[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Balikesir University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":235},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,46,72,93,111,127,151,178,204],{"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":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100644028","efficacy-of-complex-decongestive-therapy-exercise-and-diet-in-women-with-lipedema-100644028",false,"NCT07667270","Efficacy of Complex Decongestive Therapy, Exercise and Diet in Women With Lipedema","Efficacy of Complex Decongestive Therapy, Exercise, and Nutritional Interventions in Women Diagnosed With Lipedema: A Prospective, Single-Blind, Randomized Controlled Trial","Inclusion Criteria:\n\n* Female, aged 18 to 65 years.\n* Clinical and physical examination confirming Stage I, II, or III lipedema.\n* Body Mass Index (BMI) \\\u003C 45 kg\u002Fm\\^2.\n* Ability to walk without restriction.\n\nExclusion Criteria:\n\n* Presence of active malignancy.\n* Decompensated heart failure.\n* Significant lower extremity peripheral artery disease.\n* Acute deep vein thrombosis or active thromboembolism.\n* Pregnancy.\n* Significant sensory loss or severe neuropathy in the lower extremities.\n* History of lower extremity liposuction within the last 12 months.\n* Active severe infection (e.g., cellulitis).\n* Other severe systemic diseases deemed unsafe for the study by researchers.\n* Severe non-compliance with the study protocol (e.g., missing \\>30% of planned sessions) or participant requesting withdrawal.","FEMALE","18 Years","65 Years",{"count":20,"type":21},75,"ESTIMATED","INTERVENTIONAL",[24],"NA","The purpose of this study is to compare the effectiveness of standard physical therapy methods (Complex Decongestive Therapy, Pneumatic Compression, and Exercise) combined with two different nutritional approaches (personalized anti-inflammatory diet vs. standard healthy nutrition education) in women diagnosed with lower extremity lipedema.",[27],"Lipedema",[27,29,30,31,32],"diet","exercise","Complex Decongestive Therapy","Physical Therapy","NOT_YET_RECRUITING","2026-06-21",{"date":36,"type":37},"2026-06-25","ACTUAL",{"date":39,"type":21},"2026-06-15",{"date":41,"type":21},"2027-12-15",{"name":43,"class":44},"Balikesir University","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":54,"minAge":18,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":45},"100639177","figure-of-8-walk-test-in-individuals-with-motoric-cognitive-risk-syndrome-100639177","NCT07586553","Figure-of-8 Walk Test in Individuals With Motoric Cognitive Risk Syndrome","Validity and Reliability of the Figure-of-8 Walk Test (8FWT) in Individuals With Motoric Cognitive Risk Syndrome","8FWT-MCR","Inclusion Criteria:\n\nAged 65 years or older Presence of subjective cognitive complaints Gait speed ≤ 0.8 m\u002Fs (4-meter walk test) Able to walk independently without assistive devices No clinical diagnosis of dementia Able to understand and follow test instructions\n\nExclusion Criteria:\n\nMini-Mental State Examination (MMSE) score \\\u003C 24 Neurological diseases affecting gait (e.g., stroke, Parkinson's disease, multiple sclerosis) Severe musculoskeletal conditions affecting walking Lower extremity surgery within the last 6 months Severe visual or hearing impairment that interferes with testing Dependence on assistive walking devices","ALL",{"count":56,"type":21},52,"OBSERVATIONAL","This observational study aims to investigate the validity and reliability of the Figure-of-8 Walk Test (8FWT) in individuals with Motoric Cognitive Risk Syndrome (MCRS). The study will evaluate test-retest reliability, measurement error (SEM, MDC), and construct validity by examining the relationship between 8FWT performance and functional mobility measures. The findings are expected to provide evidence for the clinical applicability of 8FWT in assessing dynamic balance, gait performance, and cognitive-motor interaction in older adults.",[60,61,62],"Motoric Cognitive Risk Syndrome","Gait","Balance","RECRUITING","2026-05-07",{"date":66,"type":37},"2026-05-14",{"date":68,"type":37},"2026-04-07",{"date":70,"type":21},"2026-07-08",{"name":43,"class":44},{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":4,"eligibilityCriteria":78,"healthyVolunteers":79,"sex":54,"minAge":18,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":82,"conditions":83,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":45},"100639707","gait-and-cognitive-function-in-relation-to-foot-arch-structure-in-older-adults-100639707","NCT07582367","Gait and Cognitive Function in Relation to Foot Arch Structure in Older Adults","Relationship Between Foot Arch Structure, Spatiotemporal Gait Parameters, and Cognitive Function in Older Adults","Inclusion Criteria:\n\n* Aged 65 years or older\n* Able to walk independently for at least 10 meters without assistive devices\n* Able to understand study procedures and provide informed consent\n* Having sufficient cognitive and physical capacity to comply with the assessment protocol\n\nExclusion Criteria:\n\n* Diagnosed neurological disorders affecting gait and motor control (e.g., stroke, Parkinson's disease, multiple sclerosis)\n* Diagnosed dementia or Alzheimer's disease, or Mini-Mental State Examination (MMSE) score below 24\n* Severe visual or hearing impairment that cannot be corrected and may affect reaction time testing\n* History of major lower extremity or spinal surgery within the last 6 months Severe musculoskeletal conditions affecting gait (e.g., advanced osteoarthritis, severe pain, active inflammation, open wounds, or recent fractures in the lower extremity)\n* Presence of severe balance disorders (e.g., vertigo)",true,{"count":81,"type":21},50,"This study aims to investigate the relationship between foot arch structure and spatiotemporal gait parameters and cognitive function in older adults. Foot arch integrity will be assessed using the Navicular Drop Test, and gait performance will be evaluated using the 10-Meter Walk Test. Cognitive-motor interaction will be examined through lower extremity reaction time using a light-based system. The study is designed as an observational cross-sectional analysis.",[61,84,85],"Foot Biomechanics","Cognitive Function",{"date":87,"type":37},"2026-05-12",{"date":89,"type":37},"2026-04-15",{"date":91,"type":21},"2026-11-08",{"name":43,"class":44},{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":98,"acronym":4,"eligibilityCriteria":99,"healthyVolunteers":11,"sex":54,"minAge":18,"maxAge":4,"enrollmentInfo":100,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":102,"conditions":103,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":105,"lastUpdatePostDateStruct":106,"startDateStruct":107,"completionDateStruct":108,"leadSponsor":110,"locationsCount":45},"100636998","dual-task-effects-on-gait-and-balance-in-mcrs-100636998","NCT07572968","Dual-Task Effects on Gait and Balance in MCRS","Effects of Cognitive Load on Gait and Balance Performance in Individuals With Motoric Cognitive Risk Syndrome: A Dual-Task Analysis","Inclusion Criteria:\n\nAge ≥ 65 years Subjective cognitive complaints Slow gait speed No dementia diagnosis\n\nExclusion Criteria:\n\nSevere visual\u002Fhearing impairment Neurological diseases (stroke, Parkinson) Acute orthopedic conditions affecting walking",{"count":101,"type":21},35,"This study aims to investigate the effects of cognitive load on gait and balance performance in individuals with Motoric Cognitive Risk Syndrome (MCRS). Participants will perform Timed Up and Go (TUG) and tandem walking tests under single-task and dual-task conditions. The study evaluates cognitive-motor interference and dual-task cost to better understand early markers of cognitive decline and fall risk.",[60,104,61,62],"Dual-Task Performance","2026-05-01",{"date":64,"type":37},{"date":89,"type":37},{"date":109,"type":21},"2026-07-15",{"name":43,"class":44},{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":116,"acronym":4,"eligibilityCriteria":117,"healthyVolunteers":11,"sex":54,"minAge":18,"maxAge":4,"enrollmentInfo":118,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":119,"conditions":120,"keywords":4,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":105,"lastUpdatePostDateStruct":123,"startDateStruct":124,"completionDateStruct":125,"leadSponsor":126,"locationsCount":45},"100636996","laser-based-map-tests-in-motoric-cognitive-risk-syndrome-100636996","NCT07572942","Laser-Based Map Tests in Motoric Cognitive Risk Syndrome","Validity and Reliability of Neuroscience-Based Visual Laser Feedback Map Tests in Individuals With Motoric Cognitive Risk Syndrome","Inclusion Criteria:\n\nAged ≥65 years Diagnosis of Motoric Cognitive Risk Syndrome (subjective cognitive complaint + slow gait) Living independently in the community Able to understand and perform test procedures\n\nExclusion Criteria:\n\nDiagnosed dementia Severe psychiatric disorders Advanced visual impairments (e.g., macular degeneration, severe cataract) Neurological disorders affecting motor control Severe tremor or ataxia interfering with task performance",{"count":101,"type":21},"This study aims to evaluate the validity and reliability of neuroscience-based visual laser feedback map tests in individuals with Motoric Cognitive Risk Syndrome (MCRS). The developed assessment protocol integrates visuospatial processing, reaction time, and upper extremity motor control within a single task. Construct validity will be examined through correlations with reaction time and proprioception measurements, and test-retest reliability will be assessed to determine measurement consistency.",[60,121,122],"Cognitive-Motor Interaction","Sensorimotor Performance",{"date":64,"type":37},{"date":89,"type":37},{"date":109,"type":21},{"name":43,"class":44},{"id":128,"slug":129,"hasResults":11,"nctId":130,"briefTitle":131,"officialTitle":131,"acronym":4,"eligibilityCriteria":132,"healthyVolunteers":11,"sex":54,"minAge":133,"maxAge":18,"enrollmentInfo":134,"targetDuration":4,"studyType":22,"phases":136,"briefSummary":137,"conditions":138,"keywords":140,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":147,"completionDateStruct":148,"leadSponsor":150,"locationsCount":45},"100596640","development-of-standard-guidelines-for-relaxation-exercises-in-patients-with-chronic-neck-pain-and-determination-of-their-effectiveness-100596640","NCT07048093","Development of Standard Guidelines for Relaxation Exercises in Patients With Chronic Neck Pain and Determination of Their Effectiveness","Inclusion Criteria:\n\n* Knowledge of Turkish\n* Chronic (at least three months) neck pain\n* Neck pain level of 4 or higher on a numerical pain scale\n\nExclusion Criteria:\n\n* Neck pain caused by a tumor, trauma, or rheumatic disease\n* History of surgery involving the head, neck, shoulder, or thoracic region\n* Root compression\n* Regular use of painkillers due to another illness\n* Another illness severe enough to interfere with work","22 Years",{"count":135,"type":21},34,[24],"The goal of this observational study is to determine whether relaxation exercises performed before cranio-cervical flexion can reduce superficial neck muscle activation (specifically sternocleidomastoid and upper trapezius) in individuals with neck pain.\n\nThe main questions it aims to answer are:\n\n* Does performing relaxation exercises prior to cranio-cervical flexion reduce sternocleidomastoid (SCM) muscle activation?\n* Does it reduce upper trapezius muscle activation during the standing?\n\nResearchers will compare the group performing relaxation exercises before cranio-cervical flexion to the group performing only cranio-cervical flexion to see if there is a measurable difference in superficial neck muscle activation.\n\nParticipants will:\n\n* Perform cranio-cervical flexion exercises.\n* Perform relaxation exercises prior to the cranio-cervical flexion (intervention group only).\n* Undergo surface EMG measurements to assess muscle activity.",[139],"Non Specific Chronic Neck Pain",[141,142,143],"Relaxation Exercise","craniocervical flexion","upper trapezius","2025-09-17",{"date":146,"type":37},"2025-09-22",{"date":146,"type":21},{"date":149,"type":21},"2026-09-01",{"name":43,"class":44},{"id":152,"slug":153,"hasResults":11,"nctId":154,"briefTitle":155,"officialTitle":156,"acronym":4,"eligibilityCriteria":157,"healthyVolunteers":11,"sex":54,"minAge":17,"maxAge":4,"enrollmentInfo":158,"targetDuration":160,"studyType":57,"phases":4,"briefSummary":161,"conditions":162,"keywords":166,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":170,"lastUpdatePostDateStruct":171,"startDateStruct":173,"completionDateStruct":175,"leadSponsor":177,"locationsCount":45},"100578529","anticholinergic-burden-and-osteoporosis-in-rheumatoid-arthritis-100578529","NCT06812481","Anticholinergic Burden and Osteoporosis in Rheumatoid Arthritis","Anticholinergic Drug Use in Patients With Rheumatoid Arthritis and Its Effects on Fracture Risk","Inclusion Criteria:\n\n* Patients diagnosed with rheumatoid arthritis\n\nExclusion Criteria:\n\n* Kemik metabolizmasını etkileyen sistemik hastalıkları veya ilaçları kullanan hastalar,\n* Kemik mineral yoğunluk ölçümünü etkileyen kalça veya lomber vertebralarda metalik materyalleri olan hastalar",{"count":159,"type":21},100,"3 Months","Background: Rheumatoid arthritis (RA) is a chronic, progressive, inflammatory rheumatological disease. Use of corticosteroids for more than 3 months in RA treatment is considered an important risk factor in terms of developing secondary osteoporosis and increasing the risk of fracture. The cumulative effect of taking one or more drugs with anticholinergic properties is called anticholinergic load. It is stated that anticholinergic load also increases the risk of fracture in individuals. The aim of this study is to investigate the effects of drugs used by patients with Rheumatoid Arthritis (RA) on anticholinergic load and fracture risk. The Fracture Risk Assessment Tool (FRAX) will be used to assess fracture risk in patients.\n\nMaterials and methods: The study was planned as a prospective cohort study. The study will included 100 patients who were followed up as outpatients with rheumatoid arthritis diagnosis in the physical medicine and rehabilitation clinic between 2024-2025. Patients of both genders and over 18 years of age diagnosed with rheumatoid arthritis will be included in the study. Patients with systemic diseases or medications affecting bone metabolism and those with metallic materials in the hip or lumbar vertebrae affecting bone mineral density measurement will be excluded from the study. Demographic characteristics, systemic diseases, medications used, bone density measurement and blood test values of the patients will be recorded.\n\nPatients taking multiple medications with anticholinergic effects create an anticholinergic burden. The Anticholinergic Drug Scale, Anticholinergic Cognitive Burden Scale and Anticholinergic Risk Scale will be used to measure anticholinergic burden in the study.",[163,164,165],"Rheumatoid Arthritis (RA)","Anticholinergic Adverse Reaction","Fractures, Bone",[167,168,169],"Rheumatoid arthritis","anticholinergic load","risk of fracture","2025-09-16",{"date":172,"type":37},"2025-09-18",{"date":174,"type":37},"2025-09-15",{"date":176,"type":21},"2025-12-31",{"name":43,"class":44},{"id":179,"slug":180,"hasResults":11,"nctId":181,"briefTitle":182,"officialTitle":182,"acronym":4,"eligibilityCriteria":183,"healthyVolunteers":79,"sex":16,"minAge":17,"maxAge":184,"enrollmentInfo":185,"targetDuration":4,"studyType":22,"phases":187,"briefSummary":188,"conditions":189,"keywords":191,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":197,"lastUpdatePostDateStruct":198,"startDateStruct":200,"completionDateStruct":202,"leadSponsor":203,"locationsCount":45},"100530669","effects-of-rosa-damascena-and-frankincense-essential-oils-in-labor-100530669","NCT06189794","Effects of Rosa Damascena and Frankincense Essential Oils in Labor","Inclusion Criteria:\n\n\\- Pregnant women who are at latent phase of labor\n\nExclusion Criteria:\n\n* Complicated pregnancy (preeclampsia, hypertension, diabetes etc.)\n* Women who will have planned cesarean section\n* Asthma or any other respiratory disease\n* Allergies to Rosa Damascena or Frankincense oil","49 Years",{"count":186,"type":21},39,[24],"This randomized controlled study aims to compare effects of different essential oils in labor pain, anxiety and childbirth comfort. The main questions it aims to answer are:\n\nIs it effective using rosa damascena oil during labor? Is it effective using frankincense oil during labor? Which essential oil is more effective during labor Researchers will compare aromatherapy oils groups to see labor pain, anxiety and childbirth comfort levels of pregnant women.",[190],"Labor Pain",[192,193,194,195,196],"Aromatherapy","Childbirth Problems","Rosa damascena","Frankincense","Comfort","2025-06-14",{"date":199,"type":37},"2025-06-18",{"date":201,"type":37},"2024-01-21",{"date":176,"type":21},{"name":43,"class":44},{"id":205,"slug":206,"hasResults":11,"nctId":207,"briefTitle":208,"officialTitle":208,"acronym":4,"eligibilityCriteria":209,"healthyVolunteers":79,"sex":54,"minAge":210,"maxAge":211,"enrollmentInfo":212,"targetDuration":4,"studyType":22,"phases":214,"briefSummary":215,"conditions":216,"keywords":222,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":227,"lastUpdatePostDateStruct":228,"startDateStruct":230,"completionDateStruct":232,"leadSponsor":234,"locationsCount":4},"100581906","effect-of-using-educational-robots-during-vaccination-on-fear-and-pain-in-children-100581906","NCT06856395","Effect of Using Educational Robots During Vaccination on Fear and Pain in Children","Inclusion Criteria:\n\n* Volunteering to participate in the study\n* The child must be 4 years old\n* Must have come to a primary care center in Balıkesir city center\n* DaBT-İPA vaccination must be administered\n* Vastus Lateralis muscle must be used in vaccination\n\nExclusion Criteria:\n\n* Not volunteering to participate in the study\n* The child is not 4 years old\n* He\u002Fshe has not come to a family health center in Balıkesir city center\n* DaBT-İPA vaccination is not applied\n* Vastus Lateralis muscle will not be used in vaccination application","48 Months","60 Months",{"count":213,"type":21},74,[24],"Pain and fear are very common in children during vaccination. We are planning to conduct a study to help children go through this process more comfortably. The aim is to examine whether the educational robot has an effect on pain and fear during vaccination in 4-year-old children in a randomized controlled manner.",[217,218,219,220,221],"Fear","Fear of Pain","Pain","Vaccination","Child Behavior",[223,224,225,226],"pain","fear","vaccination","child behavior","2025-03-06",{"date":229,"type":37},"2025-03-11",{"date":231,"type":21},"2025-03-31",{"date":233,"type":21},"2026-01-31",{"name":43,"class":44},""]