[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hernia-femoral\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hernia-femoral":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":34,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":53},"100647918","recoverhome-postoperative-follow-up-study-100647918",false,"NCT07714343","Recover@Home Postoperative Follow-up Study","Incorporating Mobile Technology Into Postoperative Care: A Randomized-Control Trial on Ambulatory Surgery With Recover@Home Approach Compared to Traditional Postoperative Inpatient Stay","Inclusion criteria:\n\n* Age 18 years or older.\n* Undergoing one of the eligible surgical procedures: inguinal\u002Ffemoral hernia repair; umbilical\u002Fepigastric hernia repair; excision of soft tissue tumors; thyroidectomy; or appendectomy; varicocelectomy, hydrocelectomy.\n* Able to provide informed consent, with consent read aloud and\u002For fingerprint signature permitted where approved by local ethics authorities.\n* Available for inpatient interviews, postoperative clinic visit interviews, and postoperative telephone and\u002For home follow-up during the 30-day postoperative period.\n\nExclusion criteria:\n\n* Clinical determination by the surgeon or anesthesia team that same-day discharge is unsafe or inappropriate.\n* Inability to provide informed consent or lack of an approved surrogate\u002Falternative consent process if required by the IRB.\n* Any other exclusion required by the final approved protocol or local regulatory authority.\n* ASA 3 or higher","ALL","18 Years",{"count":19,"type":20},194,"ESTIMATED","INTERVENTIONAL",[23],"NA","This proposal describes a human subjects research study evaluating mHealth Ambulatory Surgery with Follow-up Nurse (Recovery@Home), as an alternative postoperative care pathway for selected low-acuity surgical procedures in Uganda. The Recovery@Home model discharges eligible patients home on the day of surgery and provides structured postoperative follow-up through nurse telephone calls, home visits, mobile-app documentation, escalation algorithms, and surgeon teleconsultation when clinically indicated. The proposed research includes a design to evaluate Recovery@Home against traditional postoperative inpatient care in a randomized controlled trial across three participating Ugandan surgical facilities.",[26,27,28,29,30,31,32,33],"Hernia, Inguinal","Hernia, Femoral","Hernia, Umbilical","Hernia, Ventral","Thyroidectomy","Appendectomy","Testicular Hydrocele","Varicocele",[35,36,37,38,39,40],"ambulatory surgery","nurse-led mobile health","postoperative care delivery","rural surgical facility","recovery at home","implementation science","NOT_YET_RECRUITING","2026-07-15",{"date":44,"type":45},"2026-07-20","ACTUAL",{"date":47,"type":20},"2027-03-01",{"date":49,"type":20},"2029-11-30",{"name":51,"class":52},"Icahn School of Medicine at Mount Sinai","OTHER",4]