[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100629174":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":12,"centralContacts":16,"locations":26,"responsibleParty":54,"collaborators":57,"id":61,"slug":62,"hasResults":63,"nctId":64,"briefTitle":65,"officialTitle":66,"acronym":67,"eligibilityCriteria":68,"healthyVolunteers":63,"sex":69,"minAge":70,"maxAge":7,"enrollmentInfo":71,"targetDuration":7,"studyType":74,"phases":7,"briefSummary":75,"conditions":76,"keywords":79,"overallStatus":88,"whyStopped":7,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":98},{"fullName":5,"class":6},"Bournemouth University","OTHER",null,[9],{"type":6,"name":10,"description":11,"armGroupLabels":7,"otherNames":7},"Wound Dressing Material","The study will investigate any wound dressing applied as part of routine care. Advanced wound dressings are highly absorbent, flexible and comfortable for surgical wounds, and offer up to 14 days wear time. The adhesive moulds to the skin without sticking to the wound, thus protecting the skin and wound from damage. They support patient mobilisation by being comfortable, and thereby minimising painful skin damage such as blisters.",[13],{"name":14,"affiliation":5,"role":15},"Thomas Wainwright","PRINCIPAL_INVESTIGATOR",[17,22],{"name":18,"role":19,"phone":20,"phoneExt":7,"email":21},"Tikki Immins","CONTACT","+441202 962727","timmins@bournemouth.ac.uk",{"name":23,"role":19,"phone":24,"phoneExt":7,"email":25},"Chloe Bascombe","+441202 961945","cbascombe@bournemouth.ac.uk",[27,44],{"facility":28,"status":7,"city":29,"state":30,"zip":31,"country":32,"countryCode":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":40},"Nuffield Health Hospital Bournemouth","Bournemouth","Dorset","BH1 1RW","United Kingdom","UK",{"type":35,"coordinates":36},"Point",[37,38],-1.8795,50.72048,{"lat":38,"lon":37},[41,43],{"name":42,"role":19,"phone":7,"phoneExt":7,"email":7},"Robert Middleton",{"name":42,"role":15,"phone":7,"phoneExt":7,"email":7},{"facility":5,"status":7,"city":29,"state":30,"zip":45,"country":32,"countryCode":33,"cosmosGeoPoint":46,"geoPoint":48,"contacts":49},"BH8 8EB",{"type":35,"coordinates":47},[37,38],{"lat":38,"lon":37},[50,53],{"name":14,"role":19,"phone":51,"phoneExt":7,"email":52},"+441202 961656","twainwright@bournemouth.ac.uk",{"name":14,"role":15,"phone":7,"phoneExt":7,"email":7},{"type":15,"investigatorFullName":55,"investigatorTitle":56,"investigatorAffiliation":5,"oldNameTitle":7,"oldOrganization":7},"Tom Wainwright","Professor of Orthopaedics",[58],{"name":59,"class":60},"Nuffield Health Bournemouth","UNKNOWN","100629174","dressing-related-experiences-and-surgical-site-self-care-in-hip-and-knee-replacement-an-observational-cohort-study-100629174",false,"NCT07471243","Dressing-related Experiences and Surgical Site Self-care in Hip and Knee Replacement: an Observational Cohort Study","Dressing-Related Experiences and Surgical Site Self-Care in Hip and Knee Replacement: an Observational Cohort Study (DRESS-X)","DRESS-X","Inclusion Criteria:\n\n* Adults (18+) undergoing primary total hip or knee replacement\n* Enrolled in an ERAS protocol\n* Willing and able to provide informed consent\n\nExclusion Criteria:\n\n* Requiring revision replacement\n* Unable to provide informed consent (cognitive disorder such as dementia, psychiatric illness)\n* Unable to understand written English","ALL","18 Years",{"count":72,"type":73},100,"ESTIMATED","OBSERVATIONAL","The goal of this prospective observational cohort study is to investigate dressing-related experiences and surgical site self-care in patients who are undergoing a total hip or knee replacement. The main objectives of the study are:\n\n* To evaluate patient adherence to the ISWCAP self-care checklist after total hip or knee replacement within an ERAS pathway.\n* To explore patient-reported outcomes related to the performance and comfort of advanced dressings.\n* To assess the perceived adequacy and usefulness of post-discharge wound care education.\n* To identify the incidence and types of wound-related complications in the 12 weeks following surgery.\n\nParticipants will give informed consent before surgery and will start the study once the dressing has been applied following surgery. There will be follow up study visits at discharge, 7 days, 12 days, 6 weeks and 12 weeks post-surgery. Data relating to vital signs, medical history, surgery and medication will be taken from routine data.",[77,78],"Total Hip Replacement","Total Knee Replacement",[80,81,82,83,84,85,86,87],"Hip arthroplasty","Hip replacement","Knee arthroplasty","Knee replacement","Musculoskeletal","Enhanced recovery after surgery","ERAS","Surgical wound","NOT_YET_RECRUITING","2026-03-10",{"date":91,"type":92},"2026-03-13","ACTUAL",{"date":94,"type":73},"2026-04-01",{"date":96,"type":73},"2027-08-31",{"name":5,"class":6},2]