[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100621126":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":24,"centralContacts":31,"locations":40,"responsibleParty":56,"collaborators":18,"id":59,"slug":60,"hasResults":61,"nctId":62,"briefTitle":63,"officialTitle":64,"acronym":18,"eligibilityCriteria":65,"healthyVolunteers":61,"sex":66,"minAge":67,"maxAge":18,"enrollmentInfo":68,"targetDuration":18,"studyType":71,"phases":72,"briefSummary":74,"conditions":75,"keywords":78,"overallStatus":83,"whyStopped":18,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":93},{"fullName":5,"class":6},"Trakya University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental group (with Foot Bath Device Foot Bath Application (20 min, 41-42°C)","EXPERIMENTAL","Postoperative Preparation: The intervention will commence once the effects of anesthesia have subsided and initial mobilization (routinely 6-8 hours post-surgery) has been achieved. At approximately 9:00 PM, the patient's feet will be prepared by removing socks or adjusting anti-embolic stockings above the ankle . A visual and physical examination of the feet will be conducted to screen for contraindications such as pressure injuries, wounds, or discoloration.\n\nFoot Bath Intervention: The foot bath procedure will be performed using a disinfected device lined with single-use, watertight bags to ensure hygiene.The water temperature will be strictly maintained at 41-42°C, verified by a non-contact infrared digital thermometer. Both feet will be immersed in the device for a duration of 20 minutes. Post-intervention, the researcher will thoroughly dry the patient's feet and replace their socks or anti-embolic stockings. Any adverse events or side effects observed, recorded.",[13],"Other: Foot bath device",{"label":15,"type":16,"description":17,"interventionNames":18},"Control group Control group (Standard care (no foot bath procedure)","NO_INTERVENTION","Patients in the control group will receive routine care. Patient Recruitment and Preoperative Phase: Patients admitted to the General Surgery department for abdominal surgery will be informed about the study on the morning of their procedure. Following the acquisition of both verbal and written informed consent, the Patient Information Form will be completed. To establish a baseline for sleep quality, the Richards-Campbell Sleep Questionnaire (RCSQ) will be administered preoperatively.\n\nNo foot bath application will be in question for the patients in the control group.\n\nData Collection and Conclusion: On the morning of the first postoperative day, the RCSQ, GKO (Visual Analog Scale\u002FGlobal Quality Scale), and pain scores will be administered to evaluate the intervention's impact. The data collection process will conclude following these assessments.",null,[20],{"type":6,"name":21,"description":22,"armGroupLabels":23,"otherNames":18},"Foot bath device","On the day of surgery, patients will receive a foot bath between 9:00 PM and 10:00 PM. Any socks or clothing on both feet will be removed. The feet will be visually and manually examined to determine if they show any signs of illness (pressure ulcers, discoloration, wounds, etc.). The patient will be informed that the foot bath device is disinfected before each use and that water-tight bags will be placed around the device to prevent contact between the foot and the water to facilitate repeated use. The water temperature will be adjusted to 41-42°C using an infrared thermometer (non-contact digital thermometer). Both feet will be placed inside the foot bath device. The patient's feet will remain in the foot bath device for 20 minutes. After the foot bath, the patient's feet will be thoroughly dried with a towel, and the patient will be re-dressed in their existing socks or anti-embolic stockings. Any side effects\u002Fadverse reactions, etc., related to the foot bath will be questioned and",[9],[25,28],{"name":26,"affiliation":5,"role":27},"ZEYNEP KIZILCIK ÖZKAN, Assoc.Prof","STUDY_CHAIR",{"name":29,"affiliation":5,"role":30},"Ayşe Nur Aktaş, Reg.Nurse","PRINCIPAL_INVESTIGATOR",[32,37],{"name":33,"role":34,"phone":35,"phoneExt":18,"email":36},"ZEYNEP KIZILCIK ÖZKAN, Assco.Prof","CONTACT","05056010101","zeynepozkan@trakya.edu.tr",{"name":38,"role":34,"phone":18,"phoneExt":18,"email":39},"Ayşe Nur Aktaş, Reg. Nurse","aysenuraktas24@gmail.com",[41],{"facility":42,"status":18,"city":43,"state":44,"zip":45,"country":46,"countryCode":18,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"Trakya University Hospital","Edirne","Cahit Arf Boulevard","22030","Turkey (Türkiye)",{"type":48,"coordinates":49},"Point",[50,51],26.55597,41.67719,{"lat":51,"lon":50},[54],{"name":26,"role":34,"phone":55,"phoneExt":18,"email":36},"+905056010101",{"type":30,"investigatorFullName":57,"investigatorTitle":58,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"Zeynep Kızılcık Ozkan","Associate professor","100621126","effect-of-foot-bath-on-pain-sleep-and-comfort-levels-after-abdominal-surgery-100621126",false,"NCT07366567","Effect of Foot Bath on Pain, Sleep, and Comfort Levels After Abdominal Surgery","Effect of Foot Bath on Pain, Sleep, and Comfort Levels After Abdominal Surgery: A Randomized Controlled Trial","Inclusion Criteria:\n\n* who are hospitalized in the General Surgery Clinic,\n* are on day 0 of surgery,\n* volunteer to participate in the study,\n* have no neuropsychiatric diagnosis and are not taking antipsychotic medications,\n* are over 18 years of age,\n* accept random selection,\n* and undergo abdominal surgery.\n* For the experimental group, all patients with no infectious diseases (shingles, fungal infections, eczema, warts, calluses), local infections (abscesses, etc.), open lesions\u002Fwounds, scar tissue, edema, hematomas, thrombophlebitis, deep vein thrombosis, lymphangitis, coagulation disorders, varicose veins, osteoporosis, osteomyelitis, hepatitis, degenerative joint diseases, neuropathy due to diabetes, toe deformities, recent fractures, dislocations, or ruptures of muscle fibers, tendons, or ligaments will be included in the sample.\n\nExclusion Criteria:\n\n* patients who underwent multiple simultaneous surgeries along with abdominal surgery,\n* those with postoperative complications such as delirium,\n* those who underwent reoperation,\n* those with a pain score \\>7 because it could affect sleep levels,\n* and those who received narcotic analgesics on postoperative day 0 due to pain will be excluded from the sample.","ALL","18 Years",{"count":69,"type":70},96,"ESTIMATED","INTERVENTIONAL",[73],"NA","The aim of this study was to investigate the effects of foot bath application on pain level, comfort and sleep quality in the postoperative period.\n\nH1: Foot baths have a postoperative pain-reducing effect. H2: Foot baths have a postoperative comfort-enhancing effect. H3: Foot baths have a postoperative sleep-improving effect.",[76,77],"Pain, Postoperative","Sleep",[79,80,81,82],"pain","foot bath","sleep quality","comfort","NOT_YET_RECRUITING","2026-01-16",{"date":86,"type":87},"2026-01-26","ACTUAL",{"date":89,"type":70},"2025-12-29",{"date":91,"type":70},"2026-12-30",{"name":5,"class":6},1]