[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pelvic-floor-dysfunctions\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pelvic-floor-dysfunctions":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,48,83,115],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":31,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100638371","postpartum-exercise-intervention-100638371",false,"NCT07613333","Postpartum Exercise Intervention","Influence of a Supervised Postpartum Exercise Program on Maternal Physical Activity Levels and Musculoskeletal Health","Inclusion Criteria:\n\n* 18 years of age or older\n* gave birth in the 24 months prior to study enrollment\n\nExclusion Criteria:\n\n* less than 6 weeks postpartum or not medically appropriate to engage in exercise regardless of time since childbirth (will be screened using the Get Active Questionnaire for Postpartum)\n* prescription anti-inflammatory\u002Fpain medications that are taken daily;\n* significant orthopedic conditions that would contraindicate performance of the fatigue task and participation in the exercise intervention (such as fractures, severe scoliosis, etc)\n* moderate to severe cardiovascular \\&\u002For pulmonary disease that contraindicates participation in exercise\n* neuromuscular health conditions (such as diabetes, neuropathy, multiple sclerosis, stroke, seizures, etc);\n* smoking\u002Fvaping or use of other tobacco or nicotine products (chewing tobacco, nicotine patches, nicotine gum, etc.)\n* use of any illegal drugs","FEMALE","18 Years",{"count":19,"type":20},50,"ESTIMATED","INTERVENTIONAL",[23],"NA","The postpartum period is associated with decreases in physical activity levels, muscular strength, muscular endurance, and pelvic floor muscle function, but little scientific evidence exists on how best to initiate and progress exercise in the postpartum period. This proposal aims to improve habitual physical activity levels, neuromuscular health (i.e., strength, fatigability, symptom burden) and overall wellbeing (i.e., decreased fear of movement, improved sleep quality, improved perception of quality of life) through participation in a weekly exercise program. This study will help to inform postpartum exercise recommendations and is novel as it allows participants to incorporate their children into the exercise routine, thus removing a primary barrier to physical activity\u002Fexercise.",[26,27,28,29,30],"Postpartum","Neuromuscular Adaptations","Abdominal Muscles","Pelvic Floor Dysfunctions","Physical Activity",[32,33,34],"postpartum physical activity","postpartum neuromuscular function","postpartum exercise","RECRUITING","2026-05-21",{"date":38,"type":39},"2026-05-29","ACTUAL",{"date":41,"type":39},"2026-02-19",{"date":43,"type":20},"2028-08",{"name":45,"class":46},"Carroll University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":21,"phases":57,"briefSummary":58,"conditions":59,"keywords":62,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":4},"100607280","adapted-physical-activity-and-pelvic-floor-function-for-pelvic-girdle-pain-during-pregnancy-100607280","NCT07186504","Adapted Physical Activity and Pelvic Floor Function for Pelvic Girdle Pain During Pregnancy","Impact of Adapted Physical Activity Combined With Pelvic Floor Functionality on Pelvic Girdle Pain During Pregnancy: A Randomized Controlled Exploratory Trial","Inclusion Criteria:\n\n* Pregnant women aged ≥18 years\n* Gestational age ≤27 weeks at enrollment\n* Clinically confirmed pelvic girdle pain, defined as:\n* Pain localized between the posterior iliac crest and the gluteal fold, particularly around the sacroiliac joints and\u002For pubic symphysis, Pain intensity ≥3\u002F10 on Visual Analog Scale (VAS), At least 3 positive clinical tests among: Posterior Pelvic Pain Provocation (P4) test, Patrick's FABER, Menell's test, Active Straight Leg Raise (ASLR), and palpation of long dorsal sacroiliac ligament or symphysis pubis\n* Ability to understand and provide written informed consent\n\nExclusion Criteria:\n\n* Isolated low back pain without pelvic involvement\n* Contraindications to exercise during pregnancy (e.g., severe preeclampsia, placenta previa after 26 weeks, risk of preterm labor, ruptured membranes, significant cardiac or pulmonary disease)\n* Neurological, rheumatologic, or orthopedic conditions that may interfere with participation\n* Insufficient French language proficiency to understand questionnaires and instructions\n* Participation in another interventional study that could affect outcomes",{"count":56,"type":20},40,[23],"Pelvic girdle pain (PGP) is a common condition during pregnancy, affecting up to two-thirds of women. It can cause significant discomfort, limit daily activities, and reduce quality of life. Current treatment options are limited, and many women continue to experience pain throughout pregnancy and even after childbirth.\n\nThis study will evaluate whether a structured program of adapted physical activity, with additional individualized pelvic floor rehabilitation when needed, can reduce pelvic girdle pain and improve function during pregnancy. The intervention consists of weekly 60-minute sessions of adapted physical activity, led by a pelvic health physiotherapist, from inclusion until 36-38 weeks of gestation. The exercises focus on lumbopelvic stability, mobility, strengthening, and safe aerobic activity. If a participant presents with pelvic floor dysfunction, individualized rehabilitation may be added in parallel.\n\nParticipants will be randomly assigned to either the intervention group (adapted physical activity ± pelvic floor rehabilitation) or a control group. The control group will receive standard pregnancy follow-up care plus a validated flyer with international recommendations on physical activity during pregnancy but without supervised sessions.\n\nThe primary outcomes are pain intensity and functional impact of PGP, measured using the Visual Analog Scale (VAS) and the Pelvic Girdle Questionnaire (PGQ). Secondary outcomes include self-reported physical activity, pelvic symptoms, pelvic floor function, adherence to the intervention, and acceptability of the program.\n\nA total of 40 pregnant women will be enrolled at Hospital La Tour in Geneva, Switzerland. Assessments will take place at three time points: inclusion (≤27 weeks of gestation), late pregnancy (36-38 weeks), and 3 months after delivery.\n\nThe study is expected to provide new evidence on the benefits of integrating pelvic floor functionality into physical activity programs for pregnant women with PGP. If effective, this approach could inform clinical practice and improve care for women during pregnancy",[60,61,29],"Pelvic Girdle Pain","Pregnancy",[63,64,65,66,67,68,69,70,71,72],"Pregnancy-related pelvic girdle pain","Prenatal pelvic pain","Pelvic floor function","Pelvic floor rehabilitation","Adapted physical activity","Prenatal exercise","Physiotherapy in pregnancy","Prenatal musculoskeletal pain","Maternal health","Randomized controlled trial","NOT_YET_RECRUITING","2025-09-15",{"date":76,"type":39},"2025-09-22",{"date":78,"type":20},"2025-09-30",{"date":80,"type":20},"2027-10-31",{"name":82,"class":46},"Haute Ecole de Santé Vaud",{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":89,"eligibilityCriteria":90,"healthyVolunteers":11,"sex":91,"minAge":17,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":21,"phases":94,"briefSummary":95,"conditions":96,"keywords":97,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":47},"100577586","effectiveness-of-modern-physical-agents-in-the-treatment-of-pelvic-floor-dysfunctions-100577586","NCT06800222","Effectiveness of Modern Physical Agents in the Treatment of Pelvic Floor Dysfunctions","The Effectiveness of Modern Physical Agents in Treating Pelvic Floor Dysfunctions, Improving Functional State, Life Quality, and Biosocial Functions During First-stage Pelvic Rehabilitation.","EMPHAT-PFD","Inclusion Criteria:\n\n1. Patients older than 18 years old.\n2. One or more signs characteristic of pelvic floor dysfunctions are identified: elimination function disorders, pelvic organ prolapse, scar(s) (and lack of tissue mobility) in the perineum, pelvic floor muscle tone\u002Fstrength disorders (hypoactivity\u002Fhyperactivity), neuromuscular control disorders, sexual dysfunctions, pain in the pelvis, perineum.\n3. Not a single exclusion criterion has been established.\n4. Subjects capable of signing informed consent.\n\nExclusion Criteria:\n\n1. Oncological diseases or being actively investigated for oncological diseases.\n2. Any contraindications to methods of functional state examination or physical agents in the pelvic area that will be used in the study\n3. Individuals who refuse a detailed clinical examination of the perineum and pelvic floor muscles, functional testing, and\u002For functional ultrasound examination.\n4. Patients with urinary tract, prostate, genital, and other infections.\n5. Patients with inflammatory bowel diseases (ulcerative colitis, Crohn's disease, etc.).\n6. Persons for whom other health care professionals have already planned treatment of pelvic dysfunctions or other diseases during the expected participation period in the study that may interfere with participation in the study and\u002For significantly change the health status of the patient's pelvic floor.\n7. Pregnant or planning to become pregnant during the expected period of rehabilitation interventions.","ALL",{"count":93,"type":20},250,[23],"This clinical trial aims to determine whether adding modern physical agents (high-intensity laser therapy, magnetotherapy, radial shock wave therapy, kinesiotaping) in conjunction with classical rehabilitation interventions produces superior outcomes in treating pelvic floor dysfunction compared to classical rehabilitation interventions alone. It will also assess the safety of these agents in the context of pelvic floor dysfunction rehabilitation. The main questions it aims to answer are:\n\nDoes adding modern physical agents to the treatment of pelvic floor dysfunction improve symptoms, impairments in functional state, quality of life, and biosocial functions more effectively than classical interventions alone?\n\nParticipants who experience pelvic floor dysfunction during primary rehabilitation will receive:\n\nEither an individualized rehabilitation intervention plan comprising 20 classical procedures in combination with modern physical agents or classical interventions alone. Rehabilitation will take place in the outpatient rehabilitation department. Patients will visit the clinic for a comprehensive functional state assessment and then for individualized procedures; the entire plan will be delivered over three months, after which participants will return for follow-up checkups and assessments after the procedures and again after six months.",[29],[98,99,100,101,102,103,104,105],"pelvic floor dysfunctions","pelvic pain","urgency","incontinece","vaginismus","constipation","erectile dysfunction","irritable bladder","2025-01-24",{"date":108,"type":39},"2025-01-29",{"date":110,"type":20},"2025-03-01",{"date":112,"type":20},"2029-09-09",{"name":114,"class":46},"Lithuanian University of Health Sciences",{"id":116,"slug":117,"hasResults":11,"nctId":118,"briefTitle":119,"officialTitle":120,"acronym":4,"eligibilityCriteria":121,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":122,"targetDuration":4,"studyType":21,"phases":124,"briefSummary":125,"conditions":126,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":133,"locationsCount":47},"100252339","effect-of-brief-tele-support-on-attendance-at-physiotherapy-sessions-100252339","NCT02563600","Effect of Brief-tele Support on Attendance at Physiotherapy Sessions","Effect of Brief-tele Support on Attendance at Physiotherapy Sessions for Pelvic Floor Dysfunctions","Inclusion Criteria:\n\n* Women on waiting list for pelvic floor dysfunction\n* over 18 years old\n\nExclusion Criteria:",{"count":123,"type":20},500,[23],"Patients on the waiting list for physiotherapy treatment for pelvic floor dysfunction will be randomly divided into three groups:\n\n* a group that gets a telephone call before their invitation letter is sent.\n* a group that gets a telephone call after their invitation letter is sent.\n* a group that does not receive a telephone call.\n\nThe phone call is a brief 5-10 minute call, which will be semi-structured. It will remind the patient of their appointment time, it will outline what the treatment involves and highlight the potential benefits and drawbacks, and allow the patient to ask questions about the treatment.",[29],"2024-11-27",{"date":129,"type":39},"2024-12-02",{"date":131,"type":39},"2015-09-30",{"date":78,"type":20},{"name":134,"class":46},"Swansea University"]