[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Jouf University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":182},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,42,70,95,126,152],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100635693","effect-of-physical-therapy-rehabilitation-on-gait-and-plantar-pressure-in-patients-after-total-knee-replacement-100635693",false,"NCT07556003","Effect of Physical Therapy Rehabilitation on Gait and Plantar Pressure in Patients After Total Knee Replacement","Effect of Physical Therapy Rehabilitation on Gait Temporospatial Parameters and Plantar Pressure Distribution in Patients Following Total Knee Replacement Surgery","Inclusion Criteria:\n\n* Female participants aged between 40 and 70 years\n* Patients who have undergone unilateral total knee replacement (TKR) or have knee pathology without surgical intervention\n* Ability to walk independently with or without assistive devices\n* Medically stable and able to participate in a physical therapy rehabilitation program\n\nExclusion Criteria:\n\n* Neurological disorders affecting gait (e.g., stroke, Parkinson's disease)\n* Severe musculoskeletal disorders other than knee pathology\n* History of revision knee replacement surgery\n* Significant cognitive impairment affecting the ability to follow instructions\n* Any contraindications to physical therapy rehabilitation","FEMALE","40 Years","70 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to investigate the effects of a structured physical therapy and rehabilitation program on gait temporospatial parameters and plantar pressure distribution in patients who have undergone total knee replacement surgery.\n\nPatients undergoing total knee replacement often experience alterations in gait patterns and weight distribution, which may affect functional mobility and recovery outcomes. This study will evaluate whether a targeted rehabilitation program can improve walking performance and restore more symmetrical plantar pressure distribution.\n\nParticipants will be assessed before and after the intervention using objective gait analysis and plantar pressure measurement tools. The findings of this study may help improve rehabilitation strategies and enhance functional recovery following knee replacement surgery.",[27,28],"Knee Osteoarthritis","Total Knee Replacement","RECRUITING","2026-04-21",{"date":32,"type":33},"2026-04-29","ACTUAL",{"date":35,"type":33},"2025-08-15",{"date":37,"type":21},"2027-12-30",{"name":39,"class":40},"Jouf University","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":49,"minAge":50,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":61,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":41},"100624532","virtual-reality-enhanced-parent-education-in-neonatal-intensive-care-100624532","NCT07410858","Virtual Reality-Enhanced Parent Education in Neonatal Intensive Care","Virtual Reality-Enhanced Parent Education and Its Effect on Neonatal Intensive Care Practices: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Parent or legal guardian of a neonate admitted to the Neonatal Intensive Care Unit (NICU) within 72 hours of admission\n* Age 18 years or older\n* Able to read and understand the study language (Arabic)\n* Willing to provide informed consent and participate in study procedures\n\nExclusion Criteria:\n\n* Parent with a confirmed diagnosis of epilepsy, vestibular disorder, or any medical condition that contraindicates virtual reality exposure\n* Parent of a neonate expected to be discharged or transferred within 48 hours\n* Parent unable to complete study procedures or assessments","ALL","18 Years",{"count":52,"type":21},60,[24],"This randomized pilot clinical trial aims to evaluate the effectiveness and feasibility of virtual reality (VR)-enhanced parent education in improving neonatal intensive care unit (NICU) caregiving practices among parents of hospitalized neonates. The study will also examine the safety and tolerability of VR use among parents.\n\nResearchers will compare VR-enhanced education with standard NICU parent education to determine whether immersive VR training improves parents' knowledge, confidence, and ability to perform caregiving tasks.\n\nParticipants will be randomly assigned to receive either VR-enhanced education or standard education. Participants receiving VR education will engage in short immersive sessions demonstrating NICU orientation and caregiving procedures. All participants will complete assessments and observations related to caregiving practices and VR tolerability throughout the study period.",[56,57,58,59,60],"Neonatal Intensive Care Units","Premature Infant","Parent Education","Virtual Reality","Health Knowledge, Attitudes, Practice",[59,56,58,57],"2026-02-13",{"date":64,"type":33},"2026-02-18",{"date":66,"type":33},"2026-01-01",{"date":68,"type":21},"2026-04-30",{"name":39,"class":40},{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":49,"minAge":77,"maxAge":4,"enrollmentInfo":78,"targetDuration":4,"studyType":22,"phases":80,"briefSummary":81,"conditions":82,"keywords":4,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":4},"100587399","effects-of-whole-body-vibration-therapy-on-cognitive-function-balance-and-quality-of-life-in-older-adults-with-mild-cognitive-impairment-100587399","NCT06927882","Effects of Whole Body Vibration Therapy on Cognitive Function, Balance, and Quality of Life in Older Adults With Mild Cognitive Impairment","Effects of Whole Body Vibration Therapy on Cognitive Function, Balance, and Quality of Life in Older Adults With Mild Cognitive Impairment: A Randomized, Double-Blind, Placebo-Controlled Trial","Inclusion Criteria:\n\n* Adults aged 60 years and older.\n* Diagnosed with mild cognitive impairment (Montreal Cognitive Assessment (MoCA) score of 18-25). One point is added if years of education are less than 12 years\\[2\\].\n* Able to stand independently or with minimal assistance.\n* No contraindications for WBV therapy or exercise.\n\nExclusion Criteria:\n\n* Diagnosis of dementia.\n* Severe musculoskeletal or neurological disorders.\n* Implanted electronic medical devices (e.g., pacemaker).\n* Inability to comprehend study instructions.","60 Years",{"count":79,"type":21},180,[24],"This is a double-blind, randomized controlled trial comparing WBV therapy with a placebo intervention and standard care. A total of 150 participants will be recruited and investigated from Prince Mutib Hospital. Participants will be randomly allocated to one of three groups: WBV therapy, placebo (non-vibrating platform), or control (standard care). The study duration will be 12 weeks, with assessments conducted at baseline, post-intervention (12 weeks), and at a 6-month follow-up.\n\nProtocol Parameters Summary\n\n* Session Frequency: 3 times per week.\n* Session Duration: 25 minutes per session.\n* Vibration Frequency: 30 Hz.\n* Amplitude: 1-2 mm.\n* Program Duration: 12 weeks.",[83,84,85],"Cognitive Impairment","Balance","Quality of Life","NOT_YET_RECRUITING","2025-11-14",{"date":89,"type":33},"2025-11-17",{"date":91,"type":21},"2025-11-15",{"date":93,"type":21},"2025-12-30",{"name":39,"class":40},{"id":96,"slug":97,"hasResults":11,"nctId":98,"briefTitle":99,"officialTitle":100,"acronym":4,"eligibilityCriteria":101,"healthyVolunteers":11,"sex":49,"minAge":50,"maxAge":102,"enrollmentInfo":103,"targetDuration":4,"studyType":22,"phases":105,"briefSummary":106,"conditions":107,"keywords":110,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":121,"completionDateStruct":123,"leadSponsor":125,"locationsCount":4},"100596048","kea-vs-towel-for-early-quad-activation-post-anterior-cruciate-ligament-reconstruction-100596048","NCT07040384","KEA vs Towel for Early Quad Activation Post Anterior Cruciate Ligament Reconstruction","Knee Extensors Activation Device Versus Rolled Towel for Early Quadriceps Activation After ACL Reconstruction: Protocol for a Randomized Controlled Trial","Inclusion Criteria:\n\n* Adults aged 18 to 45 years\n* Undergoing primary unilateral anterior cruciate ligament (ACL) reconstruction (any graft type, any surgical technique)\n* Able and willing to participate in postoperative rehabilitation\n* Able to provide written informed consent\n* Able to comply with study procedures and complete the 5-day inpatient exercise program\n\nExclusion Criteria:\n\n* Bilateral knee surgeries (e.g., simultaneous ACL reconstruction on both knees)\n* Significant neuromuscular disorders that may affect rehabilitation or EMG readings\n* Cognitive impairment that would interfere with understanding or performing exercises\n* History of major lower limb surgery within the past year (excluding the current ACL surgery)\n* Concomitant injuries requiring extensive repair (e.g., complex ligament reconstructions beyond minor meniscal or collateral work)\n* Any medical condition or postoperative complication that would prevent safe participation in the exercise program","45 Years",{"count":104,"type":21},40,[24],"The goal of this clinical trial is to learn if a novel Knee Extensors Activation (KEA) device can improve quadriceps muscle activation in adults after anterior cruciate ligament (ACL) reconstruction surgery. The study focuses on adults aged 18-45 years undergoing primary unilateral ACL reconstruction, a population commonly affected by this injury.\n\nThe main questions it aims to answer are:\n\nDoes using the KEA device lead to greater quadriceps muscle activation (measured via EMG) by postoperative Day 5 compared to standard care using a rolled towel?\n\nDoes the KEA device improve early knee function, reduce pain, and decrease fear of movement compared to the towel method?\n\nResearchers will compare participants using the KEA device versus a control group using the conventional rolled towel during early postoperative rehabilitation to see if the KEA device provides better outcomes.\n\nParticipants will:\n\nBegin quadriceps strengthening exercises on the first day after ACL surgery.\n\nBe randomly assigned to use either the KEA device or a rolled towel for isometric quadriceps exercises.\n\nPerform 3 sets of 10 repetitions of knee extension exercises, twice daily for 5 consecutive days.\n\nUndergo assessment of quadriceps EMG activation and complete questionnaires (KOOS, IKDC, TSK, and VAS) on Day 5.",[108,109],"ACL Surgery","Quadriceps Strength",[111,112,113,114,115,116,117],"Anterior cruciate ligament","quadriceps activation","biofeedback","rehabilitation","electromyography","knee","randomized controlled trial","2025-06-25",{"date":120,"type":33},"2025-06-27",{"date":122,"type":21},"2025-08-25",{"date":124,"type":21},"2026-12-10",{"name":39,"class":40},{"id":127,"slug":128,"hasResults":11,"nctId":129,"briefTitle":130,"officialTitle":131,"acronym":4,"eligibilityCriteria":132,"healthyVolunteers":11,"sex":49,"minAge":133,"maxAge":134,"enrollmentInfo":135,"targetDuration":4,"studyType":22,"phases":137,"briefSummary":138,"conditions":139,"keywords":141,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":145,"lastUpdatePostDateStruct":146,"startDateStruct":148,"completionDateStruct":150,"leadSponsor":151,"locationsCount":4},"100593161","effect-of-cross-legged-sitting-among-patients-with-unilateral-hip-developmental-dysplasia-100593161","NCT07002840","Effect of Cross-legged Sitting Among Patients With Unilateral Hip Developmental Dysplasia","Effect of Engaging the Cross-legged Sitting in Rehabilitation Among Patients With Unilateral Hip Developmental Dysplasia According to Gait Parameters, Foot Pressure and Muscular Electrical Activity.","Inclusion Criteria:\n\n* age group from 9 months to 10 years old\n* all participants suffer from Unilateral Hip Developmental Dysplasia (UHDD)\n* participants should be healthy in general\n\nExclusion Criteria:\n\nAny participant with a history of neurological disorders, lower extremities previous surgical intervention, lower limb deformities, flat feet or high body mass index will be excluded from this study","9 Months","10 Years",{"count":136,"type":21},16,[24],"One of the most common infant developmental diseases is Hip dysplasia which is mostly seen among female' babies and leads to hip instability due to partial or full hip dislocation \\[1\\]. Physical therapy's role plays a significant role in treating hip dysplasia by creating new walking habits as an adaptation way and compensation for the deformity \\[3\\]. Focusing on the muscles that produce hip abduction force is a basic item of the hip dysplasia rehabilitation program \\[4\\]. Cross-legged sitting position can be considered as a common and easy position that might enhance the range of motion of the lower limb joints \\[5\\].\n\nWhile unilateral hip developmental dysplasia has been widely distributed among newborns, especially in the last few years, the role of engaging the cross-legged sitting technique as a part of physical therapy and rehabilitation programs on improving the temporospatial parameters, muscular electrical activity and foot pressure distributing is still not clear. Therefore, this study aimed to analyze the effects of engaging the cross-legged sitting technique as a part of physical therapy and rehabilitation program among patients with UHDD by comparing the group who participated in rehabilitation program with CLS to the other without.\n\nTo understand the importance of including Cross-legged sitting technique in physical therapy and rehabilitation program of Unilateral Hip Developmental Dysplasia (UHDD) to enhance the spatial and temporal measures, achieving a healthy distribution of foot pressure, increasing the electrical activity of lower limb muscles and improving the overall gait pattern.\n\nNo risks at all. All instruments and techniques in this study are safe and used regularly without any hazards.\n\nThe data will be stored and archived on a password-protected computer for safety and security purposes. After accomplishing the research and getting the outcomes, the results of the research may be published as an academic article in a peer-reviewed journal. In another word, no personal data will be published at all.\n\nTaking part in the study and withdrawing at any time is completely voluntary with no need to give any reason.",[140],"Hip Developmental Dysplasia",[142,143,144,140],"Rehabilitation","Gait","Foot pressure","2025-05-26",{"date":147,"type":33},"2025-06-04",{"date":149,"type":21},"2025-06-05",{"date":93,"type":21},{"name":39,"class":40},{"id":153,"slug":154,"hasResults":11,"nctId":155,"briefTitle":156,"officialTitle":157,"acronym":4,"eligibilityCriteria":158,"healthyVolunteers":159,"sex":160,"minAge":161,"maxAge":4,"enrollmentInfo":162,"targetDuration":4,"studyType":22,"phases":164,"briefSummary":165,"conditions":166,"keywords":169,"overallStatus":86,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":175,"startDateStruct":177,"completionDateStruct":179,"leadSponsor":181,"locationsCount":41},"100565614","whole-body-vibration-in-middle-aged-men-100565614","NCT06644469","Whole Body Vibration in Middle Aged Men","Effects of Whole-Body Vibration on Bone Mineral Density, Hand Grip Strength, and Vitamin D Levels in Middle-Aged Men: a Preliminary Clinical Trial","Inclusion Criteria:\n\n* Male participants aged 50 years or older\n* Participants with physical activity or exercise program involvement\n* Participants with no history of serious medical conditions such as tumors, fractures, epilepsy, cardiac disease, or stroke within the past year.\n* Participants must be non-smokers and not receiving hormone or calcium supplement therapy\n\nExclusion Criteria:\n\n* Participants unable to stand on the WBV platform\n* Participants with conditions contraindicating vibration therapy\n* Participants participating in other clinical trials",true,"MALE","50 Years",{"count":163,"type":21},34,[24],"This study aims of this clinical trial is to evaluate the effect of an 8-week Whole Body Vibration (WBV) intervention on Bone Mineral Density (BMD), hand grip strength, and vitamin D levels in middle-aged men. Findings from this study will contribute to understanding whether WBV is a viable alternative to conventional exercise, especially for those with limitations in physical activity.\n\nStudy Objectives:\n\n• Primary Objective: To assess the effectiveness of an 8-week WBV intervention in improving BMD, hand grip strength, and vitamin D levels compared to a placebo intervention.",[167,168],"Bone Density","Muscle Weakness",[170,167,171,172,173],"Pilot Study","Vibration Therapy","Vitamin D","Muscle Strength","2024-10-16",{"date":176,"type":33},"2024-10-18",{"date":178,"type":21},"2024-10-15",{"date":180,"type":21},"2024-12-15",{"name":39,"class":40},""]