[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"stroke-6-months-or-more-after-onset\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:stroke-6-months-or-more-after-onset":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":4},"100648806","co-designed-digital-education-and-peer-support-for-young-and-middle-aged-stroke-survivors-100648806",false,"NCT07725666","Co-Designed Digital Education and Peer Support for Young and Middle-Aged Stroke Survivors","A Co-Designed Digital Education and Peer Support Intervention for Reducing Unmet Needs and Enhancing Recovery Among Young and Middle-Aged Stroke Survivors","Inclusion Criteria:\n\n* Aged 31 to 64 years.\n* Diagnosis of stroke confirmed by computed tomography (CT) or magnetic resonance imaging (MRI) and physician diagnosis.\n* Received treatment at the Stroke Center of Linkou Chang Gung Memorial Hospital.\n* Conscious and able to communicate, including individuals with mild aphasia.\n* Willing and able to provide informed consent.\n\nExclusion Criteria:\n\n* End-stage cancer.\n* Severe aphasia resulting in inability to communicate.\n* Dependent in basic activities of daily living before the index stroke (Barthel Index \\\u003C100), regardless of the underlying cause.","ALL","31 Years","64 Years",{"count":20,"type":21},148,"ESTIMATED","INTERVENTIONAL",[24],"NA","Stroke survivors often experience persistent unmet needs during long-term recovery. Young and middle-aged stroke survivors may face additional challenges in balancing rehabilitation with work and family responsibilities. Although digital health interventions have the potential to improve access to education and self-management support, existing programs are often provider-driven, provide limited peer support, and have short follow-up periods.\n\nThis study aims to evaluate the effectiveness of a patient-centered digital education and peer support intervention co-designed with young and middle-aged stroke survivors. Participants will be randomly assigned to either the intervention group or the usual care group. The intervention will be delivered through LINE communities and Google collaborative platforms over a 12-month period. The primary outcome is unmet needs. Secondary outcomes include stroke self-efficacy, depressive symptoms, quality of life, activities of daily living, instrumental activities of daily living, and return-to-work status.",[27,28],"Stroke","Stroke (6 Months or More After Onset)",[27,30,31],"Digital Health","Peer Support","NOT_YET_RECRUITING","2026-07-21",{"date":35,"type":36},"2026-07-24","ACTUAL",{"date":38,"type":21},"2026-08",{"date":40,"type":21},"2029-07",{"name":42,"class":43},"Chang Gung Memorial Hospital","OTHER",{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":5},"100645982","feasibility-evaluation-of-wear-it-for-hand-therapy-after-stroke-100645982","NCT07698067","Feasibility Evaluation of WEAR-IT for Hand Therapy After Stroke","Feasibility Evaluation of WEAR-IT (Wearable Assistive and Rehabilitation Robot Facilitating Intensive Telerehabilitation) for Hand Therapy After Stroke: A Randomized Controlled Trial","WEAR-IT","Inclusion Criteria:\n\n* Each participant must meet all of the following inclusion criteria to participate in this study:\n\nA) Persons with chronic stroke:\n\n1. Be able to attend one rehabilitation site (Toronto or Edmonton),\n2. Be 18 years of age or older,\n3. Be able to provide informed consent,\n4. Has English language proficiency,\n5. Be in the chronic stage of recovery (e.g., \\> 6 months post-stroke),\n6. Have hand recovery at Stage 1 (flaccid paralysis) to Stage 4 (inability to make a fist and then extend the fingers fully) on the Chedoke-McMaster Stroke Assessment (CMSA)\n7. Have a pain rating between 0\u002F10 (no pain) and 4\u002F10 (moderate pain) at rest and with assisted hand movement\n8. Demonstrate the ability to understand and participate in a 3-month study program,\n9. Live with someone or have someone consistently available (caregiver participant) who can help with setting up telerehabilitation equipment and assist with putting on\u002Fremoving the Glove (as needed), and\n10. Have access to a computer or tablet with a camera and a reliable internet connection for telerehabilitation sessions.\n\nB) Caregiver participants who are willing to assist people living with stroke can be included if they meet the following criteria:\n\n1. Be 18 years of age or older,\n2. Be able to provide informed consent , and\n3. Be able to support glove donning\u002Fdoffing, set-up, and therapy for people living with stroke at home.\n\nExclusion Criteria:\n\n* All participants meeting any of the following exclusion criteria at baseline will be excluded from participation in this study:\n\nA) Persons with chronic stroke:\n\n1. Have no limitations in fully extending fingers or making a fist,\n2. Are experiencing pain or cognitive impairments that prevent active participation in therapy,\n3. Be unable to communicate with therapists independently,\n4. Have had any musculoskeletal or other neurological conditions that would impact their participation in a hand rehabilitation program, or\n5. Are currently involved in another rehabilitation program aimed at improving upper limb movement.","18 Years",{"count":54,"type":21},44,[24],"The goal of this clinical trial is to understand whether a program of using a hand robot at home, supported by telerehabilitation, is feasible for people living with stroke. The study aims to answer the following questions:\n\n* What is the extent that people living with stroke complete the prescribed therapy program? (adherence)\n* Do people living with stroke continue to participate in the therapy program until follow-up? (retention)\n* How acceptable and helpful is the hand robot to be use at the outpatient rehabilitation clinic and home via telerehabilitation for people living with stroke?\n* How reliable and safe is the hand robot when used in clinical and home settings?\n* What are the costs of delivering the hand robot program compared to providing the same amount of standard therapy without the hand robot? Researchers will also compare rehabilitation using the hand robot program to a dose-matched therapy program that does not use the robot.\n\n  * Intervention group: Participants will use the hand robot for 12 weeks, with follow-up intervention and assessments at 6 months.\n  * Control (comparator) group: Participants will receive the same amount of therapy over 12 weeks, but without the hand robot, followed by 6-month follow-up.\n\nFor both groups, researchers will record information about each participant's clinical recovery, their experience with the therapy process and the cost of care.",[28],[27,59,60,61,62,63,64],"Hand function","Robotic exoskeleton","Virtual care","Rehabilitation","Neurological rehabilitation","Hand therapy","2026-07-06",{"date":67,"type":36},"2026-07-13",{"date":69,"type":21},"2026-09-01",{"date":71,"type":21},"2029-12-23",{"name":73,"class":43},"Dr. Rosalie Wang"]