[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Brooks Rehabilitation\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":64},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"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":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":5},"100605617","effect-of-neuro20-functional-electrical-stimulation-suit-on-autonomic-function-muscle-performance-and-gait-100605617",false,"NCT07164846","Effect of Neuro20 Functional Electrical Stimulation Suit on Autonomic Function, Muscle Performance, and Gait","Neuro20","Inclusion Criteria:\n\n* At least one week post amputation or neurologic injury (i.e. brain injury, stroke, spinal cord injury) and deemed medically stable to participate in rehabilitation\n* Able to provide Informed Consent by demonstrating the ability to follow a three step command\n\nExclusion Criteria:\n\n* Pacemaker \u002F Defibrillator or severe cardiac disease (Class IV according to New York Heart Association Functional Classification)\n* Implanted medical devices\n* Active DVT\u002Fthrombophlebitis\n* Active Cancer\n* Active fever, infection, or acute inflammation\n* Pregnancy\n* Epilepsy or uncontrolled seizures or seizure within the last 6 months\n* Implanted stimulator or pump that cannot be turned off externally\n* Significant, active wounds in areas stimulated by the suit\n* Inability to follow a three-step motor command\n* Bleeding tendency","ALL","18 Years",{"count":19,"type":20},30,"ESTIMATED","INTERVENTIONAL",[23],"NA","This research aims to understand the effect of the Neuro20 Functional Electrical Stimulation Suit on autonomic nervous system function, muscle performance, and gait after amputation or neurologic injury.",[26,27,28],"Spinal Cord Injury","Stroke","Amputees","RECRUITING","2025-10-30",{"date":32,"type":33},"2025-10-31","ACTUAL",{"date":35,"type":33},"2025-08-05",{"date":37,"type":20},"2026-08-01",{"name":39,"class":40},"Brooks Rehabilitation","OTHER",{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":48,"enrollmentInfo":49,"targetDuration":4,"studyType":21,"phases":51,"briefSummary":52,"conditions":53,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":63},"100604418","assessing-the-impact-of-esight-go-at-home-usage-in-individuals-with-visual-impairment-100604418","NCT07149259","Assessing the Impact of eSight Go At-Home Usage in Individuals With Visual Impairment","eSight","Inclusion Criteria:\n\n* Aged 18 to 90.\n* Best-corrected visual acuity between 20\u002F50 to 20\u002F400 in the better eye.\n* Subjects who have been diagnosed with an ocular condition causing visual impairment\n* Have a functional binocular field of view of at least 20 degrees.\n* Visual status stable for at least six months.\n* Demonstrate visual benefit from magnification.\n* Agree to wear the eSight Go in a variety of situations in the home and community.\n* Score ≥ 20 on the Short Orientation-Memory-Concentration Test of Cognitive Impairment (OMCT).\n* Subject must be able to provide an informed consent\n* Subject must agree to use eSight Eyewear only under conditions that will not jeopardize the safety of either the user or the device.\n\nExclusion Criteria:\n\n* Participant must not be currently undergoing any medical or surgical procedures resulting in unstable vision.\n* Participants who have undergone cataract, refractive, or other surgical procedures related to vision in the six-month period prior to study enrollment.\n* Severe (\\>20\u002F400) visual impairment in the better seeing eye.\n* Cognitive limitations (\\\u003C 20 on OMCT).\n* Participants who have undergone any vision-related injections (e.g. anti-VEGF) in the two-month period prior to the study because of active bleeding in the retina. Ongoing anti-VEGF treatments are permitted if the participant is in a \"Treat and Extend\" or pro re nata (\"PRN\") disease management, and macula is dry.\n* Participants are unable or unwilling to adhere to the examination schedules as they are described in the study protocol. This may also include participants already enrolled, who for whatever reason, have become unable or unwilling to continue the study. This may also include participants for whom the travel time to\u002Ffrom the study site is unacceptable.\n* Participants who self-report a history of alcoholism, drug abuse, or psychosis.\n* Participants who exhibit clinical evidence of depression, poor motivation, emotional or intellectual problems, or any other conditions which would likely limit validity of consent or appropriate responses to participate in the study or who are deemed unsuitable psychologically or physiologically for study participation by the investigator.\n* Participants who may have a conflict of interest with eSight Corp, which could reasonably influence their participation in the study.\n* Refractive error outside the range correctable by lens inserts in the device (\\> +\u002F-8.00 D sph or -4.00 cyl)","90 Years",{"count":50,"type":20},50,[23],"This research aims to test the updated version of Gentex's device, eSight Go, an image enhancing wearable device to assist those with vision impairments limiting activities of daily living.",[54],"Low Vision Aids","2025-08-27",{"date":57,"type":33},"2025-08-29",{"date":59,"type":33},"2025-06-18",{"date":61,"type":20},"2026-06-01",{"name":39,"class":40},1,""]