[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Wroclaw University of Health and Sport Sciences\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":307},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,51,76,107,136,167,197,225,258,283],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100616577","assessment-of-respiratory-dysfunction-in-obesity-and-the-use-of-imt-100616577",false,"NCT07307417","Assessment of Respiratory Dysfunction in Obesity and the Use of IMT.","Functional Respiratory Tract Dysfunctions in Individuals With Obesity Undergoing Experimental Inspiratory Muscle Training.","IMT","Inclusion Criteria:\n\n* diagnosed obesity, BMI equal to or greater than 30 kg\u002Fm2\n* age between 30 and 60 (women and men),\n* consent of the subject.\n\nExclusion Criteria:\n\n* respiratory diseases requiring pharmacological treatment,\n* acute illness that may affect the training programme: e.g. infection, renal failure,\n* mental impairment preventing cooperation,\n* mental disorders preventing contact and cooperation with the patient,\n* pacemaker,\n* pregnancy\n* implanted electronic\n* medical implants\n* epilepsy\n* metal implants.","ALL","30 Years","60 Years",{"count":21,"type":22},40,"ESTIMATED","INTERVENTIONAL",[25],"NA","The aim of the project will be to assess the functional condition of the respiratory tract and inflammation resulting from obesity, as well as the possibility of using inspiratory muscle training as a factor reducing the occurrence of dysfunction in the respiratory system.",[28,29,30],"Obesity & Overweight","Inflammation","Ventilation Disorders",[32,33,34,35,36,37],"inspiratory muscle training","obesity","ventilation disorders","inflammation","forced oscillation technique","spirometry","RECRUITING","2026-04-12",{"date":41,"type":42},"2026-04-14","ACTUAL",{"date":44,"type":42},"2025-03-25",{"date":46,"type":22},"2026-11",{"name":48,"class":49},"Wroclaw University of Health and Sport Sciences","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":23,"phases":61,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":50},"100600246","massage-therapy-for-healthcare-staff-100600246","NCT07094997","Massage Therapy for Healthcare Staff","Effectiveness of Massage Therapy Among Healthcare Workers Suffering From Low Back Pain - a Randomized Controlled Trial","Inclusion Criteria:\n\n* Adult healthcare workers\n* Aged 30-65 years with chronic nonspecific low back pain for ≥3 months\n* No medical contraindications to massage therapy\n* Body mass index (BMI) between 18.5 and 25 kg\u002Fm²\n* Provided written informed consent\n\nExclusion Criteria:\n\n* Massage therapy within the past 3 months\n* Contraindications to massage therapy\n* Ongoing physical therapy\n* Significant medical or psychiatric conditions","65 Years",{"count":60,"type":22},60,[25],"The piriformis muscle can be a contributing factor to low back pain (LBP) due to its anatomical proximity to the sciatic nerve and sacroiliac joint. When the piriformis becomes tight or irritated, it may compress or irritate the sciatic nerve-a condition often referred to as piriformis syndrome-leading to pain that radiates from the lower back to the buttock and down the leg.\n\nThe goal of this clinical trial is to examine the effectiveness of massage therapy in counteracting symptoms of low back pain (LBP) among healthcare workers. The main question it aims to answer is:\n\n\\- Can massage of the piriformis muscle and related musculature effectively reduce symptoms in individuals experiencing LBP linked to myofascial or neuromuscular dysfunction?\n\nMassage therapy targeting the piriformis and associated muscles (e.g., gluteus maximus, medius, and deep hip rotators) can help by:\n\n* Reducing muscle tension and spasms,\n* Improving local blood circulation,\n* Alleviating pressure on the sciatic nerve,\n* Restoring hip mobility and muscle balance.",[64],"Low Back Pain",[66,67],"Randomiezed controlled trial","Massage therapy","2026-02-22",{"date":70,"type":42},"2026-02-24",{"date":72,"type":42},"2025-07-31",{"date":74,"type":22},"2026-03",{"name":48,"class":49},{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":83,"maxAge":84,"enrollmentInfo":85,"targetDuration":4,"studyType":23,"phases":87,"briefSummary":88,"conditions":89,"keywords":92,"overallStatus":97,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":106},"100625351","spinal-mobility-in-children-with-cerebral-palsy-ndt-bobath-and-exergaming-100625351","NCT07421505","Spinal Mobility in Children With Cerebral Palsy: NDT-Bobath and Exergaming","Spinal Mobility in Children With Cerebral Palsy Undergoing NDT-Bobath Therapy and Exergaming-based Therapy","Inclusion Criteria:\n\n* Written informed consent from parents\u002Fguardians and the child (if capable)\n* GMFCS levels I-III (mild to moderate motor limitations)\n* Ability to maintain standing position\n* Ability to follow instructions and perform exercises\n* No prior exergaming therapy\n* No implanted electronic devices\n* No acute infections or inflammatory conditions\n* No metabolic disorders affecting bioimpedance measurements\n\nExclusion Criteria:\n\n* GMFCS levels IV-V\n* Orthopedic surgery within the past 12 months\n* Seizure episodes within the past 6 months\n* Cognitive or behavioral impairments preventing cooperation\n* Severe spinal deformities (scoliosis \\>40° or other significant changes)\n* Attendance at therapy sessions \\\u003C85%","6 Years","18 Years",{"count":86,"type":22},42,[25],"The purpose of this study is to evaluate changes in spinal mobility in the cervical, thoracic, and lumbar regions in children with cerebral palsy aged 10-15 years. The study will compare outcomes between standard NDT-Bobath therapy supplemented with exergaming in a sitting position and exergaming in a standing position. Postural stability, body composition, and functional parameters will also be assessed.\n\nParticipants will complete a socio-medical questionnaire and undergo baseline measurements of spinal mobility, cervical range of motion, postural stability (using Podoscan and Zebris platform), body height, and body composition (using SECA stadiometer and Tanita bioimpedance analyzer).\n\nThe intervention will last 3 months and include twice-weekly 60-minute therapy sessions. Group I will receive NDT-Bobath therapy supplemented with exergaming in a sitting position, while Group II will receive NDT-Bobath therapy with exergaming in a standing position.\n\nAfter the intervention, participants will undergo post-intervention measurements and a follow-up evaluation three months later to assess the persistence of any changes.",[90,91],"Spastic Diplegia Cerebral Palsy","Spastic Hemiplegia",[93,94,95,96],"Cerebral palsy","Spinal mobility","NDT-Bobath therapy","Exergaming","NOT_YET_RECRUITING","2026-02-16",{"date":100,"type":42},"2026-02-19",{"date":102,"type":22},"2026-02",{"date":104,"type":22},"2026-06",{"name":48,"class":49},2,{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":4,"eligibilityCriteria":113,"healthyVolunteers":11,"sex":17,"minAge":114,"maxAge":115,"enrollmentInfo":116,"targetDuration":4,"studyType":23,"phases":118,"briefSummary":119,"conditions":120,"keywords":122,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":106},"100606582","inspiratory-muscle-training-in-children-and-adolescents-with-idiopathic-scoliosis-undergoing-schroth-therapy-100606582","NCT07177430","Inspiratory Muscle Training in Children and Adolescents With Idiopathic Scoliosis Undergoing Schroth Therapy.","The Effect of Inspiratory Muscle Training on Respiratory Function, Exercise Tolerance and Core Stability in Children and Adolescents With Idiopathic Scoliosis Undergoing Schroth Therapy.","Inclusion Criteria:\n\n* diagnosed idiopathic scoliosis,\n* age: 11-16 years (girls after their first period, boys after voice mutation),\n* spinal curvature angle \\> 20° according to Cobb,\n* guardian's consent to participate in the study;\n\nExclusion Criteria:\n\n* chronic respiratory diseases,\n* inhalant allergies,\n* limited contact with the patient, preventing the examination from being performed;","11 Years","16 Years",{"count":117,"type":22},56,[25],"This study evaluates the effectiveness of inspiratory muscle training in children and adolescents with idiopathic scoliosis undergoing therapy with the Schroth method.\n\nThe intervention- inspiratory muscle training- aims to improve respiratory function, increase exercise tolerance, and strengthen core stability in the participants.\n\nThe proposed training may enhance the effectiveness of therapy conducted using the Schroth method and improve participants' performance in activities of daily living.\n\nThe project aims to assess the impact of inspiratory muscle training in children and adolescents with idiopathic scoliosis on respiratory system function, exercise tolerance, and core stability.",[121],"Scoliosis Idiopathic",[123,124,125,126,127],"Inspiratory Muscle Training","Schroth method","Exercise tolerance","Core stability","Respiratory function","2025-11-30",{"date":130,"type":42},"2025-12-05",{"date":132,"type":42},"2025-10-13",{"date":134,"type":22},"2027-07",{"name":48,"class":49},{"id":137,"slug":138,"hasResults":11,"nctId":139,"briefTitle":140,"officialTitle":141,"acronym":4,"eligibilityCriteria":142,"healthyVolunteers":11,"sex":17,"minAge":143,"maxAge":144,"enrollmentInfo":145,"targetDuration":147,"studyType":148,"phases":4,"briefSummary":149,"conditions":150,"keywords":153,"overallStatus":97,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":160,"startDateStruct":162,"completionDateStruct":164,"leadSponsor":166,"locationsCount":4},"100608420","effects-of-corrective-helmet-therapy-on-cervical-motion-and-thermoregulation-in-children-with-positional-deformities-100608420","NCT07201324","Effects of Corrective Helmet Therapy on Cervical Motion and Thermoregulation in Children With Positional Deformities","Analysis of the Relationships Between Cranial Remolding Orthosis Therapy, Cervical Spine Motor Function, and Thermoregulatory Responses in Children With Cranial Deformity","Inclusion Criteria:\n\n* positional head deformity of severe or very severe degree;\n* age at therapy initiation: 4-12 months;\n* minimum therapy duration of 12 weeks (for Stage 1 and Stage 2).\n\nExclusion Criteria:\n\n* craniosynostosis;\n* hydrocephalus;\n* non-adherence to 23-hour daily helmet use;\n* metabolic disorders;\n* torticollis.","4 Months","12 Months",{"count":146,"type":22},270,"6 Months","OBSERVATIONAL","The purpose of the study is to examine how cranial helmet therapy may affect neck movement and body temperature regulation in children with positional head deformity. The study will also look at factors that might influence how well the therapy works, such as the child's age, sex, and the type of head shape deformity.\n\nDuring the study, children will undergo several assessments:\n\nmeasurement of head shape using standard cranial indices, recording of body surface temperature with a thermal imaging camera, evaluation of neck mobility, focusing on rotation of the cervical spine.",[151,152],"Plagiocephaly, Nonsynostotic","Brachycephaly",[154,155,156,157,158],"positional head deformity","helmet therapy","infants","thermoregulation","range of motion of the cervical spine","2025-09-23",{"date":161,"type":42},"2025-10-01",{"date":163,"type":22},"2025-09",{"date":165,"type":22},"2027-05",{"name":48,"class":49},{"id":168,"slug":169,"hasResults":11,"nctId":170,"briefTitle":171,"officialTitle":172,"acronym":4,"eligibilityCriteria":173,"healthyVolunteers":11,"sex":174,"minAge":175,"maxAge":176,"enrollmentInfo":177,"targetDuration":4,"studyType":23,"phases":178,"briefSummary":179,"conditions":180,"keywords":183,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":189,"lastUpdatePostDateStruct":190,"startDateStruct":192,"completionDateStruct":194,"leadSponsor":196,"locationsCount":50},"100598328","virtual-reality-for-urinary-incontinence-in-women-100598328","NCT07070063","Virtual Reality for Urinary Incontinence in Women","Use of Virtual Reality in the Treatment of Various Types of Urinary Incontinence in Women","Inclusion Criteria:\n\n* Women aged 50-80 years, who are at least 12 months post-menopausal,\n* Diagnosed with urinary incontinence of grade I or IIa according to the ICS classification,\n* No contraindications to participation (e.g., acute urinary tract infections, severe neurological disorders),\n* Provision of written informed consent to participate in the research experiment.\n\nExclusion Criteria:\n\n* Urinary incontinence of grade III or higher,\n* Presence of significant neurological conditions affecting bladder control,\n* Participation in other therapeutic interventions that could interfere with study outcomes,\n* Pregnancy,\n* Refusal or inability to provide informed consent.","FEMALE","50 Years","80 Years",{"count":21,"type":22},[25],"This study evaluates the effectiveness of using virtual reality to support pelvic floor muscle training in women with urinary incontinence. The intervention aims to enhance patients' motivation, awareness, and exercise accuracy through real-time muscle visualization and immersive interaction. The project seeks to determine whether virtual reality-assisted therapy improves clinical outcomes compared to conventional approaches.",[181,182],"Urinary Incontinence","Pelvic Floor Disorder",[184,185,186,187,188],"Virtual Reality","Rehabilitation","Pelvic Floor Muscle Training","Urinary incontinence","Women's health","2025-07-22",{"date":191,"type":42},"2025-07-24",{"date":193,"type":42},"2025-07-15",{"date":195,"type":22},"2027-06-15",{"name":48,"class":49},{"id":198,"slug":199,"hasResults":11,"nctId":200,"briefTitle":201,"officialTitle":202,"acronym":4,"eligibilityCriteria":203,"healthyVolunteers":11,"sex":17,"minAge":19,"maxAge":204,"enrollmentInfo":205,"targetDuration":4,"studyType":23,"phases":206,"briefSummary":207,"conditions":208,"keywords":211,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":217,"lastUpdatePostDateStruct":218,"startDateStruct":220,"completionDateStruct":222,"leadSponsor":224,"locationsCount":50},"100596086","antigravity-treadmill-after-joint-arthroplasty-100596086","NCT07040878","Antigravity Treadmill After Joint Arthroplasty","Antigravity Treadmill Rehabilitation After Lower Limb Arthroplasty in Older Adults","Inclusion Criteria:\n\n* individuals who have recently undergone hip or knee joint arthroplasty surgeries aged 60 years and above.\n\nExclusion Criteria:\n\n* cognitive impairments that prevent independent completion of research questionnaires\n* history of consciousness disturbances, psychotic disorders, bipolar disorder, or other severe psychiatric illnesses\n* functional status preventing independent ambulation (wheelchair-bound or bedridden patients; orthopedic devices such as crutches or walker allowed)\n* refusal to participate in the study at any stage","75 Years",{"count":60,"type":22},[25],"The study aims to evaluate the efficacy of antigravity treadmill training and body weight-supported treadmill training in the rehabilitation of elderly patients (60-75 years) following hip or knee arthroplasty.",[209,210],"Arthropathy","Osteoarthritis",[212,213,214,215,216],"arthroplasty","balance","fall risk","gait rehabilitation","psychological outcomes","2025-06-26",{"date":219,"type":42},"2025-06-27",{"date":221,"type":42},"2025-05-15",{"date":223,"type":22},"2026-06-30",{"name":48,"class":49},{"id":226,"slug":227,"hasResults":11,"nctId":228,"briefTitle":229,"officialTitle":230,"acronym":231,"eligibilityCriteria":232,"healthyVolunteers":11,"sex":17,"minAge":84,"maxAge":204,"enrollmentInfo":233,"targetDuration":4,"studyType":23,"phases":235,"briefSummary":236,"conditions":237,"keywords":241,"overallStatus":97,"whyStopped":4,"lastUpdateSubmitDate":250,"lastUpdatePostDateStruct":251,"startDateStruct":253,"completionDateStruct":255,"leadSponsor":257,"locationsCount":50},"100591047","effects-of-a-protocol-of-hip-flexor-stretching-on-chronic-mechanical-non-specific-lbp-100591047","NCT06975345","Effects of a Protocol of Hip Flexor Stretching on Chronic Mechanical, Non-specific LBP.","Short, Medium and Long Term Effects of a Protocol of Hip Flexor Stretching, Exercise and Pain Managment Education, Function and Disability in Patients With Chronic, Mechanical, Non-specific Low Back Pain. Randomized Controlled Clinical Trial.","HipFlexinCLBP","Inclusion Criteria:\n\n* Age 18-75 years\n* Medical diagnosis of chronic, mechanical, non-specific pain in the lumbar spine (M54, M51) - chronic low back pain.\n* Obtaining written consent to conduct research\n* Must be able to swallow tablets\n\nExclusion Criteria:\n\n* Pregnancy\n* Pacemaker\n* Active cancer\n* To consent to conduct research\n* Difficulty communicating\n* The presence of a metal plate in the head and metal screws in the body\n* Condition after operations in the area of the lumbar spine\n* Condition after fractures in the lumbar spine\n* Contraindications to manual therapy or exercise\n* Has participated in a lumbar spine exercise or manual therapy program in the last three months\n* Present clear signs of having suffered a significant lumbar injury\n* Inability to maintain standing or a supine or prone position\n* No possibility to perform the stretching of hip flexors",{"count":234,"type":22},100,[25],"The goal of this clinical trial is to compare the effectiveness of a stretching, exercise and education protocol versus usual care in improving pain, function and disability in patients with non-specific mechanical chronic low back pain (CLBP). The research hypothesis is: A combination of hip flexors stretching, exercise and education is more effective than usual care to improve pain, function and disability in patients with CLBP.\n\nParticipants will be randomly allocated in one of the two treatment groups. Pain, function and disability will be assessed before starting treatment, after the end of the treatment and one month , three months and one year after the end of the treatment.",[238,239,240],"Pain","Musculoskeletal Manipulations","Low Back Pain, Mechanical",[242,243,244,245,246,247,248,249],"manual therapy,","spine,","low back pain,","Chronic Low Back Pain,","Muscle Stretching Exercises,","Range of Motion, Articular,","Body composition,","Numeric Pain Rating Scale (NPRS)","2025-05-07",{"date":252,"type":42},"2025-05-16",{"date":254,"type":22},"2025-07-02",{"date":256,"type":22},"2027-12-31",{"name":48,"class":49},{"id":259,"slug":260,"hasResults":11,"nctId":261,"briefTitle":262,"officialTitle":263,"acronym":264,"eligibilityCriteria":265,"healthyVolunteers":11,"sex":17,"minAge":84,"maxAge":19,"enrollmentInfo":266,"targetDuration":4,"studyType":23,"phases":268,"briefSummary":269,"conditions":270,"keywords":272,"overallStatus":97,"whyStopped":4,"lastUpdateSubmitDate":275,"lastUpdatePostDateStruct":276,"startDateStruct":278,"completionDateStruct":280,"leadSponsor":282,"locationsCount":50},"100567954","electrolysis-in-patients-with-chronic-plantar-fasciitis-100567954","NCT06674902","Electrolysis in Patients With Chronic Plantar Fasciitis","Short-term Effectiveness of High- and Low-intensity Percutaneous Electrolysis in Patients With Plantar Fasciitis","Electrolysis","Inclusion Criteria:\n\n* age 18 years or older,\n* unilateral heel pain lasting longer than 3 months,\n* a clinical diagnosis of chronic plantar fasciitis according to the clinical practice guidelines of the Orthopaedic Section of the American Physical Therapy Association (APTA), i.e., sudden onset of pain on the plantar surface of the heel after a period of non-weight bearing, pain that is worse in the morning with the first step, and tenderness to palpation at the proximal attachment site of the plantar fascia.\n\nExclusion Criteria:\n\n* previous lower extremity surgery,\n* the presence of positive neurological signs consistent with nerve root compression,\n* any medical conditions causing heel pain, such as rheumatoid arthritis, diabetes, or peripheral neuropathy,\n* receipt of any foot treatment within the past 6 weeks.",{"count":267,"type":22},16,[25],"Aim of the Study\n\nThe aim of this study is to investigate the differential effects of high-intensity and low-intensity percutaneous electrolysis (PCE) on pain perception and muscle tissue properties in individuals with chronic plantar fasciitis.\n\nResearch Questions\n\nPain Perception:\n\nDoes high-intensity PCE induce greater changes in pressure pain threshold (PPT) in the plantar fascia compared to low-intensity PCE in individuals with chronic plantar fasciitis?\n\nMuscle Tissue Properties:\n\nDoes high-intensity PCE reduce stiffness in the plantar fascia to a greater extent than low-intensity PCE in individuals with chronic plantar fasciitis?",[271],"Plantar Fasciitis",[238,264,273,274],"shear-wave elastography","pain sensitivity","2024-11-04",{"date":277,"type":42},"2024-11-05",{"date":279,"type":22},"2024-11-11",{"date":281,"type":22},"2024-11-30",{"name":48,"class":49},{"id":284,"slug":285,"hasResults":11,"nctId":286,"briefTitle":287,"officialTitle":288,"acronym":264,"eligibilityCriteria":289,"healthyVolunteers":11,"sex":17,"minAge":290,"maxAge":175,"enrollmentInfo":291,"targetDuration":4,"studyType":23,"phases":293,"briefSummary":294,"conditions":295,"keywords":296,"overallStatus":97,"whyStopped":4,"lastUpdateSubmitDate":300,"lastUpdatePostDateStruct":301,"startDateStruct":303,"completionDateStruct":304,"leadSponsor":306,"locationsCount":50},"100566891","electrolysis-in-patients-with-low-back-pain-100566891","NCT06661070","Electrolysis in Patients With Low Back Pain","Short-term Effectiveness of High- and Low-intensity Percutaneous Electrolysis in Patients With Low Back Pain","Inclusion Criteria:\n\n* to report low back pain of at least six months duration,\n* aged 35 to 50 years,\n* at least one active trigger point is present in the multifidus muscle.\n\nExclusion Criteria:\n\n* pharmacological (e.g., analgesics) or physiotherapy treatment before or during their participation in the study,\n* needle fear,\n* prior lower extremity or spine surgery, absence of pain, any musculoskeletal or neuropathic conditions (e.g., peripheral compressive neuropathy, radiculopathy, sarcopenia, fibromyalgia, muscle ruptures), traumatic injuries (e.g., fractures or fissures), or any medical condition or contraindication for needling treatment (e.g., anticoagulants).","35 Years",{"count":292,"type":22},50,[25],"The goal of this observational study is to investigate the efficacy of percutaneous electrolysis compared with dry needling on pain sensations and multifidus muscle properties in subjects with low back pain. The main questions it aims to answer are:\n\nThe high-intensity and low-intensity percutaneous electrolysis may induce pressure pain threshold (PPT) changes in myofascial trigger points in the low back during the intervention compared with dry needling.\n\nPercutaneous electrolysis interventions may reduce stiffness in the multifidus muscle during the intervention compared with dry needling.",[64],[297,238,298,299,273,274],"Low Back","Multifidus muscle","Trigger Points","2024-10-24",{"date":302,"type":42},"2024-10-28",{"date":275,"type":22},{"date":305,"type":22},"2024-11-23",{"name":48,"class":49},""]