disease With Mild Cognitive Impairment: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Age: Between 55 and 75 years.\n* Disease Diagnosis: Clinically diagnosed with Idiopathic Parkinson's Disease (PD) according to the UK Parkinson's Disease Society Brain Bank Criteria.\n* Disease Stage: Hoehn \\& Yahr (H\\&Y) stages 1 to 2.5.\n* Cognitive Function: Montreal Cognitive Assessment (MoCA) score between 23 and 26, indicating mild cognitive impairment (MCI).\n* Medication Stability: Stable doses of antiparkinsonian medications for at least 4 weeks prior to screening.\n* Subjective Cognitive Complaints: Self-reported or informant-reported cognitive decline persisting for at least 6 months.\n* Ambulatory Ability: Able to walk independently, with or without assistive devices.\n* Sensory Abilities: Adequate vision and hearing to comply with study procedures.\n* Informed Consent: Willingness to provide written informed consent and comply with study requirements.\n\nExclusion Criteria:\n\n* Other Neurological Disorders: Presence of other neurological conditions that could affect cognitive function, such as Alzheimer's disease, stroke, or brain tumors.\n* Psychiatric Conditions: Severe psychiatric disorders, including major depressive disorder or schizophrenia.\n* Substance Abuse: Recent history of drug or alcohol abuse.\n* Serious Medical Conditions: Uncontrolled hypertension, diabetes, heart disease, or other conditions that could interfere with study participation or outcomes.\n* Severe Cognitive Impairment: Diagnosis of Parkinson's Disease Dementia (PDD).\n* Other Factors Affecting Cognition: Recent head trauma, uncontrolled thyroid dysfunction, vitamin B12 deficiency, or other conditions known to affect cognitive function.\n* Deep Brain Stimulation (DBS): History of DBS treatment. Participation in Other Clinical Trials: Participation in another clinical trial that could interfere with this study within the last 3 months.","75 Years",{"count":71,"type":20},90,[23],"The goal of this clinical trial is to learn if Mindfulness-Enhanced Dual-Task Training work to treat PD-MCI in adults. The main questions it aims to answer are:\n\nDoes Mindfulness-Enhanced Dual-Task Training improve the cognitive or motor function of participants? Can the combination of Dual-Task Training and Mindfulness achieve better effects?\n\nResearchers will compare 3 groups (Dual-Task Training + Mindfulness, Dual-Task Training, and conventional motor task training) to see if Dual-Task Training and Mindfulness works to treat PD-MCI.\n\nParticipants will:\n\nReceive treatment for 4 weeks Receive scale and instrument testing before and after treatment",[27,75],"Parkinson's Disease (PD)","NOT_YET_RECRUITING","2025-04-09",{"date":79,"type":32},"2025-04-16",{"date":81,"type":20},"2025-05-01",{"date":83,"type":20},"2025-07-30",{"name":38,"class":39},{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":4,"eligibilityCriteria":91,"healthyVolunteers":11,"sex":16,"minAge":48,"maxAge":92,"enrollmentInfo":93,"targetDuration":4,"studyType":21,"phases":94,"briefSummary":95,"conditions":96,"keywords":4,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":4},"100552773","visual-feedback-balance-training-system-combined-with-rfe-in-stroke-100552773","NCT06477445","Visual Feedback Balance Training System Combined with RFE in Stroke","Effect of Visual Feedback Balance Training System Combined with Repetitive Facilitative Exercise on Fall Risk After Stroke: a Randomized Control Trial","Inclusion Criteria:\n\n* patients (18 to 74 years old) who suffered a first or second unilateral stroke\n* chronic stroke (over 6 months from the onset)\n* moderate or higher risk of falls (TUG \\> 15s, or 10-MWT ≤ 0.8m\u002Fs)\n* ability to understand and follow simple directions\n\nExclusion Criteria:\n\n* pregnant or lactating\n* lower extremity contracture, pain, or trauma\n* perceptual, apraxic, or cognitive deficits that lead to inability to follow verbal instructions\n* unable to maintain standing posture\n* cerebellar lesion\n* clinically unstable medical disorders\n* inability to provide informed consent","74 Years",{"count":19,"type":20},[23],"The goal of this clinical trial is to learn if visual feedback balance training system combined with repetitive facilitative exercise (RFE) work to treat stroke in adults. The main questions it aims to answer are:\n\nDoes visual feedback balance training system combined with RFE reduce the fall risk of participants? Can the combination of intelligent rehabilitation robot training system and RFE achieve better effects?\n\nResearchers will compare 3 groups (RFE, visual feedback balance training system under RFE, and conventional therapy) to see if visual feedback balance training system and RFE works to treat stroke.\n\nParticipants will:\n\nReceive treatment for 4 weeks Receive scale and instrument testing before and after treatment",[26],"2024-06-21",{"date":99,"type":32},"2024-06-27",{"date":101,"type":20},"2024-07",{"date":103,"type":20},"2024-10",{"name":38,"class":39},""]