[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"veteran\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:veteran":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,51,81,107,152,181],{"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":26,"conditions":27,"keywords":31,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100612277","phase-1-psilocybin-to-treat-depression-in-spinal-cord-injury-100612277",false,"NCT07251491","Psilocybin to Treat Depression in Spinal Cord Injury","Safety, Tolerability, Outcomes of Psilocybin for Depression (STOP Depression) in Veterans With Spinal Cord Injury","STOP","Inclusion Criteria:\n\n* Able and willing to provide informed consent\n* Spinal cord injury for at least 1 year\n* Confirmed diagnosis of depression\n* At least 22 years of age at time of consent\n* At least 50 kg (110 lbs.) body weight\n* Fully independent from ventilatory support (ventilator or diaphragm pacer)\n* Fluent in speaking and reading English\n* Able to swallow pills\n* Agree to have study visits recorded with audio and video\n* Agree to release outside medical and psychiatric records\n* Able and willing to taper off antidepressant, under clinician supervision\n* Agree to use adequate contraceptive methods\n\nExclusion Criteria:\n\n* Are not able to give adequate informed consent\n* Have used psilocybin or another psychedelic within 6 months\n* Have received Electroconvulsive Therapy (ECT) within 12 weeks\n* Have used ketamine within 12 weeks\n* Have a history of Bipolar I Disorder\n* Have a current eating disorder\n* Have a current severe alcohol or cannabis use disorder within the 6 months\n* Have an illicit drug or prescription drug substance use disorder within 12 months\n* Current serious suicide risk\n* History of heart attack, aneurysm, or stroke\n* Uncontrolled hypertension\n* Are pregnant or nursing","ALL","22 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24,25],"PHASE1","PHASE2","The main goal of this study is to determine if psilocybin is safe for use in people with SCI. The study will measure how people with SCI respond to three psilocybin doses: low (5mg), medium (10mg), and high (25mg).\n\nThe main question the study aims to answer is: does psilocybin increase the number and severity of adverse (bad) events reported by people with SCI? These may include pain, muscle spasms, symptoms of depression, and symptoms of low or high blood pressure. The investigators will also measure how well people with SCI tolerate the psychedelic experience, and compare responses between the low (5mg), medium (10mg), and high (25mg) doses.\n\nParticipants will:\n\n* Agree to be enrolled in the study for up to 13 months.\n* Agree to complete the seven (7) visits that are included in the psilocybin-assisted therapy.\n* Agree to complete follow-up study visits, including in-person visits to the James J Peters VA Medical Center, located in the Bronx, New York and remote visits.\n* Agree to keep a log of how they are feeling and any change in the frequency or severity of adverse events.",[28,29,30],"Spinal Cord Injury","Depression - Major Depressive Disorder","Veteran",[32,33,34,35,36,37],"Tetraplegia","Paraplegia","Psychosocial Wellbeing","Depression","Neuropathic Pain","Psychedelics","RECRUITING","2026-04-28",{"date":41,"type":42},"2026-05-04","ACTUAL",{"date":44,"type":21},"2026-05-01",{"date":46,"type":21},"2028-03-01",{"name":48,"class":49},"James J. Peters Veterans Affairs Medical Center","FED",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":17,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":22,"phases":63,"briefSummary":65,"conditions":66,"keywords":69,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":50},"100607577","goal-oriented-telehealth-rehabilitation-of-executive-functioning-for-veterans-with-chronic-tbi-100607577","NCT07190365","Goal-oriented Telehealth Rehabilitation of Executive Functioning for Veterans With Chronic TBI","Goal-oriented Rehabilitation of Executive Functioning Using Video-telehealth to Improve Community Reintegration for Veterans With Chronic TBI and Cognitive Difficulties","GOALS TH","Inclusion Criteria:\n\n* History of mild to moderate TBI \\> 6 months ago\n* Cognitive difficulties affecting daily functioning\n* Age 18-65\n* Veteran\n* At least 12th grade education or equivalent \\* Interested in improving community reintegration\n\nExclusion Criteria:\n\n* Amnesic\u002FSevere memory problems\n* Active Substance Abuse\u002FDependence\n* Medical condition that may affect mental status\u002Fdisrupt study participation\n* Active psychotropic medication changes","18 Years","65 Years",{"count":62,"type":21},80,[64],"NA","Provision of interventions that address cognitive and emotional problems faced by Veterans with history of TBI pursuing community reintegration is an important concern for VA. Using telerehabilitation, the current project will help determine whether goal-directed training of attentional control functions via personally relevant activities will improve community integration for Veterans with history of TBI and cognitive difficulties. Findings may guide rehabilitation training towards providing services to maximize success in attaining complex functional goals in which Veterans can engage in skill strengthening 'where they are' (any location).",[67,68,30],"Mild to Moderate Traumatic Brain Injury","Cognitive Rehabilitation",[67,68,70,71],"Telehealth","Community Reintegration","2026-04-02",{"date":74,"type":42},"2026-04-03",{"date":76,"type":42},"2026-04-01",{"date":78,"type":21},"2030-03-30",{"name":80,"class":49},"VA Office of Research and Development",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":17,"minAge":59,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":22,"phases":90,"briefSummary":91,"conditions":92,"keywords":93,"overallStatus":97,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":102,"leadSponsor":104,"locationsCount":50},"100629431","oprestore-ai-patient-navigator-study-100629431","NCT07474584","OpRESTORE AI-Patient Navigator Study","The OpRESTORE AI-Patient Navigator Study: Developing and Testing an AI-enhanced Patient Navigator for UK Veterans With Service-related Physical Health Problems","Inclusion Criteria:\n\n* Meets criteria for referral to OpRESTORE service\n* Age 18 years or older.\n* Capacity to consent.\n* Have a physical health need (e.g. not purely mental health, or seeking social care advice)\n\nExclusion Criteria:\n\n* Referrals processed outside standard MDT workflow.\n* Patients lacking capacity to consent.\n* Prisoners.\n* Acute presentation best managed by emergency services and not appropriate for OpRESTORE.",{"count":89,"type":21},1389,[64],"OpRESTORE is a national NHS service that supports UK veterans with complex physical health problems linked to their military service. Veterans referred to OpRESTORE often need care from many different specialists, including surgeons, pain teams, rehabilitation, and mental health services. Currently, decisions about which service is most appropriate are made by a multidisciplinary team (MDT) of clinicians. While effective, this process can be slow, resource-intensive, and sometimes difficult for patients to navigate.\n\nThis study will develop and test a new digital \"navigator\" tool that uses artificial intelligence (AI) to support these referral decisions. The aim is to see whether the tool can safely and accurately match veterans to the right care pathway, while reducing delays and improving patient experience.\n\nThe project will be carried out in several stages:\n\n* Reviewing past OpRESTORE records to design the AI model.\n* Testing the tool alongside the MDT (\"shadow testing\") to check whether its recommendations match the clinical decisions.\n* Running a case-control study to compare outcomes between patients referred using AI support and those referred by the MDT alone.\n* Creating and testing a structured self-referral form to make it easier for veterans to access care directly.\n\nThe main outcome will be whether the AI tool makes the same referral decisions as the MDT. Other outcomes include patient satisfaction, quality of life, time taken to reach the right service, and overall costs.\n\nThe study will recruit veterans aged 18 or older who are referred to OpRESTORE with a physical health need. It will run for two years. If successful, this approach could free up clinician time, shorten waits for treatment, and improve veterans' health and wellbeing, while laying the foundations for wider use of AI-supported navigation across the NHS.",[30],[94,95,96],"healthcare navigation","veteran healthcare","clinical AI","NOT_YET_RECRUITING","2026-03-11",{"date":100,"type":42},"2026-03-16",{"date":44,"type":21},{"date":103,"type":21},"2027-11-01",{"name":105,"class":106},"Imperial College Healthcare NHS Trust","OTHER",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":17,"minAge":59,"maxAge":115,"enrollmentInfo":116,"targetDuration":4,"studyType":117,"phases":4,"briefSummary":118,"conditions":119,"keywords":130,"overallStatus":97,"whyStopped":4,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":147,"completionDateStruct":148,"leadSponsor":150,"locationsCount":50},"100627766","using-integrated-care-and-wearable-technology-to-evaluate-outcomes-of-the-shields--stripes-program-for-veterans-and-first-responders-100627766","NCT07452900","Using Integrated Care and Wearable Technology to Evaluate Outcomes of the Shields & Stripes Program for Veterans and First Responders","Evaluating Integrated Care and Wearable Technology Outcomes in the Shields & Stripes Program for Veterans and First Responders: A Retrospective Mixed-Methods Study","S&S Wellness","Inclusion Criteria:\n\n* Adults aged 18-70 years\n* Current or former members of the U.S. Armed Forces or first responder professions (e.g., law enforcement, firefighting, EMS)\n* Participants who completed the Shields \\& Stripes holistic wellness program\n* Providers who worked within the Shields and Stripes program.\n\nExclusion Criteria:\n\n-None","70 Years",{"count":62,"type":21},"OBSERVATIONAL","This study aims to evaluate outcomes from the Shields \\& Stripes (S\\&S) program - a 12-week, multidisciplinary wellness intervention designed for veterans and first responders. The S\\&S program integrates occupational therapy (OT), mental health (MH), physical therapy (PT), and registered dietitian (RD) services to promote recovery, resilience, and performance in individuals who have experienced cumulative stress, trauma exposure, or occupational burnout.\n\nThis research will use a retrospective mixed-methods observational design to analyze data collected from previous S\\&S participants who consent to research use of their de-identified information. No intervention or treatment changes will occur as part of this study.\n\nQuantitative data will include biometric information (e.g., sleep, activity, and heart rate variability via Oura Ring), standardized self-report measures (GAD-7, PHQ-9, PCL-5, RAND-36, PSQI, ISI), satisfaction surveys, and laboratory nutrition panels. Qualitative data will include semi-structured interviews with consenting participants and S\\&S providers following program completion.\n\nThe purpose of the study is to identify patterns of improvement in physical, psychological, and occupational functioning and to explore how integrated, team-based care supports holistic recovery. Findings may inform the development of future evidence-based wellness programs for military and first-responder populations.\n\nParticipation involves minimal risk, and all data will be de-identified before analysis.",[120,121,122,123,29,124,125,126,127,128,30,129],"Holistic Care","Mental Health","Sleep","PTSD","Anxiety","Resilience","Recovery","Occupation","Biometrics Measurement","Quality of Life",[131,132,133,134,121,135,136,137,138,139,122,140,123,124,35,129,141,142,143],"Shields & Stripes","Veterans","First Responders","Occupational Therapy","Physical Therapy","Registered Dietitian","Integrated Wellness","Biometric Data","Oura Ring","Heart Rate Variability","Holistic Health","Multidisciplinary Rehabilitation","Functional Outcomes","2026-03-06",{"date":146,"type":42},"2026-03-10",{"date":76,"type":21},{"date":149,"type":21},"2027-04-30",{"name":151,"class":106},"Baylor University",{"id":153,"slug":154,"hasResults":11,"nctId":155,"briefTitle":156,"officialTitle":157,"acronym":4,"eligibilityCriteria":158,"healthyVolunteers":159,"sex":160,"minAge":161,"maxAge":4,"enrollmentInfo":162,"targetDuration":4,"studyType":117,"phases":4,"briefSummary":164,"conditions":165,"keywords":168,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":172,"lastUpdatePostDateStruct":173,"startDateStruct":175,"completionDateStruct":177,"leadSponsor":179,"locationsCount":50},"100595064","the-relationship-between-training-dynamics-and-general-health-status-in-veteran-football-players-100595064","NCT07027592","The Relationship Between Training Dynamics and General Health Status in Veteran Football Players","The Relationship Between Training Dynamics and General Health Status With Injury Risk in Veteran Football Players","Inclusion Criteria:\n\n* Playing football as a veteran\n\nExclusion Criteria:\n\n* Not participating in a regular training program",true,"MALE","40 Years",{"count":163,"type":21},130,"The goal of this observational study is to learn how training habits and general health status are related to injury risk in veteran football players (men over 35 years old who play recreational football). The main questions it aims to answer are:\n\nDo specific training patterns (such as frequency, intensity, and duration) increase or lower the risk of injury?\n\nHow does general health status (including factors like sleep, nutrition, and existing health conditions) affect injury risk?\n\nParticipants will:\n\nComplete questionnaires about their training habits, lifestyle, and general health\n\nReport any injuries they experience during the football season\n\nAttend periodic health assessments",[166,167,30],"Football","Injury",[169,170,171],"FIFA 11+","Veteran Football Players","Injury risk","2026-01-28",{"date":174,"type":42},"2026-01-30",{"date":176,"type":42},"2025-06-01",{"date":178,"type":21},"2026-05",{"name":180,"class":106},"Izmir Bakircay University",{"id":182,"slug":183,"hasResults":11,"nctId":184,"briefTitle":185,"officialTitle":186,"acronym":4,"eligibilityCriteria":187,"healthyVolunteers":159,"sex":17,"minAge":18,"maxAge":188,"enrollmentInfo":189,"targetDuration":4,"studyType":22,"phases":191,"briefSummary":192,"conditions":193,"keywords":200,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":210,"lastUpdatePostDateStruct":211,"startDateStruct":213,"completionDateStruct":215,"leadSponsor":217,"locationsCount":50},"100548358","nightware-and-cardiovascular-health-in-veterans-with-ptsd-100548358","NCT06419959","NightWare and Cardiovascular Health in Veterans With PTSD","Improving Cardiovascular Health in Veterans With PTSD by Treating Trauma-Related Nightmares With NightWare","Inclusion Criteria:\n\n1. Diagnosis of PTSD via American Psychiatric Association PTSD diagnostic criteria in the fifth edition of its Diagnostic and Statistical Manual of Mental Disorders (DSM-5).\n2. Self-report having repetitive nightmares contributing to disrupted sleep;\n3. Age 22 years (rationale is because the device has only been used in adults in 22 years and older);\n4. Resting blood pressure (BP, \\\u003C160\u002F100 mmHg);\n5. Fasted glucose \\\u003C126 mg\u002FdL;\n6. Poor overall sleep quality as indicated by a Pittsburgh Sleep Quality Index (PSQI) score 6 or higher;\n7. Epworth Sleepiness Scale (ESS): Question #8 score above \"0\" will prompt an additional question: Do you drive (\"get behind the wheel\") when you are drowsy? The answer must be \"No\" to be enrolled in the study due to safety concerns;\n8. Wireless Internet and two power outlets in sleeping location;\n9. Willingness not to use any other application which collects heart rate data on the phone and watch that is used for NightWare;\n\nExclusion Criteria:\n\n1. Unstable medical condition (e.g., uncontrolled hypertension or active CVD or cancer);\n2. Active infection (note, anyone with an active infection would become eligible once the infection has ended);\n3. Thyroid dysfunction, defined as an ultrasensitive TSH \\\u003C0.5 or \\>5.0 mU\u002FL; volunteers with abnormal TSH values will be re-considered for participation in the study after follow-up evaluation by the PCP with initiation or adjustment of thyroid hormone replacement; or other problems that would interfere with participation in the study;\n4. Use of insulin or sulfonylureas\n5. Pregnancy or currently breast feeding;\n6. Current history (past 3 months) of substance (excluding marijuana) or alcohol abuse per the SCID-5. Adults with past substance or alcohol use disorders will be allowed to participate;\n7. Participants will be excluded if they report elevated acute risk for suicidal self-directed violence warranting immediate hospitalization (e.g., suicidal ideation with intent, evaluated by the Columbia-Suicide Severity Rating Scale \\[C-SSRS\\]).\n8. Shift workers (due to circadian rhythm disruption);\n9. Diagnosis of active disorder of arousal from non-rapid eye movement sleep, rapid eye movement sleep behavior disorder, or narcolepsy;\n10. Nocturia that causes awakening from sleep;\n11. Known sleep walking or acting out dreams (contraindication to NW use);\n12. Diagnosis or suspicion of dementia;\n13. Seizure disorder\n14. Participants experiencing severe cognitive impairment or current psychiatric symptoms of such severity that would preclude participation (e.g., active psychosis, imminently suicidal)","88 Years",{"count":190,"type":21},125,[64],"The purpose of this study is to learn more about the effectiveness of a prescription wrist-wearable device called NightWare (NW) on improving sleep in Veterans with nightmares related to posttraumatic stress disorder (PTSD). The investigators also want to learn whether it improves cardiovascular health among this population.",[194,195,196,197,198,199,30],"Post-traumatic Stress Disorder (PTSD)","Cardiovascular Diseases","Autonomic Dysfunction","Vascular Stiffness","Nightmare","Endothelial Dysfunction",[122,201,202,203,30,204,205,206,207,208,195,209],"Oxidative stress","aging, inflammation","sex\u002Fgender","Trauma and Stressor Related Disorders","Mental Disorders","Nervous System Diseases","Autonomic Nervous System Diseases","Primary Dysautonomias","Stress Disorders, Post-Traumatic","2025-09-11",{"date":212,"type":42},"2025-09-12",{"date":214,"type":42},"2025-09-10",{"date":216,"type":21},"2026-12-31",{"name":80,"class":49}]