[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100658510":3},{"organization":4,"outcomesModule":7,"designInfo":21,"detailedDescription":29,"studyPopulation":20,"armGroups":30,"interventions":43,"overallOfficials":51,"centralContacts":56,"locations":62,"responsibleParty":82,"collaborators":20,"id":84,"slug":85,"hasResults":86,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":90,"eligibilityCriteria":91,"healthyVolunteers":86,"sex":92,"minAge":93,"maxAge":94,"enrollmentInfo":95,"targetDuration":20,"studyType":98,"phases":99,"briefSummary":101,"conditions":102,"keywords":105,"overallStatus":112,"whyStopped":20,"lastUpdateSubmitDate":113,"lastUpdatePostDateStruct":114,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":122},{"fullName":5,"class":6},"Halic University","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":16,"otherOutcomes":20},[9,13],{"measure":10,"description":11,"timeFrame":12},"Change in Self-Care Agency Score","Self-care agency will be assessed using the Exercise of Self-Care Agency Scale. The scale consists of 35 items scored from 0 to 4, with a total score ranging from 0 to 140. Higher scores indicate greater self-care agency. The change in scores from baseline to the tenth day after discharge will be compared between the intervention and control groups.","Baseline and 10 days after discharge",{"measure":14,"description":15,"timeFrame":12},"Change in General Comfort Score","General comfort will be assessed using the General Comfort Questionnaire. The questionnaire consists of 48 items evaluating physical, psychospiritual, sociocultural, and environmental dimensions of comfort. Higher scores indicate a higher level of comfort. The change in scores from baseline to the tenth day after discharge will be compared between the intervention and control groups.",[17],{"measure":18,"description":19,"timeFrame":12},"Change in Pain Intensity","Pain intensity will be assessed using a 10-centimeter Visual Analog Scale ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity. The change in pain scores from baseline to the tenth day after discharge will be compared between the intervention and control groups.",null,{"allocation":22,"interventionModel":23,"interventionModelDescription":24,"primaryPurpose":25,"observationalModel":20,"timePerspective":20,"maskingInfo":26},"RANDOMIZED","PARALLEL","Participants will be randomly assigned in a 1:1 ratio to either the Teach-Back-supported discharge education group or the routine discharge education control group.","SUPPORTIVE_CARE",{"masking":27,"maskingDescription":28,"whoMasked":20},"NONE","Participants and the researcher delivering the intervention will not be blinded due to the nature of the educational intervention. Statistical analyses will be performed by an independent statistician blinded to the group codes.","This study is designed as a parallel-group randomized controlled trial and will be conducted at Istanbul Büyükçekmece Mimar Sinan State Hospital. The study will include 68 adult patients aged 18-64 years who undergo elective surgery for pilonidal sinus disease. Participants will be randomly assigned to the intervention group or the control group in a 1:1 ratio using block randomization with variable block sizes. Allocation concealment will be ensured through sequentially numbered, opaque, sealed envelopes.\n\nBefore the intervention, participants in both groups will complete the Patient Information Form, Exercise of Self-Care Agency Scale, General Comfort Questionnaire, and Visual Analog Scale for pain. Participants in the intervention group will receive Teach-Back-supported discharge education covering wound care, personal hygiene, pain management, sitting and mobility, activities of daily living, bowel elimination, signs of complications, and situations requiring medical consultation. Participants will be asked to explain the information in their own words, and any misunderstood or incomplete information will be clarified until correct understanding is demonstrated. Participants in the control group will receive the hospital's routine discharge education and standard care. All outcome measures will be repeated during the follow-up visit on the tenth day after discharge.",[31,37],{"label":32,"type":33,"description":34,"interventionNames":35},"Teach-Back-Supported Discharge Education","EXPERIMENTAL","Participants will receive Teach-Back-supported discharge education in addition to standard care. The education will cover wound care, personal hygiene, pain management, sitting and mobility, activities of daily living, bowel elimination, signs of complications, and situations requiring medical consultation. Participants will be asked to repeat the information in their own words, and misunderstood or incomplete information will be explained again.",[36],"Behavioral: Teach-Back-Supported Discharge Education",{"label":38,"type":39,"description":40,"interventionNames":41},"Routine Discharge Education","ACTIVE_COMPARATOR","Participants will receive the hospital's routine discharge education and standard postoperative care. No additional education based on the Teach-Back method will be provided by the researchers.",[42],"Behavioral: Routine Discharge Education",[44,48],{"type":45,"name":32,"description":46,"armGroupLabels":47,"otherNames":20},"BEHAVIORAL","Participants will receive individualized discharge education using the Teach-Back method. The education will cover wound care, personal hygiene, pain management, sitting and mobility, activities of daily living, bowel elimination, signs of complications, and situations requiring medical consultation. Participants will be asked to explain the information in their own words. Any misunderstood or incomplete information will be clarified and reassessed until correct understanding is demonstrated.",[32],{"type":45,"name":38,"description":49,"armGroupLabels":50,"otherNames":20},"Participants will receive the hospital's routine discharge education and standard postoperative care. No additional education using the Teach-Back method will be provided by the researchers.",[38],[52],{"name":53,"affiliation":54,"role":55},"fatma eti aslan","Bahcesehir","STUDY_CHAIR",[57],{"name":58,"role":59,"phone":60,"phoneExt":20,"email":61},"Kübra can, MSc","CONTACT","+90 5438711795","kubracan@halic.edu.tr",[63],{"facility":64,"status":20,"city":65,"state":20,"zip":66,"country":67,"countryCode":20,"cosmosGeoPoint":68,"geoPoint":73,"contacts":74},"Istanbul Buyukcekmece Mimar Sinan State Hospital","Istanbul","34100","Turkey (Türkiye)",{"type":69,"coordinates":70},"Point",[71,72],28.94966,41.01384,{"lat":72,"lon":71},[75,78],{"name":76,"role":59,"phone":77,"phoneExt":20,"email":61},"kübra can, MSc","+90 543 8711795",{"name":79,"role":59,"phone":80,"phoneExt":20,"email":81},"gaye mutlu, MSc","+90 534 5132197","gayeeemutluuu@gmail.com",{"type":83,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100658510","teach-back-discharge-education-after-pilonidal-sinus-surgery-100658510",false,"NCT07851285","Teach-Back Discharge Education After Pilonidal Sinus Surgery","The Effect of Teach-Back-Supported Discharge Education on Self-Care Agency, Pain, and Comfort Levels After Pilonidal Sinus Surgery: A Randomized Controlled Trial","TB-PSS","Inclusion Criteria:\n\n* Being between 18 and 64 years of age Having undergone elective surgery for pilonidal sinus disease Being clinically stable after surgery Being able to read and understand Turkish and communicate verbally in Turkish Having no cognitive, hearing, or visual impairment severe enough to prevent participation in the education process or completion of the data collection forms Being scheduled to attend the follow-up visit on the tenth day after discharge Volunteering to participate in the study and providing written informed consent\n\nExclusion Criteria:\n\nBeing 65 years of age or older Having undergone emergency surgery for pilonidal sinus disease Having undergone another surgical procedure during the same operative session in addition to pilonidal sinus surgery Having previously undergone pilonidal sinus surgery and being reoperated on because of recurrence Requiring postoperative intensive care or being clinically unsuitable to participate in the education Having a diagnosed severe cognitive disorder, psychiatric disorder, or neurological condition that prevents effective communication Being unable to communicate in Turkish Having a physical or cognitive impairment that prevents independent management of self-care and the discharge process Being unable to complete the scales or data collection forms used in the study\n\n\\-","ALL","18 Years","65 Years",{"count":96,"type":97},68,"ESTIMATED","INTERVENTIONAL",[100],"NA","This randomized controlled trial will evaluate the effect of Teach-Back-supported discharge education on self-care agency, pain intensity, and comfort levels in patients undergoing surgery for pilonidal sinus disease. A total of 68 participants will be randomly assigned in a 1:1 ratio to either the intervention group or the control group. The intervention group will receive discharge education using the Teach-Back method, while the control group will receive routine discharge education and standard care. Self-care agency, pain intensity, and comfort levels will be assessed at baseline and on the tenth day after discharge.",[103,104],"Pilonidal Sinus Disease","Pilonidal Sinus Treatment",[106,107,108,109,110,111],"Teach-Back Method","Pilonidal Sinus Surgery","Patient Comfort","Postoperative Pain","Self-Care Agency","Discharge Education","NOT_YET_RECRUITING","2026-09-25",{"date":115,"type":116},"2026-10-01","ACTUAL",{"date":118,"type":97},"2026-09-15",{"date":120,"type":97},"2026-12-31",{"name":5,"class":6},1]