[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"rehabilitation-after-neurological-or-orthopaedic-injuries\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:rehabilitation-after-neurological-or-orthopaedic-injuries":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,56],{"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":36,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":44,"lastUpdatePostDateStruct":45,"startDateStruct":48,"completionDateStruct":50,"leadSponsor":52,"locationsCount":55},"100613601","assess-the-efficacy-of-tailored-patient-information-and-voluntary-patient-managed-outpatient-digital-follow-up-i-pod-as-an-adjunct-to-standard-treatment-according-to-national-guidelines-in-the-national-trauma-plan-among-adult-trauma-patients-in-norway-100613601",false,"NCT07268716","Assess the Efficacy of Tailored Patient Information and Voluntary Patient-managed Outpatient Digital Follow-up (I-POD) as an Adjunct to Standard Treatment According to National Guidelines in the National Trauma Plan Among Adult Trauma Patients in Norway.","A Randomized Controlled Clinical Trial to Assess the Efficacy of Tailored Patient Information and Voluntary Patient-Managed Outpatient Digital Follow-Up as an Adjunct to Standard Treatment According to National Guidelines in Adult Trauma Patients in Norway (The POSTRAUMA Trial).","POSTRAUMA","Inclusion Criteria:\n\n* 16 years or older\n* Fulfils the national criteria for TTA and admitted to HUS following trauma\n* Included in NTR database\n* Able to give informed consent\n\nExclusion Criteria:\n\n* 15 years or younger\n* Not included in NTR database\n* Deceased before discharge from the hospital.\n* Not able to give informed consent\n* Insufficient command of the Norwegian language\n* Foreign tourists or nationals\n* Suicide attempt or serious self-inflicted trauma\n* Serious psychiatric disorders or serious ongoing substance abuse","ALL","16 Years",{"count":20,"type":21},256,"ESTIMATED","INTERVENTIONAL",[24],"NA","The POSTRAUMA trial is a clinical trial at The Regional trauma centre of Western Norway, Haukeland University Hospital.\n\nTrauma is the leading cause of death worldwide in patients aged 1-45 years. In Norway, approximately 10,000 patients are admitted to hospital annually due to trauma, with 66% being male. The mean age is 43 years for male and 48 years for female, indicating a relatively young patient population.\n\nWhile mortality rates are decreasing, a significant proportion of trauma survivors experience long-term disabilities, reduced quality of life, and difficulties in returning to work. These consequences impose substantial burdens on individuals, families, and society. Considering these issues, a shift in focus is needed-from survival alone to long-term functional recovery and quality of life after trauma.\n\nSevere trauma often requires long-term follow-up, both physically and psychosocially. Traditional follow-up can be fragmented and not tailored to individual needs. Digital patient monitoring and tailored information have the potential to improve patient pathways, but knowledge about how these are experienced by patients is limited.\n\nThe goal is to find out if Norwegian trauma patients who receive tailored patient information and patient-managed outpatient digital follow-up, in addition to standard treatment have:\n\n* Less disability\n* Return more often to work\n* Improved quality of life\n\nThe study population are Norwegian trauma patients, 16 years or older at date of inclusion, who are admitted to Haukeland University hospital (HUS) following trauma with trauma team activation. 256 patients will be included in this trial.\n\nParticipants will:\n\n* Answer a questionnaire at inclusion, one month, 6 months and 12 months.\n* Participants in the intervention group will be invited to digital outpatient follow up one month after the accident.\n* Some participants will be interviewed about how they experienced their trauma follow up.",[27,28,29,30,31,32,33,34,35],"Trauma Centers","Trauma Patients","Trauma (Including Fractures)","Trauma Injury","Rehabilitation After Neurological or Orthopaedic Injuries","Rehabilitation","Return to Work","HRQOL (Health Related Quality Of Life)","EQ5D5L-VAS",[37,38,39,40,41,42],"multitrauma","trauma","rehabilitation","return to work","HRQOL","EQ5D","NOT_YET_RECRUITING","2025-12-16",{"date":46,"type":47},"2025-12-22","ACTUAL",{"date":49,"type":21},"2026-03-02",{"date":51,"type":21},"2029-12-31",{"name":53,"class":54},"Haukeland University Hospital","OTHER",1,{"id":57,"slug":58,"hasResults":11,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":4,"eligibilityCriteria":62,"healthyVolunteers":11,"sex":17,"minAge":63,"maxAge":4,"enrollmentInfo":64,"targetDuration":4,"studyType":22,"phases":66,"briefSummary":67,"conditions":68,"keywords":69,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":4},"100606990","feasibility-of-unsupervised-therapy-after-neurological-or-orthopaedical-injury-in-the-home-setting-with-a-hand-rehabilitation-device-rehandybot-and-an-assistive-smartphone-application-rehabcoach-100606990","NCT07182734","Feasibility of Unsupervised Therapy After Neurological or Orthopaedical Injury in the Home Setting With a Hand Rehabilitation Device (ReHandyBot) and an Assistive Smartphone Application (RehabCoach)","Feasibility of Unsupervised Therapy After Neurological or Orthopaedical Injury in the Home Setting With a Hand Rehabilitation Device (ReHandyBot) and an Assistive Smartphone Application (RehabCoach): an Exploratory Study","Eligibility criteria for neurological patients\n\nInclusion criteria:\n\n* Informed Consent signed by the subject.\n* Female and male patients between 18 and 90 years old.\n* Stroke or traumatic brain injury (recruitment within 6 months from event onset).\n* Presence of a motor and\u002For sensory impairment of the upper limb as assessed by the responsible therapist.\n* Possibility (e.g., enough space) to set up the ReHandyBot at home.\n\nExclusion criteria:\n\n* Modified Ashworth Scale \\> 2 for one or more of the following muscles: shoulder adductors, forearm pronator and supinator, flexors and extensors of elbow, wrist and fingers.\n* Moderate to severe aphasia: Goodglass-Kaplan's scale \\\u003C 3.\n* Moderate to severe cognitive deficits: levels of cognitive functioning-revised (LCF-R) \\\u003C 9.\n* Functional impairment of the upper limb due to other pathologies.\n* Severe pain in the affected arm: visual analogue scale for pain (VASp) ≥ 5.\n* Other pathologies which may interfere with the study.\n* After discharge, the patient will go to an assisted living facility (e.g., care home).\n\nEligibility criteria for orthopedic patients\n\nInclusion criteria:\n\n* Informed Consent signed by the subject.\n* Female and male patients between 18 and 90 years old.\n* Clinic stay due to an orthopedic-related condition (e.g., surgery, trauma, burns).\n* Presence of a motor and\u002For sensory impairment of the upper limb as assessed by the responsible therapist.\n* Possibility (e.g., enough space) to set up the ReHandyBot at home.\n\nExclusion criteria:\n\n* Moderate to severe aphasia: Goodglass-Kaplan's scale \\\u003C 3.\n* Moderate to severe cognitive deficits: levels of cognitive functioning-revised (LCF-R) \\\u003C 9.\n* Functional impairment of the upper limb due to other pathologies.\n* Severe pain in the affected arm: visual analogue scale for pain (VASp) ≥ 5.\n* Other pathologies which may interfere with the study.\n* After discharge, the patient will go to an assisted living facility (e.g., care home).","18 Years",{"count":65,"type":21},30,[24],"The goal of this clinical trial is to evaluate whether using the ReHandyBot hand rehabilitation device together with the RehabCoach smartphone app can support safe, independent, and effective home therapy in patients with stroke, traumatic brain injury, or orthopedic problems.\n\nThe main questions it aims to answer are:\n\n* Can patients safely and independently use ReHandyBot and RehabCoach after leaving the clinic?\n* Will patients follow the recommended daily therapy schedule when using these tools at home?\n* How do patients experience the usability and acceptability of ReHandyBot and RehabCoach in everyday life?\n* Can this type of home-based therapy be extended to populations beyond stroke, such as traumatic brain injury and orthopedic patients?\n\nParticipants will:\n\n* Complete a screening and baseline assessment with a therapist.\n* Use ReHandyBot in a supervised phase at the clinic (3 sessions of 30 minutes).\n* Continue with a minimally supervised phase at the clinic (3-7 sessions of 30 minutes, with daily app use).\n* If ready, enter the unsupervised phase, taking ReHandyBot home for daily 30-minute training sessions, supported by RehabCoach.\n* Return for a final assessment including clinical and robotic evaluations and usability feedback.",[31],[39,70,71,72,73,74,75],"stroke","traumatic brain injury","robotic devices","unsupervised therapy","hand training","upper limb therapy","2025-09-12",{"date":78,"type":47},"2025-09-19",{"date":80,"type":21},"2025-09-15",{"date":82,"type":21},"2028-08-01",{"name":84,"class":54},"Swiss Federal Institute of Technology"]