[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100621369":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":31,"locations":37,"responsibleParty":55,"collaborators":26,"id":59,"slug":60,"hasResults":61,"nctId":62,"briefTitle":63,"officialTitle":64,"acronym":26,"eligibilityCriteria":65,"healthyVolunteers":66,"sex":67,"minAge":68,"maxAge":69,"enrollmentInfo":70,"targetDuration":26,"studyType":73,"phases":74,"briefSummary":76,"conditions":77,"keywords":81,"overallStatus":39,"whyStopped":26,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"KTO Karatay University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Group","PLACEBO_COMPARATOR","Women in the control group will receive routine intervention. They will be mobilized at 6 hours. Decaffeinated coffee will be served at 6-hour intervals.",[13],"Dietary Supplement: Decaffeinated coffee",{"label":15,"type":16,"description":17,"interventionNames":18},"intervention group","EXPERIMENTAL","They will be mobilized at 4 hours.They will consume Turkish coffee containing caffeine every six hours.",[19],"Dietary Supplement: caffeine consumption",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DIETARY_SUPPLEMENT","caffeine consumption","The women in the intervention group will be mobilised at the 4-hour mark. The intervention group will be given caffeinated Turkish coffee at 6-hour intervals.",[15],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Decaffeinated coffee","The women in the control group will be mobilised at the 6-hour mark. The control group will be given decaffeinated Turkish coffee at 6-hour intervals.",[9],[32],{"name":33,"role":34,"phone":35,"phoneExt":26,"email":36},"Hafize D Dağ TÜZMEN","CONTACT","5357446142","hafize.dag.tuzmen@karatay.edu.tr",[38],{"facility":5,"status":39,"city":40,"state":26,"zip":41,"country":42,"countryCode":26,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"RECRUITING","Konya","42208","Turkey (Türkiye)",{"type":44,"coordinates":45},"Point",[46,47],32.48464,37.87135,{"lat":47,"lon":46},[50,52],{"name":51,"role":34,"phone":35,"phoneExt":26,"email":36},"Hafize Dağ Tüzmen D Dr.Öğrt.Üyesi",{"name":53,"role":54,"phone":26,"phoneExt":26,"email":26},"Esma Kovalı, Yükseklisans Öğrencisi","SUB_INVESTIGATOR",{"type":56,"investigatorFullName":57,"investigatorTitle":58,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Hafize Dağ Tüzmen","DOCTORAL PROFESSOR","100621369","effects-of-mobilization-and-caffeine-after-cesarean-100621369",false,"NCT07369726","Effects of Mobilization and Caffeine After Cesarean","The Effect of Early Post-Cesarean Mobilization and Caffeine Consumption on Bowel Motility, Pain, and Psychological Well-being: A Randomized Controlled Trial","Inclusion Criteria:\n\n1. Being between 18 and 35 years of age,\n2. Women who underwent cesarean delivery under spinal anesthesia,\n3. Having a post-cesarean pain level of 4 or higher,\n4. Being able to understand and write Turkish and communicate effectively with researchers.\n\nExclusion Criteria:\n\n1. Women who underwent emergency cesarean delivery,\n2. Those with pregnancy complications (preeclampsia, placenta previa, etc.),\n3. Those with a history of chronic gastrointestinal disease (e.g., irritable bowel syndrome, Crohn's disease, ulcerative colitis),\n4. Those with sensitivity or allergy to caffeine,\n5. Those with a history of chronic pain syndrome or dependence on analgesics,\n6. Regular coffee drinkers (≥2 cups per day),\n7. Intraoperative complications such as bowel or bladder injury,\n\ni) Those who cannot comply with the study protocol or complete the follow-up process.\n\nRemoval Criteria:\n\n1. Participants are excluded from the study under the following conditions:\n2. During surgery If complications occur (e.g., bladder or bowel injury, excessive bleeding),\n3. Postoperative complications requiring admission to the intensive care unit (ICU) for the mother or newborn,\n4. Development of severe postoperative nausea, vomiting, or intolerance to oral intake,\n5. Inability to consume or refusal to consume coffee according to the study protocol,\n6. Withdrawal of consent by the participant at any point during the study,\n7. Failure to comply with surgical procedures or loss of follow-up,\n8. Development of medical conditions during follow-up that may affect study results (e.g., acute infections, neurological disorders).",true,"FEMALE","18 Years","35 Years",{"count":71,"type":72},60,"ESTIMATED","INTERVENTIONAL",[75],"NA","This study Maims to assess bowel motility, pain and psychological well-being in women in the post-cesarean period by mobilizing them early and encouraging them to consume coffee.",[78,79,80],"Gastrointestinal Motility","Postoperative Pain","Psychological Well-Being",[82,83,80,84],"gastrointestinal motility","postoperatif pain","Early Ambulation","2026-02-05",{"date":87,"type":88},"2026-02-09","ACTUAL",{"date":90,"type":88},"2025-11-25",{"date":92,"type":72},"2026-05-01",{"name":5,"class":6},1]