[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pain-back\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pain-back":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,44,68,110,144,167,194],{"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":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100443736","phase-3-lumbar-steroid-use-in-patients-undergoing-posterior-lumbar-decompression-100443736",false,"NCT05058287","Lumbar Steroid Use in Patients Undergoing Posterior Lumbar Decompression","Topical Epidural Steroid Usage in Patients Undergoing Posterior Lumbar Decompression: A Randomized Control Trial","Inclusion Criteria:\n\n* Patients scheduled to undergo 1 to 2 level laminectomy\n* Between the ages of 18-85\n\nExclusion Criteria:\n\n* Minimally invasive surgery\n* Prior daily opioid usage within 6 months.\n* Use of concomitant procedures such as spinal fusion, revision procedure at the same level.\n* History of a chronic pain syndrome, uncontrolled diabetes defined as A1C \\> 6.5, immunocompromised condition such as active cancer treatment, history of transplant, benign prostatic hyperplasia or history of urinary retention, and other conditions which require chronic steroid therapy or immunosuppressants.\n* Non-English speakers\n* Patients allergic to Depo-Medrol and\u002For glucocorticoids, or other steroids","ALL","18 Years","85 Years",{"count":20,"type":21},150,"ESTIMATED","INTERVENTIONAL",[24],"PHASE3","This study seeks to evaluate the impact of intra-operative topical epidural steroid usage in patients undergoing 1-2 level lumbar laminectomy. The study will examine post-operative opioid usage, length of stay, return to work, and patient reported outcomes following these procedures.",[27,28,29,30],"Opioid Use","Lumbar Spinal Stenosis","Pain, Postoperative","Pain, Back","RECRUITING","2026-04-23",{"date":34,"type":35},"2026-04-28","ACTUAL",{"date":37,"type":35},"2021-11-05",{"date":39,"type":21},"2026-12-31",{"name":41,"class":42},"Hospital for Special Surgery, New York","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":66,"locationsCount":43},"100474683","early-phase-1-regional-nerve-blocks-to-improve-analgesia-and-recovery-in-older-adults-undergoing-spinal-fusion-100474683","NCT05461092","Regional Nerve Blocks to Improve Analgesia and Recovery in Older Adults Undergoing Spinal Fusion","Inclusion Criteria:\n\n* Are 65 or older\n* Indicated for lumbar spinal fusion of less than or equal to 3 levels\n* Undergoing elective surgery\n* no contraindications to local anesthetic or procedures\n* no severe cardiac or respiratory disease\n* no preexisting cognitive dysfunction\u002Fdementia\n\nExclusion Criteria:\n\n* 64 years old and younger\n* emergency treatment\n* pathologic fractures\n* seeking revision surgery\n* major liver or kidney dysfunction\n* coexisting hematological disorder or irreversible abnormal coagulation\n* patients with previous diagnosis of dementia or SLUMS score \\\u003C20\n* patient unable to communicate\u002Fcooperate\u002Flanguage barrier\n* BMI\\>40\n* allergy to study medications\n* opioid tolerant (oral opioid intake morphine equivalent =\\\u003C 60 mg\u002Fday)\n* other sources of chronic pain like fibromyalgia\n* patients with associated significant CNS or respiratory disease (home oxygen requirements)\n* incarcerated patients\n* psychiatric illnesses preoperative neurological deficits greater than one motor group, less than three out of five motor functions\n* pregnant or breast feeding","65 Years",{"count":52,"type":21},50,[54],"EARLY_PHASE1","This initial study is a feasibility study for implementing thoracolumbar interfascial plane, or TLIP, blocks in older adults undergoing spinal fusion. TLIP blocks are done by using anesthesia. In this case, it will be done to either side of the back where surgery will be performed. This has been shown to decrease pain the patients have post-operatively in previous research. In this study, the investigators will examine recruitment rates, completion of assessments, dropout rate, gather patient feedback, and identify barriers to performing TLIP. Further, this feasibility study will provide data to determine adequate sample size and refine methods and outcomes for a future randomized clinical trial. The ultimate goal is to perform a large, appropriately powered randomized control trial to determine the effect of TLIP blocks on pain, physical function and disability, opioid consumption, and delirium in older adult undergoing spinal fusion.",[57,30,58,59],"Delirium","Spinal Fusion","Thoracolumbar Interfascial Plane Block","2026-03-24",{"date":62,"type":35},"2026-03-27",{"date":64,"type":35},"2024-01-01",{"date":39,"type":21},{"name":67,"class":42},"University of Iowa",{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":4,"eligibilityCriteria":74,"healthyVolunteers":11,"sex":75,"minAge":17,"maxAge":76,"enrollmentInfo":77,"targetDuration":4,"studyType":22,"phases":79,"briefSummary":81,"conditions":82,"keywords":87,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":43},"100575860","effects-of-reformer-pilates-in-pregnant-women-100575860","NCT06777771","Effects of Reformer Pilates in Pregnant Women","The Effects of Reformer Pilates on Pain, Functional Capacity, Lumbopelvic Stabilization, Abdominal Muscles, Respiratory Functions, Pelvic Floor Function, and Venous Insufficiency in Pregnant Women","Inclusion Criteria:\n\n* Single pregnancy\n* Primiparous pregnancy\n* Adult pregnant women (between 18-35 years old)\n* Pregnant women whose gestational week is 11-22 weeks\n* Pregnant women with a body mass index \\\u003C30\n* Ability to read and write\n\nExclusion Criteria:\n\n* Multiple pregnancies\n* Having a history of abdominal surgery\n* Having one of the conditions in which exercise is contraindicated, such as heart disease, severe lung disease, continuous bleeding in the second and third trimesters, placenta previa, risk of premature birth, rupture of membranes, preeclampsia, severe anemia\n* Not volunteering to participate in the study\n* Not participating in more than 90% of the training sessions","FEMALE","35 Years",{"count":78,"type":21},30,[80],"NA","Pregnancy is known as a period associated with important physiological and psychological changes in women's lives. There is moderately sufficient evidence in the literature to recommend supplementing prenatal physical activity for maternal health benefits. It has been reported that physical exercise by pregnant women in the absence of obstetric contraindications will not pose a risk to the health of the mother and fetus. In the literature, there are no studies examining the effects of reformer pilates on pain, functional capacity, lumbopelvic stabilization, diastasis recti abdominis, abdominal muscle thickness, respiratory functions, pelvic floor dysfunction, urinary incontinence, sexual function, and venous insufficiency in pregnant women. Therefore, this study aimed to investigate the effects of reformer pilates on pain, functional capacity, lumbopelvic stabilization, diastasis recti abdominis, abdominal muscle thickness, respiratory functions, pelvic floor dysfunction, urinary incontinence, sexual function, and venous insufficiency in pregnant women.",[83,84,30,85,86],"Pregnancy Related","Pelvic Floor Disorders","Pain, Neck","Pregnancy, Abdominal",[88,89,90,91,92,93,94,95,96,97,98,99,100],"Pregnancy","Exercise","Reformer Pilates","Pilates","Pelvic Floor Dysfunction","Lumbopelvic Stabilization","Functional Capacity","Respiratory Function","Abdominal Muscle Thickness","Venous Insufficiency","Urinary Incontinence","Sexual Function","Pain","2025-01-15",{"date":103,"type":35},"2025-01-16",{"date":105,"type":35},"2024-02-06",{"date":107,"type":21},"2025-09",{"name":109,"class":42},"Izmir Democracy University",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":116,"eligibilityCriteria":117,"healthyVolunteers":11,"sex":16,"minAge":118,"maxAge":4,"enrollmentInfo":119,"targetDuration":4,"studyType":22,"phases":121,"briefSummary":122,"conditions":123,"keywords":129,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":43},"100462821","preventing-pain-after-surgery-100462821","NCT05306665","PREventing Pain After Surgery","PREventing Pain After Surgery: a Feasibility and Acceptability Study of Acceptance and Commitment Therapy for the Prevention of Chronic Post-surgical Pain (PREPS)","PREPS","Inclusion Criteria:\n\n* scheduled to undergo fusion, discectomy, vertebroplasty, kyphoplasty, or foraminotomy\n* age 22 and older\n* able to communicate fluently in English\n\nExclusion Criteria:\n\n* inability to complete study procedures due to delirium, dementia, psychosis, or other cognitive impairment\n* have a history of severe neurologic movement disorder\n* are pregnant or intent to become pregnant during study\n* have undergone previous spinal surgery\n* have spinal deformity, pseudarthrosis, trauma, infection, or tumor as primary indication for surgery\n* have undergone Acceptance and Commitment Therapy in last 2 years","22 Years",{"count":120,"type":21},140,[80],"The present study aims to adapt and modify a brief presurgical Acceptance and Commitment Therapy (ACT) intervention aimed at preventing the transition to Chronic Post-Surgical Pain (CPSP) and reducing long-term opioid use. Investigators will then assess the acceptability, feasibility, and preliminary efficacy of the finalized intervention to prevent the transition to CPSP and reduce post-surgical opioid use six months following lumbar spine surgery. Finally, investigators will identify psychosocial and psychophysical phenotypes associated with response to this intervention.",[30,124,125,126,127,128],"Spinal Stenosis","Disc Herniation","Spondylosis","Spondylolisthesis","Back Injuries",[130,131,132,133,134],"Chronic pain","Surgery","opioid","acceptance and commitment therapy","Prevention","2024-10-25",{"date":137,"type":35},"2024-10-28",{"date":139,"type":35},"2023-01-13",{"date":141,"type":21},"2026-08-01",{"name":143,"class":42},"Brigham and Women's Hospital",{"id":145,"slug":146,"hasResults":11,"nctId":147,"briefTitle":148,"officialTitle":148,"acronym":4,"eligibilityCriteria":149,"healthyVolunteers":150,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":151,"targetDuration":4,"studyType":22,"phases":153,"briefSummary":154,"conditions":155,"keywords":4,"overallStatus":157,"whyStopped":4,"lastUpdateSubmitDate":158,"lastUpdatePostDateStruct":159,"startDateStruct":161,"completionDateStruct":163,"leadSponsor":165,"locationsCount":4},"100554877","the-effect-of-automatic-massage-applied-to-healthcare-workers-on-pain-fatigue-and-psychological-well-being-100554877","NCT06504797","The Effect of Automatic Massage Applied to Healthcare Workers on Pain, Fatigue and Psychological Well-being","Inclusion Criteria:\n\n* Working in the delivery room\n\nExclusion Criteria:\n\n* Being receiving psychiatric treatment (Pharmacotherapy or psychotherapy),\n* having a wound on the waist and back that prevents the application.",true,{"count":152,"type":21},25,[80],"To determine the effect of automatic massage applied to healthcare workers on pain, fatigue and psychological well-being. This research is planned as a pretest-posttest type study. It will be held in the Osmaniye State Hospital maternity ward. The application will be applied by one person in the rest room. Data will be collected using the Introductory Information Form, Psychological Well-Being Scale, Perceived Stress Scale (ASÖ\u002FPSÖ-14), State-Trait Anxiety Inventory (STAI), and Piper Fatigue Scale.",[156,30],"Massage","NOT_YET_RECRUITING","2024-07-16",{"date":160,"type":35},"2024-07-17",{"date":162,"type":21},"2024-07-25",{"date":164,"type":21},"2024-08-02",{"name":166,"class":42},"Emine Yıldırım",{"id":168,"slug":169,"hasResults":11,"nctId":170,"briefTitle":171,"officialTitle":171,"acronym":4,"eligibilityCriteria":172,"healthyVolunteers":11,"sex":16,"minAge":173,"maxAge":174,"enrollmentInfo":175,"targetDuration":4,"studyType":22,"phases":177,"briefSummary":178,"conditions":179,"keywords":182,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":185,"lastUpdatePostDateStruct":186,"startDateStruct":188,"completionDateStruct":190,"leadSponsor":192,"locationsCount":43},"100387550","brown-adipose-tissue-activation-by-spinal-cord-stimulation-100387550","NCT04326192","Brown Adipose Tissue Activation by Spinal Cord Stimulation","Inclusion Criteria:\n\n1. Age: 21-70 years\n2. Persistent neuropathic leg and back pain\n3. Subjects who are already planning to undergo SCS for pain\n4. Subjects who have not received a prior SCS trial for pain\n5. Subjects with a BMI of 25-45, using formula; weight (lb) \u002F \\[height (in)\\]2 x 703\n\nExclusion Criteria:\n\n1. Not considering SCS for pain\n2. Forensic patient\n3. Taking beta blockers\n4. Weight change \\> 5% within last 3 months\n5. Habitual tobacco use\n6. Habitual excessive alcohol use\n7. Pregnancy\n8. Decisionally impaired adults\n9. Children\n10. Neonates\n11. Subjects with a BMI of \\\u003C25 or \\>45","21 Years","70 Years",{"count":176,"type":21},10,[80],"The objective of this study is to investigate and utilize spinal cord stimulation (SCS) as an effective approach to eliciting weight loss and potentially alleviating Type 2 diabetes mellitus (DM), as evidenced by increasing metabolism of adipose tissue.",[30,180,181],"Obesity, Morbid","Type 2 Diabetes",[183,184],"Obesity","Diabetes","2024-04-01",{"date":187,"type":35},"2024-04-03",{"date":189,"type":35},"2021-02-19",{"date":191,"type":21},"2026-10",{"name":193,"class":42},"Oregon Health and Science University",{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":4,"eligibilityCriteria":200,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":201,"targetDuration":4,"studyType":22,"phases":203,"briefSummary":205,"conditions":206,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":209,"lastUpdatePostDateStruct":210,"startDateStruct":212,"completionDateStruct":214,"leadSponsor":216,"locationsCount":43},"100411695","phase-4-trigger-point-injections-in-anterior-cervical-surgery-100411695","NCT04640896","Trigger Point Injections in Anterior Cervical Surgery","Comparison of Trigger Point Injections Versus Traditional Therapies in the Management of Postsurgical Pain in Patients Who Had Anterior Cervical Surgery","Inclusion Criteria:\n\n* Elective anterior cervical surgery\n\nExclusion Criteria:\n\n* Emergency surgery\n* Local anesthetic allergy\n* Long term opioid usage (not including tramadol and codeine)\n* Intra-operative complication (e.g. unstable cervical spine)",{"count":202,"type":21},60,[204],"PHASE4","To achieve appropriate exposure for an anterior neck surgery (for example an Anterior Cervical Discectomy and Fusion or ACDF), patients are positioned supine with their neck extended. Due to being in this position, patients frequently complain of posterior neck stiffness and pain postoperatively in addition to the anterior incisional pain. This posterior cervical pain can be classified as myofascial pain.\n\nCervical myofascial pain is thought to be the result of overuse or trauma to the supporting muscles of the neck and shoulders. Trigger point injections are one of the methods used to treat myofascial pain. The trigger point injection procedure is where a physician (typically an anesthesiologist) performs an exam of the patient neck and upper back and finds areas of point tenderness. The physician will then inject a small amount of numbing medication (such as bupivacaine) into the muscle or tissue in that area.\n\nTrigger point injections have been shown to be superior to botox injections or dry needling, and equivalent to physical therapy. However, these studies were performed on patients with chronic neck pain. There are no studies evaluating the effectiveness of trigger point injections on post anterior cervical surgery patients.\n\nAt our institution, trigger point injections with local anesthetic are used as part of a multimodal pain control regimen for post-anterior cervical surgery patients. Our hypothesis is if the addition of trigger point injections to standard of care multi-modal post-operative pain control will decrease patients' myofascial pain, and thereby decrease the amount of narcotic pain medication used.",[207,85,30,208],"Myofacial Pain","Cervical Fusion","2022-12-07",{"date":211,"type":35},"2022-12-08",{"date":213,"type":35},"2020-11-05",{"date":215,"type":21},"2023-12-31",{"name":217,"class":42},"George Washington University"]