[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Nurcan Gökgöz\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":48},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":33,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":5},"100595625","effects-of-mindfulness-based-self-efficacy-development-program-on-postmenopausal-women-100595625",false,"NCT07034885","Effects of Mindfulness-Based Self-Efficacy Development Program on Postmenopausal Women","Effects of Mindfulness-Based Self-Efficacy Development Program on Menopausal Symptoms and Quality of Life in Postmenopausal Women: A Randomized Controlled Trial","MOPKA","Inclusion Criteria:\n\nInclusion criteria:\n\n* Individuals who are in the +1a or +1b substage of early postmenopause according to the STRAW+10 system (at least 12 months and at most 24 months have passed since their last menstrual period)\n* Are proficient in reading and writing Turkish\n* Are in a spouse or partner\n* Have entered menopause naturally\n* Do not have a physical disability such as a severe musculoskeletal disorder, neurological disease, or mobility limitation that would prevent the use of mindfulness techniques (e.g., seated meditation, breathing exercises, gentle body awareness exercises)\n* Have not used MBSR techniques in the last six months\n* Own a smartphone or internet-enabled device.\n\nExclusion Criteria:\n\n* Those who completed the pretest data collection forms incompletely,\n* Those who had any psychological disorder or experienced a traumatic event in the last two to one years,\n* Those who received hormone replacement therapy during menopause,\n* Those who had any gynecological cancer","FEMALE","45 Years","57 Years",{"count":21,"type":22},70,"ESTIMATED","INTERVENTIONAL",[25],"NA","The aim of this randomized controlled clinical trial is to evaluate the effects of a mindfulness-based self-efficacy development program on menopausal symptoms and quality of life in postmenopausal women. The main questions it aims to answer are:\n\nDoes the mindfulness-based program reduce the severity of menopausal symptoms?\n\nDoes the mindfulness-based program improve the quality of life of postmenopausal women?\n\nDoes the mindfulness-based program significantly increase participants' overall self-efficacy?\n\nThe researchers will compare whether there are differences between the mindfulness-based training program applied to the intervention group and the control group in terms of menopausal symptoms, quality of life, and self-efficacy scores.\n\nThe main tasks that will be asked of the participants are as follows:\n\nThose in the intervention group will participate in a face-to-face mindfulness-based self-efficacy development program, each session lasting at least 120 minutes, once a week for 8 weeks, with a maximum of 10 people per group.\n\nThe control group will not receive any intervention.\n\nParticipants in both groups will be evaluated with a personal information form and measurement tools such as the Menopause Symptoms Assessment Scale, the Menopause Specific Quality of Life Scale, and the General Self-efficacy Scale.",[28,29,30,31,32],"Postmenopausal Period","Menopausal Symptoms","Quality of Life","Stress Management","Self-Efficacy",[34,32,30,35],"Menopause","Mindfulness","NOT_YET_RECRUITING","2025-07-17",{"date":39,"type":40},"2025-07-22","ACTUAL",{"date":42,"type":22},"2025-09-15",{"date":44,"type":22},"2026-02-28",{"name":46,"class":47},"Nurcan Gökgöz","OTHER_GOV",""]