[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100541640":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":23,"locations":32,"responsibleParty":102,"collaborators":10,"id":104,"slug":105,"hasResults":106,"nctId":107,"briefTitle":108,"officialTitle":109,"acronym":110,"eligibilityCriteria":111,"healthyVolunteers":106,"sex":112,"minAge":113,"maxAge":10,"enrollmentInfo":114,"targetDuration":10,"studyType":117,"phases":10,"briefSummary":118,"conditions":119,"keywords":121,"overallStatus":34,"whyStopped":10,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":135},{"fullName":5,"class":6},"Nantes University Hospital","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Assessment of pain during pelvic positioning",null,"48-hour follow-up of patients included in the study, with data collected on two pelvis fittings per 24 hours of follow-up (one fitting = one installation and one removal).",[13],"Other: Questioning the patient during hygiene care",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":10},"Questioning the patient during hygiene care","The study examines how patients and caregivers feel when using the bedpan. Over the course of a day, collecting all this information would take just under 7 minutes. Over the duration of patient participation (2 days), we estimate that it would take a total of 15 minutes per patient to collect this information. The objectives are focused on pain and discomfort, and on the alteration of the (patient's) skin condition through objective observation of redness or stage I pressure sores by the caregiver.",[9],[20],{"name":21,"affiliation":5,"role":22},"Pia SECHER","PRINCIPAL_INVESTIGATOR",[24,29],{"name":25,"role":26,"phone":27,"phoneExt":10,"email":28},"Jules Galy","CONTACT","(+33) 253482835","jules.galy@chu-nantes.fr",{"name":30,"role":26,"phone":10,"phoneExt":10,"email":31},"Thomas RULLEAU, PhD","Thomas.rulleau@chu-nantes.fr",[33,50,63,76,89],{"facility":5,"status":34,"city":35,"state":36,"zip":37,"country":38,"countryCode":39,"cosmosGeoPoint":40,"geoPoint":45,"contacts":46},"RECRUITING","Nantes","Loire Atlantique","44093","France","FR",{"type":41,"coordinates":42},"Point",[43,44],-1.55336,47.21725,{"lat":44,"lon":43},[47],{"name":48,"role":26,"phone":10,"phoneExt":10,"email":49},"Pia SECHER-CAILLETEAU","pia.secher@chu-nantes.fr",{"facility":51,"status":34,"city":52,"state":10,"zip":10,"country":38,"countryCode":39,"cosmosGeoPoint":53,"geoPoint":57,"contacts":58},"CHU Cholet","Cholet",{"type":41,"coordinates":54},[55,56],-0.87974,47.05893,{"lat":56,"lon":55},[59],{"name":60,"role":26,"phone":61,"phoneExt":10,"email":62},"Stéphanie NOURISSON","(+33) 2 41 49 69 85","stephanie.nourisson@ch-cholet.fr",{"facility":64,"status":34,"city":65,"state":10,"zip":10,"country":38,"countryCode":39,"cosmosGeoPoint":66,"geoPoint":70,"contacts":71},"CHU Laval","Laval",{"type":41,"coordinates":67},[68,69],-0.77019,48.07247,{"lat":69,"lon":68},[72],{"name":73,"role":26,"phone":74,"phoneExt":10,"email":75},"ROMAIN CHAMPAGNE","(+33) 672091548","Romain.CHAMPAGNE@chlaval.fr",{"facility":77,"status":34,"city":78,"state":10,"zip":10,"country":38,"countryCode":39,"cosmosGeoPoint":79,"geoPoint":83,"contacts":84},"CH Le Mans","Le Mans",{"type":41,"coordinates":80},[81,82],0.20251,48.0021,{"lat":82,"lon":81},[85],{"name":86,"role":26,"phone":87,"phoneExt":10,"email":88},"Emmanuelle Lecompte","(+33) 681220543","gsicot@ch-lemans.fr",{"facility":90,"status":34,"city":91,"state":10,"zip":10,"country":38,"countryCode":39,"cosmosGeoPoint":92,"geoPoint":96,"contacts":97},"CHU Orleans","Orléans",{"type":41,"coordinates":93},[94,95],1.90407,47.90248,{"lat":95,"lon":94},[98],{"name":99,"role":26,"phone":100,"phoneExt":10,"email":101},"Guillaume FOSSAT","(+33) 2 38.65.13.18","guillaume.fossat@chu-orleans.fr",{"type":103,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100541640","research-project-on-the-risk-of-discomfort-pain-alteration-of-skin-condition-in-bedpan-use-by-patients-and-caregivers-100541640",false,"NCT06332495","Research Project on the Risk of Discomfort, Pain, Alteration of Skin Condition in Bedpan Use by Patients and Caregivers","Research Project on the Risk of Discomfort, Pain and Alteration of Skin Condition in Bedpan Use by Patients and Caregivers","RIDAECUBA","Inclusion Criteria:\n\n* Patient of legal age (age ≥ 18 years).\n* Patient with reduced and very reduced mobility, bedridden requiring the use of a bedpan.\n* Estimated length of hospital stay on the ward ≥ 2 days.\n* Patient affiliated to a social security system.\n* Patient able to understand the protocol.\n* Patient having given oral non-opposition to participate.\n* Patient who has received the study information note.\n* Patient who had never participated in this study.\n\nExclusion Criteria:\n\n* Patients with cognitive impairment preventing objective pain assessment or with neurological pathologies.\n* Patients under guardianship, curatorship or safeguard of justice.","ALL","18 Years",{"count":115,"type":116},300,"ESTIMATED","OBSERVATIONAL","The hypothesis is that the current bedpan is not adapted to the diversity of patients encountered. It is necessary to collect the opinions of patients themselves on the current pool in different departments in order to validate our hypothesis.\n\nThe objective is to evaluate pain in patients with reduced or very reduced mobility caused by the bedpan currently used in current practice through an observational study.",[120],"Nurse-Patient Relations",[122,123,124,125],"Bedpan","Discomfort","Alteration of Skin","Pain","2025-05-30",{"date":128,"type":129},"2025-05-31","ACTUAL",{"date":131,"type":129},"2024-08-03",{"date":133,"type":116},"2026-08-03",{"name":5,"class":6},5]