[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100649222":3},{"organization":4,"armGroups":7,"interventions":30,"overallOfficials":35,"centralContacts":35,"locations":48,"responsibleParty":68,"collaborators":35,"id":72,"slug":73,"hasResults":74,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":35,"eligibilityCriteria":78,"healthyVolunteers":74,"sex":79,"minAge":80,"maxAge":81,"enrollmentInfo":82,"targetDuration":35,"studyType":85,"phases":86,"briefSummary":88,"conditions":89,"keywords":91,"overallStatus":51,"whyStopped":35,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":106},{"fullName":5,"class":6},"Istanbul Medipol University Hospital","OTHER",[8,15,20,25],{"label":9,"type":10,"description":11,"interventionNames":12},"Vibration Therapy Group","EXPERIMENTAL","Participants will receive standardized education on primary dysmenorrhea and vibration therapy using a vibrating massage ball applied to the abdominal and lumbosacral regions. The intervention will be administered twice weekly for 12 weeks, covering three menstrual cycles.",[13,14],"Device: Vibration Therapy Group","Other: Education",{"label":16,"type":10,"description":17,"interventionNames":18},"Abdominal Massage Group","Participants will receive standardized education on primary dysmenorrhea and abdominal massage applied to the lower abdominal and suprapubic regions using standardized massage techniques. The intervention will be administered twice weekly for 12 weeks, covering three menstrual cycles.",[19,14],"Other: Abdominal Massage",{"label":21,"type":10,"description":22,"interventionNames":23},"Myofascial Release Group","Participants will receive standardized education on primary dysmenorrhea and myofascial release applied to the abdominal, lumbopelvic, and sacral regions. The intervention will be administered twice weekly for 12 weeks, covering three menstrual cycles.",[24,14],"Other: Myofascial Release",{"label":26,"type":27,"description":28,"interventionNames":29},"Education Control Group","ACTIVE_COMPARATOR","Participants will receive standardized education on primary dysmenorrhea and menstrual pain management, including information about daily activities and non-pharmacological approaches. No additional vibration-based or manual treatment will be administered during the 12-week study period.",[14],[31,36,40,44],{"type":32,"name":9,"description":33,"armGroupLabels":34,"otherNames":35},"DEVICE","Vibration will be applied to the abdominal and lumbar-sacral regions. This treatment will be performed twice a week for 12 weeks.",[9],null,{"type":6,"name":37,"description":38,"armGroupLabels":39,"otherNames":35},"Abdominal Massage","A standardized abdominal massage protocol will be applied manually to the lower abdominal and suprapubic regions. The intervention will be delivered twice weekly for 12 weeks.",[16],{"type":6,"name":41,"description":42,"armGroupLabels":43,"otherNames":35},"Myofascial Release","Manual myofascial release techniques will be applied to the abdominal, lumbopelvic, and sacral regions using a standardized treatment protocol. The intervention will be delivered twice weekly for 12 weeks.",[21],{"type":6,"name":45,"description":46,"armGroupLabels":47,"otherNames":35},"Education","Standardized education will include information about menstrual pain management, considerations during daily activities, and general non-pharmacological approaches. The same education will be provided to participants in all four study arms.",[16,26,21,9],[49],{"facility":50,"status":51,"city":52,"state":52,"zip":53,"country":54,"countryCode":35,"cosmosGeoPoint":55,"geoPoint":60,"contacts":61},"Istanbul Medipol University","RECRUITING","Istanbul","34815","Turkey (Türkiye)",{"type":56,"coordinates":57},"Point",[58,59],28.94966,41.01384,{"lat":59,"lon":58},[62],{"name":63,"role":64,"phone":65,"phoneExt":66,"email":67},"Gizem Boztaş Elverişli","CONTACT","05439076494","90 5439076494","gboztas@medipol.edu.tr",{"type":69,"investigatorFullName":70,"investigatorTitle":71,"investigatorAffiliation":5,"oldNameTitle":35,"oldOrganization":35},"PRINCIPAL_INVESTIGATOR","gizem boztas","Assistant professor","100649222","vibration-massage-and-myofascial-release-in-primary-dysmenorrhea-100649222",false,"NCT07731243","Vibration, Massage, and Myofascial Release in Primary Dysmenorrhea","Comparison of Vibration Therapy, Classical Abdominal Massage, and Myofascial Release Applications in Primary Dysmenorrhea","* Inclusion Criteria:\n* Female participants aged 18 to 30 years.\n* Having regular menstrual cycles during the previous 6 months.\n* Having a diagnosis consistent with primary dysmenorrhea following evaluation by an obstetrician and gynecologist.\n* Experiencing menstrual pain in at least 2 of the previous 3 menstrual cycles.\n* Having menstrual pain intensity of 4 or higher on a 0-10 Visual Analog Scale.\n* Voluntarily agreeing to participate in the study and providing written informed consent.\n\nExclusion Criteria:\n\n* Secondary dysmenorrhea.\n* Diagnosis of endometriosis, uterine fibroids, ovarian cysts, or pelvic inflammatory disease.\n* History of gynecological surgery.\n* Pregnancy or suspected pregnancy.\n* Having given birth within the previous 6 months.\n* Recent initiation of hormonal treatment.\n* Chronic pelvic pain or a neurological, rheumatological, or systemic inflammatory disease.\n* Having received manual therapy or physiotherapy targeting the abdominal or lumbopelvic region within the previous 3 months.\n* Skin lesions, infection, open wounds, or other dermatological conditions in the treatment regions.\n* Any clinical condition considered a contraindication to vibration therapy.\n* Inability to comply with the study protocol -","FEMALE","18 Years","30 Years",{"count":83,"type":84},96,"ESTIMATED","INTERVENTIONAL",[87],"NA","This randomized, assessor-blinded, four-arm, parallel-group controlled trial aims to compare the effects of vibration therapy, abdominal massage, and myofascial release with an education-only control intervention in women with primary dysmenorrhea. Seventy-two women aged 18 to 30 years will be randomized in a 1:1:1:1 ratio. All participants will receive standard education about primary dysmenorrhea. The three intervention groups will additionally receive their assigned treatment twice weekly for 12 weeks, covering three menstrual cycles. Menstrual pain, pain characteristics, pressure pain threshold, menstrual symptoms, and symptoms associated with central sensitization will be evaluated at baseline and after the intervention by a blinded assessor.",[90],"Dysmenorrhea Primary",[92,93,94,95,96],"Primary dysmenorrhea","menstrual pain","vibration therapy","abdominal massage","myofascial release","2026-07-23",{"date":99,"type":100},"2026-07-28","ACTUAL",{"date":102,"type":100},"2026-07-14",{"date":104,"type":84},"2026-11-15",{"name":5,"class":6},1]