[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"occupational-therapy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:occupational-therapy":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,45,72,109,129,157,186,212,237,261],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100579148","trapeziectomy-and-suture-suspensionplasty-for-thumb-carpometacarpal-arthritis---is-in-clinic-therapy-needed-100579148",false,"NCT06820528","Trapeziectomy and Suture Suspensionplasty for Thumb Carpometacarpal Arthritis - Is In-Clinic Therapy Needed?","Inclusion Criteria:\n\n* Patients over the age of 18 years\n* Patients undergoing CMC Arthroplasty\n* Ability to read and write in English\n* Ability to provide informed consent\n\nExclusion Criteria:\n\n* Patients undergoing revision CMC arthroplasty\n* Acute traumatic dislocation of the CMC joint as indication for surgery\n* Concomitant treatment of MCP hyperextension","ALL","18 Years",{"count":18,"type":19},180,"ESTIMATED","INTERVENTIONAL",[22],"NA","The study is a randomized, controlled trial to evaluate the efficacy of formal occupational therapy on outcomes following CMC arthroplasty",[25,26,27],"CMC Arthritis","Occupational Therapy","Hand Arthritis",[29,30,31],"CMC Arthroplasty","Thumb Arthritis","Hand Therapy","RECRUITING","2026-06-03",{"date":35,"type":36},"2026-06-05","ACTUAL",{"date":38,"type":36},"2025-04-17",{"date":40,"type":19},"2028-01-01",{"name":42,"class":43},"Julie Nuelle","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":55,"conditions":56,"keywords":59,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":44},"100600038","studying-rehabilitation-treatments-using-video-to-improve-recovery-for-adults-with-physical-disabilities-100600038","NCT07092293","Studying Rehabilitation Treatments Using Video to Improve Recovery for Adults With Physical Disabilities","Using the Rehabilitation Treatment Specification System (RTSS) to Maximize Rehabilitation Research Impact: A Video-Based Observational Study","Occupational Therapy Inclusion Criteria:\n\n* Must be a licensed OT practitioner (occupational therapist or occupational therapy assistant),\n* The OT practitioner must treat at least one adult stroke or spinal cord injury patient with UE sensorimotor impairment per month\n* The OT practitioner must be willing to be video recorded while treating their enrolled stroke or SCI patients.\n\nStroke Patients Inclusion Criteria:\n\n* Must have a medical diagnosis of ischemic or hemorrhagic stroke\n* Must be ≥ 18 years old\n* Must have at least one OT goal related to UE hemiparesis\n* Must have at least one remaining OT treatment session after enrollment\n* The patient's OT must be enrolled in the study.\n\nSpinal Cord Injury (SCI) Patients Inclusion Criteria:\n\n* Must have a medical diagnosis of cervical spinal cord injury\n* Must be ≥ 18 years old\n* Must have at least one OT goal related to UE sensorimotor impairment\n* Must have at least one remaining OT treatment session after enrollment\n* The patient's OT must be enrolled in the study.",{"count":53,"type":19},90,"OBSERVATIONAL","This study aims to better understand how occupational therapists provide rehabilitation for adults recovering from stroke or spinal cord injury (SCI), with a focus on improving arm and hand function. Using video recordings of real outpatient therapy sessions, researchers will identify the key elements of treatment, such as the types of activities, the therapist's techniques, and how patients respond. The study will use the Rehabilitation Treatment Specification System (RTSS), a framework designed to clearly describe rehabilitation methods. By analyzing these sessions, the research team will develop a practical toolkit to help therapists and researchers deliver and study more effective rehabilitation treatments in the future.",[57,58,26],"Stroke","Spinal Cord Injury",[60,61,62],"occupational therapy","stroke","spinal cord injury","2026-05-05",{"date":65,"type":36},"2026-05-07",{"date":67,"type":36},"2025-02-11",{"date":69,"type":19},"2026-12-31",{"name":71,"class":43},"Ohio State University",{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":20,"phases":82,"briefSummary":83,"conditions":84,"keywords":88,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":44},"100627588","virtual-activities-of-living-for-occupational-rehabilitation-100627588","NCT07450586","Virtual Activities of Living for Occupational Rehabilitation","Virtual Activities of Living for Occupational Rehabilitation (VALOR)","VALOR","Criteria for inclusion:\n\n1. Participant has had a right or left hemispheric stroke affecting normal hand function.\n2. At least 3 months have passed since the last stroke.\n3. Participant has sufficient active finger flexion at the MCP joint in at least one finger to be detected by visual observation by a study therapist.\n4. Participant has visual acuity with corrective lenses of 20\u002F50 or better.\n5. Participant must have active movement against gravity of at least 30 degrees shoulder flexion, 45 degrees elbow flexion, elbow extension to within 30 degrees of full extension, and 15 degrees shoulder internal and external rotation.\n6. In the opinion of a study therapist, participant can independently and safely use the system at home or has an at-home caregiver who is willing and able to assist.\n7. In the opinion of a study therapist, participant has a suitable and safe space in their home for using the VALOR system.\n8. Participant is willing and able to provide informed consent.\n\nCriteria for exclusion:\n\n1. Withholding or withdrawal of consent by the participant.\n2. Inability to understand and follow verbal directions.\n3. Determination by the Principal Investigator that participation would result in overexertion or significant discomfort or pain.\n4. A psychological diagnosis that in the determination of the Principal Investigator could significantly impact subject's participation or that could be aggravated by study participation (Principal Investigator will consult with candidate's personal physician as appropriate).\n5. Determination by the Principal Investigator that participation would result in significant agitation or elevated stress.\n6. Visual field deficit in either eye that impairs the ability to view the VR display.\n7. Significant contractures of the muscles, joints, tendons, ligaments, or skin that restrict normal upper extremity movement.\n8. More than mild tone\u002Fspasticity (measured on modified Ashworth, 5-point scale);\n9. Severe pre-stroke co-morbidities, such as cardiovascular, neurological, orthopedic, or rheumatoid impairments before stroke that may interfere with task performance.\n10. Severe sensory deficits from the involved UE; or\n11. Hemispatial neglect that impairs the ability to process and perceive visual stimuli provided through the VR display.\n\nAs the system will be adaptable to a wide range of hand dexterity, no restriction will be made for fine control of digits. Patients will not be excluded due to inability to use the VR headset. If at any time the study therapist, in consultation with the Duke PI, determines the patient is not tolerating VR headset use, the patient will be given the option to use a non-immersive version of the VALOR system which employs a TV monitor and depth sensor in lieu of the headset. Please see Potential Risks section for additional details on controls and mitigations for potential cyber sickness.",{"count":81,"type":19},48,[22],"Duke University will serve as the clinical research site for the Phase II RCT of the VALOR system, which enables telehealth delivery of evidence-based upper extremity (UE) stroke therapy in a patient's home using immersive VR headset technology for guided practice of activities of daily living (ADLs) and instrumental ADLs (IADLs). The study compares VALOR Home Exercise Program (HEP) to Usual Care Treatment (UCT) in adults with stroke-related UE impairment.",[57,26,85,86,87],"Activities of Daily Living","Rehabilitation","Virtual Reality",[89,87,90,91,92,85,93,94,95,96,97,26],"Stroke Rehabilitation","Upper Extremity","Telehealth","Home Exercise Program","Fugl-Meyer Assessment","Wolf Motor Function Test","Motor Activity Log","Hand Function","Hemiplegia","NOT_YET_RECRUITING","2026-04-22",{"date":101,"type":36},"2026-04-27",{"date":103,"type":19},"2026-06-15",{"date":105,"type":19},"2027-07-29",{"name":107,"class":108},"Barron Associates, Inc.","INDUSTRY",{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":113,"acronym":4,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":115,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":117,"conditions":118,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":44},"100541412","validation-of-the-screen-of-cancer-survivorship---occupational-therapy-services-socs-ots-tool-for-use-in-a-physical-medicine-rehabilitation-clinic-100541412","NCT06329531","Validation of the Screen of Cancer Survivorship - Occupational Therapy Services (SOCS-OTS) Tool for Use in a Physical Medicine Rehabilitation Clinic","Inclusion Criteria:\n\n1. Must be 18 years an older\n2. Currently medically followed in the PMR clinic (with or without acute disease)\n3. Must speak and read English. The AM-PAC is currently validated in adults only. Additionally, the assessment tools are in English without translation into other languages, therefore only clients who do speak and read English will be included. Pregnant participants are not excluded.\n\nExclusion Criteria:\n\n1\\. Potential participants with confusion and cognitive impairments that might hinder their ability to sign an informed consent form or participate in the study.",{"count":116,"type":19},80,"To compare the results of the SOCS-OTS to another standardized screening measure that is currently being used by rehabilitation services at MD Anderson Cancer Center and to ensure that the SOCS-OTS correctly identifies those individuals needing OT services in cancer care.",[119,26],"Cancer","2026-04-13",{"date":122,"type":36},"2026-04-16",{"date":124,"type":36},"2024-07-12",{"date":126,"type":19},"2027-12-01",{"name":128,"class":43},"M.D. Anderson Cancer Center",{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":136,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":137,"targetDuration":139,"studyType":54,"phases":4,"briefSummary":140,"conditions":141,"keywords":144,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":148,"lastUpdatePostDateStruct":149,"startDateStruct":151,"completionDateStruct":153,"leadSponsor":155,"locationsCount":44},"100631534","development-of-a-clinical-skills-teaching-video-database-in-occupational-therapy-100631534","NCT07501936","Development of a Clinical Skills Teaching Video Database in Occupational Therapy","Development of an Occupational Therapy Clinical Skills Teaching and Assessment Video Database","Inclusion Criteria:\n\n* Occupational therapists involved in clinical teaching activities\n* Occupational therapy interns or postgraduate trainees receiving clinical training\n* Adult patients (aged 20 years or older) or family members who receive occupational therapy services provided by participating therapists or trainees\n* Able and willing to provide informed consent for video or audio recording\n\nExclusion Criteria:\n\n* Individuals who are unwilling or unable to provide informed consent for video or audio recording\n* Individuals with significant cognitive impairment or communication difficulties that prevent informed consent\n* Individuals who decline participation or request withdrawal at any stage of the study",true,{"count":138,"type":19},2020,"1 Day","This study aims to develop a video and audio database for teaching and learning clinical skills in occupational therapy. The database will include recordings of clinical teaching sessions, skill demonstrations, student practice, and interactions between occupational therapists, trainees, and patients or family members.\n\nParticipants may include occupational therapists involved in clinical teaching, occupational therapy interns or postgraduate trainees, and adult patients or family members who receive occupational therapy services. Participation involves voluntary video or audio recording of clinical teaching or therapy-related activities after informed consent is obtained.\n\nThis study does not involve any experimental treatment, intervention, or comparison of outcomes. The collected materials will be securely stored, anonymized, and organized for future educational use and research on clinical skills teaching and assessment in occupational therapy.",[142,26,143],"Occupational Therapy Education","Clinical Competence",[145,146,147],"Occupational therapy education","Clinical skills training","Clinical competence","2026-03-24",{"date":150,"type":36},"2026-03-30",{"date":152,"type":36},"2026-02-01",{"date":154,"type":19},"2034-12-31",{"name":156,"class":43},"Chang Gung Memorial Hospital",{"id":158,"slug":159,"hasResults":11,"nctId":160,"briefTitle":161,"officialTitle":162,"acronym":4,"eligibilityCriteria":163,"healthyVolunteers":11,"sex":15,"minAge":164,"maxAge":165,"enrollmentInfo":166,"targetDuration":4,"studyType":20,"phases":168,"briefSummary":169,"conditions":170,"keywords":173,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":177,"lastUpdatePostDateStruct":178,"startDateStruct":180,"completionDateStruct":182,"leadSponsor":184,"locationsCount":44},"100535149","effectiveness-of-online-program-and-task-related-training-for-parkinsons-disease-100535149","NCT06248073","Effectiveness of Online Program and Task-related Training for Parkinson's Disease","Comparing the Effectiveness of Online Self-management Program and On-site Task-related Training for People With Early Stage Parkinson's Disease on Activity Participation and Quality of Life","Inclusion criteria:\n\n1. Willingness to sign the informed consent form.\n2. Age between 45 and 70 years, with mild idiopathic Parkinson's disease and Hoehn and Yahr stage 1-2.\n3. No cognitive impairment.\n4. No severe depression that could affect the motivation to participate in the study.\n5. No history of shoulder dislocation or fracture that could affect body proprioception.\n6. No diseases that could affect the ability to reach for objects, such as stroke.\n7. No diseases that could affect peripheral sensation, such as diabetes.\n8. No severe tremors; patients whose hands, when relaxed and placed on the apparatus, still exhibit significant tremor interfering with the experiment will not be included.\n9. Able to follow instructions and complete the assessment process.\n10. Have not received physical or occupational therapy in the past year.\n\nExclusion criteria:\n\n1. Other central nervous system diseases, such as stroke.\n2. Have major surgery on the head or upper limbs.\n3. Inability to perform the reaching task while sitting.","45 Years","70 Years",{"count":167,"type":19},100,[22],"The goal of this clinical trial is to compare the effectiveness of online self-management program and on-site task-related training for people with early stage Parkinson's disease.\n\npeople with early stage of Parkinson's disease (age range: 45-70 years) will be randomly assigned into the following three groups: control group, online self-management program group and on-site task-related training group.The control group will receive no treatment during the experimental period. For the other two groups, participants will receive the intervention twice a week, one hour per session and 12 sessions in total.\n\nThe main questions it aims to answer are:\n\n1. the potential impact of motor and non-motor symptoms on activity participation and quality of life for people with early stage of Parkinson's disease (PD).\n2. compare and examine the the effectiveness of online self-management program and on-site task-related training for people with early stage Parkinson's disease on activity participation and quality of life.",[171,26,172,85],"Parkinson Disease","Telerehabilitation",[172,174,175,176],"early intervention","patient-reported outcome assessment","self-perception","2026-03-18",{"date":179,"type":36},"2026-03-20",{"date":181,"type":36},"2024-03-01",{"date":183,"type":19},"2027-12-31",{"name":185,"class":43},"Chang Gung University",{"id":187,"slug":188,"hasResults":11,"nctId":189,"briefTitle":190,"officialTitle":190,"acronym":191,"eligibilityCriteria":192,"healthyVolunteers":11,"sex":193,"minAge":194,"maxAge":16,"enrollmentInfo":195,"targetDuration":4,"studyType":20,"phases":197,"briefSummary":198,"conditions":199,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":202,"lastUpdatePostDateStruct":203,"startDateStruct":205,"completionDateStruct":207,"leadSponsor":209,"locationsCount":44},"100547051","gamified-occupational-therapy-for-adolescents-with-duchenne-muscular-dystrophy-100547051","NCT06402942","Gamified Occupational Therapy for Adolescents With Duchenne Muscular Dystrophy","DMD","Inclusion Criteria:\n\n* Being diagnosed with Duchenne muscular dystrophy\n* To be literate in Turkish\n* To have scored 27 points or more on the Modified Mini Mental Test\n* Having a computer, tablet and internet connection\n* Volunteering to participate in the study by their parents and reading and signing the informed consent form\n\nExclusion Criteria:\n\n* Having a neurological disease other than Duchenne muscular dystrophy and\u002For another diagnosed neurological disease accompanying Duchenne muscular dystrophy\n* Having a cooperation problem that prevents completing the assessments for any reason\n* Difficulty understanding and speaking the Turkish language","MALE","13 Years",{"count":196,"type":19},20,[22],"This research aims to improve the quality of life, occupational performance, occupational satisfaction and emotional health of young people with Duchenne muscular dystrophy compared to the classical occupational therapy program. The findings are planned to shed light on the development of new and effective strategies in the rehabilitation of adolescents with Duchenne muscular dystrophy.",[200,201,26],"Duchenne Muscular Dystrophy","Gamification","2026-01-24",{"date":204,"type":36},"2026-01-27",{"date":206,"type":36},"2025-05-01",{"date":208,"type":19},"2026-12-08",{"name":210,"class":211},"Başak Çağla Arslan","OTHER_GOV",{"id":213,"slug":214,"hasResults":11,"nctId":215,"briefTitle":216,"officialTitle":216,"acronym":217,"eligibilityCriteria":218,"healthyVolunteers":136,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":219,"targetDuration":139,"studyType":54,"phases":4,"briefSummary":221,"conditions":222,"keywords":225,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":228,"lastUpdatePostDateStruct":229,"startDateStruct":231,"completionDateStruct":233,"leadSponsor":235,"locationsCount":4},"100612296","understanding-the-lived-experience-and-bereavement-of-caregivers-of-people-with-alzheimers-disease-100612296","NCT07251738","Understanding the Lived Experience and Bereavement of Caregivers of People With Alzheimer's Disease","ALCARE","Inclusion Criteria:\n\n* Inclusion criteria for Group 1: relatives of people diagnosed with AD by a neurologist or geriatrician, who have suffered the loss of a relative with AD; who have lived with and\u002For cared for the person with AD until the end of their life; who agree to participate voluntarily in the project and who have signed the informed consent form.\n* Inclusion criteria for Group 2: relatives of people diagnosed with AD by a neurologist or geriatrician; who live with and\u002For care for the person with AD; who attend the Day Centre and who agree to participate voluntarily in the project and have signed the informed consent form.\n* Inclusion criteria for Group 3: relatives of people diagnosed with AD by a neurologist or geriatrician; who have their relative institutionalised in a nursing home and who agree to participate voluntarily in the project and have signed the informed consent form.\n\nExclusion Criteria:\n\n* Those who have not lived with or cared for relatives with AD and who do not agree to participate in the study will be excluded from the project.",{"count":220,"type":19},66,"The main objective of this study is to explore the lived experience of caregivers and family members of people with Alzheimer's disease (AD), from the beginning of caregiving through the bereavement process following the patient's death. Using a mixed-methods design, qualitative data will be collected through in-depth interviews and combined with quantitative data obtained from standardized scales. The results will aim to determine whether prolonged caregiving significantly affects the caregiver's or family member's personal, emotional, and occupational well-being, as well as whether it leads to a reorganization of activities of daily living (ADL), an increased perception of burden, and\u002For a decreased quality of life. The study will also examine the presence of positive adaptation experiences.",[223,26,224],"Alzheimer Disease (AD)","Family Caregivers",[226,26,227],"Alzheimer's disease","occupational balance","2025-11-18",{"date":230,"type":36},"2025-11-26",{"date":232,"type":19},"2025-12-01",{"date":234,"type":19},"2026-07-31",{"name":236,"class":43},"Universidad Rey Juan Carlos",{"id":238,"slug":239,"hasResults":11,"nctId":240,"briefTitle":241,"officialTitle":242,"acronym":43,"eligibilityCriteria":243,"healthyVolunteers":11,"sex":15,"minAge":244,"maxAge":4,"enrollmentInfo":245,"targetDuration":4,"studyType":20,"phases":247,"briefSummary":248,"conditions":249,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":251,"lastUpdatePostDateStruct":252,"startDateStruct":254,"completionDateStruct":256,"leadSponsor":258,"locationsCount":260},"100504968","effect-of-occupational-therapy-at-home-e-rehabilitation-other-for-persons-post-stroke-100504968","NCT05855226","Effect of Occupational Therapy at Home E-Rehabilitation (OTHER) for Persons Post-stroke","Supporting Daily Functioning of Persons With a Neurological Disorder: (Cost)Effectiveness of Occupational Therapy at Home E-Rehabilitation (OTHER) for Persons Post-stroke","Inclusion Criteria:\n\n* be able to walk a few steps with or without a walking device.\n* 60 years or older\n* an assessment score of at least 16 on the Montreal Cognitive Assessment (MoCA)\n* an indication for follow up GR at home\n\nExclusion Criteria:\n\n* Who are terminally ill\n* Who have severe aphasia; problems with understanding.\n* Who has been assessed legally incapable by a geriatric doctor","60 Years",{"count":246,"type":19},171,[22],"The goal of this (cost)effectiveness study is to compare care as usual with OTHER-intervention in Cerebro Vascular Accident (CVA) older adults in Geriatric Rehabilitation (GR). The main question\\[s\\] it aims to answer are:\n\n1. What is the effectiveness of OTHER, as compared to occupational therapy as usual (CAU), on improving the self-perceived performance in daily activities of community-dwelling older persons post-stroke over a 24-week period after initiation of OTHER or CAU, as measured longitudinally (at week 4, 13 and 26)?\n\n   Secondary:\n2. What is the effectiveness of OTHER on improving satisfaction with the perceived daily performance of community-dwelling persons post-stroke, 26 weeks after start compared to usual OT? (quantitative approach)\n3. What is the effectiveness of OTHER on improving physical activity of community-dwelling persons post-stroke, 26 weeks after start compared to usual OT? (quantitative approach)\n4. What is the effectiveness of OTHER on improving self-management of community-dwelling persons post-stroke, 26 weeks after start compared to usual OT? (quantitative approach)\n5. How do persons post-stroke and OT's experience and how do they reflect on OTHER in supporting a sense of self-management, safety and improving daily functioning? (qualitative approach).\n6. What factors influenced the intervention delivery and the perceived benefits in the OTHER study (process evaluation)? 1) monitoring treatment fidelity, barriers and facilitators for implementation; 2) gain insight into the impact of OTHER on the GR transition to home; 3) to gain insight into what stroke survivors and OT's think of OTHER. 4) how participants, and professionals experience and thoughts they have on the OTHER-intervention in supporting daily functioning and self-management\n\n   Cost-effectiveness\n7. What is the cost-effectiveness of OTHER on improving self-perceived performance in daily activities and Quality Adjusted Life Years (QALYs) of community-dwelling persons post-stroke, 26 weeks after start compared to usual OT? (quantitative approach)\n\nParticipants will get the OTHER-intervention treatment given by de occupational therapist which consists of activity monitoring, coaching and videoconferencing to optimalise the transition from clinical care to home.\n\nResearchers will compare care as usual to see if there is a effect on improving the self-perceived performance in daily activities, self-management and improving physical activity .",[57,250,26],"eHealth","2025-09-04",{"date":253,"type":36},"2025-09-10",{"date":255,"type":36},"2023-03-13",{"date":257,"type":19},"2026-01",{"name":259,"class":43},"Amsterdam University of Applied Sciences",9,{"id":262,"slug":263,"hasResults":11,"nctId":264,"briefTitle":265,"officialTitle":266,"acronym":4,"eligibilityCriteria":267,"healthyVolunteers":11,"sex":15,"minAge":268,"maxAge":4,"enrollmentInfo":269,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":271,"conditions":272,"keywords":277,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":283,"lastUpdatePostDateStruct":284,"startDateStruct":286,"completionDateStruct":288,"leadSponsor":290,"locationsCount":44},"100602251","the-effects-of-a-dynamic-arm-support-in-daily-life-100602251","NCT07121075","The Effects of a Dynamic Arm Support in Daily Life","The Effects of a Dynamic Arm Support in Daily Life. A Mixed Methods Study Including the Different Components of the ICF","Inclusion Criteria:\n\n* Age: 16 and oler\n* Being able to understand and comprehend test instructions\n* Using a DAS from Focal Meditech (Balancer, Flowing, Dowing, Gowing 2 or Top Help)\n\nExclusion Criteria:\n\n\u002F","16 Years",{"count":270,"type":19},50,"The goal of this mixed method study is to learn about how a dynamic arm support device (DAS) helps people with everyday activities. The study focuses on people with neuro(-muscular) conditions, age 16 and older. The research questions that are formulated, are:\n\n* How does a person experience their daily activities, with and without a DAS?\n* What are the contextual (external and personal) factors that influence the use of a DAS?\n\nParticipants will take part in three testing sessions. In each session, they must complete a few questionnaires and participate in an interview. The first time, without DAS. In the second and third session, they will be using their DAS (resp. 3 to 4 weeks and 3 months). The data collection will be executed by phone, digital questionnaires and\u002For paper.",[273,274,275,85,26,276],"Neuromuscular Disease","Neuromuscular Disability","Assistive Technology","Upper Limb",[278,279,280,281,282],"dynamic arm support","dynamic arm support device","ICF","daily life","outcome measures","2025-08-12",{"date":285,"type":36},"2025-08-13",{"date":287,"type":36},"2024-12-02",{"date":289,"type":19},"2026-08",{"name":291,"class":43},"Hasselt University"]