[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100621307":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":21,"locations":27,"responsibleParty":42,"collaborators":20,"id":46,"slug":47,"hasResults":48,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":20,"eligibilityCriteria":52,"healthyVolunteers":48,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":20,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":67,"overallStatus":30,"whyStopped":20,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},{"fullName":5,"class":6},"Xijing Hospital","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Transcutaneous Electrical Stimulation (TENS)）","EXPERIMENTAL","All enrolled participants in this arm will receive transcutaneous electrical nerve stimulation (TENS) therapy 5 times per week for 4 consecutive weeks. Treatment will be delivered according to a standardized protocol, with stimulation intensity adjusted within a safe range based on individual tolerance. Outcomes will be assessed at baseline and weekly during the 4-week treatment period, and adverse events will be recorded.",[13],"Device: Transcutaneous Electrical Nerve Stimulation (TENS)",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","Transcutaneous Electrical Nerve Stimulation (TENS)","TENS will be delivered via surface electrodes placed bilaterally around the area of maximal low back pain. Each session will last 20-30 minutes, administered 5 times per week for 4 weeks. Stimulation intensity will be titrated to a strong but comfortable sensation without pain, and parameters may be adjusted based on participant tolerance. Safety will be monitored throughout treatment and follow-up.",[9],null,[22],{"name":23,"role":24,"phone":25,"phoneExt":20,"email":26},"Bo Gao MD, PhD","CONTACT","029-84775507","gaobofmmu@hotmail.com",[28],{"facility":29,"status":30,"city":31,"state":32,"zip":33,"country":34,"countryCode":35,"cosmosGeoPoint":36,"geoPoint":41,"contacts":20},"Xjing hospital","RECRUITING","Xi'an","Shaanxi","710032","China","CN",{"type":37,"coordinates":38},"Point",[39,40],108.92861,34.25833,{"lat":40,"lon":39},{"type":43,"investigatorFullName":44,"investigatorTitle":45,"investigatorAffiliation":5,"oldNameTitle":20,"oldOrganization":20},"PRINCIPAL_INVESTIGATOR","Bo Gao, MD","principal investigator","100621307","transcutaneous-electrical-nerve-stimulation-tens-for-the-treatment-of-low-back-pain-lbp-in-adults-100621307",false,"NCT07368920","Transcutaneous Electrical Nerve Stimulation (TENS) for the Treatment of Low Back Pain (LBP) in Adults","A Prospective, Open-Label, Single-Arm, Self-Controlled Study of Transcutaneous Electrical Nerve Stimulation (TENS) for Adult Low Back Pain","Inclusion Criteria:\n\n1. Adults aged 18-65 years\n2. Diagnosis consistent with myofascial low back pain (localized low back pain with a palpable taut band; referred pain and\u002For sensory changes near a specific trigger point; an identifiable tender spot within the taut band; mild muscle weakness and\u002For some limitation of joint range of motion)\n3. Mild pain intensity at baseline (VAS \\\u003C 4 on a 0-10 scale)\n4. Symptom duration \\> 1 month\n5. Able to understand the study procedures and demonstrate good compliance\u002Fcooperation\n6. Written informed consent provided\n\nExclusion Criteria:\n\n1. Low back pain due to other causes, including but not limited to lumbar disc herniation, lumbar spinal stenosis, ankylosing spondylitis, spinal tumor, spinal tuberculosis, or spinal infection\n2. Received physical therapy, interventional procedures, or medication treatment within 4 weeks prior to enrollment that may affect pain or function assessment\n3. Systemic disease or organ dysfunction\n4. Skin\u002Fsoft tissue breakdown or infection at\u002Fnear the planned treatment area\n5. Use of sedative medications or opioid analgesics within 6 months prior to enrollment, or currently receiving other treatments that may affect study outcomes\n6. Severe psychiatric disorder or inability to cooperate with study procedures\n7. Pregnant or breastfeeding women","ALL","18 Years","65 Years",{"count":57,"type":58},40,"ESTIMATED","INTERVENTIONAL",[61],"NA","The goal of this clinical trial is to assess the effects and safety of transcutaneous electrical nerve stimulation (TENS) in adults with myofascial low back pain. Eligible participants will receive TENS treatment 5 times per week for 4 weeks. Pain intensity and functional outcomes will be assessed at baseline and weekly during the 4-week treatment period, and adverse events will be recorded.",[64,65,66],"Low Back Pain","Paraspinal Muscles","CLBP - Chronic Low Back Pain",[68,69,70],"Low back pain","Transcutaneous electrical stimulation","Self-controlled clinical trial","2026-03-19",{"date":73,"type":74},"2026-03-20","ACTUAL",{"date":76,"type":74},"2026-02-01",{"date":78,"type":58},"2029-01-01",{"name":5,"class":6},1]