[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Quiropraxia y Equilibrio\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":103},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,79],{"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":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100602583","low-level-laser-auriculotherapy-in-the-treatment-of-myogenic-temporomandibular-disorders-and-anxiety-100602583",false,"NCT07125404","Low-Level Laser Auriculotherapy in the Treatment of Myogenic Temporomandibular Disorders and Anxiety","Effectiveness of Low-Level Laser Auriculotherapy in the Treatment of Myogenic Temporomandibular Disorders and Anxiety: A Randomized Clinical Trial","Inclusion Criteria:\n\n* Age ≥ 18 years.\n* Clinical diagnosis of unilateral or bilateral myogenic temporomandibular disorder (TMD) based on DC\u002FTMD criteria.\n* Presence of myalgia or myofascial pain in the masticatory muscles, either spontaneous or induced by clinical palpation.\n* At least one episode of local, referred, or radiating masticatory pain in the past 30 days, lasting at least one hour.\n* Score ≥ 5 on the Generalized Anxiety Disorder 7-item scale (GAD-7), indicating generalized anxiety.\n\nExclusion Criteria:\n\n* Recent musculoskeletal injury in the cervical region.\n* Skin lesions or dermatological conditions on the auricle.\n* Regular use of medications such as corticosteroids, non-steroidal anti-inflammatory drugs (NSAIDs), or photosensitizing agents (e.g., tetracyclines, quinolones, sulfonamides).\n* Tattoos on or near the auricular area.\n* History of cancer or tumors within the past five years.\n* Fitzpatrick skin phototype V or VI.\n* Autoimmune diseases (e.g., lupus erythematosus, hepatic porphyria, pellagra).\n* Epilepsy.\n\nDiscontinuation Criteria\n\n\\- The participant's withdrawal or non-attendance results in the failure to complete the evaluation or treatment protocol.","ALL","18 Years",{"count":19,"type":20},32,"ESTIMATED","INTERVENTIONAL",[23],"NA","Summary:\n\nLow-level laser auriculotherapy (LLLT-AT) is a non-invasive technique that has gained attention for managing musculoskeletal pain and anxiety. Given the painful and emotional components of temporomandibular disorders (TMD), LLLT-AT may offer therapeutic benefits by stimulating auricular points associated with pain modulation and anxiety reduction. This randomized, placebo-controlled, two-arm clinical trial with blinded outcome assessors aims to evaluate the effects of LLLT-AT in individuals diagnosed with myogenic TMD (Axis I, Group I of the DC\u002FTMD classification) and anxiety. The study will be conducted at the Physical Agents Laboratory of Universidad Andrés Bello. Eligible participants will include members of the university community with myogenic TMD (Axis I, Group I of the DC\u002FTMD classification) and anxiety. Participants will be stratified by sex and randomly assigned to either an experimental group receiving LLLT-AT combined with a standardized myofascial release protocol or a control group receiving sham LLLT-AT with the same myofascial protocol. Interventions will be administered twice weekly for three weeks. Outcome measures will be collected at baseline, post-intervention, and at a four-week follow-up. Primary outcomes include pressure pain threshold (PPT), assessed by algometry, and anxiety level, measured using the GAD-7 scale. Secondary outcomes include maximum mouth opening range of motion (MMOROM) and mandibular functional limitation (MFL), assessed using the Jaw Functional Limitation Scale 8 (JFLS-8).",[26,27],"Temporomandibular Disorder","Anxiety State",[29,30,31,32,33,34],"Laser Therapy","Low-level Light Therapy","Auriculotherapy","Joint Disorders","Temporomandibular Joint Dysfunction Syndrome","Anxiety","NOT_YET_RECRUITING","2025-08-12",{"date":38,"type":39},"2025-08-15","ACTUAL",{"date":41,"type":20},"2025-09-01",{"date":43,"type":20},"2026-05-01",{"name":45,"class":46},"Quiropraxia y Equilibrio","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":55,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":21,"phases":58,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},"100492257","high-intensity-laser-therapy-for-neck-pain-100492257","NCT05689788","High-intensity Laser Therapy for Neck Pain","Effect of High-intensity Laser Therapy in Patients With Chronic Nonspecific Neck Pain. Randomized Clinical Trial","Inclusion Criteria:\n\n* Participants must be at least 18 years old.\n* Both sexes (men and women)\n* Non-specific, chronic neck pain, defined as pain or discomfort in the cervical region between the superior nuchal line and the spinous process of T1 or the shoulder girdle, with the following criteria: neck pain in the last 3 months or more; a questionnaire score of cervical disability (NDI) equal to or greater than 5; and cervical pain of 3 or greater on the numerical pain scale (NPRS).\n\nExclusion Criteria:\n\n* Neck or shoulder musculoskeletal injuries in the last 3 months (fractures, sprains, tendinopathies, dislocations, or muscle tears).\n* Osteosynthesis materials close to the shoulders, neck, or surrounding areas.\n* Wounds or skin changes in the shoulder and\u002For neck region (such as psoriasis, scars, or burns).\n* Analgesic, anti-inflammatory, or muscle relaxant drugs for permanent use.\n* Neurological alterations such as paresthesia, loss of sensation (partial or complete), decrease in strength, or color changes in the neck, arms, forearms, or hands.\n* Diagnosed photosensitivity.\n* Presence of solar urticaria or adverse reactions to sunlight.\n* The presence of dermatomyositis, systemic lupus erythematosus, hepatic porphyria, cutaneous carcinoid syndrome, or pellagra.\n* Cancer or tumors of some type have been diagnosed in the last 5 years.\n* Epilepsy.",true,{"count":57,"type":20},72,[23],"Chronic nonspecific neck pain is a common musculoskeletal disorder recognized for its high rates of disability and economic losses, ranking second in musculoskeletal conditions after low back pain. There are several effective physical therapy interventions to treat chronic nonspecific neck pain, such as laser therapy. High-intensity laser therapy (HILT) is a recent treatment proposed to reduce musculoskeletal pain; however, there are few studies that prove its effects in reducing neck pain.\n\nThe aim of this randomized clinical trial is to evaluate the effect of high-intensity laser therapy on pain intensity in patients with chronic nonspecific neck pain.\n\nThe research will be carried out in the laboratory of physical agents at the Andrés Bello University, Campus Casona de las Condes. Participants will be employers and volunteer students with non-specific chronic neck pain. Participants will be randomized and allocated into 2 study groups: group 1 (HILT and stretching exercises) and group 2 (simulated HILT and stretching exercises). Treatments will be performed twice a week for 4 weeks with 3 assessments: before treatment, at the end of treatment, and 12 weeks after treatment (follow-up). The main results will be the differences in pain pressure threshold (ΔPPT), intensity of pain at rest (ΔRPI) and intensity of pain on movement (ΔMPI). Secondary outcome measures, on the other hand, will include differences in cervical spine range (ΔCROM) and cervical disability (ΔND).",[61],"Non-specific Chronic Neck Pain",[63,64,65,66,67,68],"Lasers","Laser therapy","Chronic pain","Neck pain","Physical Therapy Modalities","Clinical trial","RECRUITING","2025-08-06",{"date":72,"type":39},"2025-08-07",{"date":74,"type":39},"2024-03-31",{"date":76,"type":20},"2025-12-28",{"name":45,"class":46},2,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":55,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":21,"phases":89,"briefSummary":90,"conditions":91,"keywords":93,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":98,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":102,"locationsCount":78},"100396702","high-intensity-laser-therapy-hilt-on-myofascial-trigger-points-100396702","NCT04445545","High Intensity Laser Therapy (HILT) on Myofascial Trigger Points.","Effectiveness of High Intensity Laser Therapy (HILT) and Stretching Exercises on Cervical Flexibility and Pain Reduction in Myofascial Trigger Points. Randomized Clinical Trial (RCT).","HILT","Inclusion Criteria:\n\n* Participants over 18 years of age.\n* Officials and students of the Casona las Condes Campus of the Andrés Bello University.\n* Presence of myofascial trigger points in the shortened upper trapezius muscle evaluated (expert consensus establishing criteria for the diagnosis of MTrPs, Delphi study).25\n\nExclusion Criteria:\n\n* Musculoskeletal problems or pathologies of the neck or shoulders in the last 3 months (fractures, sprains, tendinopathies, dislocations, or muscle tears).\n* Presence of osteosynthesis materials near shoulders, neck, or surrounding areas.\n* Presence of wounds or skin changes in the shoulder and\u002For neck region (such as psoriasis, scars, or burns).\n* Use of analgesic, anti-inflammatory, or muscle relaxant medications for permanent use.\n* Neurological changes such as paresthesia, loss of sensitivity (partial or complete), decreased strength, and color changes in the neck, arms, forearms, or hands.\n* Diagnosed photosensitivity.\n* Presence of solar urticaria or adverse reactions to sunlight.\n* Presence of the following conditions: dermatomyositis, systemic lupus erythematosus, hepatic porphyria, cutaneous carcinoid syndrome or pellagra\n* Cancer or tumors of any type diagnosed.\n* Epilepsy.",{"count":88,"type":20},24,[23],"The aim of the study is to evaluate the effects of HILT on cervical flexibility and pain reduction in myofascial trigger points. The research will be carried out in the Physiotherapy laboratory of Andrés Bello University. The participants will be civil servants and volunteer university students with the presence of latent MTrPs of the upper trapezius muscle. Participants will be randomized and divided into 3 study groups: group 1 (HILT and stretching exercises), group 2 (sham HILT and stretching exercises), and group 3 (the conventional US and stretching exercises). The treatments will be carried out twice a week for 4 weeks accompanied by 2 evaluations during the treatment and 1 post-treatment follow-up. The main result will be considered the differences in pain intensity (ΔPI), pain pressure threshold (ΔPPT), cervical spine range (ΔCROM), and cervical disability (ΔND) between the evaluation sessions.",[92],"Myofascial Trigger Point Pain (MTrP)",[63,29,94,95,96,97],"Trigger Points","Myofascial Pain Syndromes","Analgesia","Clinical Trial",{"date":72,"type":39},{"date":100,"type":39},"2025-05-01",{"date":41,"type":20},{"name":45,"class":46},""]