[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"serious-mental-illness\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:serious-mental-illness":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,47,73,107,139,175,199,229,259],{"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":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100633655","abriendo-caminos-engaging-latinos-100633655",false,"NCT07529509","Abriendo Caminos: Engaging Latinos","Abriendo Caminos: Engaging Latino Communities Through Culturally Responsive Peer Delivered Motivational Interviewing","AC","Inclusion Criteria:\n\n* Meet criteria for serious mental illness\n* Not in treatment\n* 18 years of age or older\n* Reside in CT\n* Self-identify as Latino\n* Speak English and\u002For Spanish\n* History of trauma\n* Have not received any treatment in the past 30 days\n* Willing and able to be contacted for follow-up\n\nExclusion Criteria:\n\n* Individuals in formal mental health treatment in the past 30 days\n* Have a life-threatening or unstable medical, surgical, or psychiatric condition\n* Inability to provide \\> 1 form of contact information\n* Anticipate being unable to return for a follow-up assessment\n* Reported active risk of suicide or homicide\n* Fail capacity to consent\n* Cognitively impaired\n* Currently in jail or other overnight facilities as required by courts or law","ALL","18 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn if a culturally responsive peer-delivered motivational interviewing intervention can enhance mental health treatment engagement in Latinos with serious mental illness. The main questions it aims to answer are:\n\n* How feasible is it to recruit 30 Latinos with serious mental illness into a 6 week treatment engagement intervention?\n* How acceptable is the intervention to Latinos with serious mental illness?\n\nParticipants will:\n\n* Receive six sixty-minute sessions\n* Complete weekly measures, along with pre-, post-, 30-day, and 60-day post-intervention assessments",[27],"Serious Mental Illness",[29,30,31,32,33],"SMI","Latino","Peer","Recovery","Engagement","RECRUITING","2026-06-09",{"date":37,"type":38},"2026-06-10","ACTUAL",{"date":40,"type":21},"2026-07",{"date":42,"type":21},"2027-08",{"name":44,"class":45},"Yale University","OTHER",2,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":72},"100501331","rct-of-an-intersectional-stigma-intervention-to-sustain-viral-suppression-among-women-living-with-serious-mental-illness-and-hiv-in-botswana-100501331","NCT05807867","RCT of an Intersectional Stigma Intervention to Sustain Viral Suppression Among Women Living With Serious Mental Illness and HIV in Botswana","(A) WOMEN WITH SMI AND HIV\n\nAt Sbrana Psychiatric Hospital, the investigators will recruit women with SMI and HIV who are receiving treatment at that facility. Women with SMI and HIV will be receiving psychiatric care and ART and must:\n\n1. Meet DSM-5 criteria for current psychotic disorder or mood disorders or other disorders causing functional impairment except substance use disorders and developmental disorders, per clinician interview based on the MINI\n2. Have confirmed HIV positive status\n3. Be 18-55 years of age\n4. Be female\n5. Have capacity to provide consent and written informed consent\n6. Speak English or Setswana\n7. Be a Botswana citizen\n\n   The investigators will also recruit 6 to 8 women with SMI and HIV as peer co-leaders to facilitate the intervention. For women who are peer co-leaders, inclusion criteria include #1 to #7 above in addition to:\n8. Remaining adherent to psychiatric medications\n9. Being symptomatically stable for \\>2 years\n10. Maintaining consistent ART adherence.\n\n(B) FAMILY MEMBERS OF WOMEN WITH SMI AND HIV.\n\nIn Botswana, families are usually contacted and engaged in psychiatric treatment planning during inpatient stay or on admission. The involvement of family continues during outpatient follow-ups since most patients are accompanied by some relative or caregiver on such visits. Eligible participants include:\n\n1. Identified by participant and\u002For clinician as the relative 'most involved in the client's care'.\n2. Be 18-65 years of age\n3. English or Setswana speaking\n4. Botswana citizen.\n\n(C) POLICY MAKERS AND OTHER STAKEHOLDERS.\n\nPolicy makers will be\n\n1. Be 18-55 years of age\n2. Include: (a) bureaucratic officials of Botswana, public sector ministries (government) at the national level holding appointment to senior offices that develop, interpret and\u002For implement national mental health and HIV programs (prevention and treatment) or related clinical services; (b) senior bureaucratic officials of the National AIDS and Health Promotion Agency (NAHPA); and (c) senior members of civil society organizations (CSOs), nongovernment organizations (NGOs) or other entities that support the national Botswana government to implement services to People Living With HIV (PLWH) and mental health patients.","65 Years",{"count":55,"type":21},360,[24],"The study goal is to promote viral load suppression among women with serious mental illness (SMI) and HIV in Botswana, given that these women are especially vulnerable to psychiatric medication nonadherence and symptom exacerbation, which are made worse by stigma and threaten antiretroviral therapy (ART) adherence.\n\nThe investigators propose to test an intervention to reduce stigma due to the statuses of SMI and HIV, against an attention control condition, in the high-risk transition period after discharge from an initial psychiatric hospitalization. Specifically, the investigators are conducting a two-arm randomized controlled trial (RCT) with a 4-month follow-up to compare the effectiveness of 1) What Matters Most (WMM)-based intersectional stigma intervention delivered as clients transition from psychiatric hospitalization to outpatient care; and 2) an attention placebo control condition that follows a similar format to isolate the effects of the intervention.\n\nThe investigators will also assess policymaker workshops where peer women with SMI and HIV co-lead the reporting of RCT findings via lived experience to policymakers to initiate structural change.\n\nEnabling women with SMI and HIV to resist stigma has the potential to improve their HIV outcomes and empower these women to elicit broader, structural-level change.",[59,27],"Hiv",[61,62],"HIV","Stigma","2026-04-20",{"date":65,"type":38},"2026-04-23",{"date":67,"type":38},"2024-08-01",{"date":69,"type":21},"2027-12",{"name":71,"class":45},"New York University",1,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":81,"targetDuration":4,"studyType":22,"phases":83,"briefSummary":84,"conditions":85,"keywords":87,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":72},"100627968","facilitation-to-increase-tobacco-treatment-100627968","NCT07455526","Facilitation to Increase Tobacco Treatment","External Facilitation to Expand Reach of Tobacco Treatment to SMI Veterans","FITT","Inclusion Criteria:\n\nProviders:\n\n* VA Maryland Health Care System patient care providers serving Veterans in Critical Time Intervention, Psychosocial Rehabilitation and Recovery Center, Mental Health Integrative Case Management, or outpatient psychiatry clinics\n\nVeterans receiving direct letters:\n\n* Had an appointment in VA Maryland Health Care System, Critical Time Intervention, Psychosocial Rehabilitation and Recovery Center, Mental Health Integrative Case Management, or outpatient psychiatry clinics in the last 30 days\n* Diagnosed with a serious mental illness\n* Positive tobacco use screen\n* Appointment scheduled with an outpatient psychiatric prescriber in the next 30 days\n\n  * Of note, study staff are not directly recruiting Veterans for this implementation intervention component\n\nVeteran chart review:\n\n* All Veterans actively enrolled in VAMHCS medical facilities with at least one encounter during a given period with available smoking health factor data\n\n  * Of note, study staff are not directly recruiting veterans for this data analysis\n\nExclusion Criteria:\n\nProviders:\n\n* None\n\nVeterans receiving direct letters:\n\n* Active prescription for bupropion, varenicline, or any nicotine replacement therapy",{"count":82,"type":21},65,[24],"Smoking disproportionally impacts Veterans, and VA spends $2.7 billion annually on smoking-related health conditions. Veterans with serious mental illness (SMI) smoke tobacco products at triple the rate of Veterans without any mental illness and die 10-15 years earlier as a result. SMI Veterans who smoke want to quit and FDA-approved tobacco cessation medications are safe, effective, and readily available in VA. However, mental health providers are hesitant to treat smoking and just 11-18% of Veterans with SMI who smoke receive tobacco medication. External facilitation is an effective implementation strategy that can overcome barriers to integrating evidence-based treatment into routine clinical practice. In collaboration with local and operational partners, the proposed CDA-2 will evaluate and refine an external facilitation strategy to improve tobacco medication prescribing in VA SMI clinics. This proposal aligns with VA priorities to enhance timely access to care and improve Veteran outcomes.",[27,86],"Tobacco Use Disorder",[88,89,90,91,92,93,94,95],"veterans health services","mental health services","tobacco use disorder","delivery of health care, integrated","attitude of health personnel","qualitative research","implementation science","mental disorders","NOT_YET_RECRUITING","2026-03-02",{"date":99,"type":38},"2026-03-06",{"date":101,"type":21},"2026-10-01",{"date":103,"type":21},"2031-10-01",{"name":105,"class":106},"VA Office of Research and Development","FED",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":115,"targetDuration":4,"studyType":22,"phases":117,"briefSummary":118,"conditions":119,"keywords":123,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":135,"leadSponsor":137,"locationsCount":72},"100620556","changing-lives-and-changing-outcomes-9-at-worcester-recovery-center-and-hospital-100620556","NCT07359157","Changing Lives and Changing Outcomes-9 at Worcester Recovery Center and Hospital","Changing Lives and Changing Outcomes-9 at Worcester Recovery Center and Hospital: Implementing and Evaluating A Mental Illness and Criminal Risk Focused Intervention for People With Serious Mental Illness","CLCO-9","Inclusion Criteria:\n\n* Currently hospitalized at Worcester Recovery Center and Hospital (WRCH)\n* At least 18 years old\n* Self-reported current or past legal involvement\n* Speaks English\n* For patients without a legally authorized representative (LAR): demonstrate capacity to consent per the Capacity Assessment Record (CAR).\n* For patients with an LAR: assent to participate.\n\nExclusion Criteria:\n\n* Hospital status that does not permit group attendance (e.g., room-based seclusion)",{"count":116,"type":21},40,[24],"People with serious mental illness (depression, bipolar, and schizophrenia spectrum disorders) have high rates of repeated criminal legal involvement and psychiatric hospitalizations. Longstanding research shows that in addition to treating clients' symptoms of mental illness, targeting risk factors for legal involvement can help reduce their chances of future incarcerations. Because hospitals are becoming increasingly forensic, treatment programs that address both mental illness and risk factors for legal involvement may be especially helpful in a state hospital setting, like Worcester Recovery Center and Hospital (WRCH). This treatment study offers an adjunctive 9-session intervention, Changing Lives and Changing Outcomes-9 (CLCO-9), for patients at WRCH; this program is designed to help people with serious mental illness who are involved in the legal system increase their awareness of their mental health and reduce their chances of future legal involvement.\n\nThe investigators are proposing a treatment study testing the use of the CLCO-9 group intervention with patients with serious mental illness with current or previous criminal legal involvement at Worcester Recovery Center and Hospital (WRCH). The study has three aims:\n\n1. Evaluate feasibility, fidelity, and patient satisfaction during the implementation of the CLCO-9 group treatment at WRCH\n2. Evaluate CLCO-9's effectiveness on improving patient's self-reported mental health, and behavioral indicators of mental health and risk factors for legal involvement\n3. Explore changes in WRCH clinicians' knowledge and attitudes about treating risk factors for criminal legal involvement.\n\nTo test these aims, the research team will employ a two-phase study. In the first phase, the researchers will implement the intervention and make necessary adjustments to maximize the success of the implementation. In the second phase, the researchers will evaluate the treatment program's effectiveness in producing change from pre- to post-treatment.\n\nAll patient participants in this study will receive the intervention. The projected sample size is about 20 treatment completers and 4 to 8 group leaders.",[27,120,121,122],"Psychotic Disorder","Depression","Bipolar",[124,125,126,127,128,129],"serious mental illness","criminogenic risk","criminal legal involvement","treatment","forensic","state hospital","2026-02-12",{"date":132,"type":38},"2026-02-17",{"date":134,"type":38},"2026-02-05",{"date":136,"type":21},"2026-07-01",{"name":138,"class":45},"Massachusetts General Hospital",{"id":140,"slug":141,"hasResults":11,"nctId":142,"briefTitle":143,"officialTitle":144,"acronym":4,"eligibilityCriteria":145,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":146,"enrollmentInfo":147,"targetDuration":4,"studyType":22,"phases":149,"briefSummary":150,"conditions":151,"keywords":157,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":170,"completionDateStruct":172,"leadSponsor":174,"locationsCount":72},"100561131","enhancing-rehabilitation-for-veterans-with-serious-mental-illness-100561131","NCT06586164","Enhancing Rehabilitation for Veterans With Serious Mental Illness","Enhancing Rehabilitation for Veterans With Serious Mental Illness Via Biomarker-Informed Cognitive Training","Inclusion Criteria:\n\n* Veterans with SMI (e.g., schizophrenia, schizoaffective disorder, bipolar disorder, PTSD) being treated at PRRCs or co-located rehabilitative services.\n* Age 18 and 83 years.\n* Fluency in spoken and written English.\n* Ability to detect 1000 Hz tones binaurally at a 40-dB sound pressure level.\n* Ability to see with an acuity of 20\u002F40 with both eyes tested together (corrected if applicable) by a standard printed Snellen eye chart reading card.\n\nExclusion Criteria:\n\n* Estimated premorbid IQ below 70, as estimated via the WRAT-4 Reading subtest.\n* Active substance use other than cannabis within the last 30 days as determined by CPRS review, self- report, or positive urine drug screen (obtained as part of the screening process).\n* History of significant medical or neurological illness.\n* Inability to comprehend or provide informed consent.","83 Years",{"count":148,"type":21},80,[24],"This study addresses the critical need for innovative therapeutic interventions in Veterans with serious mental illnesses (SMI) receiving care in VA Psychosocial Rehabilitation and Recovery Centers (PRRCs). The vast majority of individuals with SMI suffer from cognitive impairments, leading to chronic functional disability, and impaired outcomes, causing a significant strain on support networks and the VA healthcare system. This study aims to introduce an innovative mental health therapy, Targeted Cognitive Training (TCT), to Veterans struggling with serious mental illnesses (SMI). TCT works to improve basic sensory information processing and, ultimately, clinical, cognitive, and psychosocial functioning. By using EEG biomarkers to identify Veterans with SMI receiving care within VA Psychosocial Rehabilitation and Recovery Centers who are most likely to benefit from this treatment, and by understanding how best to implement this therapy, the investigators hope to enhance care and improve life quality for Veterans with SMI.",[152,153,27,154,155,156],"Schizophrenia","Psychosis","PTSD","Schizoaffective Disorder","Bipolar Disorder",[158,159,160,161,162,154,163,164,165,166],"schizophrenia","psychosis","cognition","EEG","Serious mental illness","Schizoaffective disorder","Bipolar disorder","clinical symptoms","function","2026-01-28",{"date":169,"type":38},"2026-01-30",{"date":171,"type":38},"2025-02-25",{"date":173,"type":21},"2028-10-31",{"name":105,"class":106},{"id":176,"slug":177,"hasResults":11,"nctId":178,"briefTitle":179,"officialTitle":179,"acronym":4,"eligibilityCriteria":180,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":181,"targetDuration":4,"studyType":22,"phases":183,"briefSummary":184,"conditions":185,"keywords":186,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":190,"lastUpdatePostDateStruct":191,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":72},"100594903","piloting-and-evaluation-of-a-group-intervention-for-people-with-psychosis-designed-to-boost-access-and-usage-of-ict-100594903","NCT07025499","Piloting and Evaluation of a Group Intervention for People With Psychosis Designed to Boost Access and Usage of ICT","Inclusion Criteria:\n\n* Specific inclusion criteria for participants in this study will include being diagnosed with a psychotic disorder, living in the Hamilton area, ability to communicate in English, and having more than one episode of psychosis. Every effort will be made to recruit participants from study with HiREB approvals #17367 and #18549, as indicated in that study's previous consent form, for those that have consented to be contacted for future research.\n\nExclusion Criteria:\n\n* Exclusion criteria include currently experiencing an acute psychotic episode or medical condition that would render them incapable of meaningfully participating in the study.",{"count":182,"type":21},18,[24],"Participants will be given access to a tablet. With this technology, participants will be invited to set personal goals related to using this technology to foster social connection and community participation. Participants will attend a group led by two occupational therapy students and an occupational therapist focused on digital literacy and how to use technology to meet their goals. In the group, participants will learn how to use their device and how to safely access various online resources and tools to support their recovery. Participants will keep their provided devices upon conclusion of the group sessions. Participants will complete quantitative outcome measures at the start and end of the group intervention. Participants will be invited to attend a semi-structured interview one month after the completion of the group about their experiences with the program.",[27],[187,32,188,189],"Information and Communication Technology","social connection","community participation","2025-06-09",{"date":192,"type":38},"2025-06-17",{"date":194,"type":21},"2025-07-15",{"date":196,"type":21},"2025-12-31",{"name":198,"class":45},"McMaster University",{"id":200,"slug":201,"hasResults":11,"nctId":202,"briefTitle":203,"officialTitle":204,"acronym":205,"eligibilityCriteria":206,"healthyVolunteers":11,"sex":17,"minAge":207,"maxAge":4,"enrollmentInfo":208,"targetDuration":4,"studyType":22,"phases":210,"briefSummary":211,"conditions":212,"keywords":214,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":220,"lastUpdatePostDateStruct":221,"startDateStruct":223,"completionDateStruct":225,"leadSponsor":227,"locationsCount":46},"100588395","a-pilot-randomized-controlled-trial-of-the-hopeful-and-healthy-living-program-100588395","NCT06940843","A Pilot Randomized Controlled Trial of the Hopeful and Healthy Living Program","Enhancing Social Connection, Health, and Aging in Older Persons: A Pilot Randomized Trial of the Hopeful and Healthy Living (HHL) Program","(HHL)","Inclusion Criteria:\n\n50 years or older, diagnosis of a serious mental illness, and a member of Center Club or Transitions of Boston\n\nExclusion Criteria:\n\nDiagnosis of dementia or other progressive neurological disorder","50 Years",{"count":209,"type":21},60,[24],"The goal of this clinical trial is to learn if a novel psychosocial intervention is effective in helping adults over 50 with serious mental illness (SMI) increase their social connections and participate in more healthy lifestyle activities. The Hopeful and Healthy Living (HHL) intervention combines social skills training and training in cognitive self-management strategies in order to help older adults build healthy lifestyle and social routines. We predict that:\n\n* Individuals who participate in the HHL intervention will improve more in perceived social support (i.e., what people get from relationships such as reliance, reassurance of worth, attachment) and loneliness at the 4-, 8-, and 12-month follow-up assessments than those who receive treatment as usual (TAU).\n* Individuals who participate in the HHL intervention will improve more in overall psychosocial functioning at the 4-, 8-, and 12-month follow-up assessments than those who receive TAU.\n* Individuals who participate in the HHL intervention will improve more in cognitive functioning at the 4-, 8-, and 12-month follow-up assessments than those who receive TAU.\n* Individuals who participate in the HHL intervention will improve more in healthy behaviors (sleep, activity, diet) at the 4-, 8-, and 12-month follow-up assessments than those who receive TAU.\n\nIn this trial, participants will be either receive the HHL intervention or participate in their regular treatment activities (treatment as usual). HHL vs. TAU will be compared to see if there are any differences in social support, cognition, loneliness, psychosocial functioning, or healthy lifestyle activities including physical activity, sleep, and diet.\n\nParticipants will be asked to complete an interview-based assessment at baseline, 4-months, 8-months, and 12-months. After completing the baseline assessment, those who are in the experimental group will participate in the 16-week long HHL group intervention.",[27,213],"Older Adults",[215,216,217,218,219],"psychosocial interventions","cognitive interventions","social skills interventions","healthy lifestyle interventions","older adults with SMI","2025-04-23",{"date":222,"type":38},"2025-04-25",{"date":224,"type":38},"2025-03-12",{"date":226,"type":21},"2028-07-31",{"name":228,"class":45},"Boston University Charles River Campus",{"id":230,"slug":231,"hasResults":11,"nctId":232,"briefTitle":233,"officialTitle":234,"acronym":235,"eligibilityCriteria":236,"healthyVolunteers":11,"sex":17,"minAge":237,"maxAge":4,"enrollmentInfo":238,"targetDuration":4,"studyType":22,"phases":240,"briefSummary":241,"conditions":242,"keywords":244,"overallStatus":96,"whyStopped":4,"lastUpdateSubmitDate":249,"lastUpdatePostDateStruct":250,"startDateStruct":252,"completionDateStruct":254,"leadSponsor":256,"locationsCount":46},"100582111","improving-health-and-wellness-for-people-with-serious-mental-illness-in-puerto-rico-100582111","NCT06859060","Improving Health and Wellness for People With Serious Mental Illness in Puerto Rico","Testing Bridges to Better Health and Wellness for People Living With Serious Mental Illness in Puerto Rico","BRIDGES","Inclusion criteria:\n\nAdults receiving psychiatric or psychological services at the Wellness Center or the Mayaguez Medical Center - Primary Care Diagnosed with at least one serious mental illness SMI (e.g., schizophrenia, bipolar disorder, major depression, etc.) Have at least one risk factor or a diagnosis of a chronic health condition (e.g., diabetes, overweight, hypertension, etc.).\n\nBe willing to receive or continue preventive medical care with a primary care physician.\n\nExclusion criteria:\n\nHave started psychiatric or mental health services at least one month before Have been diagnosed with a general mental health condition (e.g., Depression or Anxiety).","21 Years",{"count":239,"type":21},300,[24],"This study evaluates the effectiveness of a culturally tailored intervention, Bridges to Better Health and Wellness (BRIDGES), aimed at reducing chronic disease disparities among Puerto Ricans with serious mental illness (SMI). Participants receive monthly sessions with health care managers to address patient-provider stigma and care coordination.",[243,27],"Chronic Disease",[245,62,246,247,248],"Bridges","Preventive Primary Care","Healthcare Managers","Wellness","2025-02-27",{"date":251,"type":38},"2025-03-05",{"date":253,"type":21},"2025-08",{"date":255,"type":21},"2029-02-28",{"name":257,"class":258},"Ponce Medical School Foundation, Inc.","INDUSTRY",{"id":260,"slug":261,"hasResults":11,"nctId":262,"briefTitle":263,"officialTitle":264,"acronym":4,"eligibilityCriteria":265,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":53,"enrollmentInfo":266,"targetDuration":4,"studyType":22,"phases":268,"briefSummary":269,"conditions":270,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":271,"lastUpdatePostDateStruct":272,"startDateStruct":274,"completionDateStruct":276,"leadSponsor":278,"locationsCount":72},"100544583","peer-facilitated-waitlist-controlled-transportation-study-100544583","NCT06370767","Peer Facilitated Waitlist Controlled Transportation Study","Enhancing Community Mobility in Individuals With Serious Mental Illnesses Through Peer-Facilitated Travel Training: A Two-armed Waitlist Controlled Trial","Inclusion Criteria:\n\n* are between the ages of 18 and 65\n* are diagnosed with a SMI (confirmed via the MINI)\n* score at least an 8 on a travel skills assessment\n* indicates that they can ride a bicycle\n* have expressed interest in using a bikeshare and public transportation\n* are able to provide informed consent\n\nExclusion Criteria:\n\n* score less than 8 on a travel skills assessment\n* express no interest in independent transportation\n* are non-English speaking individuals\n* are unable to provide consent\n* are living in a setting where mobility and participation is restricted\n* have a limiting physical condition that would prevent their ability to ride a bicycle independently",{"count":267,"type":21},180,[24],"The goal of this clinical trial is to test the effectiveness of a peer-facilitated travel intervention in adults with serious mental illnesses. This project aims to address the following hypotheses:\n\n1. Individuals with SMI receiving either of the two peer-mediated travel training transportation interventions will experience an increase in transportation self-efficacy and transportation skills.\n2. Participants in the intervention arms will increase their transport utilization, participate in significantly more activities in the community, and make significantly more trips in the community.\n3. Individuals with SMI receiving peer-mediated travel training interventions will retain post-test levels of community participation and self-efficacy 2 months after intervention.\n\nParticipants will be assigned to an 8-week travel-training intervention either using a bike-share program or public transportation. All participants will complete three data-collection research interviews.",[27],"2024-10-30",{"date":273,"type":38},"2024-11-01",{"date":275,"type":38},"2024-09-12",{"date":277,"type":21},"2025-05",{"name":279,"class":45},"Temple University"]