[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100571890":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":12,"centralContacts":17,"locations":10,"responsibleParty":26,"collaborators":30,"id":32,"slug":33,"hasResults":34,"nctId":35,"briefTitle":36,"officialTitle":37,"acronym":10,"eligibilityCriteria":38,"healthyVolunteers":39,"sex":40,"minAge":10,"maxAge":10,"enrollmentInfo":41,"targetDuration":44,"studyType":45,"phases":10,"briefSummary":46,"conditions":47,"keywords":57,"overallStatus":67,"whyStopped":10,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":10},{"fullName":5,"class":6},"Nottingham University Hospitals NHS Trust","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":10},"Experts in the field of rehabilitation with knowledge in outcome monitoring and service evaluation",null,"This study has one study cohort, consisting of a diverse panel of expert clinicians, researchers and managers from a variety of professional backgrounds.\n\nThese study participants will be purposefully selected based on their knowledge of which demographic, socio-economic and healthcare related variables, as well as any associated outcome measure instruments should be collected as part of a rehabilitation dataset to evaluate the clinical efficacy and cost effectiveness of inpatient multidisciplinary rehabilitation.",[13],{"name":14,"affiliation":15,"role":16},"Thomas Corbett, MSc","Research at the National Rehabilitation Centre (part of Nottingham University Hospital NHS Trust)","PRINCIPAL_INVESTIGATOR",[18,23],{"name":19,"role":20,"phone":21,"phoneExt":10,"email":22},"Pauline Hyman-Taylor","CONTACT","0115 924 9924","pauline.hymantaylor@nhs.net",{"name":24,"role":20,"phone":21,"phoneExt":10,"email":25},"Alison Loyd","nuhnt.researchsponsor@nhs.net",{"type":27,"investigatorFullName":28,"investigatorTitle":29,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"SPONSOR_INVESTIGATOR","ThomasCorbett","Chief Investigator",[31],{"name":5,"class":6},"100571890","the-nrc-dataset-developing-a-minimum-dataset-for-multidisciplinary-rehabilitation-a-modified-e-delphi-study-100571890",false,"NCT06726135","The NRC Dataset. Developing a Minimum Dataset for Multidisciplinary Rehabilitation: a Modified E-Delphi Study","The National Rehabilitation Centre Dataset. Development of a Minimum Dataset for Multidisciplinary Rehabilitation: a Modified E-Delphi Study","Inclusion Criteria:\n\nThe panel will aim to include clinicians with a minimum of 5 years' experience from a variety of professional backgrounds within the following specialist areas:\n\n* Neuro Rehab\n* Trauma Rehab\n* Community Rehab\n* Outpatient Rehabilitation services\n* Defence medical services\n* Psychology services\n* Amputee Rehab\n* Speech and Language therapy\n* Emergency department\n* Critical Care\n* Trauma and Orthopaedics\n* Rehabilitation Medicine\n\nIt is expected that the expert panel will include:\n\n* Medical Doctors\n* Dietitians\n* Physiotherapists\n* Psychologists\n* Prosthetists\n* Occupational therapists\n* Speech and Language therapists\n* Data-base managers\n* Researchers\u002FAcademics\n* Commissioners\n* Local service managers\n* A department of work and pensions representative\n* An epidemiologist\u002Fdata-scientist with healthcare financial modelling experience\n\nExclusion Criteria:\n\nIndividuals will be excluded from the expert panel for any of the following reasons:\n\n1. They do not have 5 years' experience in their specialist field\n2. They do not have an understanding of various health indicators and the appropriate outcome measure instruments required to evaluate these health indicators.\n3. They have no understanding of how demographic and socio-economic variables impact health outcomes\n4. They have no understanding of how to evaluate clinical effectiveness and cost efficiency of inpatient rehabilitation services.\n5. Their professional background is not represented in the above noted specialist areas",true,"ALL",{"count":42,"type":43},50,"ESTIMATED","6 Months","OBSERVATIONAL","Several rehabilitation datasets are presently in use for specific patient groups in England. The 'National Clinical Audit of Specialist Rehabilitation for patients with complex needs following major injury' (NCASRI) evaluated outcomes within a cohort of Major Trauma patients between 2015 and 2018 using data from two of these datasets. The NCASRI project outlined some of the shortcomings of the pre-existing datasets and highlighted the need for a single National Rehabilitation Dataset to provide long term evaluation of a variety of patient presentations.\n\nThe proposed study will seek to develop such a dataset by means of an E-delphi study. This study will seek consensus from a panel of experts on the data items required to measure the effectiveness and socio-economic impact of multidisciplinary inpatient rehabilitation. Providing commissioners, researchers and clinicians with the data required to improve patient care, conduct research and develop rehabilitation services.\n\nThere are three potential phases to this study:\n\n* Phase one involves the establishment of a core domain set, outlining what information (data) should be included in the NRC core dataset.\n* Phase one will consist of at least 2 rounds of voting, with successive rounds of voting undertaken until an a-priori consensus of 70% is reached for all core data items marked as mandatory\u002Fcritical data in fitting OMERACT guidelines.\n* After 2 rounds, any data item that have reached consensus will be included in the final dataset. These core domain (data items) will then be excluded from subsequent rounds of voting.\n* A maximum of 4 rounds will be allowed in Phase 1. At which point the highest-ranking data items remaining with a consensus above 60% from each of the pre-identified categories will be included in the final dataset.\n* Phase two will explore what tools should be used to collect the core domains (outcome measure instruments) for each category outlined in phase 1.\n* Phase 2 will follow the same protocol for including outcome measure instruments into the core outcome set as were required to include core data items from phase 1.\n* If a consensus of equal or greater than 60% cannot be reached using an E-Delphi method in either phase 1 or phase 2 then a virtual meeting will be held amongst all expert panel members to reach consensus using a nominal group technique (phase 3).",[48,49,50,51,52,53,54,55,56],"Pain","Traumatic Brain Injury","Major Trauma","Multiple Sclerosis","Amputees \u002F Rehabilitation","Spinal Cord Injuries (SCI)","Functional Neurological Disorder","Intensive Care Unit (ICU) Acquired Weakness (ICU - AW)","Trauma Related Injuries",[58,59,60,61,62,63,64,65,66],"E-delphi","Delphi","Multidisciplinary","Rehabilitation","Core outcome set","Dataset","national rehabilitation centre","outcome measure instruments","inpatient","NOT_YET_RECRUITING","2024-12-15",{"date":70,"type":71},"2024-12-19","ACTUAL",{"date":73,"type":43},"2025-01",{"date":75,"type":43},"2025-06",{"name":28,"class":6}]