[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100601366":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":23,"centralContacts":28,"locations":37,"responsibleParty":52,"collaborators":18,"id":55,"slug":56,"hasResults":57,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":18,"eligibilityCriteria":61,"healthyVolunteers":62,"sex":63,"minAge":64,"maxAge":65,"enrollmentInfo":66,"targetDuration":18,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":18,"overallStatus":40,"whyStopped":18,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":87},{"fullName":5,"class":6},"University of Yalova","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Baduanjin","EXPERIMENTAL","Participants in this arm will receive supervised Baduanjin exercises in addition to routine postoperative care. The Baduanjin protocol will begin on Postoperative Day 1 and continue for 3 weeks, with daily practice under guidance. Data collection will be performed at four time points using the Visual Analog Scale (VAS), the General Comfort Questionnaire, and the Quality of Recovery-40 (QoR-40).\n\nInterview and Application Schedule:\n\nInterview I (Preoperative): Face-to-face interview one day before surgery; informed consent and sociodemographic data collection\n\nInterview II (Postoperative Day 1): Start of Baduanjin; baseline assessment with VAS, QoR-40, and Comfort Questionnaire\n\nInterview III (Postoperative Week 4): Follow-up assessment with VAS, QoR-40, and Comfort Questionnaire\n\nInterview IV (Postoperative Week 8): Final assessment with VAS, QoR-40, and Comfort Questionnaire",[13],"Other: Baduanjin",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard care","NO_INTERVENTION","Description:\n\nParticipants in this arm will receive standard postoperative nursing care and physical therapy, without any complementary intervention. Data will be collected at the same four time points as in the intervention group for comparison purposes.\n\nInterview and Application Schedule:\n\nInterview I (Preoperative): Face-to-face interview one day before surgery; informed consent and sociodemographic data collection\n\nInterview II (Postoperative Day 1): Baseline assessment with VAS, QoR-40, and Comfort Questionnaire\n\nInterview III (Postoperative Week 4): Follow-up assessment with VAS, QoR-40, and Comfort Questionnaire\n\nInterview IV (Postoperative Week 8): Final assessment with VAS, QoR-40, and Comfort Questionnaire",null,[20],{"type":6,"name":9,"description":21,"armGroupLabels":22,"otherNames":18},"Baduanjin exercise",[9],[24],{"name":25,"affiliation":26,"role":27},"NİRAN ÇOBAN","https:\u002F\u002Fakademik.yok.gov.tr\u002FAkademikArama\u002Fview\u002FviewAuthor.jsp","STUDY_DIRECTOR",[29,33],{"name":25,"role":30,"phone":31,"phoneExt":18,"email":32},"CONTACT","05301586912","nirancoban@gmail.com",{"name":34,"role":30,"phone":35,"phoneExt":18,"email":36},"Seçkin Özcan","05418078632","seckin.ozcan@yalova.edu.tr",[38],{"facility":39,"status":40,"city":41,"state":18,"zip":42,"country":43,"countryCode":18,"cosmosGeoPoint":44,"geoPoint":49,"contacts":50},"Niran Çoban","RECRUITING","Yalova","77000","Turkey (Türkiye)",{"type":45,"coordinates":46},"Point",[47,48],29.27693,40.65501,{"lat":48,"lon":47},[51],{"name":34,"role":30,"phone":35,"phoneExt":18,"email":36},{"type":53,"investigatorFullName":39,"investigatorTitle":54,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"SPONSOR_INVESTIGATOR","Asst.Prof.","100601366","the-effect-of-baduanjin-on-patients-undergoing-knee-replacement-surgery-100601366",false,"NCT07109557","The Effect of Baduanjin on Patients Undergoing Knee Replacement Surgery","The Effect of Baduanjin on Pain, Comfort, and Quality of Recovery in Patients Undergoing Knee Replacement Surgery","Inclusion Criteria:\n\n* Having undergone Knee Replacement Surgery under general anesthesia\n\n  • 18 years old and over,\n* Are in stable condition after surgery,\n* Are conscious, and\n* Volunteer to participate in the study.\n\nExclusion Criteria:\n\n* Patients with contraindications to Baduanjin exercises,\n\n  -• Over 70 years old,\n\n  • Using anxiolytic and sedative drugs,\n* Patients with any mental illness and those who do not meet the inclusion criteria will not be included in the study.",true,"ALL","18 Years","70 Years",{"count":67,"type":68},60,"ESTIMATED","INTERVENTIONAL",[71],"NA","This randomized controlled trial aims to evaluate the effects of Baduanjin, a traditional Chinese mind-body exercise, on pain, comfort, and quality of recovery in patients undergoing total knee arthroplasty (TKA). The study will be conducted between July 2025 and July 2026 at Yalova Training and Research Hospital's Orthopedics Clinic. Sixty patients will be randomly assigned into two groups: an intervention group practicing Baduanjin and a control group receiving standard postoperative care. The intervention will begin on the first postoperative day and continue for three weeks. Outcome measures include the Visual Analog Scale (VAS) for pain, the General Comfort Questionnaire, and the Quality of Recovery-40 (QoR-40) questionnaire. These assessments will be conducted weekly for three weeks. The control group will follow routine postoperative care without Baduanjin. The primary objective is to determine whether Baduanjin can improve postoperative outcomes in terms of pain reduction, increased comfort, and better recovery quality.",[74,75,76,77],"Pain, Postoperative","Surgery","Knee Replacement","Nurse's Role","2025-08-07",{"date":80,"type":81},"2025-08-12","ACTUAL",{"date":83,"type":81},"2025-07-01",{"date":85,"type":68},"2026-12-01",{"name":39,"class":6},1]