[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Federal University of Paraíba\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":130},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,51,78,110],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"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},"100607703","immediate-effects-of-flossband-and-mobilization-with-movement-on-shoulder-mobility-in-volleyball-athletes-100607703",false,"NCT07192003","Immediate Effects of Flossband and Mobilization With Movement on Shoulder Mobility in Volleyball Athletes","Comparison of the Immediate Effect of Flossband and Mobilization With Movement on Shoulder Mobility in Volleyball Athletes: A Randomized Clinical Trial","Inclusion Criteria:\n\n* Age between 18 and 50 years.\n* Male or female volleyball athletes (indoor or beach), at amateur or professional level.\n* Regular training routine of at least two sessions per week.\n* No shoulder pain at the time of testing or during the previous three months.\n\nExclusion Criteria:\n\n* History of shoulder surgery, structural shoulder injuries (e.g., fractures, labrum tear), or recurrent glenohumeral dislocation.\n* Skin disorders contraindicating the intervention, including active dermatitis, inflammatory-phase psoriasis, cutaneous infections (e.g., folliculitis), open wounds, burns, eczema, or hypersensitivity in the shoulder region.\n* Vascular disorders contraindicating the intervention, including history or diagnosis of deep vein thrombosis, symptomatic varicose veins, peripheral arterial disease, lymphedema, or advanced chronic venous insufficiency.\n* Other conditions contraindicating intervention: peripheral neuropathies with significant sensory loss, presence of a pacemaker in the region of band application, known allergy to elastic band material, or pain during shoulder movement at assessment.\n* Development of shoulder or elbow injuries during the study, especially requiring surgical intervention.\n* Participants who voluntarily withdraw from the study at any time.",true,"ALL","18 Years","50 Years",{"count":21,"type":22},36,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to learn if Floss Band application works as effectively as mobilization with movement (MWM) to improve shoulder mobility in volleyball athletes. It will also explore whether these techniques affect athletes' perception of movement fluency and sport-specific performance.\n\nThe main questions it aims to answer are:\n\nDoes Floss Band application immediately improve shoulder range of motion in volleyball athletes? Does Floss Band application change the perception of movement fluency compared to MWM? Does Floss Band application impact sport-specific performance tests compared to MWM?\n\nParticipants will:\n\nBe randomly assigned to receive either Floss Band or mobilization with movement Have their shoulder mobility, perception of movement, and sport performance tested before and immediately after the intervention",[28,29,30],"Healthy Athlete","Shoulder Mobility","Musculoskeletal Health",[32,33,34,35,36,37],"Range of Motion","Shoulder","Sports","Physical Therapy Modalities","Mobilization with Movement","Volleyball","NOT_YET_RECRUITING","2025-09-21",{"date":41,"type":42},"2025-09-25","ACTUAL",{"date":44,"type":22},"2025-10-20",{"date":46,"type":22},"2026-04-18",{"name":48,"class":49},"Federal University of Paraíba","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":58,"maxAge":4,"enrollmentInfo":59,"targetDuration":4,"studyType":23,"phases":61,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":50},"100583594","impact-of-educational-intervention-protocol-on-the-level-of-knowledge-clinical-control-and-lung-function-of-people-with-asthma-100583594","NCT06878352","Impact of Educational Intervention Protocol on the Level of Knowledge, Clinical Control and Lung Function of People With Asthma","Impact of Educational Intervention Protocol on the Level of Knowledge, Clinical Control and Lung Function of People With Asthma: Randomized Controlled Clinical Trial","Inclusion Criteria:\n\n* Clinical diagnosis of asthma\n* Assisted by the Pulmonary Function Clinic\n* Ventilatory dysfunction assessed by spirometry\n\nExclusion Criteria:\n\n* Obesity\n* Treatment with systemic corticosteroids\n* Previous chest surgery\n* Unable to perform any of the proposed assessment steps","8 Years",{"count":60,"type":22},28,[25],"The goal of this randomized controlled clinical trial is to evaluate the effects of a proposed educational intervention on people with asthma. The main question it aims to contribute to a better understanding of the effectiveness of educational intervention strategies in people with asthma.\n\nParticipants allocated to the control group will receive standard follow-up according to the clinic routine. Participants allocated to the experimental group will undergo an educational intervention BUNDLE, prepared in accordance with the recommendations of the Global Initiative for Asthma- GINA (2024).",[64],"Asthma",[64,66,67,68],"Heath Education","Spirometry","Respiratory Tract Disease","RECRUITING","2025-03-12",{"date":72,"type":42},"2025-03-14",{"date":74,"type":22},"2025-03",{"date":76,"type":22},"2025-10",{"name":48,"class":49},{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":23,"phases":88,"briefSummary":89,"conditions":90,"keywords":94,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":107,"leadSponsor":109,"locationsCount":50},"100566938","cognitive-functional-therapy-for-treating-individuals-with-chronic-shoulder-pain-100566938","NCT06661681","Cognitive Functional Therapy for Treating Individuals With Chronic Shoulder Pain","Cognitive Functional Therapy Versus Therapeutic Exercises for the Treatment of Individuals With Chronic Shoulder Pain: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Men or women;\n* Age between 18 and 60 years;\n* Presence of shoulder pain for more than 3 months;\n* Pain intensity of 4 points or more on the 11-point Numeric Pain Rating Scale.\n* High level of disability or moderate level of irritability.\n\nExclusion Criteria:\n\n* History of fracture or surgery of the clavicle, scapula, and\u002For humerus, surgical stabilization or rotator cuff repair;\n* History of dislocation, instability (positive sulcus sign or apprehension test), and\u002For rotator cuff tear (positive drop arm test);\n* Adhesive capsulitis verified by the presence of gradual onset pain associated with stiffness and reduced passive and active mobility;\n* Ongoing pregnancy;\n* Reproduction of shoulder pain radiating to the entire upper limb during cervical or thoracic spine tests (positive Spurling test);\n* Neurological or systemic diseases that may alter muscle strength and sensitivity such as rheumatoid arthritis, fibromyalgia, lupus, gout, and diabetes;\n* Corticosteroid injection in the shoulder region in the last 3 months;\n* Physiotherapy treatment in the last 6 months.\n* Active treatment for cancer","60 Years",{"count":87,"type":22},72,[25],"Shoulder pain is a debilitating musculoskeletal condition with functional, physical, and psychological impacts. Interventions for chronic shoulder pain should address the biopsychosocial model, with Cognitive Functional Therapy emerging as a promising physiotherapy approach. Cognitive Functional Therapy approaches the multidimensional nature of pain, integrating physical and cognitive aspects.\n\nThe aim of this randomized controlled trial is to compare the effects of Cognitive Functional Therapy with therapeutic exercise on biological aspects of pain (pain intensity, disability, function, perception of improvement\u002Fdeterioration, and central pain processing), and psychosocial aspects of pain (sleep quality, self-efficacy, and biopsychosocial factors). The hypothesis of this study is that CFT will lead to greater improvements in these outcomes compared to therapeutic exercise.",[91,92,93],"Chronic Shoulder Pain","Exercise Therapy","Psychosocial Rehabilitation",[95,96,97,98,99,100,101,102],"Shoulder pain","Subacromial pain","Rotator cuff related shoulder pain","Shoulder Impingement","Chronic pain","Psychosocial","Rehabilitation","Biopsychosocial","2025-02-17",{"date":105,"type":42},"2025-02-19",{"date":103,"type":42},{"date":108,"type":22},"2026-11-25",{"name":48,"class":49},{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":85,"enrollmentInfo":117,"targetDuration":4,"studyType":23,"phases":119,"briefSummary":120,"conditions":121,"keywords":122,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":124,"startDateStruct":126,"completionDateStruct":127,"leadSponsor":129,"locationsCount":50},"100557788","cognitive-functional-therapy-for-chronic-shoulder-pain-pilot-and-feasibility-study-100557788","NCT06542666","Cognitive Functional Therapy for Chronic Shoulder Pain: Pilot and Feasibility Study","Cognitive Functional Therapy Versus Therapeutic Exercises for Treating Individuals With Chronic Shoulder Pain: A Pilot and Feasibility Study","Inclusion Criteria:\n\n* Men and women;\n* Age between 18 and 60 years;\n* Presence of shoulder pain for more than 3 months;\n* Pain intensity of 4 points or more on the 11-point Numeric Pain Rating Scale during the past week.\n* High level of disability or moderate level of irritability.\n\nExclusion Criteria:\n\n* History of fracture or surgery of the clavicle, scapula, and\u002For humerus, surgical stabilization or rotator cuff repair;\n* History of dislocation, instability (positive sulcus sign or apprehension test), and\u002For rotator cuff tear (positive drop arm test);\n* Adhesive capsulitis verified by the presence of gradual onset pain associated with stiffness and reduced passive and active mobility;\n* Ongoing pregnancy;\n* Reproduction of shoulder pain radiating to the entire upper limb during cervical or thoracic spine tests (positive Spurling test);\n* Neurological or systemic diseases that may alter muscle strength and sensitivity such as rheumatoid arthritis, fibromyalgia, lupus, gout, and diabetes;\n* Corticosteroid injection in the shoulder region in the last 3 months;\n* Physiotherapy treatment in the last 6 months.",{"count":118,"type":22},24,[25],"This pilot randomized controlled clinical trial (RCT) will assess the feasibility and identify the key components necessary for conducting the main RCT, which will involve the comparison of Cognitive Functional Therapy with Therapeutic Exercises in individuals with chronic shoulder pain. The main questions it aims to answer are:\n\n* What barriers to the participation of the included individuals might arise?\n* Will the assessment procedures and outcome measures be feasible and suitable?\n* What time will be necessary to conduct the assessments?\n* Will participants be willing to be randomized to the proposed treatment groups?\n* What barriers to the clinical delivery of Cognitive Functional Therapy in the healthcare system might exist?\n* Will the treatment(s) be acceptable to patients?\n* Will participants adhere to the treatment?\n* What will the recruitment rates be per week\u002Fmonth?\n* Will there be any selection bias?\n* Will participant retention be high among the allocation groups?\n* Will the data be complete?\n* What will the data variability be?\n* Will the treatment effects\u002Foutcomes be consistent with expectations and previous literature?",[91,92,93],[95,96,123,98,99,100,101,102],"Rotator cuff related pain",{"date":125,"type":42},"2025-02-18",{"date":103,"type":42},{"date":128,"type":22},"2025-09-01",{"name":48,"class":49},""]