[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100550339":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":18,"locations":18,"responsibleParty":25,"collaborators":18,"id":29,"slug":18,"hasResults":30,"nctId":31,"briefTitle":32,"officialTitle":33,"acronym":18,"eligibilityCriteria":34,"healthyVolunteers":30,"sex":35,"minAge":36,"maxAge":37,"enrollmentInfo":38,"targetDuration":18,"studyType":41,"phases":42,"briefSummary":44,"conditions":45,"keywords":47,"overallStatus":49,"whyStopped":18,"lastUpdateSubmitDate":50,"lastUpdatePostDateStruct":51,"startDateStruct":54,"completionDateStruct":56,"leadSponsor":58,"locationsCount":18},{"fullName":5,"class":6},"Islamia University of Bahawalpur","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Group A","EXPERIMENTAL","It will receive 12 sessions of Cognitive Behavior Therapy for Chronic Pelvic Pain.",[13],"Behavioral: Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp",{"label":15,"type":16,"description":17,"interventionNames":18},"Group B","NO_INTERVENTION","Group B will be control group.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"BEHAVIORAL","Cognitive Behavior Therapy for Chronic Pelvic Pain-CBT-cp","CBT-cp will be administered weekly sessions for 12 weeks.",[9],{"type":26,"investigatorFullName":27,"investigatorTitle":28,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Bushra Akram","PhD Scholar","100550339",false,"NCT06445790","Efficacy of Cognitive Behavior Therapy in the Treatment of Chronic Pelvic Pain in Women","Efficacy of Cognitive Behavior Therapy in the Treatment of Chronic Pelvic Pain in Women: A Randomized Controlled Trial","Inclusion Criteria:\n\n1. Women of reproductive age.\n2. Women with Chronic Pelvic Pain having no pathological or anatomical causes.\n3. Women with Overactive Bladder Syndrome.\n4. Women with Vulvodynia. -\n\nExclusion Criteria:\n\n1. Women experiencing perimenopause or menopause.\n2. Women with medical, or gynecological or hormonal abnormalities.\n3. Women with mental disorders.\n4. Women who use substances. -","FEMALE","18 Years","45 Years",{"count":39,"type":40},60,"ESTIMATED","INTERVENTIONAL",[43],"NA","This will be the pilot study trial. The target population will be 30 individuals with Chronic Pelvic Pain (CCP). There will be 02 groups, Experimental Group and Control Group. The primary outcome measure will be Impact of Female Chronic Pelvic Pain Questionnaire (IF-CPPQ). The experimental group will receive CBT spread over 12 sessions.",[46],"Chronic Pelvic Pain Syndrome",[48],"Chronic Pelvic Pain, Pelvic Pain, Women","NOT_YET_RECRUITING","2024-06-05",{"date":52,"type":53},"2024-06-06","ACTUAL",{"date":55,"type":40},"2024-06-20",{"date":57,"type":40},"2024-10-20",{"name":5,"class":6}]