[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"recovery-method\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:recovery-method":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"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":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100631902","early-mobilization-following-elective-spine-surgery-trial-of-in-bed-cycling-100631902",false,"NCT07506720","Early Mobilization Following Elective Spine Surgery: Trial of In-bed Cycling","Early Mobilization Following Elective Spine Surgery: Prospective Randomized Trial of In-bed Cycling on Postoperative Day 1","Inclusion Criteria\n\nMale or female ≥ 18 years old.\n\nPostoperative #0 following elective spinal surgery: decompression with or without fusion, or fusion.\n\nPatient able to walk independently before surgery (does not require assistance from another person and does not use a wheelchair).\n\nPatient admitted directly from the operating room to the ward.\n\nHemodynamically stable:\n\nSystolic blood pressure (SBP): ≥ 90 mmHg and \\\u003C 140 mmHg\n\nOxygen saturation \\> 94%\n\nHeart rate: 50-100 bpm\n\nPatient approved for surgery after preoperative internal medicine evaluation.\n\nPatient alert and conscious.\n\nValid informed consent obtained.\n\nExclusion Criteria\n\nNon-ambulatory preoperatively.\n\nBody Mass Index (BMI) \\> 40 kg\u002Fm².\n\nAcute neurological spinal trauma.\n\nNon-neurological musculoskeletal impairment of the lower limbs (e.g., severe osteoarthritis, hip fracture, amputation) limiting the ability to pedal in bed.\n\nUncontrolled comorbidities preventing surgery or intervention (cardiovascular, respiratory, diabetes).\n\nExpected hospital stay of less than 2 days after surgery.\n\nSurgery-related complications: acute neurological deficit, dural tear, cerebrospinal fluid (CSF) leak, residual spinal instability.\n\nTransfer to intensive care unit or hemodynamic instability.\n\nPersistent hemodynamic instability: SBP \\\u003C 90 mmHg or \\> 200 mmHg, oxygen saturation \\\u003C 88%, heart rate \\\u003C 50 or \\> 100 bpm, temperature \\> 38°C.\n\nCapillary blood glucose outside target values: \\\u003C 4.0 or \\> 7.0 mmol\u002FL fasting or pre-meal, \\\u003C 5.0 and \\> 10.0 mmol\u002FL 2 hours post-meal.\n\nPatient confused, disoriented, or agitated.\n\nPatient already evaluated by physiotherapy for discharge planning or intensive functional rehabilitation.\n\nPatient in isolation.\n\nPatient already discharged.","ALL","18 Years",{"count":19,"type":20},88,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical trial is to learn if early mobilization using an in-bed cycling device can reduce the amount of time patients spend in bed after elective spine surgery in adults.\n\nThe main questions it aims to answer are:\n\nDoes in-bed cycling on the day after surgery reduce the amount of time patients spend in bed over the next 24 hours?\n\nDoes in-bed cycling reduce the length of hospital stay and improve participation during physiotherapy assessment?\n\nResearchers will compare patients who receive an in-bed cycling session plus standard postoperative care to patients who receive standard postoperative care alone to see if early in-bed cycling improves mobility and recovery after spine surgery.\n\nParticipants will:\n\nBe randomly assigned to either a standard care group or an in-bed cycling group\n\nWear a fitness tracker to measure activity levels and time spent in bed\n\nReceive standard postoperative care\n\nComplete a 30-minute in-bed cycling session on the day after surgery (intervention group only)\n\nBe monitored for pain and vital signs during the study period\n\nUndergo a physiotherapy assessment to evaluate mobility and participation",[26,27,28],"Spine","Post Surgery Patients","Recovery Method",[30,31,32,33,34],"Spine Surgery","Postoperative Recovery","Early Mobilization","In-Bed Cycling","Kinesiophobia","RECRUITING","2026-06-17",{"date":38,"type":39},"2026-06-22","ACTUAL",{"date":41,"type":39},"2025-08-01",{"date":43,"type":20},"2029-01",{"name":45,"class":46},"Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":55,"sex":16,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":21,"phases":60,"briefSummary":61,"conditions":62,"keywords":63,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":47},"100564875","comparison-of-the-effects-of-intermittent-pneumatic-compression-graston-technique-and-percussive-therapy-100564875","NCT06634862","Comparison of the Effects of Intermittent Pneumatic Compression, Graston Technique and Percussive Therapy","Comparison of the Effects of Intermittent Pneumatic Compression, Graston Technique and Percussive Therapy on Muscle Pain, Muscle Tone and Balance After Quadriceps Fatigue Protocol","Inclusion Criteria:\n\n* To be between 25-45 years old.\n* Not having any chronic disease.\n* Not doing active sports for at least 6 months.\n* Not having any previously diagnosed lower extremity pathology.\n* Not having a chronic lower extremity problem and not having a major trauma (fracture, anterior cruciate ligament injury, etc.).\n* Not having any cognitive problem that prevents them from following and adapting to a specific exercise programme.\n* No visual, vestibular and neurological disorders.\n\nExclusion Criteria:\n\n* Having a chronic disease.\n* Any musculoskeletal problem in the lower extremities.\n* Use of sedative medication due to chronic disease (rheumatism, lung and\u002For heart etc.)\n* Regular use of painkillers, muscle relaxants or anti-inflammatory drugs.\n* Any history of surgery on the lower extremity.\n* Any history of pain in the lower extremity during the fatigue protocol.\n* Pregnancy.",true,"25 Years","45 Years",{"count":59,"type":20},60,[23],"The aim of this study was to compare the effects of intermittent pneumatic pressure, percussive therapy and graston after a fatigue protocol applied to the leg muscles.",[28],[64,65,66,67,68,69,70],"Recovery","Quadriceps Fatigue Protocol","Intermittent pneumatic pressure","Soft Tissue Mobilization Technique","Percussive therapy","Muscle Fatigue","Muscle Tone","NOT_YET_RECRUITING","2024-10-10",{"date":74,"type":39},"2024-10-15",{"date":76,"type":20},"2024-12-02",{"date":78,"type":20},"2025-05-18",{"name":80,"class":46},"Okan University"]