[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Universitat de Lleida\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":395},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,14,0,[8,45,80,103,134,164,196,223,252,279,308,330,353,373],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":25,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100585274","knowledge-attitudes-and-beliefs-about-musculoskeletal-pain-among-primary-care-health-professionals-in-spain-100585274",false,"NCT06900231","Knowledge, Attitudes, and Beliefs About Musculoskeletal Pain Among Primary Care Health Professionals in Spain.","Knowledge, Attitudes, and Beliefs About Musculoskeletal Pain Among Primary Care Health Professionals in Different Autonomous Communities of Spain: A Cross-Sectional Study","CACDAPES","Inclusion Criteria:\n\n* Graduates in medicine or residents specializing in family and community medicine.\n\nGraduates in physiotherapy. Graduates in nursing or residents specializing in family and community nursing. Graduates in psychology. Graduates in nutrition.\n\nExclusion Criteria:\n\n\\-","ALL",{"count":19,"type":20},300,"ESTIMATED","OBSERVATIONAL","Pain is influenced by psychological and emotional factors, and healthcare professionals may unintentionally contribute to chronic disability by reinforcing fear and limiting normal activity. Patients with chronic pain often feel they lack adequate information to manage their condition.\n\nThis study aims to:\n\n* Assess primary care professionals' knowledge of pain neurophysiology in Spain.\n* Evaluate their attitudes and beliefs about chronic low back pain.\n* Examine their fear-avoidance beliefs related to pain. A cross-sectional study will gather data from primary care providers. The results will help guide educational strategies and policies to improve musculoskeletal pain management. This will be the first study in Spain to analyze these aspects among primary care professionals.",[24],"Fear Avoidance",[26,27,28,29,30,31],"Pain Management","Primary Health Care","Musculoskeletal Pain","Health Professionals","Fear-Avoidance","Pain Neurophysiology Knowledge","NOT_YET_RECRUITING","2026-04-27",{"date":35,"type":36},"2026-05-01","ACTUAL",{"date":38,"type":20},"2026-06",{"date":40,"type":20},"2027-03",{"name":42,"class":43},"Universitat de Lleida","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":17,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":66,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":44},"100622304","gel-aid-safe-and-effective-hydration-for-institutionalized-older-adults-100622304","NCT07381881","GEL-AID: Safe and Effective Hydration for Institutionalized Older Adults","Efficacy and Efficiency of GEL-AID Gelled Water for Hydration in Institutionalized Older People","Inclusion Criteria:\n\n* Age equal to or greater than 65 years.\n\nExclusion Criteria:\n\n* No exclusion criteria have been established.",true,"65 Years",{"count":55,"type":20},156,"INTERVENTIONAL",[58],"NA","The objective of this clinical trial is to assess whether hydration with gelled water (GEL-AID) can improve fluid intake and reduce cases of dehydration, as well as the incidence of urinary and respiratory infections in institutionalized elderly individuals in nursing homes.\n\nThe main question this trial aims to answer is:\n\n• Do institutionalized elderly individuals hydrated with GEL-AID increase their daily fluid intake and reduce the incidence of dehydration, urinary infections, and respiratory infections?\n\nParticipants:\n\nThe control group will follow the center's usual hydration plan. Individuals with swallowing difficulties will receive thickened liquids and\u002For gelatin, while those without swallowing difficulties will be hydrated with unmodified liquids or gelatin.\n\nThe intervention group will receive hydration with GEL-AID. For participants with swallowing difficulties, thickened liquids and gelatin will be replaced by GEL-AID, with texture adapted to their needs. Those without swallowing difficulties will receive unmodified liquids and GEL-AID instead of gelatin.",[61,62,63,64,65],"Dehydration","Urinary Infections","Respiratory Infections","Daily Fluid Intake","Mortality",[67,68,69,70,71],"dehydration","aged","nursing homes","fluid intake","gelled water","2026-01-27",{"date":74,"type":36},"2026-02-02",{"date":76,"type":20},"2026-02-23",{"date":78,"type":20},"2027-12-31",{"name":42,"class":43},{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":86,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":17,"minAge":88,"maxAge":4,"enrollmentInfo":89,"targetDuration":4,"studyType":56,"phases":91,"briefSummary":92,"conditions":93,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":44},"100608357","telerehabilitation-for-core-stability-and-strength-in-hereditary-ataxia-100608357","NCT07200505","Telerehabilitation for Core Stability and Strength in Hereditary Ataxia","A Telerehabilitation Intervention Targeting Core Stability and Muscular Strength in Individuals With Moderate-to-Advanced Hereditary Ataxia: A Pilot Study","TRCORE-AH2","Inclusion Criteria:\n\n* Confirmed diagnosis of spinocerebellar hereditary ataxia.\n* Moderate severity defined by the SARA scale (10-20 points, Traschütz et al., 2023).\n* Stable internet access and suitable electronic devices.\n\n  * Basic digital literacy.\n  * Signed informed consent.\n\nExclusion Criteria:\n\n* Mild (\\\u003C10) or severe (\\>20) scores on the SARA scale.\n* Severe comorbidities preventing safe exercise participation.\n* Severe cognitive impairment that would preclude program adherence.","18 Years",{"count":90,"type":20},24,[58],"This is a two-arm, controlled clinical trial with a parallel design. Participants will be randomly assigned to an intervention or control group. The study is single-blind, as outcome assessors will be blinded to group allocation, while participants and physiotherapists cannot be blinded due to the nature of the intervention. Consecutive sampling will be applied.\n\nFor the evaluation of intervention effects (primary and secondary outcomes), the study will follow the Consolidated Standards of Reporting Trials (CONSORT) for non-pharmacological interventions. For the assessment of satisfaction and adherence, a qualitative study will be conducted following the COREQ EQUATOR 17 guidelines to ensure methodological rigor.\n\nThe intervention will consist of a 12-week home-based exercise program supervised via mixed telerehabilitation (TR). The control group will perform the same program but receive only telephone follow-up. Four assessments will be conducted: baseline (T0), post-intervention (T1), three months follow-up (T2), and six months follow-up (T3).",[94],"Hereditary Ataxia","2025-09-26",{"date":97,"type":36},"2025-10-01",{"date":99,"type":20},"2026-02-09",{"date":101,"type":20},"2026-12-21",{"name":42,"class":43},{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":4,"eligibilityCriteria":109,"healthyVolunteers":11,"sex":17,"minAge":53,"maxAge":4,"enrollmentInfo":110,"targetDuration":4,"studyType":56,"phases":112,"briefSummary":113,"conditions":114,"keywords":119,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":4},"100608704","freefrail-project-a-multicomponent-intervention-for-the-management-of-frailty-in-primary-care-a-randomized-controlled-trial-100608704","NCT07205016","FreeFrail Project: A Multicomponent Intervention for the Management of Frailty in Primary Care: A Randomized Controlled Trial","FreeFrail Project: Effectiveness of a Multicomponent Intervention Including Dual-task Exercise to Increase Functionality and Cognitive Performance in Frail and Pre-frail Individuals Over 65 Years Aged in Primary Care Compared to Usual Care: Protocol for a Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged 65 or older\n* Frailty according to Fragil-VIG index (\\>0,20)\n* Barthel index \\> 60\n* Able to perform physical exercise\n* Able to understand and communicate in Catalan or Spanish\n\nExclusion Criteria:\n\n* Decompensated \u002F Unstable cardiovascular disease or recent diagnosed\n* Upper or lower injury with functional impairment\n* Institutionalized patient.\n* Terminal or tumoral processes\n* People who participated in another clinical trial or exercise programme during last year\n* Diagnosis of severe dementia",{"count":111,"type":20},220,[58],"The primary aim is to assess the effectiveness of a multicomponent intervention including dual-task exercise in improving functionality and cognitive performance and in reducing frailty among community-dwelling adults aged ≥65 years compared to usual care. Secondary objectives include evaluating its impact on pain, anxiety or depression, sleep quality, quality of life, physical activity, handgrip strength, and polypharmacy.\n\nA double-blind, randomized, parallel-group controlled trial will be conducted in primary care centers in Lleida. Frail older adults (≥65 years) will be recruited and randomly allocated to either the intervention group, receiving a structured cognitive-motor dual-task based multicomponent program, or the control group, receiving usual care. Outcomes will be assessed using validated tools at baseline and follow-up.",[115,116,117,118],"Frail Elderly","Dual Task Exercises in Elderly People","Exercise Training","Frailty",[120,121,122,123,124,125],"primary care Health [MeSH]","multicomponent intervention","exercise therapy [MeSH]","cognitive-motor dual-task","frail elderly [MeSH]","frailty [MeSH]","2025-09-24",{"date":128,"type":36},"2025-10-03",{"date":130,"type":20},"2026-01",{"date":132,"type":20},"2026-10",{"name":42,"class":43},{"id":135,"slug":136,"hasResults":11,"nctId":137,"briefTitle":138,"officialTitle":139,"acronym":4,"eligibilityCriteria":140,"healthyVolunteers":52,"sex":17,"minAge":88,"maxAge":141,"enrollmentInfo":142,"targetDuration":4,"studyType":56,"phases":144,"briefSummary":145,"conditions":146,"keywords":149,"overallStatus":155,"whyStopped":4,"lastUpdateSubmitDate":156,"lastUpdatePostDateStruct":157,"startDateStruct":159,"completionDateStruct":161,"leadSponsor":163,"locationsCount":44},"100544151","an-algorithm-for-approaching-temporomandibular-disorders-with-osteopathic-manual-therapy-in-patients-with-fibromyalgia-100544151","NCT06365151","An Algorithm for Approaching Temporomandibular Disorders With Osteopathic Manual Therapy in Patients With Fibromyalgia","Effectiveness of an Algorithm for Approaching Temporomandibular Disorders With Osteopathic Manual Therapy in Patients With Fibromyalgia","Inclusion Criteria:\n\n* be diagnosed as suffering from fibromyalgia,\n* present moderate pain or dysfunction of more than 3 months' duration in the temporomandibular joint,\n* be over 18 years old,\n* understand Spanish and\u002For Catalan correctly,\n* and read and accept the informed consent form\n\nExclusion Criteria:\n\n* history of trauma or recent surgery to the head, face or neck;\n* systemic, rheumatic or central nervous system diseases;\n* diagnosis of malignant tumors or cancer in the orofacial region;\n* participate in other studies at the same time.","75 Years",{"count":143,"type":20},114,[58],"Nowadays, fibromyalgia is the rheumatic disorder with the highest levels of deterioration in quality of life. Among the comorbidities it presents, one of the most frequent is temporomandibular disorders. A randomized clinical study will be conducted to evaluate the effectiveness of an osteopathic manual therapy approach algorithm in a group of patients with fibromyalgia and temporomandibular disorders.",[147,148],"Fibromyalgia","Temporomandibular Disorder",[150,151,152,153,154],"temporomandibular joint disorders","fibromyalgia","Osteopathic medicine","chronic pain","musculoskeletal manipulations","RECRUITING","2025-08-27",{"date":158,"type":36},"2025-09-04",{"date":160,"type":36},"2024-04-05",{"date":162,"type":20},"2026-04-05",{"name":42,"class":43},{"id":165,"slug":166,"hasResults":11,"nctId":167,"briefTitle":168,"officialTitle":169,"acronym":170,"eligibilityCriteria":171,"healthyVolunteers":52,"sex":17,"minAge":172,"maxAge":173,"enrollmentInfo":174,"targetDuration":4,"studyType":56,"phases":176,"briefSummary":177,"conditions":178,"keywords":182,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":188,"lastUpdatePostDateStruct":189,"startDateStruct":191,"completionDateStruct":193,"leadSponsor":195,"locationsCount":44},"100578330","management-of-non-pharmacologic-delirium-with-the-use-of-a-nursing-led-e-health-project-a-randonmized-controlled-trial-100578330","NCT06809894","Management of Non-pharmacologic Delirium With the Use of a Nursing-led E-health Project: a Randonmized Controlled Trial","Improvement of the Delirium Management in Adult Patients Hospitalized Through the Use of Non-pharmacological Interventions","Delirium","Inclusion criteria:\n\n* Age over 80 years\n* Three risk factor to develop delirium, for example: sex (men), polypharmacy,urinary tract infections (UTIs) or strictures.\n* Admission in geriatric unit.\n* Have social support\n\nExclusion criteria:\n\n* Age under 80 years\n* Eseeable death on admission not caused by delirium or delirium diagnosis on admission.","80 Years","130 Years",{"count":175,"type":20},65,[58],"Application of an action protocol focused on the application of non-pharmacological interventions for managing delirium in the process of prevention, diagnosis and treatment, evaluated using an e-health intervention, with a tablet to introduce on it the data about the prevention, diagnostic and treatment process of each recluted patient, in the Igualada Hospital Center, once a day.",[179,180,181],"Delirium Treatment","Delirium Confusional State","Delirium in Old Age",[170,183,184,185,186,187],"SCA","CAM","Older pacient","non-pharmacologic treatment","nurse","2025-05-22",{"date":190,"type":36},"2025-05-29",{"date":192,"type":20},"2026-04-01",{"date":194,"type":20},"2027-06-15",{"name":42,"class":43},{"id":197,"slug":198,"hasResults":11,"nctId":199,"briefTitle":200,"officialTitle":201,"acronym":202,"eligibilityCriteria":203,"healthyVolunteers":11,"sex":17,"minAge":88,"maxAge":53,"enrollmentInfo":204,"targetDuration":4,"studyType":56,"phases":206,"briefSummary":207,"conditions":208,"keywords":209,"overallStatus":155,"whyStopped":4,"lastUpdateSubmitDate":214,"lastUpdatePostDateStruct":215,"startDateStruct":217,"completionDateStruct":219,"leadSponsor":221,"locationsCount":222},"100481928","body-awareness-therapy-and-biomarkers-in-fibromyalgia-100481928","NCT05555394","Body Awareness Therapy and Biomarkers in Fibromyalgia","Effectiveness of a Rehabilitation Programme Based on Lifestyle Changes and Self-care in Patients Diagnosed With Fibromyalgia: Neuroinflammatory and Neuropsychological Biomarkers.","BATBF","Inclusion Criteria:\n\n* whose diagnosed of fibromyalgia almost 6 months before\n* whose could be in different position such as lying, sitting, and stand-up\n\nExclusion Criteria:\n\n* whose are diagnosed of disease that it worse the pain\n* pregnancy\n* whose are diagnosed of other disease such as rheumatology, neurology, cardiac problems o another internal medical condition,malignant disease or acute infections",{"count":205,"type":20},110,[58],"A randomized trial of Basic Body Awareness Therapy (BBAT) is applied in fibromyalgia patients as compared with a control intervention consisting of stretching. Sessions of BBAT lasted 90 min each and took place twice a week form 12 weeks. The primary end point is a change in the biomarkers and neurotransmitters and the Fibromyalgia Impact Questionnaire and the secondary end points include Visual Analog Scale, State Trait Anxiety inventory, Beck Depression Inventory. All assessments will be repeated at post treatment, 12 and 24 weeks and 1 year follow-up.",[147],[210,211,212,213],"Body awareness therapy","physical therapy","serotonin","cortisol","2025-05-05",{"date":216,"type":36},"2025-05-08",{"date":218,"type":36},"2024-05-08",{"date":220,"type":20},"2025-09-01",{"name":42,"class":43},2,{"id":224,"slug":225,"hasResults":11,"nctId":226,"briefTitle":227,"officialTitle":228,"acronym":229,"eligibilityCriteria":230,"healthyVolunteers":52,"sex":17,"minAge":88,"maxAge":53,"enrollmentInfo":231,"targetDuration":4,"studyType":56,"phases":233,"briefSummary":234,"conditions":235,"keywords":239,"overallStatus":155,"whyStopped":4,"lastUpdateSubmitDate":244,"lastUpdatePostDateStruct":245,"startDateStruct":247,"completionDateStruct":249,"leadSponsor":251,"locationsCount":44},"100580799","protocol-to-improve-the-representation-of-the-reproductive-process-in-spanish-fiction-100580799","NCT06842004","Protocol to Improve the Representation of the Reproductive Process in Spanish Fiction.","Protocol to Improve the Representation of the Reproductive Process in Spanish Fiction: Sequential Transformative Approach, With Qualitative Predominance and Participatory Action.","MaterScreen","Inclusion Criteria Users:\n\n* Participated in the group health education program at the primary sexual and reproductive health care centers (ASSIR), attended at least 3 sessions.\n* Signed the informed consent form.\n\nExclusion Criteria Users:\n\n\\- Language barrier (Spanish\u002FCatalan) that limits their ability to have a relaxed conversation.\n\nInclusion Criteria Health Professionals:\n\n* Employed by the Institut Català de la Salut, specifically within the obstetrics and gynecology team at the Hospital Universitari Arnau de Vilanova (HUAV) or primary health care (ASSIR)\n* Signed the informed consent form.\n\nExclusion Criteria Health Professionals:\n\n\\- No exclusion criteria were applied.",{"count":232,"type":20},60,[58],"The aim of this study is to promote the inclusive and plural representation of reproductive processes in Spanish fiction, in order to generate knowledge, emotional well-being and improve the quality of life of people in similar situations. The question to be answered is\n\nWill a handbook of good practices used in the training of scriptwriters and audiovisual creators, based on the testimonies of people experiencing reproductive processes and developed with the collaboration of experts (gynaecologists, midwives -ACL-, audiovisuals -Dones Visuals- and scriptwriters -Guionistes Associats-) promote the inclusive and updated representation of reproductive processes?\n\nFocus groups with people involved in reproductive processes and in-depth interviews with professionals involved in these processes will be carried out. A manual of good practices will then be developed in collaboration with audiovisual experts and scriptwriters.",[236,237,238],"Sexual Health","Community Participation","Social Norms",[240,241,242,243],"sexual health","motion pictures","community participation","social norms","2025-04-14",{"date":246,"type":36},"2025-04-18",{"date":248,"type":36},"2025-04-01",{"date":250,"type":20},"2026-12",{"name":42,"class":43},{"id":253,"slug":254,"hasResults":11,"nctId":255,"briefTitle":256,"officialTitle":257,"acronym":4,"eligibilityCriteria":258,"healthyVolunteers":11,"sex":17,"minAge":88,"maxAge":4,"enrollmentInfo":259,"targetDuration":261,"studyType":21,"phases":4,"briefSummary":262,"conditions":263,"keywords":266,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":272,"lastUpdatePostDateStruct":273,"startDateStruct":275,"completionDateStruct":276,"leadSponsor":278,"locationsCount":4},"100586207","experiences-outcomes-and-unmet-needs-of-caregivers-of-children-with-cerebral-palsy-100586207","NCT06912373","Experiences, Outcomes and Unmet Needs of Caregivers of Children With Cerebral Palsy","Experiences, Outcomes and Unmet Needs of Caregivers of Children With Cerebral Palsy in Spain: A Mixed-Method Study","Inclusion Criteria:\n\n* \\>18 years old\n* Being a caregiver of a child with Cerebral Palsy\n* Spanish\u002FCatalan speaking\n* Willing to talk about their experiences and be audio\u002Fvideo-recorded.\n* Accept and sign the informed consent form",{"count":260,"type":20},30,"1 Day","Cerebral palsy (CP ) is one of the most prevalent motor disabilities in childhood, significantly impacting both children and their caregivers. This study explores the experiences, psychological well-being, and unmet needs of caregivers of children with CP. Using an explanatory sequential design (QUAN → QUAL), first it will be assessed burden, stress levels, and quality of life of caregivers through standardized questionnaires (PedsQL-FIM , ZBI , PSS-14 ).",[264,265],"Cerebral Palsy Infantile","Caregiver",[267,268,269,270,271],"Caregivers","Cerebral Palsy","Mixed-Method Research","Quality of Life","Parenting Stress","2025-03-30",{"date":274,"type":36},"2025-04-04",{"date":248,"type":20},{"date":277,"type":20},"2025-08-01",{"name":42,"class":43},{"id":280,"slug":281,"hasResults":11,"nctId":282,"briefTitle":283,"officialTitle":284,"acronym":4,"eligibilityCriteria":285,"healthyVolunteers":52,"sex":286,"minAge":88,"maxAge":53,"enrollmentInfo":287,"targetDuration":261,"studyType":21,"phases":4,"briefSummary":289,"conditions":290,"keywords":296,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":300,"lastUpdatePostDateStruct":301,"startDateStruct":303,"completionDateStruct":305,"leadSponsor":307,"locationsCount":4},"100563837","hemonirs-a-paradigm-shift-in-the-process-of-musculoskeletal-rehabilitation-of-acl-injuries-in-cyclic-sports-athletes-100563837","NCT06621355","HemoNIRS: a Paradigm Shift in the Process of Musculoskeletal Rehabilitation of ACL Injuries in Cyclic Sports Athletes.","HemoNIRS: Un Cambio De Paradigma En El Proceso De Rehabilitación Musculoesquelética De Lesiones De Ligamento Cruzado Anterior Mediante Dispositivos NIRS En Deportistas Que Realizan Deportes Cíclicos","General inclusion criteria\n\n* Men aged 18 to 65\n* An adipose layer of \\<2 cm in areas of NIRS placement, assessed with a plicometer\n* Understand written, read and spoken Spanish, English or Catalan.\n\nGeneral exclusion criteria\n\n* Having any cardio-metabolic, hormonal, neurological or other comorbidities that could affect participation in the study (e.g. severe mental illness, end-stage disease).\n\nEligibility criteria (LCA1 group)\n\n* Regular athlete with training and\u002For competition \\>3 days\u002Fwk prior to injury.\n* ACL injury \\<6 months after surgery.\n* Able to perform an incremental intervallic test on a cycloergometer or treadmill.\n\nEligibility criteria (LCA2 group)\n\n* Regular athlete with training and\u002For competition \\>3 days a week.\n* ACL injury \\>2 years after surgery.\n* Able to perform an incremental intervallic test on a cycloergometer or treadmill.\n\nEligibility criteria (CON group)\n\n* Regular athlete with training and\u002For competition \\>3 days a week.\n* Never suffered an ACL injury in any knee - Able to perform incremental intervallic test on cycleergometer or treadmill.\n\nAll the groups exclusion criteria\n\n\\- Incapacitating pain that prevents assessment","MALE",{"count":288,"type":20},129,"Muscle haemodynamics has so far been assessed using at most 2-3 near-infrared spectroscopy devices on isolated muscles and without correlating variables. At the same time, research on musculoskeletal pathologies is limited, and there are no studies that analyse the haemodynamic changes that occur when the anterior cruciate ligament (ACL) is injured and whether these changes last over time. The aim of the study is to monitor and evaluate the physiological changes produced by ACL injury on muscle performance using non-invasive near-infrared spectroscopy (NIRS) devices in trained athletes. This descriptive cross-sectional observational multicentre multicentre study, with Balearic Islands ethics committee IB 5585\u002F24PI, will include males aged 18-65 years who have undergone ACL surgery, divided into 3 groups that: have an evolution of less than 6 months (ACL1), more than 2 years since the surgical intervention and are already practising normal physical-sports activities (ACL2) and the control group (CON) that has never suffered an ACL affectation to date. The 3 groups will perform an incremental intervallic test (4:1) on a cycloergometer or treadmill (according to the specificity of their sport), where different muscular haemodynamic variables will be assessed using 12-24 NIRS devices. The main study variables will be the muscular haemodynamic values of each muscle analysed and their correlation between them: muscular oxygen saturation, absolute capillary haemoglobin, loaded and unloaded with oxygen and relative muscular haemoglobin blood flow, loaded and unloaded with oxygen. Secondary variables will be heart rate, socio-demographic variables (age, toxic habits, injury and sports history) and subjective perception of effort (RPE-20).",[291,292,293,294,295],"ACL - Anterior Cruciate Ligament Rupture","ACL Injury","Hemodynamics","Oxygen Consumption Based Assessment of Hemodynamics","Exercise",[297,293,295,298,299],"Spectroscopy, Near-Infrared","Vascular resistance","Oxygen consumption","2024-09-27",{"date":302,"type":36},"2024-10-01",{"date":304,"type":20},"2024-12-02",{"date":306,"type":20},"2026-12-02",{"name":42,"class":43},{"id":309,"slug":310,"hasResults":11,"nctId":311,"briefTitle":312,"officialTitle":313,"acronym":4,"eligibilityCriteria":314,"healthyVolunteers":11,"sex":17,"minAge":315,"maxAge":316,"enrollmentInfo":317,"targetDuration":4,"studyType":56,"phases":318,"briefSummary":319,"conditions":320,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":322,"lastUpdatePostDateStruct":323,"startDateStruct":325,"completionDateStruct":327,"leadSponsor":329,"locationsCount":44},"100454544","the-effectiveness-of-repetitive-transcranial-magnetic-stimulation-for-spastic-diplegia-cerebral-palsy-100454544","NCT05198921","The Effectiveness of Repetitive Transcranial Magnetic Stimulation for Spastic Diplegia Cerebral Palsy","The Effectiveness of Repetitive Transcranial Magnetic Stimulation for the Treatment of Spastic Diplegia Cerebral Palsy Based on the Gross Motor Function in School-aged Children: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Primary school children with diagnose of Spastic Diplegia CP\n* \\> 1 on Mas in hip flexors, adductors and tibialis anterior of both lower extremities.\n* Parents\u002Flegal guardians signed the Informed consent\n\nExclusion Criteria:\n\n* Severe mental retardation\n* Present epilepsy\n* Present any remedial surgery\u002Fmedication\n* Less than 1 year post orthopaedic surgery\n* Less than 6 months post botulinum toxin type A injection\n* Present metallic implants\n* Present any comorbidity unfit for the study\n* Congenital disorders such as Down's syndrome, fragile-x syndrome or congenital anomalies","6 Years","12 Years",{"count":260,"type":20},[58],"Cerebral palsy describes a group of permanent disorders of the development of movement and posture, causing activity limitation that are attributed to non-progressive disturbances that occurred in the developing fetal or infant brain.\n\nNowadays, CP is not fully curable, and physiotherapy should be used in conjunction with other interventions such as oral drugs, botulinum toxin type A, continuous pump-administered intrathecal baclofen, orthopaedic surgery and selective dorsal rhizotomy. However, several systematic reviews conclude that there is low evidence that these invasive therapies are more effective than placebo.\n\nRepetitive transcranial magnetic stimulation (rTMS) is a type of neuromodulatory technique through magnetic impulses. The effect of rTMS depends on the frequency of the emitted electromagnetic field; low frequencies (≤1 Hz) lead to an inhibition of neuronal electrical activity at the stimulation site, while high frequencies (≥3 Hz) cause neuronal depolarization.\n\nThe objective of the project is to evaluate the effectiveness of a repetitive Transcranial Magnetic Stimulation (rTMS) protocol, as an adjunct treatment to neurorehabilitation to improve gross motor function and quality of life in school-age children with spastic diplegia-type infantile cerebral palsy.",[321],"Cerebral Palsy, Spastic","2024-09-13",{"date":324,"type":36},"2024-09-19",{"date":326,"type":20},"2025-01",{"date":328,"type":20},"2025-06",{"name":42,"class":43},{"id":331,"slug":332,"hasResults":11,"nctId":333,"briefTitle":334,"officialTitle":335,"acronym":4,"eligibilityCriteria":336,"healthyVolunteers":11,"sex":17,"minAge":88,"maxAge":4,"enrollmentInfo":337,"targetDuration":4,"studyType":56,"phases":339,"briefSummary":340,"conditions":341,"keywords":343,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":347,"lastUpdatePostDateStruct":348,"startDateStruct":349,"completionDateStruct":351,"leadSponsor":352,"locationsCount":4},"100557327","intervention-to-reduce-infectious-complications-of-peritoneal-dialysis-100557327","NCT06536673","Intervention to Reduce Infectious Complications of Peritoneal Dialysis","Educational Intervention Aimed At Reducing Infectious Complications Related to Peritoneal Dialysis","Inclusion Criteria:\n\n* Patients \\>18 years of age\n* Medically stable\n* Who can perform dialysis themselves or with the help of a caregiver willing to participate in the study and sign the informed consent will be included\n\nExclusion Criteria:\n\n* Patients with psychiatric, psychological disorders and social (language barrier included)\n* Who do not have a formal\u002Finformal caregiver\n* Those who due to medical needs cannot continue with the standard schedule, pregnant women, participants who suffered peritonitis before receiving the educational intervention",{"count":338,"type":20},80,[58],"Peritonitis is a common and serious complication of peritoneal dialysis (PD) and is one of the main causes of peritoneal dialysis technique failure and long-term hemodialysis conversion.",[342],"Peritoneal Infection",[344,345,346],"Educational intervention","Peritoneal dialysis","Peritonitis","2024-09-06",{"date":324,"type":36},{"date":350,"type":20},"2024-09-15",{"date":220,"type":20},{"name":42,"class":43},{"id":354,"slug":355,"hasResults":11,"nctId":356,"briefTitle":357,"officialTitle":358,"acronym":4,"eligibilityCriteria":359,"healthyVolunteers":11,"sex":17,"minAge":88,"maxAge":4,"enrollmentInfo":360,"targetDuration":4,"studyType":56,"phases":361,"briefSummary":362,"conditions":363,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":367,"lastUpdatePostDateStruct":368,"startDateStruct":370,"completionDateStruct":371,"leadSponsor":372,"locationsCount":44},"100558927","the-effects-of-mindfulness-based-stress-reduction-program-for-family-or-caregivers-of-children-with-motor-disabilities-100558927","NCT06557486","The Effects of Mindfulness-Based Stress Reduction Program for Family or Caregivers of Children With Motor Disabilities","The Effects of Mindfulness-Based Stress Reduction Program on the Psychological and Physiological Stress of Family or Caregivers of Children With Motor Disabilities Due to a Neurological Disorder: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Not having attended previously a mindfulness course\n* A score equal to or greater than 23 points at the PSS.\n* \\>18 years old\n* Children \\\u003C18y with motor\u002Fphysical disability due to a Neurological disorder.\n* Spanish\u002FCatalan speaking\n\nExclusion Criteria:\n\n* Currently using drugs or any kind of medication related to stress, depression, anxiety or sleeping pills, such as steroid medicines.\n* Regular meditation practice (once a week in the past 12 months)\n* Diagnose of hypertension stage 2\n* Pregnancy in the case of mothers\n* Present hyperthyroidism\n* Primary adrenal insufficiency syndromes such as Cushing syndrome or Addison disease\n* Present any kind of infection or inflammation process, different from the interestingly to the present study that could differ the results",{"count":338,"type":20},[58],"The present study aims to investigate the effect of a mindfulness-based program on perceived stress, severity of anxiety, parents'\u002Fcaregivers' quality of life and their children, cortisol and IL-6 blood concentrations.",[364,365,366],"Stress, Psychological","Stress, Emotional","Stress","2024-08-13",{"date":369,"type":36},"2024-08-16",{"date":326,"type":20},{"date":328,"type":20},{"name":42,"class":43},{"id":374,"slug":375,"hasResults":11,"nctId":376,"briefTitle":377,"officialTitle":378,"acronym":4,"eligibilityCriteria":379,"healthyVolunteers":11,"sex":17,"minAge":380,"maxAge":172,"enrollmentInfo":381,"targetDuration":4,"studyType":56,"phases":383,"briefSummary":384,"conditions":385,"keywords":4,"overallStatus":155,"whyStopped":4,"lastUpdateSubmitDate":387,"lastUpdatePostDateStruct":388,"startDateStruct":390,"completionDateStruct":392,"leadSponsor":394,"locationsCount":44},"100550254","effects-of-table-tennis-for-people-with-parkinsons-disease-100550254","NCT06444685","Effects of Table Tennis for People With Parkinson's Disease","Motor and Cognitive Effects of Table Tennis on Parkinson's Disease: Pilot Controlled Trial","Inclusion Criteria:\n\n* Diagnosis of Parkinson's Disease based on the UK PD Society Brain Bank Criteria\n* Stage I to III on the Hoehn and Yahr scale\n* Ability to walk for 10 minutes unassisted\n\nExclusion Criteria:\n\n* Score of under 23 on the Mini-Mental State Examination\n* Severe Visual or Auditory deficits\n* Cardiovascular conditions that impede physical activity\n* Brain surgery","40 Years",{"count":382,"type":20},20,[58],"Quasi-experimental, controlled, non-randomised two-arm pilot, with an experimental group (table tennis exercise) and an active control group (cognitive training based on board games).",[386],"Parkinson Disease","2024-05-30",{"date":389,"type":36},"2024-06-05",{"date":391,"type":36},"2023-10-01",{"date":393,"type":20},"2026-06-30",{"name":42,"class":43},""]