[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"ostomy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:ostomy":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,40,63,93,121,150,173,200],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":21,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":4},"100637362","cp384---ostomy-care-oc-pro-panel-plan-100637362",false,"NCT07589907","CP384 - Ostomy Care (OC) PRO Panel Plan","384 PRO Panel","Inclusion Criteria:\n\n* 18 years of age or above\n* full legal capacity\n* willing and able to complete online questionnaires\n* have either an ileostomy, a colostomy, or a urostomy\n\nExclusion Criteria:\n\n* Cannot have a scheduled stoma reversal surgery\n* Cannot have more than one stoma","ALL","18 Years",{"count":19,"type":20},1000,"ESTIMATED","5 Years","OBSERVATIONAL","The aim is to create an electronic patient reported outcome (e-PRO) based registry, specifically for subjects living with a stoma (ileostomy, colostomy or urostomy).",[25,26,27],"Ostomy","Ileostomy - Stoma","Urostomy","NOT_YET_RECRUITING","2026-05-11",{"date":31,"type":32},"2026-05-15","ACTUAL",{"date":34,"type":20},"2026-06-01",{"date":36,"type":20},"2032-10-31",{"name":38,"class":39},"Coloplast A\u002FS","INDUSTRY",{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":44,"acronym":4,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":46,"enrollmentInfo":47,"targetDuration":4,"studyType":49,"phases":50,"briefSummary":52,"conditions":53,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":54,"lastUpdatePostDateStruct":55,"startDateStruct":57,"completionDateStruct":59,"leadSponsor":61,"locationsCount":4},"100628337","study-of-tre-seals-on-early-post-operative-subjects-100628337","NCT07460323","Study of TRE Seals on Early Post-operative Subjects","Inclusion Criteria:\n\n1. At least 18 years of age\n2. Has their ostomy surgery and post-operative care in the United Kingdom (UK)\n3. Has a colostomy, ileostomy, or urostomy and no reversal planned during the study evaluation period\n4. Able to have first study product applied at first pouch change after surgery (or up to 4 days post-op)\n5. Is appropriate to use a barrier seal per the Investigator\n6. Able to provide an informed consent for study participation\n7. Willing to follow protocol procedures, including participating in study visits, as demonstrated by signing the informed consent\n\nExclusion Criteria:\n\n1. Is over 85 years of age\n2. Has received chemotherapy or radiation in the past 30 days or reports beginning chemotherapy or radiation during the study.\n3. A score of 1, 2, or 3 for any of the three OCSI Tool PSC-related domains (i.e., peristomal irritant dermatitis, peristomal bleeding, and hyperplasia) at time of enrollment\n4. Has a fistula in the peristomal area at time of enrollment\n5. Has an open draining wound (not including mucocutaneous separation) in the peristomal area at time of enrollment\n6. Has a suspected infection in the peristomal area at time of enrollment\n7. Is pregnant or lactating at time of enrollment (as determined by interview only)\n8. Is unable to speak, read, and understand English.\n9. Is currently participating in another clinical study using ostomy products\n10. Is currently an employee of Hollister Incorporated or any ostomy manufacturer","85 Years",{"count":48,"type":20},107,"INTERVENTIONAL",[51],"NA","This study will evaluate two Ostomy Seals\u002FRings in a group of post-operative patients.",[25],"2026-03-03",{"date":56,"type":32},"2026-03-10",{"date":58,"type":20},"2026-06",{"date":60,"type":20},"2027-03",{"name":62,"class":39},"Hollister Incorporated",{"id":64,"slug":65,"hasResults":11,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":69,"eligibilityCriteria":70,"healthyVolunteers":11,"sex":16,"minAge":71,"maxAge":4,"enrollmentInfo":72,"targetDuration":4,"studyType":49,"phases":74,"briefSummary":75,"conditions":76,"keywords":79,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":4},"100625634","effect-of-word-search-and-case-based-puzzle-use-in-stoma-care-education-of-nursing-students-100625634","NCT07425184","Effect of Word Search and Case-Based Puzzle Use in Stoma Care Education of Nursing Students","The Effect of Using Word Searches and Case-Based Puzzles in Stoma Care Education for Nursing Students","PUZZLE-STOMA","Inclusion Criteria:\n\n* Nursing students enrolled in the Surgical Nursing course for the first time,\n* Students who voluntarily agree to participate in the study.\n\nExclusion Criteria:\n\n* Students who have previously received stoma care training through another educational platform,\n* Students who provide incomplete responses to data collection forms,\n* Students who do not attend the theoretical course sessions,\n* Students who do not participate in any stage of the knowledge assessment,\n* Students who do not complete puzzle and word search activities included in the intervention.","17 Years",{"count":73,"type":20},87,[51],"Objective: This study aims to determine the effect of using word search and case-based puzzles in stoma care education on nursing students' knowledge levels. Given that traditional teaching methods may have limited effectiveness in helping students acquire knowledge and skills, the study aims to demonstrate the contribution of integrating active learning and gamification-based approaches into education.\n\nDesign: The study is planned as a randomized controlled experimental design and will use a pre-test-post-test measurement approach.\n\nMethod: The study will be conducted with second-year students from the Nursing Department at Gazi University. This research will be prepared under the guidance of the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) protocol, and the reporting of the randomized controlled study will be carried out under the Consolidated Standards of Reporting Trials (CONSORT). In the study, students will be randomly assigned to the experimental and control groups. The experimental group will receive training that includes word search and case-based puzzles during the stoma care training process, while the control group will receive training using traditional teaching methods. Students' knowledge levels will be assessed with measurements applied before and after the training, and student opinions regarding the training method will also be analyzed. The \"Stoma Care Knowledge Level Assessment Test\" will be used to evaluate knowledge levels, and the \"Student Opinions on the Use of Puzzles and Word Searches in Stoma Education\" form will be used to determine student opinions.\n\nHypothesis: The null hypothesis (H0) of the study states that the use of word search and case-based puzzles in stoma care education has no effect on students' knowledge level; the alternative hypothesis (H1) states that this educational method significantly affects students' knowledge level.",[25,77,78],"Nursing Education","Stoma Care Education in Nursing Students",[77,80,81,82],"Case-Based Learning","stoma care","Puzzle-Based Learning","2026-02-13",{"date":85,"type":32},"2026-02-20",{"date":87,"type":20},"2026-02-16",{"date":89,"type":20},"2026-03-19",{"name":91,"class":92},"Gazi University","OTHER",{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":98,"acronym":99,"eligibilityCriteria":100,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":101,"targetDuration":4,"studyType":49,"phases":103,"briefSummary":104,"conditions":105,"keywords":108,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":113,"lastUpdatePostDateStruct":114,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":119,"locationsCount":4},"100620489","mobile-education-and-comfort-in-ostomy-patients-100620489","NCT07358286","MOBILE EDUCATION AND COMFORT IN OSTOMY PATIENTS","THE EFFECT OF KOLCABA'S COMFORT THEORY-BASED MOBILE EDUCATION ON COMFORT LEVELS OF OSTOMY PATIENTS: A RANDOMIZED CONTROLLED TRIAL","STOMA-PLUS","Inclusion Criteria:\n\n* Adults aged 18 years and older\n* Patients with a stoma (colostomy or urostomy)\n* Ability to use a smartphone or mobile device\n* Willingness to participate in the study\n* Ability to provide informed consent\n\nExclusion Criteria:\n\n* Cognitive impairment that prevents understanding of the study procedures\n* Severe psychiatric disorders\n* Inability to use mobile technology\n* Participation in another interventional study during the study period",{"count":102,"type":20},68,[51],"Purpose of the Study\n\nThis study aims to understand whether a mobile education program can improve comfort levels in people living with a stoma. A stoma is a surgical opening created on the abdomen to allow stool or urine to leave the body. Living with a stoma can affect daily life in many ways, including physical comfort, emotional well-being, social life, and the home environment.\n\nThe education program used in this study is based on Kolcaba's Comfort Theory. This theory focuses on comfort as a whole and includes physical, emotional, social, and environmental aspects of a person's life. The study will compare people who receive mobile education with those who receive standard hospital care only.\n\nWho Can Take Part\n\nAdults aged 18 years and older who are scheduled to have colostomy, ileostomy, or urostomy surgery may take part in this study. Participants must be able to communicate in Turkish, read and understand written information, and agree to join the study voluntarily.\n\nPeople with severe cognitive problems, serious communication difficulties, or major vision or hearing problems will not be included.\n\nWhat Will Happen in the Study\n\nParticipants will be randomly assigned to one of two groups:\n\nMobile Education Group\n\nStandard Care Group\n\nBoth groups will receive routine care provided by the hospital.\n\nParticipants in the mobile education group will also receive access to a mobile application designed specifically for people with a stoma. This application includes:\n\nEasy-to-understand information about stoma care\n\nAnimated educational videos showing step-by-step stoma care practices\n\nGuidance on skin care, pouch changing, and hygiene\n\nInformation on common problems and when to seek medical help\n\nReminders to support daily stoma care routines\n\nThe mobile application can be used on smartphones and does not include diagnosis or treatment. It is for education and support only.\n\nParticipants in the standard care group will receive usual hospital education and care. After the study is completed, they will also be offered the mobile education program.\n\nWhat Participants Will Be Asked to Do\n\nAll participants will be asked to answer questionnaires that measure comfort levels at several time points:\n\nBefore surgery\n\nOne day after surgery\n\nFifteen days after discharge (by phone)\n\nOne month after surgery (during a clinic visit)\n\nParticipants in the mobile education group will be shown how to use the application and may use it as often as they wish. Researchers may contact participants to ask about their experience using the app and to identify any difficulties.\n\nPossible Benefits\n\nParticipants may gain better understanding of stoma care and feel more confident managing daily life with a stoma. The mobile education program may help reduce discomfort, support emotional well-being, and improve overall quality of life.\n\nThe results of this study may help healthcare professionals develop better education tools and support programs for people living with a stoma.\n\nRisks and Safety\n\nThis study does not involve experimental medical treatments. The mobile application provides education only. Personal data will not be collected through the app, and all information will be kept confidential. Participants may leave the study at any time without affecting their medical care.\n\nWhy This Study Is Important\n\nAccess to stoma care education can be limited due to time constraints, staff availability, and hospital resources. Mobile education may provide an easy and accessible way for people to receive reliable information whenever they need it.\n\nThis study will help determine whether a comfort-focused mobile education program can support people living with a stoma and improve their overall comfort and well-being.",[106,25,107],"Stoma","Mobile Application",[109,110,111,112],"Ostomy Care","Mobile Health","Kolcaba's Comfort Theory","Nursing","2026-01-14",{"date":115,"type":32},"2026-01-22",{"date":117,"type":20},"2026-01",{"date":58,"type":20},{"name":120,"class":92},"Ege University",{"id":122,"slug":123,"hasResults":11,"nctId":124,"briefTitle":125,"officialTitle":125,"acronym":4,"eligibilityCriteria":126,"healthyVolunteers":127,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":128,"targetDuration":4,"studyType":49,"phases":130,"briefSummary":131,"conditions":132,"keywords":133,"overallStatus":139,"whyStopped":4,"lastUpdateSubmitDate":140,"lastUpdatePostDateStruct":141,"startDateStruct":143,"completionDateStruct":145,"leadSponsor":147,"locationsCount":149},"100532487","improving-the-quality-of-life-and-self-sufficiency-of-individuals-with-stoma-pecha-kucha-training-via-smartphone-100532487","NCT06213441","Improving the Quality of Life and Self-sufficiency of Individuals With Stoma: Pecha Kucha Training Via Smartphone","Inclusion Criteria:\n\n* Having a stoma for the first time,\n* Can speak Turkish,\n* Can understand Turkish,\n\nExclusion Criteria:\n\n* A stoma has been opened before,\n* Having difficulty in speaking Turkish\n* Having difficulty in understanding Turkish",true,{"count":129,"type":20},52,[51],"This study was planned as a randomized controlled trial to determine the effect of stoma care training given by the Pecha Kucha method to improve the quality of life and self-sufficiency of individuals with stoma.",[25],[134,135,136,137,138],"education","ostomy","care","Quality of Life","Self-sufficiency","RECRUITING","2025-09-26",{"date":142,"type":32},"2025-10-01",{"date":144,"type":32},"2023-12-23",{"date":146,"type":20},"2025-09-29",{"name":148,"class":92},"MAİDE YEŞİLYURT",1,{"id":151,"slug":152,"hasResults":11,"nctId":153,"briefTitle":154,"officialTitle":154,"acronym":4,"eligibilityCriteria":155,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":156,"targetDuration":4,"studyType":49,"phases":158,"briefSummary":159,"conditions":160,"keywords":162,"overallStatus":139,"whyStopped":4,"lastUpdateSubmitDate":164,"lastUpdatePostDateStruct":165,"startDateStruct":167,"completionDateStruct":169,"leadSponsor":171,"locationsCount":149},"100556384","novel-post-surgical-incision-management-to-prevent-ostomy-complications-100556384","NCT06524401","Novel Post-Surgical Incision Management to Prevent Ostomy Complications","Inclusion Criteria:\n\n* Participant is greater than 18 years of age, inclusive\n* Participant is undergoing ileostomy surgery or,\n* has an enterocutaneous fistula with output over 500cc in 24 hours\n* Participants stoma will have a maximum diameter of 1.5 inches based on measurements from the Investigator or Sponsor.\n* Area around the stoma must have no injury through the dermis (i.e., intact skin)\n* Participant is willing and able to comply with all protocol-specified requirements\n* Participant is capable of reading and understanding English and will provide written informed consent to participate.\n\nExclusion Criteria:\n\n* Unable\u002Funwilling to attend the follow-up appointments\n* Participant has a life expectancy \\\u003C 30 days.\n* Participant has a stature too small for use of the Limpet in the opinion of the Investigator or Sponsor.\n* Participant has an enteroatmospheric fistula (enteric fistula to an open wound)\n* Participant is scheduling\u002Fplanning concurrent chemotherapy or other radiation treatment during the study follow-up period\n* Participant has a history of sensitivity or allergy to hydrocolloids or other materials in the Limpet device.\n* Participant is pregnant or planning to become pregnant (verbal report).\n* Participant is unable or unwilling to provide informed consent.\n* Participant is currently participating in an investigational drug or another device study that clinically interferes with the current study endpoints.\n* Participant has any other disease or medical condition that, in the opinion of the Investigator or Sponsor, could endanger the participant, interfere with the evaluation of the study device's efficacy or safety, or compromise the participant's ability to comply with\u002Fcomplete the study.",{"count":157,"type":20},92,[51],"The goal of this clinical trial is to evaluate the safety and effectiveness of the Limpet, as compared to standard of care ostomy pouches, in reducing complications for ostomy and fistula patients. Secondary objectives include evaluating dressing leak rates and causes of complications (e.g., edema, tissue oxygen saturation, and poor stoma eversion). The main questions it aims to answer are:\n\nPrimary Hypothesis 1: Peristomal Skin Complications will decrease\n\nPrimary Hypothesis 2: Dressing Leak Rates will decrease\n\nParticipants will:\n\n* Receive either the Limpet device or standard of care adhesive ostomy pouch dressing\n* Return every 7 days for study visits for 30 days to receive device replacement, wound imaging, blood tests, and quality of life surveys.",[25,161],"Enterocutaneous Fistula",[106,163],"Ileostomy","2025-09-24",{"date":166,"type":32},"2025-09-25",{"date":168,"type":32},"2024-11-18",{"date":170,"type":20},"2029-03",{"name":172,"class":92},"HealthPartners Institute",{"id":174,"slug":175,"hasResults":11,"nctId":176,"briefTitle":177,"officialTitle":178,"acronym":4,"eligibilityCriteria":179,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":180,"targetDuration":4,"studyType":49,"phases":182,"briefSummary":183,"conditions":184,"keywords":186,"overallStatus":139,"whyStopped":4,"lastUpdateSubmitDate":191,"lastUpdatePostDateStruct":192,"startDateStruct":194,"completionDateStruct":196,"leadSponsor":198,"locationsCount":149},"100560932","ostomy-simulation-for-patient-education-prior-to-urologic-bowel-diversion-surgeries-100560932","NCT06583577","Ostomy Simulation for Patient Education Prior to Urologic Bowel Diversion Surgeries","3D Ostomy Simulation for Patient Education","Inclusion Criteria:\n\n* Age\\>18, undergoing bowel diversion urologic surgery.\n\nExclusion Criteria:\n\n* Current or prior ostomy formation, cognitive function causing inability to care for stoma, current pregnancy.",{"count":181,"type":20},40,[51],"The purpose of this study is to evaluate the feasibility of using a realistic and anatomically accurate 3D printed simulation model for urologic bowel diversion patient education. Using a randomized two group design, we aim to determine whether the use of this model enhances patient knowledge, self-care skills, and confidence in ostomy care. We will also evaluate changes in quality of life (QOL) and patient satisfaction comparing patients exposed to the 3D model to those receiving standard of care.\n\nThe secondary aim of the study is to examine the differences between groups on patient outcomes including hospital duration, mortality, emergency\u002Furgent health care visits, readmissions, and infections.\n\nParticipants will be educated using 3D model simulation as part of their preoperative education (experimental group) or have standard education without using the simulation model (comparator group). Both groups will complete quality of life (QOL), ostomy adjustment, and satisfaction with education surveys during their preoperative education visit and again during their routine follow-up visits (a) within 3 weeks after surgery, (b) between 5- 8 weeks after surgery, and (c) at approximately 3 months after surgery.",[25,185],"Ileal Conduit",[187,188,189,190],"Patient education","Simulation","Quality of life","Ostomy adjustment","2025-08-06",{"date":193,"type":32},"2025-08-08",{"date":195,"type":32},"2024-07-30",{"date":197,"type":20},"2026-07-15",{"name":199,"class":92},"University of Minnesota",{"id":201,"slug":202,"hasResults":11,"nctId":203,"briefTitle":204,"officialTitle":204,"acronym":205,"eligibilityCriteria":206,"healthyVolunteers":127,"sex":16,"minAge":17,"maxAge":207,"enrollmentInfo":208,"targetDuration":4,"studyType":49,"phases":210,"briefSummary":211,"conditions":212,"keywords":4,"overallStatus":139,"whyStopped":4,"lastUpdateSubmitDate":215,"lastUpdatePostDateStruct":216,"startDateStruct":218,"completionDateStruct":220,"leadSponsor":222,"locationsCount":149},"100539917","3d-printed-personalized-ostomy-appliance-100539917","NCT06310070","3D Printed Personalized Ostomy Appliance","3DPPOA","Inclusion Criteria:\n\n* 18-100 years old\n* Must have had current ostomy appliance for \\> 6 weeks - if patients with stomas less than 6 weeks are included, their personalized templates will not be useful once the stoma size has changed after their initial scan.\n* Must have experienced \\> 1 leakage in the week leading up to day of consent. - If patients are not experiencing leakages, then there will be no baseline data to compare effectiveness of the post-3D appliance intervention.\n* Participants must be able to consent for themselves\n* Access to phone AND computer with internet access. Patient must be able to provide electronic mailing address for e-consent documentation and REDCap surveys.\n\nExclusion Criteria:\n\n* Concern for patient being able to be reached over the phone or reliable internet access for REDCap survey completion\n* Existing peri-stomal skin breakdown including ulceration or mucocutaneous separation.\n* Diagnosis of infection around the peristomal region. (erythema is NOT an exclusion criteria)","100 Years",{"count":209,"type":20},30,[51],"The goal of this clinical trial is to learn about the effectiveness of using a 3D scan for a personal ostomy appliance. The main question it aims to answer is:\n\n• Whether or not a 3D scan of a stoma reduces leakages and improves patient quality of life in regard to using a personalized ostomy appliance.\n\nParticipants will\n\n* Spend 2 weeks with their standard of care ostomy appliance\n* Spend 2 weeks with their personalized ostomy appliance made from a 3D scan\n* Participate in daily surveys and weekly quality of life surveys conducted over the phone",[213,25,214],"3D Printing","Leakage","2025-01-20",{"date":217,"type":32},"2025-01-22",{"date":219,"type":32},"2024-05-10",{"date":221,"type":20},"2025-06-05",{"name":223,"class":92},"Carilion Clinic"]