[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"University of Sharjah\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":277},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,44,72,98,135,169,198,225,252],{"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":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":4},"100626505","effects-of-a-combined-home-based-exercise-program-on-menstrual-pain-dual-task-gait-performance-and-eeg-markers-of-cognitive-motor-control-in-females-with-primary-dysmenorrhea-100626505",false,"NCT07436507","Effects of a Combined Home-Based Exercise Program on Menstrual Pain, Dual-Task Gait Performance, and EEG Markers of Cognitive-Motor Control in Females With Primary Dysmenorrhea","Effects of a Combined Home-Based Exercise Program on Menstrual Pain, Dual-Task Gait Performance, and Neurophysiological Outcomes in Primary Dysmenorrhoea: A Randomised Controlled Trial Protocol","Inclusion Criteria:\n\n* single\n* 18-25 years\n* meet the diagnostic criteria for PD as outlined in the Primary Dysmenorrhea Consensus Guidelines - first onset of menstrual pain 6-24 months after menarche, pain lasting 8-72h in a cycle, and the most severe pain on the 1st or 2nd day of menstruation\n* having a regular menstrual cycle (28 ± 7 days)\n* menstrual pain intensity ≥4 cm on VAS in the previous 6 months\n* absence of any known medical condition\n\nExclusion Criteria:\n\n* history of pelvic surgery\n* history and\u002For findings of secondary dysmenorrhea\n* history of mental or physical diseases\n* history of joint, motion, muscle, or bone diseases which reduce the abilities to exercise\n* being a professional athlete\n* taking analgesic or non-pharmacological agents other than NSAID for menstrual pain\n* used an intrauterine device or oral contraceptive pill\n* metal implants, including pacemaker\n* history of non-normal brain activity, including seizures","FEMALE","18 Years","25 Years",{"count":20,"type":21},86,"ESTIMATED","INTERVENTIONAL",[24],"NA","What is this study about? Dysmenorrhea, commonly known as painful period, is a common gynecological symptom experienced by several women of reproductive age. This particular type of pain arises during the menstrual cycle, often negatively impacting the quality of life and ability to successfully carry out daily activities and academic or work performance. This is study will involve physiotherapy treatment in the form of a home-based exercise program for those experiencing dysmenorrhea. The purpose of this study is to determine how effective this exercise intervention is by assessing the pain score, menstrual symptoms, gait performance and cognitive-motor control.",[27],"Dysmenorrhea Primary",[27,29,30,31],"Home exercise program","Dual-Task Gait Performance","Cognitive Motor Control","NOT_YET_RECRUITING","2026-05-10",{"date":35,"type":36},"2026-05-13","ACTUAL",{"date":38,"type":21},"2026-07-06",{"date":40,"type":21},"2027-05-31",{"name":42,"class":43},"University of Sharjah","OTHER",{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":52,"minAge":17,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":61,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},"100636438","forward-head-posture-correction-on-cerebral-oxygenation-during-dual-task-in-symptomatic-subjects-100636438","NCT07565688","Forward Head Posture Correction on Cerebral Oxygenation During Dual-task in Symptomatic Subjects","Effects of Forward Head Posture Correction on Prefrontal Cerebral Oxygenation During Cognitive-Motor Interference in Symptomatic Subjects With Forward Head Posture: A Randomized Controlled Trial","FHP","Inclusion Criteria:\n\n* Young adults of both sexes aged 18-35 years\n* Individuals with forward head posture (a craniovertebral angle (CVA) \\\u003C 50°)\n* Presence of neck pain with an intensity of ≥3 on the Visual Analog Scale (VAS)\n* Ability to understand and follow basic English instructions\n* No cognitive impairment (score \\>18 on the Montreal Cognitive Assessment (MoCA))\n\nExclusion Criteria:\n\n* History of cervical spine surgery or significant cervical trauma\n* Currently receiving physiotherapy or rehabilitation for cervical spine conditions\n* Individuals on medications (diagnosed neurological disorders)","ALL","35 Years",{"count":55,"type":21},45,[24],"This study aims to investigate the effects of forward head posture correction on neck pain, brain activity, and cognitive-motor performance. Forward head posture is a common postural problem, especially among young adults who spend long hours using smartphones and computers. It is frequently associated with neck pain, reduced mobility, and functional limitations. Emerging evidence also suggests that this postural deviation may influence brain function and increase the mental effort required during tasks that involve both thinking and movement.\n\nParticipants with forward head posture and neck pain will be recruited and randomly assigned to one of three groups: an intervention group using a cervical traction device (Denneroll), a sham group using a towel roll, or a control group receiving no intervention. The intervention will be performed at home over a six-week period, with sessions conducted five times per week. The duration of each session will gradually increase based on participant tolerance to ensure safety and comfort.\n\nAll participants will undergo assessments at baseline and after the intervention period. Pain intensity will be measured using a standardized pain scale. Brain activity will be assessed using a non-invasive technique called functional near-infrared spectroscopy (fNIRS), which measures changes in oxygen levels in the brain. Participants will also perform balance tasks under single-task and dual-task conditions, where they will be asked to maintain balance while performing simple cognitive tasks. In addition, cognitive function will be evaluated using standardized tests of attention, memory, and overall cognitive performance.\n\nThis study will help determine whether correcting forward head posture can reduce pain and improve brain and cognitive function. The findings may provide valuable insights into the relationship between posture, pain, and brain activity, and may contribute to the development of more effective and comprehensive rehabilitation approaches for individuals with forward head posture.",[59,60],"Forward Head Posture","Neck Pain",[59,62],"Neck Pain Musculoskeletal","2026-05-04",{"date":65,"type":36},"2026-05-08",{"date":67,"type":21},"2027-05-01",{"date":69,"type":21},"2028-09-01",{"name":42,"class":43},1,{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":52,"minAge":17,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":22,"phases":82,"briefSummary":83,"conditions":84,"keywords":86,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":97,"locationsCount":71},"100626384","augmented-reality-based-dual-task-training-in-people-with-multiple-sclerosis-100626384","NCT07434934","Augmented Reality-Based Dual-Task Training in People With Multiple Sclerosis","Development of Augmented Reality-Based Dual-Task Training to Enhance Cognitive and Motor Function in People With Multiple Sclerosis","MS","Inclusion Criteria:\n\n* Neurologist-confirmed diagnosis of MS according to the revised McDonald criteria and PDDS score of ≤6\n* Age above 18 years;\n* Affected by relapsing remitting and secondary progressive MS\n* Successful completion of Physical Activity Readiness Questionnaire (PAR-Q)\n* Presence of mild\u002Fmoderate cognitive impairment (Montreal Cognitive Assessment - MoCA \\>18)\n* Ambulatory for indoor and outdoor mobility with or without an assistive device but without physical assistance\n\nExclusion Criteria:\n\n* Acute illness or injury that would prevent safe participation in an exercise program\n* Presence of any other neurological conditions (e.g., stroke),\n* Presence of severe psychiatric illness other than anxiety or depression\n* According to the Diagnostic and Statistical Manual of Mental Disorders, 5th -Edition (DSM- V),\n* Presence of disabling sensory alterations (i.e. auditory and visual disturbances)\n* Relapse in the 3 months before enrollment\n* Current engagement in 3 days a week or more of moderate\u002Fvigorous exercise",{"count":81,"type":21},40,[24],"Multiple Sclerosis (MS) is the most common NDD affecting young people worldwide. MS can seriously affect quality of life and hinder daily functional activities. Therefore, living with MS is a daunting task for both patients and their families. With the prediction of an increase in life expectancy, it is also expected that MS will pose major challenges to healthcare providers in the UAE and globally in terms of its clinical management and financial implications. This proposed project aims to develop structured AR scenarios that integrate dual-tasking exercises commonly used in MS physiotherapy, specifically designed to meet the needs of PwMS. The primary goal is to evaluate the feasibility, acceptability, and potential benefits of these AR scenarios as a rehabilitation tool for PwMS.",[85],"Multiple Sclerosis",[87,88,89,90],"dual task","rehabilitation","augmented reality","motor function","2026-04-28",{"date":93,"type":36},"2026-05-05",{"date":95,"type":21},"2026-08-01",{"date":69,"type":21},{"name":42,"class":43},{"id":99,"slug":100,"hasResults":11,"nctId":101,"briefTitle":102,"officialTitle":103,"acronym":104,"eligibilityCriteria":105,"healthyVolunteers":11,"sex":52,"minAge":17,"maxAge":4,"enrollmentInfo":106,"targetDuration":4,"studyType":22,"phases":107,"briefSummary":108,"conditions":109,"keywords":110,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":71},"100635645","bilateral-anodal-cerebellar-tdcs-for-multidomain-dysfunctions-in-patients-with-multiple-sclerosis-100635645","NCT07555379","Bilateral Anodal Cerebellar tDCS for Multidomain Dysfunctions in Patients With Multiple Sclerosis","Bilateral Anodal Cerebellar tDCS for Multidomain Dysfunctions in Patients With Multiple Sclerosis: A Randomized Controlled Trial Study","CerebellertDCS","Inclusion Criteria:\n\n* Confirmed diagnosis of Multiple Sclerosis according to the revised McDonald criteria\n* Adult Age \\> 18 years\n* Expanded Disability Status Scale (EDSS) score between 2.0 and 6.0\n* Clinically stable disease status for at least 3 months prior to enrollment\n* On stable disease-modifying therapy (DMT) for at least 3 months\n* Ability to understand study procedures and provide informed consent\n* Ability to ambulate independently or with assistive devices sufficient to complete motor assessments\n\nExclusion Criteria:\n\n* Multiple sclerosis relapse within the past 3 months\n* History of epilepsy or seizures\n* Presence of implanted electronic devices (e.g., pacemaker, neurostimulator)\n* Metallic implants in the head or skull incompatible with transcranial magnetic stimulation (TMS)\n* Severe cognitive impairment preventing participation in assessments\n* Pregnancy or planned pregnancy during the study period\n* Other neurological or psychiatric disorders that may confound study outcomes\n* Severe musculoskeletal or orthopedic conditions interfering with motor performance testing\n* Contraindications to non-invasive brain stimulation or TMS",{"count":81,"type":21},[24],"The goal of this clinical trial is to learn if brain stimulation can improve movement and daily function in people with multiple sclerosis (MS). The study will also look at how this treatment affects fatigue, sleep, memory and attention, and quality of life.\n\nThe main questions this study aims to answer are the following:\n\nDoes this treatment improve coordination and balance? Does it reduce fatigue and improve sleep and daily life? Does it change brain activity?\n\nResearchers will compare active brain stimulation to sham stimulation (a look-alike treatment that does not deliver real stimulation) to see if the treatment works.\n\nParticipants will:\n\nReceive brain stimulation sessions for two weeks Attend assessment sessions before and after treatment Return for a follow-up visit after four weeks Complete tests of movement, fatigue, sleep, and thinking",[85],[111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126],"Multiple sclerosis","cerebellar transcranial direct current stimulation","ctDCS","bilateral cerebellar stimulation","neuromodulation","ataxia","balance","gait","fatigue","cognition","sleep quality","quality of life","EEG","transcranial magnetic stimulation","corticospinal excitability","neurorehabilitation","2026-04-23",{"date":129,"type":36},"2026-04-29",{"date":131,"type":21},"2026-09-01",{"date":133,"type":21},"2028-06-01",{"name":42,"class":43},{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":141,"eligibilityCriteria":142,"healthyVolunteers":11,"sex":52,"minAge":17,"maxAge":4,"enrollmentInfo":143,"targetDuration":4,"studyType":22,"phases":145,"briefSummary":146,"conditions":147,"keywords":152,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":163,"startDateStruct":165,"completionDateStruct":166,"leadSponsor":168,"locationsCount":71},"100635923","mirror-image-spine-correction-exercises-versus-conservative-physiotherapy-for-lumbar-radiculopathy-100635923","NCT07558993","Mirror Image Spine Correction Exercises Versus Conservative Physiotherapy for Lumbar Radiculopathy","Randomized, Parallel-Group, Superiority Trial of Mirror Image Spine Correction Exercises Versus Conservative Physiotherapy for Lumbar Nerve Root Microstructural Integrity Assessed by Diffusion Tensor Imaging in Adults With Lumbar Radiculopathy","MIRROR-LR","Inclusion Criteria:\n\n* Adults aged 18 years or older. Clinical diagnosis of unilateral lumbar radiculopathy. Presence of at least two of the following: dermatomal radiating leg pain, neurological deficit, positive neural tension test.\n\nMRI-confirmed lumbar nerve root compression or irritation consistent with symptoms.\n\nPain intensity of 3\u002F10 or greater. Able to undergo MRI and Diffusion Tensor Imaging (DTI). Able to understand study procedures and provide written informed consent.\n\nExclusion Criteria:\n\n* Previous lumbar spine surgery. Bilateral radiculopathy or unclear diagnosis. Tumor, infection, fracture, inflammatory spinal disease, or cauda equina syndrome.\n\nSevere progressive neurological deficit requiring urgent treatment. Contraindications to MRI (pacemaker, incompatible implants, severe claustrophobia).\n\nRecent lumbar injections or surgery. Other neurological or musculoskeletal disorders affecting outcomes. Pregnancy if MRI contraindicated by local policy. Cognitive impairment or inability to follow instructions.",{"count":144,"type":21},64,[24],"Lumbar radiculopathy is a common condition caused by irritation or compression of a lumbar nerve root, often resulting in radiating leg pain, numbness, weakness, and functional limitation. Conservative physiotherapy is commonly used as first-line treatment, but outcomes vary among patients.\n\nThis randomized controlled trial will compare Mirror Image Spine Correction Exercises with standardized conservative physiotherapy in adults with lumbar radiculopathy. Participants will be randomly assigned to one of two treatment groups for 12 weeks.\n\nThe primary outcome is lumbar nerve root microstructural integrity measured using Diffusion Tensor Imaging (DTI), including Fractional Anisotropy and other diffusion parameters. Secondary outcomes include pain intensity, disability, spinal alignment, and adverse events.\n\nThe purpose of this study is to determine whether a targeted posture-correction exercise approach provides greater improvement than conventional physiotherapy.",[148,149,150,151],"Radiculopathy","Radiculopathy Lumbar","Sciatica","Disc Disease Lumbar",[153,154,155,156,157,158,159,160,161,162],"Mirror Image Exercise","Physiotherapy","Diffusion Tensor Imaging","DTI","Conservative Physiotherapy","Low Back Pain","Nerve Root Compression","Postural Correction","Randomized Controlled Trial","Rehabilitation",{"date":164,"type":36},"2026-04-30",{"date":131,"type":21},{"date":167,"type":21},"2027-09-30",{"name":42,"class":43},{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":174,"acronym":4,"eligibilityCriteria":175,"healthyVolunteers":176,"sex":52,"minAge":17,"maxAge":177,"enrollmentInfo":178,"targetDuration":4,"studyType":22,"phases":180,"briefSummary":181,"conditions":182,"keywords":184,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":190,"lastUpdatePostDateStruct":191,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":71},"100593678","cortical-excitability-and-typing-performance-after-action-observation-and-motor-execution-100593678","NCT07009561","Cortical Excitability and Typing Performance After Action Observation and Motor Execution","Comparison of Cortical Excitability and Typing Performance Across Action Observation, Motor Execution, and Control Conditions","Inclusion Criteria:\n\n* Age between 18 and 26 years\n* Healthy university students with no known neurological, psychiatric, or musculoskeletal conditions\n* Intact motor functioning of the upper limbs\n* Basic typing proficiency using a 10-finger typing method\n* Ability to understand study procedures and provide informed consent\n\nExclusion Criteria:\n\n* Typing speed less than 16 words per minute\n* Use of hunt-and-peck or single-finger typing style\n* History of seizures or epilepsy\n* Current use of neuroactive medications\n* Presence of metallic implants in the head or upper body\n* Any contraindications to Transcranial Magnetic Stimulation (TMS)\n* Left-handed individuals using non-standard typing techniques (unless provided with adapted materials)",true,"26 Years",{"count":179,"type":21},60,[24],"Goal:\n\nThis study will aim to investigate the effects of different motor stimulation strategies-motor execution (ME) and action observation (AO)-on cortical excitability and typing performance in healthy individuals.\n\nRecruitment:\n\nA total of 60 healthy university students will be recruited and randomly assigned into three groups:\n\nMotor Execution group (n=20) Action Observation group (n=20) Control group (n=20)\n\nEvaluation Tools:\n\nTranscranial Magnetic Stimulation (TMS) using DEYMED DuoMAG XT will be used to measure Resting Motor Threshold (RMT), Motor Evoked Potential (MEP) Amplitude, and MEP Latency of the First Dorsal Interosseous (FDI) muscle.\n\nOnline Typing Test will be used to assess typing speed (words per minute) and accuracy (percentage of correct characters).\n\nIntervention:\n\nThe ME group will perform a 3-minute typing task. The AO group will observe a 3-minute first-person video of typing. The Control group will not receive any intervention between assessments.\n\nAll participants will undergo TMS and typing assessments twice, once before and once after the intervention.",[183],"Young Adults",[185,186,187,188,189],"Transcranial magnetic stimulation","Cortical excitability","Action observation","Motor execution","Typing","2025-05-29",{"date":192,"type":36},"2025-06-06",{"date":194,"type":21},"2025-06-15",{"date":196,"type":21},"2025-07-30",{"name":42,"class":43},{"id":199,"slug":200,"hasResults":11,"nctId":201,"briefTitle":202,"officialTitle":203,"acronym":4,"eligibilityCriteria":204,"healthyVolunteers":176,"sex":52,"minAge":17,"maxAge":205,"enrollmentInfo":206,"targetDuration":4,"studyType":22,"phases":208,"briefSummary":209,"conditions":210,"keywords":212,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":217,"lastUpdatePostDateStruct":218,"startDateStruct":220,"completionDateStruct":222,"leadSponsor":224,"locationsCount":71},"100574717","the-short-term-effect-of-low-load-resistance-training-with-blood-flow-restriction-on-somatosensory-evoked-potentials-in-healthy-young-adults-100574717","NCT06762912","The Short-term Effect of Low-load Resistance Training with Blood-flow Restriction on Somatosensory-evoked Potentials in Healthy Young Adults","The Short-term Effect of Low-load Resistance Training with Blood-flow Restriction on Somatosensory-evoked Potentials in Healthy Young Adults - a Randomized Crossover Trial","Inclusion Criteria:\n\n* Participants will be included if they are aged 18-30 years of both genders, with no history of cardiovascular problems or osteo-articular problems in the lower limbs, and if they responded negatively to all items of the Physical Activity Readiness Questionnaire (PAR-Q).\n* Participants will be included if they have a body mass index (BMI) less than 25 or non-overweight individuals.\n* Use of the long international physical activity questionnaire (L-IPAQ) to ensure all participants have equal physical activity levels.\n\nExclusion Criteria:\n\n* Participants will be excluded if they did not meet the inclusion criteria, and if they had a history of deep vein thrombosis (DVT), congenital heart disease, varicose veins, currently pregnant, or any contraindications to exercise.\n* Participants will be excluded if they were diagnosed with any neurological disease.\n* Participants will be excluded if they have had any musculoskeletal injury in the past 3 months to avoid potential effect on their physical activity levels.","30 Years",{"count":207,"type":21},30,[24],"The goal of this clinical trial is to investigate the short-term effect of lower limb BFRT on the somatosensory processing and related changes in SSEP amplitude and latency. The main questions it aims to answer are:\n\n* Is there an effect of short-term application of BFRT on the somatosensory system?\n* How do different cuff widths affect the somatosensory system?\n* How do three different cuff widths affect perceived pain? Researchers will compare 3 different cuff widths to see if different cuff widths affect the somatosensory system and perceived pain.\n\nParticipants will:\n\n* Undergo 3 experimental sessions, sessions will be separated by 72 hours and the order of the sessions to be randomly selected.\n* Perform low-load resistance training with blood flow restriction.",[211],"The Current Study Focuses on Investigating the Short-term Effect of BFRT on the Somatosensory System Among Healthy Young Adults",[213,214,215,216],"Blood Flow Restriction Training","Somatosensory Evoked Potentials","Neuroplasticity","Pain","2025-01-01",{"date":219,"type":36},"2025-01-08",{"date":221,"type":21},"2025-01-20",{"date":223,"type":21},"2025-07-31",{"name":42,"class":43},{"id":226,"slug":227,"hasResults":11,"nctId":228,"briefTitle":229,"officialTitle":230,"acronym":4,"eligibilityCriteria":231,"healthyVolunteers":176,"sex":52,"minAge":17,"maxAge":177,"enrollmentInfo":232,"targetDuration":4,"studyType":22,"phases":234,"briefSummary":235,"conditions":236,"keywords":239,"overallStatus":243,"whyStopped":4,"lastUpdateSubmitDate":244,"lastUpdatePostDateStruct":245,"startDateStruct":247,"completionDateStruct":249,"leadSponsor":251,"locationsCount":71},"100550700","compare-the-effects-of-different-avns-parameters-on-neck-pain-hrv-balance-in-collegiate-atheletes-100550700","NCT06450483","Compare the Effects of Different AVNS Parameters on Neck Pain, HRV, Balance in Collegiate Atheletes","Comparing the Effects of Different Auricular Vagus Nerve Stimulation (AVNS) Parameters on Neck Pain Intensity, Heart Rate Variability (HRV), and Balance in Collegiate Athletes: A Randomized Comparative Effectiveness Design","Inclusion Criteria:\n\n* Gender: Male and female Healthy collegiate athletes based in UAE\n* Age range: 18-26 years\n* Physical activity level: High score on the International Physical Activity Questionnaire\n* BMI: Within the range of 20-25\n* Neck pain level: Mild to moderate score on the Neck Pain Disability Index Questionnaire\n\nExclusion Criteria:\n\n* Recent injury: Had an injury within the last three months\n* Age: Over 26 years or below 18 years\n* Physical activity level: Scored moderate or low on the International Physical Activity Questionnaire\n* BMI: Above 25 or below 20\n* Neck pain level: Scored severe on the Neck Pain Disability Index Questionnaire",{"count":233,"type":21},70,[24],"This study looks at how auricular vagus nerve stimulation (AVNS) affects neck pain, heart rate variability, and balance in college athletes, additionally, if different settings of auricular vagus nerve stimulation (AVNS) affect neck pain, heart rate variability, and balance in college athletes. The participants will be split into two groups, each receiving AVNS with different settings.\n\nThe study hypothesizes that vagus nerve stimulation (VNS) will reduce pain perception in college athletes. It is expected that auricular vagus nerve stimulation (AVNS) will decrease heart rate variability (HRV) in this population. Additionally, it is anticipated that college athletes undergoing AVNS will exhibit improved balance. The Investigators also believe that AVNS will decrease neck pain and enhance neck function. Finally, it is proposed that different AVNS parameters will have varying effects on pain intensity, HRV, and balance in collegiate athletes.",[60,237,238],"Heart Rate Variability","Balance",[240,241,238,60,242],"AVNS","HRV","Collegiate athletes","RECRUITING","2024-06-12",{"date":246,"type":36},"2024-06-13",{"date":248,"type":36},"2024-05-29",{"date":250,"type":21},"2024-07-08",{"name":42,"class":43},{"id":253,"slug":254,"hasResults":11,"nctId":255,"briefTitle":256,"officialTitle":257,"acronym":4,"eligibilityCriteria":258,"healthyVolunteers":176,"sex":52,"minAge":17,"maxAge":205,"enrollmentInfo":259,"targetDuration":4,"studyType":22,"phases":261,"briefSummary":262,"conditions":263,"keywords":265,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":269,"lastUpdatePostDateStruct":270,"startDateStruct":272,"completionDateStruct":274,"leadSponsor":276,"locationsCount":71},"100540968","exploring-heart-rate-variability-eeg-pattern-and-corticomuscular-coherence-after-cervical-sagittal-alignment-restoration-100540968","NCT06323746","Exploring Heart Rate Variability, EEG Pattern, and Corticomuscular Coherence After Cervical Sagittal Alignment Restoration","Exploring Heart Rate Variability, EEG Pattern, and Corticomuscular Coherence After Cervical Sagittal Alignment Restoration: A Randomized Controlled Trial Investigation","Inclusion Criteria:\n\n* Anterior head translation (AHT) \\>15 mm\n* Absolute rotatory angle C2 to C7 is \\\u003C25°\n* Athletic student\n\nExclusion Criteria:\n\n* Inflammatory joint disease or other systemic pathologies\n* Prior history of overt injury and surgery relating to the musculoskeletal system, or disorder related to the spine and extremities\n* Musculoskeletal pain in the previous three months.",{"count":260,"type":21},80,[24],"The goal of this Randomized clinical trial is to learn about how fixing neck curvature and head posture right away affects heart rate, brainwaves, and muscle coordination in college athletes. The main question it aims to answer:\n\n\\- Whether forward head posture (FHP) may play a crucial role in affecting heart rate variability, brainwaves, and muscle coordination.",[264],"Cervical Lordosis",[264,266,267,268],"Athlete","Electroencephalography","Heart Rate","2024-05-28",{"date":271,"type":36},"2024-05-30",{"date":273,"type":21},"2024-05",{"date":275,"type":21},"2026-12",{"name":42,"class":43},""]