[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Ufuk University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":92},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,70],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":4},"100648556","evaluation-of-the-effects-of-a-hysterectomy-adherence-education-program-based-on-the-roy-adaptation-model-on-hysterectomy-adherence-self-esteem-and-quality-of-life-in-women-undergoing-hysterectomy-100648556",false,"NCT07721727","Evaluation of the Effects of a Hysterectomy Adherence Education Program Based on the Roy Adaptation Model on Hysterectomy Adherence, Self-Esteem, and Quality of Life in Women Undergoing Hysterectomy","HYSTADAPT","Inclusion Criteria:\n\n* Women who have completed at least primary school education. Premenopausal women who have undergone hysterectomy. Have access to the internet and possess a device (smartphone, tablet, or computer) capable of participating in online education sessions.\n\nHave an adequate level of health literacy to understand the educational materials, access online information, and follow the intervention.\n\nBe sexually active.\n\nExclusion Criteria:\n\n* Diagnosed with a sleep disorder. Have a physical and\u002For mental disability. Have communication difficulties (e.g., speech, language, comprehension, or cognitive impairment).\n\nHave a diagnosis of cancer. Currently receiving hormone therapy.",true,"FEMALE","18 Years",{"count":20,"type":21},108,"ESTIMATED","INTERVENTIONAL",[24],"NA","\\*\\*Brief Summary\\*\\*\n\nThis randomized controlled trial aims to evaluate the effectiveness of a Roy Adaptation Model-based hysterectomy adaptation education program on adaptation to hysterectomy, self-esteem, and quality of life in women who have undergone hysterectomy. A total of 110 participants will be randomly assigned to either the intervention group (n = 55) or the control group (n = 55). The intervention group will receive the Roy Adaptation Model-based education program, while the control group will receive routine care. Outcomes will be assessed using the Hysterectomy Adaptation Scale, Rosenberg Self-Esteem Rating Scale, and WHOQOL-BREF. The study will determine whether the education program improves adaptation, self-esteem, and quality of life compared with routine care.",[27,28],"Hysterectomy","Women",[30,31,32,33],"hysterektomy","life quality","women health","adaptation","NOT_YET_RECRUITING","2026-07-20",{"date":37,"type":38},"2026-07-23","ACTUAL",{"date":40,"type":21},"2026-08-01",{"date":42,"type":21},"2026-11-30",{"name":44,"class":45},"Ufuk University","OTHER",{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":69},"100607491","evaluation-of-fibromyalgia-frequency-and-pain-parameters-in-women-with-polycystic-ovary-syndrome-100607491","NCT07189247","Evaluation of Fibromyalgia Frequency and Pain Parameters in Women With Polycystic Ovary Syndrome","Evaluation of Fibromyalgia Frequency and Pain Parameters in Women With Polycystic Ovary Syndrome: A Prospective Single-Blind Study","Inclusion Criteria:\n\n1. Women aged 18-40\n2. Those diagnosed with Polycystic Ovary Syndrome by a Gynecologist and Obstetrician (according to the Rotterdam Criteria)\n3. Those who agreed to participate in the study and signed the informed consent form\n\nExclusion Criteria:\n\n1. Patients with underlying uterine or adnexal pathologies (endometrial polyps, adenomyosis, uterine fibroids, adnexal masses, etc.) identified by ultrasound\n2. Patients with previous pelvic surgery\n3. Secondary causes of hirsutism and oligomenorrhea (non-classical congenital adrenal hyperplasia, Cushing's syndrome, hypothyroidism, prolactinoma, androgen-synthesizing tumor)\n4. Pregnant women\n5. Patients with a history of muscular or rheumatological diseases\n6. Patients with uncontrolled diabetes\n7. Patients with severe psychiatric illnesses or a history of psychiatric medication\u002Fsubstance abuse","40 Years",{"count":55,"type":21},140,"OBSERVATIONAL","The primary objective was to determine the prevalence of fibromyalgia in women with PCOS and to examine the relationship between fibromyalgia and psychological status (depression and anxiety). Secondary objectives were to explore the potential link between fibromyalgia and insulin resistance, taking into account phenotypic differences. To assess the relationship between fibromyalgia severity and quality of life and pressure pain threshold measurements. To analyze the impact of pain and mood disorders on PCOS phenotypes and to demonstrate the role of insulin resistance in predicting fibromyalgia.\n\nParticipants will be women aged 18-40 diagnosed with PCOS according to the Rotterdam criteria, and a healthy control group of a similar age. When making a PCOS diagnosis, clinical (hirsutism, acne, menstrual irregularity), biochemical (free testosterone, DHEAS, androstenedione, etc.), and ultrasonographic (polycystic ovary morphology) findings will be evaluated. The control group will consist of healthy volunteers presenting with gynecological complaints other than PCOS and without chronic diseases.\n\nExamination and Assessment Process Obstetrics and Gynecology Outpatient Clinic: PCOS diagnosis, demographic data, biochemical tests (glucose, insulin, HOMA-IR, etc.), and phenotyping.\n\nPhysical Therapy and Rehabilitation: Application of the 2016 ACR fibromyalgia criteria in a single-blind trial, including measurement of pressure pain threshold (algometer), fibromyalgia severity scale, and recording of Fibromyalgia Impact Questionnaire scores.\n\nPsychological Assessment The HADS (Hospital Anxiety and Depression Scale) will be administered to assess depression and anxiety levels.\n\nScores obtained will be compared with fibromyalgia diagnosis and PCOS phenotypes to examine the influence of psychological factors on pain perception.",[59,60],"Fibromyalgia","PCOS (Polycystic Ovary Syndrome) of Bilateral Ovaries","2025-09-16",{"date":63,"type":38},"2025-09-23",{"date":65,"type":21},"2025-11-01",{"date":67,"type":21},"2026-11-01",{"name":44,"class":45},1,{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":53,"enrollmentInfo":76,"targetDuration":4,"studyType":56,"phases":4,"briefSummary":78,"conditions":79,"keywords":81,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":69},"100562720","assessment-of-the-uterus-using-ultrasonographic-elastography-in-women-with-dysmenorrhea-100562720","NCT06606834","Assessment of the Uterus Using Ultrasonographic Elastography in Women with Dysmenorrhea","Inclusion Criteria:\n\n1. Women aged 18-40 years.\n2. Women with primary dysmenorrhea who are willing to participate in the study.\n3. Women without primary or secondary dysmenorrhea who agree to participate as a control group.\n\nExclusion Criteria:\n\n1. Women with secondary dysmenorrhea.\n2. Patients with underlying uterine or adnexal pathologies (e.g., endometrial polyps, adenomyosis, uterine fibroids, adnexal masses, ovarian pathologies and cysts) identified via ultrasonography.\n3. Individuals with a history of uterine surgery.\n4. Individuals with a history of pelvic surgery.\n5. Individuals who have delivered via normal spontaneous vaginal delivery or cesarean section.",{"count":77,"type":21},100,"The aim of this study is to perform sonoelastographic assessment of the uterus in patients diagnosed with primary dysmenorrhea and to compare these measurements with sonoelastographic evaluations of the uteri in asymptomatic individuals. This will enable, for the first time, the demonstration of whether the elasticity of the myometrial tissue contributes to the etiology of primary dysmenorrhea.\n\nSecondary Objectives: To determine whether there is a correlation between the severity of primary dysmenorrhea and ultrasonographic markers.",[80],"Primary Dysmenorrhea",[82,83],"Dysmenorrhea","Sonoelastography","2024-09-19",{"date":86,"type":38},"2024-09-23",{"date":88,"type":21},"2024-09-20",{"date":90,"type":21},"2025-06-15",{"name":44,"class":45},""]