[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Pôle Saint Hélier\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":89},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,42,66],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100631155","pracoh-prevention-breakdown-support-advice-guidance-disability-100631155",false,"NCT07496996","PRACOH Prevention Breakdown Support Advice Guidance Disability","Single-center Prospective Interventional Study Evaluating a Device for Preventing Breakdown Situations in People With Disabilities and Their Primary Caregivers","PRACOH","Inclusion Criteria:\n\n* Patients:\n\n  * People with disabilities requiring a 4-week stay in a dedicated transitional care unit at POLE MPR ST HELIER\n  * Men or women, of legal age (over 18)\n  * Affiliated with a social security scheme or entitled to benefits\n  * Having given their free and informed consent\n* Caregivers:\n\n  * Primary caregiver from the circle of a person with a disability who has agreed to participate in the study.\n  * Male or female, of legal age (over 18)\n  * Affiliated with a social security scheme or entitled to benefits\n  * Having given their free and informed consent\n\nExclusion Criteria:\n\n* Patients:\n\n  * Pregnant women, women in labor, or women who are breastfeeding\n  * Individuals deprived of their liberty by judicial (excluding guardianship or curatorship) or administrative decision\n  * Individuals undergoing severe psychiatric treatment that may impact the conduct of the protocol, at the investigator's discretion\n  * Individuals in an emergency situation who are unable to give their prior consent.\n  * Individuals already admitted to a healthcare or social care facility for purposes other than research.\n* Caregivers:\n\n  * Professional caregivers of participants with disabilities who have agreed to participate in the study.\n  * Pregnant women, women in labor, or women who are breastfeeding,\n  * Individuals deprived of their liberty by a judicial (excluding guardianship or curatorship) or administrative decision.\n  * Individuals undergoing severe psychiatric treatment that may impact the conduct of the protocol, at the investigator's discretion\n  * Individuals in an emergency situation who are unable to give their prior consent.","ALL","18 Years",{"count":20,"type":21},100,"ESTIMATED","INTERVENTIONAL",[24],"NA","The main objective of this prospective interventional study is to evaluate the impact of the stay in the dedicated transitional care unit, through the achievement of the patient's primary objective set at admission, directly related to their specific needs.\n\nIt is expected to improve knowledge regarding the prevention of situations of breakdown and exhaustion in the living environment of people with disabilities.\n\n* This would improve the life and care pathways as well as the support provided to these individuals and their families and friends.\n* It would limit the use of unscheduled care services in crisis situations, thereby improving the quality of care and life.",[27,28],"Person With a Disability","Caregiver","NOT_YET_RECRUITING","2026-04-03",{"date":32,"type":33},"2026-04-09","ACTUAL",{"date":35,"type":21},"2026-04",{"date":37,"type":21},"2028-12",{"name":39,"class":40},"Pôle Saint Hélier","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":49,"sex":17,"minAge":18,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":41},"100610624","effects-of-moderatesevere-traumatic-brain-injury-in-the-subacute-or-chronic-phase-on-locomotor-strategies-involved-in-navigation-in-complex-virtual-environments-100610624","NCT07230002","Effects of Moderate\u002FSevere Traumatic Brain Injury in the Subacute or Chronic Phase on Locomotor Strategies Involved in Navigation in Complex Virtual Environments","NAVIGO","Inclusion Criteria for Traumatic Brain Injury group :\n\n* 18 ≤ Age ≤ 55 years old\n* Male\u002Ffemale\n* Having suffered a first non-penetrating head injury\n* Moderate to severe severity with initial Glasgow Coma Scale score 5\\\u003CGCS\\\u003C13\n* In the subacute or chronic phase (≥ 3 months at the date of the experiment, relative to the date of the injury)\n* Able to walk (10WMT speed ≥ 0.8 m\u002Fs, able to walk at least 20 m without technical or human assistance, PM ≥ 300 m)\n* Able to maintain dynamic balance while standing (TUG\\\u003C16s)\n* Able to answer simple questionnaires, according to the investigator's judgment\n* Having given their free, informed, expressed (written) consent\n* Registered with a social security system\n* Individuals under legal protection measures such as guardianship may be eligible\n\nInclusion Criteria for healthy control group :\n\n* 18 ≤ Age ≤ 55 years old\n* Male\u002Ffemale\n* Able to walk (≥ 0.8 m\u002Fs, able to walk at least 20 m without technical or human assistance, PM ≥ 300 m)\n* Able to answer simple questionnaires, according to the investigator's judgment\n* Having given free, informed, expressed (written) consent\n* Registered with a social security system\n\nExclusion Criteria specific to patients in the traumatic brain injury group :\n\n\\- Person under legal protection (excluding guardianship) or unable to express consent\n\nExclusion Criteria for both groups :\n\n* Severe patho-psychiatric care underway, which may impact the conduct of the protocol, at the investigator's discretion\n* Presence of neurological signs suggestive of a neurodegenerative disease responsible for gait disturbance (Parkinson's syndrome, Alzheimer's disease, etc.)\n* Individuals with musculoskeletal disorders that impact their locomotor abilities\n* Presence of uncontrolled epilepsy at the time of inclusion\n* Presence of visual impairments that make experimentation impossible, at the discretion of the investigator\n* Pregnant, parturient, or breastfeeding women\n* Participants in another ongoing research protocol involving human subjects\n\nExclusion Criteria for healthy control group :\n\n* Presence of fatigue, trauma, or a condition affecting mobility, posture, balance, or walking\n* Persons deprived of their liberty by a judicial or administrative decision\n* Persons deprived of their liberty by judicial or administrative decision\n* Persons under legal protection (guardianship, curatorship, judicial protection) or unable to express their consent\n* Persons undergoing severe psychiatric treatment or admitted to a health or social care facility for purposes other than research.",true,"55 Years",{"count":52,"type":21},40,[24],"While clinical assessment of locomotor function in this population is carried out using tasks involving walking in a straight line without any obstacles, it does not take into account ecological situations (i.e., situations comparable to real-life situations) in which the person interacts with their environment, such as walking down a street with other pedestrians, which is fundamental to everyday life. This research therefore aims to study the social navigation skills during locomotion of people who have suffered a moderate or severe head injury in the chronic phase in more ecological tasks. This will provide a better understanding of the difficulties encountered by these patients during locomotor interactions in everyday life.",[56],"Traumatic Brain Injury","RECRUITING","2025-11-14",{"date":60,"type":33},"2025-11-17",{"date":62,"type":21},"2025-11-30",{"date":64,"type":21},"2026-10-30",{"name":39,"class":40},{"id":67,"slug":68,"hasResults":11,"nctId":69,"briefTitle":70,"officialTitle":71,"acronym":72,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":74,"targetDuration":4,"studyType":22,"phases":76,"briefSummary":77,"conditions":78,"keywords":4,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},"100503466","clinical-investigation-of-the-quality-of-life-benefit-of-using-a-home-walking-exoskeleton-for-a-population-of-multiple-sclerosis-patients-100503466","NCT05835622","Clinical Investigation of the Quality of Life Benefit of Using a Home Walking Exoskeleton for a Population of Multiple Sclerosis Patients.","Clinical Investigation of the Quality of Life Benefit of Using a Home Walking Exoskeleton for a Population of Multiple Sclerosis Patients With Gait Disorders.","EXHOMESEP","Inclusion Criteria:\n\n* Patient with multiple sclerosis according to the revised Mac Donald diagnostic criteria (2017) in the relapsing-remitting form more than 6 months from a relapsing or progressive period.\n* An Expanded Disability Status Scale (EDSS) between 5 and 6.5 on the EDSS scale (Kurtzke 1983)\n* Living at home\n* Using a walking aid\n* 18 years old or older\n* Have freely consented to participate in this study\n* To be more than 1m52 tall\n* Hip Manual Muscle Testing (MMT) score ≥ 3+ (flexors and expanders)\n* Knee Manual Muscle Testing (MMT) score ≥ 2 (flexors and expanders)\n* Berg scale (BBS) score \\> 20\n* Patient affiliated with a social security plan or beneficiary of such a plan.\n\nNon-Inclusion Criteria:\n\n* Impaired comprehension preventing completion of the protocol\n* Inability to walk without assistance for 10 minutes\n* Have a rehabilitation stay scheduled during the follow-up period of the clinical investigation\n* Diagnosed psychiatric conditions that may have an impact on the experience of withdrawal of technical assistance at the end of the protocol\n* Severe cognitive impairment (MMSE\\\u003C24)\n* Person deprived of liberty by a judicial or administrative decision\n* A person under psychiatric care or admitted to a health or social institution for purposes other than research.\n* Spasticity \\>3 on the Held and Tardieu scale affecting the hamstring, quadriceps, adductor or sural triceps muscles\n* Complete paralysis of the lower limbs\n* Severe osteoporosis\n* Hip and\u002For knee replacements that would sufficiently limit range of motion for walking and sitting or squatting\n* Severe vascular disorders of the lower limbs\n* Existing wounds or skin lesions where the device is worn\n* Pregnant woman or postpartum woman who has not completed lumbopelvic recovery\n* Orthopedic disorders of the lower limb that may prevent satisfactory adjustment of Keeogo\n* Uncontrolled epilepsy or tremors\n* Uncontrolled autonomic dysreflexia\n* Severe balance disorders, neurological disorders (any condition that prevents the safe control of balance and\u002For movement of the limbs at all times while wearing the Keeogo System)\n* Conditions that prevent safe moderate-intensity exercise",{"count":75,"type":21},28,[24],"The goal of this clinical investigation is to evaluate the effectiveness of home use of a lightweight robotic lower limb exoskeleton as a walking aid device on quality of life in patients with multiple sclerosis with gait disorders.\n\nParticipants will wear an exoskeleton (Keeogo) for 8 weeks at home during the experimental phase. This phase is compared to an 8-week control phase at home with advice on regular physical activity adapted to their abilities.",[79],"Multiple Sclerosis","2025-04-08",{"date":82,"type":33},"2025-04-09",{"date":84,"type":33},"2024-02-01",{"date":86,"type":21},"2026-10-02",{"name":39,"class":40},6,""]