[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100632310":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":25,"locations":18,"responsibleParty":31,"collaborators":18,"id":35,"slug":36,"hasResults":37,"nctId":38,"briefTitle":39,"officialTitle":40,"acronym":18,"eligibilityCriteria":41,"healthyVolunteers":37,"sex":42,"minAge":43,"maxAge":44,"enrollmentInfo":45,"targetDuration":18,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":54,"overallStatus":60,"whyStopped":18,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":18},{"fullName":5,"class":6},"Muş Alparslan University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Intervention Group (Video-Assisted Early Mobilization Training)","EXPERIMENTAL","Participants in the experimental arm will receive a structured video-assisted early mobilization training program in addition to standard postoperative care. The intervention includes two professionally produced educational videos. The first is a preoperative theoretical video explaining the physiological benefits of early mobilization in clear, patient-friendly language. The second is a postoperative demonstrative video recorded in an actual patient room, showing ERAS-based step-by-step mobilization techniques. After the patient awakens from anesthesia, the demonstrative video will be shown again, and mobilization will begin as demonstrated. To objectively monitor activity, a passive pedometer will be worn to record step count, ambulation duration, and time to first mobilization. The device does not provide feedback, reminders, or alerts, ensuring that behavioral influence derives only from the video-based intervention",[13],"Behavioral: Video-Assisted Early Mobilization Training",{"label":15,"type":16,"description":17,"interventionNames":18},"Control Group (Standard Postoperative Care)","NO_INTERVENTION","Participants in the control arm will receive standard postoperative care routinely provided in the surgical unit. They will not receive the video-assisted early mobilization training. To ensure objective comparison with the experimental group, participants in the control group will also wear a passive pedometer that records step count, ambulation duration, and time to first mobilization. The device will not provide feedback, reminders, alerts, or motivational messages. This ensures that any behavioral influence on mobilization originates exclusively from the intervention applied to the experimental group.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"BEHAVIORAL","Video-Assisted Early Mobilization Training","A behavioral intervention consisting of a structured, professionally produced video-based early mobilization training program delivered preoperatively and postoperatively. The intervention aims to enhance patient engagement, improve mobilization performance, and reduce postoperative physiological stress responses.",[9],[26],{"name":27,"role":28,"phone":29,"phoneExt":18,"email":30},"Barış ÖZDERE, PhD (Candidate)","CONTACT","+90 539 7675964","b.ozdere6565@gmail.com",{"type":32,"investigatorFullName":33,"investigatorTitle":34,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","BARIŞ ÖZDERE","Principal Investigator","100632310","effects-of-postoperative-video-assisted-early-mobilization-on-recovery-outcomes-100632310",false,"NCT07512024","Effects of Postoperative Video-assisted Early Mobilization on Recovery Outcomes","The Effect of Video-assisted Early Mobilization Training on Patient Outcomes in Individuals Undergoing Laparoscopic Cholecystectomy: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Adults aged 18 to 65 years.\n* Scheduled for elective laparoscopic cholecystectomy.\n* Classified as ASA I or ASA II according to the American Society of Anesthesiologists Physical Status Classification.\n* Ability to read and understand Turkish.\n* Adequate cognitive capacity to understand video education and operate the wearable activity tracker.\n* Willingness to participate and signing the informed consent form\n\nExclusion Criteria:\n\n* Chronic pain syndrome or severe chronic orthopedic\u002Frheumatologic pain conditions.\n* Pre-existing mobility limitations.\n* Endocrine or metabolic diseases affecting cortisol or glucose (e.g., diabetes, thyroid disorders, Addison's disease, Cushing's syndrome).\n* Use of medications affecting the HPA axis (e.g., systemic corticosteroids, chronic opioids, high-dose benzodiazepines).\n* Diagnosed severe psychiatric or cognitive disorders (e.g., dementia, major depression).\n* Skin allergies or medical device contraindications preventing use of the activity tracker.\n* Conversion to open surgery or major intraoperative complications.","ALL","18 Years","65 Years",{"count":46,"type":47},44,"ESTIMATED","INTERVENTIONAL",[50],"NA","This randomized controlled trial aims to evaluate the effects of video-assisted early mobilization education on postoperative recovery in patients undergoing laparoscopic cholecystectomy. As part of the intervention, structured and professionally produced educational videos will be used to explain the physiological benefits of early mobilization in the preoperative period and to demonstrate step-by-step mobilization techniques in the postoperative period.\n\nPatients in the intervention group will receive video-assisted mobilization education in addition to standard postoperative care, while patients in the control group will receive standard care alone. Physical activity levels will be objectively monitored using wearable activity tracking devices during the first 24 hours after surgery.\n\nThe study will assess the effects of video-assisted early mobilization education on postoperative physiological stress response, pain, nausea and vomiting, blood glucose levels, mobilization performance, gastrointestinal recovery, length of hospital stay, and patient satisfaction. In addition, postoperative complications, emergency department visits, and hospital readmissions within 30-days after surgery will be evaluated as exploratory outcomes.",[53],"Cholelithiasis",[55,56,57,58,59],"Postoperative Recovery","Enhanced Recovery After Surgery (ERAS)","Early Mobilization","Surgical Stress Response","Postoperative Pain","NOT_YET_RECRUITING","2026-04-04",{"date":63,"type":64},"2026-04-09","ACTUAL",{"date":66,"type":47},"2026-05",{"date":68,"type":47},"2027-01",{"name":5,"class":6}]