[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Western University of Health Sciences\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":77},{"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":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100658329","impact-of-omt-on-the-symptoms-of-dysmenorrhea-100658329",false,"NCT07849140","Impact of OMT on the Symptoms of Dysmenorrhea","Assessing the Impact of Osteopathic Manipulative Treatment on Dysmenorrhea","Inclusion Criteria:\n\n* Female Western University of Health Sciences students, faculty, or staff who experience dysmenorrhea symptoms.\n\nExclusion Criteria:\n\n* Individuals who are pregnant or breastfeeding.\n* Individuals under the age of 20 and over the age of 51.\n* Individuals with a history of endometriosis or PCOS.\n* Individuals with a history of thyroid conditions.\n* Individuals who change or plan ot change birth control during the course of the study.\n* Individuals receiving outside OMT or physical therapy treatment.","FEMALE","20 Years","51 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","This pilot study will span two months per participant and include a baseline evaluation, a control period, the treatment itself, and an after-treatment evaluation. After getting informed consent, participants will be asked to fill out surveys about their menstrual cycles and health histories, including pain levels, timing, and the types and length of symptoms they may have. Participants will then go through a month control period where they will have their cycle without any osteopathic manipulative treatment (OMT) being given, followed by a standard osteopathic exam. They will be asked to fill out all surveys again at this time. They will then go through OMT 3-7 days before their next period. After their second cycle, they will complete a final survey. Participants' pain and symptoms will be assessed at each time point by comparing survey responses and checking for improvement. The goal of this study is to see whether osteopathic manipulative treatment reduces pain and eases symptoms, and whether this approach is practical for future studies.",[27],"Dysmenorrhea",[29,27,30,31],"OMT","Osteopathic Manipulative Treatment","Osteopathic Manipulative Medicine","RECRUITING","2026-09-23",{"date":35,"type":36},"2026-09-30","ACTUAL",{"date":38,"type":36},"2026-04-30",{"date":40,"type":21},"2027-12-31",{"name":42,"class":43},"Western University of Health Sciences","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":54,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":44},"100626776","the-cervical-stretch-study-100626776","NCT07440030","The Cervical \"STRETCH\" Study","The Cervical \"STRETCH\" (Stretching Trials for Range, Ease, and Teaching Curriculum Health) Study","STRETCH","Inclusion Criteria:\n\n* Must be currently enrolled OMSI or OMSII student at the Western University of Health Sciences (WUHS), College of Osteopathic Medicine of the Pacific (COMP).\n* Demonstrates a range of motion restriction or presents with cervical pain or both. (Normal range of motion in the cervical spine is Flexion and Extension of 60 degrees, Sidebending of 45 degrees, and Rotation of 8090 degrees.)\n* Reports mild to moderate cervical pain (VAS score between 2 and 5 or mild to moderate).\n* Agrees to complete daily cervical stretching exercises as instructed and will adhere to all study protocols.\n* Must be 18 years or older.\n\nExclusion Criteria:\n\n* History of severe cervical spine injuries (e.g., fractures, herniated discs requiring surgical intervention, cervical radiculopathy, or myelopathy).\n* Diagnosed inflammatory or degenerative conditions (e.g., rheumatoid arthritis, ankylosing spondylitis).\n* Contraindications to stretching exercises, such as recent surgery or other physical therapy restrictions.\n* Conditions that affect neuromuscular function or ROM measurements, such as multiple sclerosis or muscular dystrophy.\n* VAS score \\> 7 or pain severe enough to inhibit participation in daily stretching exercises.\n* Below the age of 18",true,"ALL","18 Years",{"count":57,"type":21},75,[24],"Neck pain and reduced cervical range of motion (ROM) are common musculoskeletal concerns that can significantly impact an individual's quality of life and daily routine. This is especially true for medical students who spend a disproportionate amount of time on their computers or mobile devices, as is required by their long study hours. A simple stretching routine is often recommended by physicians and physical therapists alike, but there is little research examining short-term changes in cervical range of motion (ROM) and pain when a brief, structured daily stretching program is used.\n\nThe goal of this single-group study is to test feasibility and determine how well a daily cervical stretching regimen affects cervical ROM and self-reported pain in osteopathic medical students with cervical ROM restrictions. Researchers will measure changes in cervical ROM using a goniometer and changes in pain levels via the Visual Analog Scale (VAS).\n\nParticipants will be asked to complete a 7-day period of no stretching, during which natural measurements will be taken, followed by 7 days of completing the 5-minute stretching routine, after which more measurements will be taken. Participants will also be asked to complete a post-study survey and a 1-month follow-up survey to provide feedback on the study and the stretching routine.",[61],"Cervical Spine",[63,64,65,66,67],"cervical spine","stretching","flexion","extension","cervical restrictions","NOT_YET_RECRUITING","2026-02-23",{"date":71,"type":36},"2026-02-27",{"date":73,"type":21},"2026-03-10",{"date":75,"type":21},"2026-08-30",{"name":42,"class":43},""]