[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"mindfulness-compassionate-living-training\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:mindfulness-compassionate-living-training":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100649027","menopause-and-compassionate-living-education-100649027",false,"NCT07728461","Menopause and Compassionate Living Education","The Effect of Compassionate Living Education on Symptom Management and Quality of Life in Menopausal Women: A Randomized Controlled Study","Inclusion Criteria:\n\n* Women who are in the menopausal period.\n* Aged 45 years or older.\n* Registered at the participating primary healthcare center.\n* Able to read and understand Turkish.\n* At least a primary school graduate.\n* Willing to participate and provide written informed consent.\n* Able to attend the online Compassionate Living Education sessions.\n* Able to complete the study questionnaires.\n\nExclusion Criteria:\n\n* Failure to complete the study questionnaires.\n* Failure to attend the Compassionate Living Education sessions.\n* Withdrawal of informed consent at any stage of the study.\n* Inability to complete the post-intervention assessment.","FEMALE",{"count":18,"type":19},68,"ESTIMATED","INTERVENTIONAL",[22],"NA","Menopause is a natural stage in a woman's life characterized by the permanent cessation of ovarian function and is frequently accompanied by vasomotor, psychological, urogenital, and sleep-related symptoms that can substantially impair quality of life. Although pharmacological treatments are available, many women seek non-pharmacological interventions to manage menopausal symptoms and improve their overall well-being. Mindfulness- and compassion-based interventions have shown promising effects on psychological health, stress reduction, and quality of life in different populations; however, evidence regarding the effectiveness of Mindfulness-Based Compassionate Living (MBCL) for women experiencing menopause remains limited.\n\nThis randomized controlled trial aims to evaluate the effectiveness of a Compassionate Living Education Program based on the principles of Mindfulness-Based Compassionate Living in improving symptom management and quality of life among menopausal women. The study will be conducted with menopausal women recruited from primary healthcare settings in Kars, Türkiye. Participants who meet the eligibility criteria will be randomly assigned to either an intervention group or a control group.\n\nParticipants in the intervention group will receive an eight-session online Compassionate Living Education Program delivered by a certified instructor. The program includes mindfulness practices, self-compassion exercises, breathing and relaxation techniques, compassionate imagery, loving-kindness meditation, and home practice assignments designed to strengthen emotional regulation, self-kindness, and adaptive coping skills. The control group will receive routine care only.\n\nPrimary outcomes will include menopausal symptom severity and menopause-specific quality of life. Secondary outcomes will include self-compassion, mindfulness, anxiety, depression, and stress. Data will be collected using validated self-report questionnaires before and after the intervention and analyzed using appropriate statistical methods.\n\nThe findings of this study are expected to provide evidence regarding the effectiveness of Compassionate Living Education as an accessible, low-cost, non-pharmacological intervention for improving symptom management and enhancing the quality of life of menopausal women. The results may contribute to the development of evidence-based nursing and women's health interventions in primary healthcare settings.",[25],"Mindfulness Compassionate Living Training",[27,28,29,30,31],"mindfulness","self-compassion","Quality of life","Menopause","Women","NOT_YET_RECRUITING","2026-07-22",{"date":35,"type":36},"2026-07-27","ACTUAL",{"date":38,"type":19},"2026-09-30",{"date":40,"type":19},"2027-01-30",{"name":42,"class":43},"Ataturk University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":20,"phases":55,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":4},"100627652","the-effect-of-mindfulness-compassionate-living-training-on-unwanted-pregnancies-100627652","NCT07451418","The Effect of Mindfulness Compassionate Living Training on Unwanted Pregnancies","The Effect of Mindfulness Compassionate Living Training on Depression, Anxiety, Stress, Self-compassion, and Acceptance Levels in Pregnant Women With Unwanted Pregnancies: A Randomized Controlled Trial.","Inclusion Criteria:\n\n* The pregnancy must be unwanted or unplanned,\n* The pregnancy must be between the ages of 18 and 45,\n* The pregnancy must involve having at least one child,\n* The pregnancy must involve having a smartphone and internet access,\n* The pregnancy must not involve any other significant illnesses.\n\nExclusion Criteria:\n\n* Having a diagnosis of a mental disorder,\n* Having any obstacle that would impair communication,\n* Being the first pregnancy,\n* Being a desired pregnancy,\n* Having a significant chronic illness (the presence of another disease that could pose a risk to pregnancy)","18 Years","45 Years",{"count":18,"type":19},[22],"This study will be conducted as a single-blind, randomized controlled trial with pregnant women who do not want or plan a pregnancy and do not intend to terminate it, and who apply for pregnancy examination at the Obstetrics and Gynecology outpatient clinic of a training and research hospital in Turkey. Data will be collected at the Obstetrics and Gynecology outpatient clinic of the Training and Research Hospital in Ağrı between March 2026 and June 2026. The study population will consist of pregnant women aged 18 to 45 who apply to the Obstetrics and Gynecology outpatient clinic during the specified period, and who have an unwanted or unplanned pregnancy. The sample size was calculated using the GPower computer program. Using power analysis at the α=0.05 level, the effect size was calculated as 150, 153 (d=0.8) and the study power as 90%, indicating that at least 68 pregnant women should be included in the sample. Pregnant women who meet the research criteria and agree to participate in the study will be randomly assigned to an experimental group and a control group. The study will use a pregnancy profile form prepared by the researcher in accordance with the literature, containing socio-demographic data of pregnant women who applied to the Obstetrics and Gynecology outpatient clinic; the Self-Acceptance Scale for Pregnant Women (SAPS) to determine the pregnant woman's level of self-acceptance; the Depression, Anxiety, and Stress Scale (DASS-21) to evaluate the symptoms of depression, anxiety, and stress; and the Self-Compassion Scale Short Form (SCI-S) to evaluate self-compassion.",[25],[27,28,59,60,61,62,63,64],"acceptance","depression","anxiety","stress","pregnancy","psychoeducation","2026-02-28",{"date":67,"type":36},"2026-03-05",{"date":69,"type":19},"2026-03-15",{"date":71,"type":19},"2026-08-15",{"name":42,"class":43}]