[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Universidad de Extremadura\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":111},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,81],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":4},"100640751","study-protocol-the-jerte-valley-as-an-inclusive-outdoor-classroom-smart-and-active-tourism-100640751",false,"NCT07609459","Study Protocol: The Jerte Valley as an Inclusive Outdoor Classroom. Smart and Active Tourism.","Inclusion Criteria:\n\n* 12 -16 years\n* Enrollment in public schools and special education centers\n* Informed consent signed by tutors\n\nExclusion Criteria:\n\n* Have health issues that prevent them from participating in physical activity or pose a safety risk to participants\n* Not having a signed informed consent",true,"ALL","12 Years",{"count":19,"type":20},35,"ESTIMATED","INTERVENTIONAL",[23],"NA","To promote the inclusion of people with disabilities, an outdoor intervention will be conducted involving physical activities with adolescents with and without disabilities. The study will be designed as a randomized controlled trial (RCT) with a control group that will not participate in these activities, and will include three time points (pre-intervention, post-intervention, and follow-up). The study will assess sociodemographic, accessibility, socio-emotional, and group cohesion variables.",[26,27],"Disabilities","Visual Impairment and Blindness (Excl Colour Blindness)",[29,30,31,32,33],"visual impairment","disability","inclusion","physical activity","smart tourism","NOT_YET_RECRUITING","2026-05-19",{"date":37,"type":38},"2026-05-27","ACTUAL",{"date":40,"type":20},"2026-06-01",{"date":42,"type":20},"2026-08-01",{"name":44,"class":45},"Universidad de Extremadura","OTHER",{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":15,"sex":16,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":21,"phases":58,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},"100614193","study-on-the-effect-of-a-gamified-health-education-programme-on-primary-school-children-100614193","NCT07276412","Study on the Effect of a Gamified Health Education Programme on Primary School Children","Study on the Effect of a Health Education Programme Based on Gamification Strategies on Diet, Sedentary Behaviour and Daily Physical Activity in Primary School Children.","BELLOTEX-SALUD","Inclusion Criteria:\n\n* Pupils enrolled in primary education at schools in Extremadura.\n\nExclusion Criteria:\n\n* All pupils diagnosed with special educational needs will be excluded.\n* Pupils who join after the programme has started.\n* Absence of informed consent signature to participate in the study and use of the BELLOTEX-SALUD application by the child's parents or legal guardians.\n* Any condition that, in the opinion of the investigators, would disqualify the subject from participation in the study.","6 Years","7 Years",{"count":57,"type":20},500,[23],"This randomised study evaluates the effectiveness of Health Education through a Gamified Health Programme on diet, sedentary behaviour and daily physical activity in primary school children.",[61,62],"Gamification in Health Education","Health Education",[64,65,66,67,62,68,69,70],"school","child","obesity","physical activities","Quality of Life","Gamification","sedentary","RECRUITING","2025-11-28",{"date":74,"type":38},"2025-12-11",{"date":76,"type":38},"2024-09-02",{"date":78,"type":20},"2026-09-07",{"name":44,"class":45},1,{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":87,"eligibilityCriteria":88,"healthyVolunteers":11,"sex":89,"minAge":90,"maxAge":4,"enrollmentInfo":91,"targetDuration":4,"studyType":21,"phases":93,"briefSummary":94,"conditions":95,"keywords":97,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":80},"100594291","cognitive-training-and-exercise-for-women-with-breast-cancer-and-cognitive-impairment-100594291","NCT07017530","Cognitive Training and Exercise for Women With Breast Cancer and Cognitive Impairment","Combined Intervention of Cognitive Training and Supervised Physical Exercise for Women With Breast Cancer and Chemotherapy-Related Cognitive Impairment: Study Protocol for a Randomized Controlled Trial","CHEMO-CogEx","Inclusion Criteria:\n\n* Women aged 18 years or older who were diagnosed with stage 0 to IV breast cancer.\n* Women undergoing chemotherapy (at least two cycles) or having completed it at least six months earlier.\n* Cognitive impairment must be reported, with scores below 54 on the FACT-Cog scale\n\nExclusion Criteria:\n\n* Women with significant neurological conditions.\n* Women with psychiatric conditions.\n* Women with contraindications for physical exercise.","FEMALE","18 Years",{"count":92,"type":20},220,[23],"Chemotherapy-related cognitive impairment is a prevalent and distressing condition among breast cancer survivors, adversely affecting memory, attention, and overall cognitive function, thereby diminishing quality of life. Emerging evidence suggests that multimodal interventions combining cognitive training and adapted physical exercise may mitigate these cognitive deficits and associated symptoms. This study aims to evaluate the efficacy of a 12-week structured intervention integrating cognitive training and supervised physical exercise in improving cognitive function, fatigue, sleep quality, psychological distress, and overall well-being in women with breast cancer. Furthermore, it seeks to determine the optimal timing for such interventions to maximize their effectiveness. A randomized controlled trial involving 220 participants will assess subjective and objective cognitive outcomes, brain activity, and physical performance. The findings from this research may contribute to the development of evidence-based rehabilitation strategies, enhancing cognitive health and quality of life in breast cancer patients.",[96],"Breast Cancer",[98,99,100,101,102],"Breast cancer","Chemotherapy-Related Cognitive Impairment","Cognitive Training","Exercise","Oncology Nursing","2025-06-03",{"date":105,"type":38},"2025-06-12",{"date":107,"type":20},"2025-09-01",{"date":109,"type":20},"2028-08-31",{"name":44,"class":45},""]