[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100647806":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":30,"centralContacts":40,"locations":30,"responsibleParty":51,"collaborators":55,"id":58,"slug":59,"hasResults":60,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":30,"eligibilityCriteria":64,"healthyVolunteers":60,"sex":65,"minAge":66,"maxAge":30,"enrollmentInfo":67,"targetDuration":30,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":76,"overallStatus":82,"whyStopped":30,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":30},{"fullName":5,"class":6},"University of Valladolid","OTHER",[8,15,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Online Therapeutic Exercise and Education Group","EXPERIMENTAL","Participants will carry out an eight-week protocol consisting of education on managing the condition and therapeutic exercises for the lumbopelvic and abdominal muscles. This will be performed progressively. All exercises will be performed at a perceived exertion level of 6-7 out of 10, leaving approximately three repetitions in reserve per exercise. If exertion values are lower, the exercise intensity will increase. If the intensity exceeds 7, the exercise intensity will decrease. Elastic bands and exercise variations will be used to achieve this. Rest periods between sets and exercises will be 1.5 minutes. These sessions will be carried out synchronously online using the Google Meets platform. This allows the physiotherapist to supervise and guide four to six participants per group online.",[13,14],"Other: Therapeutic Exercise","Behavioral: Education on the self-management of low back pain",{"label":16,"type":10,"description":17,"interventionNames":18},"Face-to-Face Therapeutic Exercise and Education Group","This group will receive the same educational protocol for condition management and therapeutic exercise as the previous one, but it will be carried out in a face-to-face group format supervised by a physiotherapist from the Primary Care Physiotherapy Units.",[13,14],{"label":20,"type":21,"description":22,"interventionNames":23},"Conventional Treatment Group","ACTIVE_COMPARATOR","This group will undergo interventions typically applied in primary care physiotherapy units, including electrotherapy and exercise training. The following electrotherapy techniques will be applied:\n\n* Microwave therapy: 15 minutes at 100 watts, continuous TENS: 80 Hz, 150 microseconds, 20 minutes. Regarding exercises, a general program incorporating mobility, strength, and stretching work will be included. The physiotherapist will explain the program during the first treatment session, after which the patient will perform the exercises independently in subsequent sessions. During these sessions, patients will receive a sheet with a complete list of exercises and their explanations. They will also have the opportunity to consult the physiotherapist if they have any questions.",[24],"Other: Usual Care",[26,31,36],{"type":6,"name":27,"description":28,"armGroupLabels":29,"otherNames":30},"Therapeutic Exercise","This intervention consists of applying a therapeutic exercise protocol to the lumbopelvic and abdominal muscles. The included exercises are:\n\n* Core: Isometric Dead Bug, Dead Bug Leg Lowering, Contralateral Dead Bug, Dead Bug with Leg Abduction and Straight Arm Drop, Band-Resisted Dead Bug.\n* Core + Abs: Fire Hydrant, Band-Resisted Fire Hydrant, and Band-Resisted Fire Hydrant on Toes\n* Quadriceps: Chair squat, air squat, asymmetric chair squat, lunge, and chair squat with heel drive.\n* Gluteus exercises include sun salutation, single-leg dead foot drag, deadlift, skater (extension, external rotation, and abduction), standing donkey kick, and single-leg deadlift.\n\nExercises will be performed at an effort level of 6-7\u002F10 (rate of perceived exertion), leaving three repetitions in reserve per exercise. Participants will perform four to six sets of 15 repetitions for each exercise, with two sessions conducted per week. Rest periods between sets and exercises will be 1.5 minutes.",[16,9],null,{"type":32,"name":33,"description":34,"armGroupLabels":35,"otherNames":30},"BEHAVIORAL","Education on the self-management of low back pain","Participants will receive four weekly education sessions on self-management of low back pain during the first four weeks of the intervention. The contents of these sessions will be as follows:\n\n* The multifactorial origin of the condition and the natural course of the disease\n* The consequences of rest and the benefits of movement\n* Ergonomic adaptations applicable to daily, work, and sports activities\n* Interpretation of imaging tests in relation to patient functionality.",[16,9],{"type":6,"name":37,"description":38,"armGroupLabels":39,"otherNames":30},"Usual Care","Participants will receive a total of 16 sessions of usual care, two per week. The interventions included are as follows:\n\n* Microwave therapy: 15 minutes at 100 watts, continuous\n* Transcutaneous electrical nerve stimulation (TENS): 80 Hz, 150 microseconds, 20 minutes\n* An unsupervised exercise program including mobility, strength, and stretching exercises",[20],[41,47],{"name":42,"role":43,"phone":44,"phoneExt":45,"email":46},"Héctor Hernández-Lázaro, PhD","CONTACT","+34975220850","38841","hector.hernandez.lazaro@uva.es",{"name":48,"role":43,"phone":49,"phoneExt":30,"email":50},"Luis Ceballos-Laita, PhD","+34975129100","luis.ceballos@uva.es",{"type":52,"investigatorFullName":53,"investigatorTitle":54,"investigatorAffiliation":5,"oldNameTitle":30,"oldOrganization":30},"PRINCIPAL_INVESTIGATOR","Héctor Hernández Lázaro","Associate Professor",[56],{"name":57,"class":6},"Castilla-León Health Service","100647806","therapeutic-exercise-and-education-for-low-back-pain-100647806",false,"NCT07713082","Therapeutic Exercise and Education for Low Back Pain","Therapeutic Exercise and Education for Patients With Non-Specific Low Back Pain in Primary Health Care: A Multicenter Clinical Trial","Inclusion criteria:\n\n* Patients with non-specific low back pain, aged 18 years or older.\n* Pain duration of more than six weeks\n* Onset or modification of low back pain with maintenance of positions and\u002For movements\n* Presenting a mild-to-moderate level of disability, as determined by the Oswestry Disability Index (ODI) questionnaire.\n* Presence of limitations or symptoms in at least two range of motion (ROM) or coordination assessment tests, as described in clinical guidelines:\n* Lumbar and\u002For hip range of motion (ROM) measured with inclinometry Prone instability test\n* Presence of aberrant movements:\n\n  * Painful arc with flexion or return from flexion\n  * Instability catch\n  * Gower sign\n  * Reversal of lumbopelvic rhythm\n* Strength and endurance of the abdominal musculature\n* Email access and a device with an internet connection are required.\n* Availability and willingness to participate in all study sessions.\n\nExclusion criteria:\n\n* Presence of acute, nociplastic, radicular, and\u002For referred pain\n* Presence of red flags\n* Previous surgeries in the spine, pelvis, or hip\n* Presence of concomitant cardiovascular, neurological, endocrine, or immune pathologies that prevent physical activity\n* Presence of psychiatric disorders\n* Pregnancy\n* Having received physiotherapy treatment, analgesic blocks, corticosteroid injections, or any other type of intervention within the last three months\n* Changes in lifestyle habits, work conditions, or physical activity levels within the last three months\n* Inability to meet the program's physical or cognitive demands during the eight weeks","ALL","18 Years",{"count":68,"type":69},132,"ESTIMATED","INTERVENTIONAL",[72],"NA","This study will evaluate a new treatment program for patients with ongoing or long-term low back pain who receive care at primary care physiotherapy units. Participants with subacute or chronic nonspecific low back pain will be randomly divided into three groups for comparison of their progress. The first group will receive an eight-week program of therapeutic exercise and health education, which will be delivered entirely online. The second group will receive the same exercise and education program in face-to-face sessions. The third group will receive standard physiotherapy care. The study will last eight weeks, and researchers will follow up with participants three months later. The project's main goal is to measure changes in participants' daily disability levels. The researchers will also examine other important factors, such as pain intensity, fear of movement, anxiety, depression, quality of life, and overall satisfaction with the care received. Measurements will be taken before the study begins, immediately after the eight-week program ends, and at the three-month follow-up. This trial aims to find more accessible, evidence-based ways to treat back pain, reduce hospital waiting lists, and improve patient well-being by combining digital and in-person care.",[75],"Low Back Pain",[77,78,79,80,81],"low back pain","therapeutic exercise","pain education","primary health care","randomized controlled trial","NOT_YET_RECRUITING","2026-07-17",{"date":85,"type":86},"2026-07-21","ACTUAL",{"date":88,"type":69},"2027-03",{"date":90,"type":69},"2028-09",{"name":5,"class":6}]