[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100582037":3},{"organization":4,"armGroups":7,"interventions":15,"overallOfficials":26,"centralContacts":33,"locations":42,"responsibleParty":59,"collaborators":61,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":70,"eligibilityCriteria":71,"healthyVolunteers":66,"sex":72,"minAge":73,"maxAge":20,"enrollmentInfo":74,"targetDuration":20,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":85,"overallStatus":89,"whyStopped":20,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":99},{"fullName":5,"class":6},"University of Manchester","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Entire cohort","EXPERIMENTAL","All participants (both transplant donor and recipients) will be assigned a 6 week graded pre operative outpatient exercise regimen (prehabilitation) delivered by video instruction. Participants will also be monitored 24\u002F7 by a wearable smart device for a total 14 week period (2 week baseline data collection, 6 weeks during prehabilitation and 6 weeks post op).",[13,14],"Other: Exercise programme","Device: Wearable smart device",[16,21],{"type":6,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"Exercise programme","6 week pre-operative graded prehabilitation programme, delivered by video and performed by participant up to 4 times a week at home or in a gym setting",[9],null,{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":20},"DEVICE","Wearable smart device","Participants will wear a wearable smart device (wrist or ring worn) for a period for 14 weeks; 2 weeks prior to prehabilitation, 6 weeks during pre-operative prehabilitation and 6 weeks post operative monitoring,",[9],[27,30],{"name":28,"affiliation":5,"role":29},"Gareth Kitchen","PRINCIPAL_INVESTIGATOR",{"name":31,"affiliation":32,"role":29},"Hussein Khambalia","Manchester University NHS Foundation Trust",[34,38],{"name":28,"role":35,"phone":36,"phoneExt":20,"email":37},"CONTACT","+447977280019","gareth.kitchen@manchester.ac.uk",{"name":39,"role":35,"phone":40,"phoneExt":20,"email":41},"Sophie Collinson","+447766827099","sophie.collinson1@nhs.net",[43],{"facility":44,"status":20,"city":45,"state":20,"zip":46,"country":47,"countryCode":48,"cosmosGeoPoint":49,"geoPoint":54,"contacts":55},"Manchester Royal Infirmary","Manchester","M13 9WL","United Kingdom","UK",{"type":50,"coordinates":51},"Point",[52,53],-2.23743,53.48095,{"lat":53,"lon":52},[56,58],{"name":31,"role":35,"phone":20,"phoneExt":20,"email":57},"hussein.khambalia@mft.nhs.uk",{"name":39,"role":35,"phone":20,"phoneExt":20,"email":41},{"type":29,"investigatorFullName":28,"investigatorTitle":60,"investigatorAffiliation":5,"oldNameTitle":20,"oldOrganization":20},"Chief Investigator",[62],{"name":32,"class":63},"OTHER_GOV","100582037","outcomes-of-a-pre-operative-exercise-programme-for-live-donor-and-recipient-kidney-transplant-patients-100582037",false,"NCT06858098","Outcomes of a Pre-operative Exercise Programme for Live Donor and Recipient Kidney Transplant Patients","Outcomes of a Pre-operative Exercise Regimen for Patients Undergoing Hand-assisted Liver Donor Nephrectomy and Transplantation","OPERATe","Inclusion Criteria:\n\n* Aged 18 years and over\n* Live kidney donor or transplant recipient\n\nExclusion Criteria:\n\n* Deceased donor transplant recipient\n* Patient unable to wear or tolerate wearable device\n* Unstable angina, recent myocardial infarction, recent cerebrovascular accident or new arrythmia\n* Patient declines or is unable to participate in the exercise programme\n* Lacks capacity to give informed consent to participate in trial\n* Non-English speaking\n* No access to a smart device to download application","ALL","18 Years",{"count":75,"type":76},40,"ESTIMATED","INTERVENTIONAL",[79],"NA","The goal of this clinical trial is to learn if a pre-operative outpatient exercise programme, monitored by a smart wearable device is acceptable to live kidney donor and recipient transplant patients. It will also look at the impact of prehabilitation on post operative outcomes. The main questions it aims to answer are:\n\nIs it feasible for renal transplant patients and live kidney donors to participate in a prehabilitation programme in combination with a piece of wearable technology?\n\nAre transplant outcomes improved by prehabilitation regimens delivered by video instruction?\n\nAre there discernible perioperative digital signatures provided by the wearable that link to surgical outcomes?\n\nIs the quality of perioperative sleep linked to surgical outcomes?\n\nParticipants will:\n\nWear a wrist or ring worn wearable device for a total of 14 weeks (2 week baseline, 6 week pre op and 6 week post op) Engage in a 6 week pre operative exercise programme at home\u002Fgym Keep a diary and answer surveys on their experience of the exercise regimen and wearable device",[82,83,84],"Kidney Transplant","Kidney Transplant Donor","Kidney Transplant Recipient",[86,87,88],"live kidney transplant","prehabilitation","wearable devices","NOT_YET_RECRUITING","2025-03-24",{"date":92,"type":93},"2025-03-25","ACTUAL",{"date":95,"type":76},"2025-05-01",{"date":97,"type":76},"2026-09-01",{"name":5,"class":6},1]