[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Universidad Catolica de Temuco\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":105},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,77],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":31,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100639538","cross-education-of-skill-and-strength-in-healthy-people-subjected-to-an-upper-limb-disuse-model-100639538",false,"NCT07615062","Cross-education of Skill and Strength in Healthy People Subjected to an Upper-limb Disuse Model","Cross-education of Skill and Strength Through Contralateral Manual Dexterity Training in Healthy Young Adults Subjected to an Upper-limb Disuse Model: A Randomized Controlled Trial.","IMMO-CROSS","Inclusion Criteria:\n\n* Individuals will be eligible for inclusion if they are right-handed adults aged 18 to 35 years with a body mass index (BMI) between 18.5 and 30 kg\u002Fm².\n* Individuals must be classified as physically inactive, defined as not meeting the World Health Organization criteria of at least 150 minutes of moderate-intensity physical activity or 75 minutes of vigorous-intensity physical activity per week.\n\nExclusion Criteria:\n\n* Individuals who have engaged in physical training (e.g., any form of strength or aerobic exercise) or specific manual dexterity training within the past 6 months. - Individuals who regularly participate in artistic, occupational, or sporting activities requiring high levels of manual dexterity (e.g., musicians, gamers, craftspeople).\n* Individuals with a history of orthopedic or traumatic injuries affecting either upper extremity. Individuals with pathologies or conditions that preclude safe training (e.g., uncontrolled hypertension, or visual, auditory, or cognitive impairments \\[for example, dyscalculia\\]).\n* Individuals currently using nutritional supplements or medications that interfere with the regulation of skeletal muscle mass and strength (e.g., whey protein, creatine) or the central nervous system (e.g., antidepressants, anxiolytics, hypnotics).",true,"ALL","18 Years","35 Years",{"count":22,"type":23},34,"ESTIMATED","INTERVENTIONAL",[26],"NA","This randomized controlled trial aims to compare manual dexterity and strength between a group undergoing a contralateral manual dexterity training program and a no-intervention control group in healthy, physically inactive individuals subjected to an induced upper-limb disuse model.",[29,30],"Disuse Atrophy","Immobilization",[32,30,33,34],"Cross-education","contralateral training","interlimb transfer","NOT_YET_RECRUITING","2026-05-22",{"date":38,"type":39},"2026-05-29","ACTUAL",{"date":41,"type":23},"2026-05-25",{"date":43,"type":23},"2027-01-30",{"name":45,"class":46},"Universidad Catolica de Temuco","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":24,"phases":58,"briefSummary":59,"conditions":60,"keywords":63,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":47},"100626464","cor-protocol-for-the-treatment-of-binge-eating-in-chilean-adults-cor-100626464","NCT07435974","COR Protocol for the Treatment of Binge Eating in Chilean Adults (COR)","A Pilot Study on the Feasibility and Acceptability of the COR (Body Compassion-Emotional Regulation-Conscious Reconnection With Eating) Protocol for Addressing Binge Eating in Chilean Adults","COR","Inclusion Criteria:\n\n* Adults aged 18 years or older.\n* Overweight or obesity, based on self-report.\n* At least three binge-eating episodes in the past 30 days, associated with psychological distress.\n* The presence of chronic medical conditions commonly associated with overweight or obesity (e.g., hypothyroidism, hyperthyroidism, dyslipidemia, hypertension, type 2 diabetes mellitus, or polycystic ovary syndrome) is permitted, provided that such conditions are medically stable.\n* If present, chronic medical conditions must be medically stable, defined as:\n* stable medical treatment for at least 12 weeks,\n* no recent changes in medication,\n* no acute clinical decompensation or recent major cardiovascular events,\n* at least one related medical follow-up visit in the past 12 months.\n* If present, psychopharmacological treatment must be stable, defined as no changes in medication type or dosage during the 12 weeks prior to enrollment.\n* Daily access to the internet and to a computer or smartphone that allows participation in online sessions and assessments.\n\nExclusion Criteria:\n\n* Current compensatory behaviors associated with binge eating, such as self-induced vomiting and\u002For regular use of laxatives, within the past 60 days.\n\n  * Pregnancy or breastfeeding at the time of the initial assessment.\n  * History of bariatric surgery.\n  * Active suicidal ideation\n  * Current symptoms consistent with severe mental disorders, such as psychotic disorders, bipolar disorder, complex post-traumatic stress disorder, or severe personality disorders, when associated with marked functional impairment or the need for specialized or higher-intensity clinical care.\n  * Current substance use pattern that, due to its severity or functional impact, requires specialized clinical treatment.\n  * Ongoing psychological and\u002For nutritional treatment at the time of enrollment, defined as regular sessions or an active treatment plan, regardless of treatment focus or therapeutic approach.\n  * Presence of active or medically unstable conditions, characterized by clinically significant symptoms, lack of medical follow-up, or recent changes in medication, that could interfere with participation in the intervention or substantially affect eating behavior or mood.\n  * Significant functional impairment that, in the clinical judgment of the research team, would limit the participant's ability to engage safely and consistently in the intervention.",{"count":57,"type":23},30,[26],"The goal of this clinical study is to learn whether a brief online psychological program called COR can be delivered in a feasible and acceptable way for adults who experience recurrent binge eating.\n\nThe main questions this study aims to answer are:\n\n* Is the COR program acceptable to participants, in terms of satisfaction, adherence, and dropout rates?\n* Is the COR program feasible to deliver online, including recruitment, retention, and completion of sessions and questionnaires?\n* Do participants show preliminary changes over time in binge eating-related distress and emotional well-being?\n\nParticipants in this study are adults who experience recurrent episodes of binge eating. They will take part in an individual online intervention that includes eight weekly sessions, a brief pre-session, and a follow-up session one month after the end of treatment.\n\nDuring the study, participants will:\n\n* Attend weekly online sessions focused on understanding binge eating, emotions, and the relationship with food and the body\n* Practice simple exercises to help manage emotional distress and food-related urges\n* Complete short questionnaires before, during, and after the intervention to describe their experiences\n\nThe information from this study will help researchers understand whether this type of intervention can be used in future, larger studies and in real-world clinical settings.",[61,62],"Binge Eating Disorder","Binge Eating",[64,61,65,66,67],"Binge eating","Body compassion","Emotion regulation","Intuitive eating","RECRUITING","2026-04-20",{"date":71,"type":39},"2026-04-22",{"date":73,"type":39},"2026-04-01",{"date":75,"type":23},"2026-07-30",{"name":45,"class":46},{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":18,"minAge":84,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":24,"phases":88,"briefSummary":89,"conditions":90,"keywords":93,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":47},"100569755","unilateral-training-of-the-uninjured-limb-on-clinical-outcomes-in-patients-with-surgically-treated-radius-fracture-100569755","NCT06698367","Unilateral Training of the Uninjured Limb on Clinical Outcomes in Patients with Surgically Treated Radius Fracture","Addition of Unilateral Training of the Uninjured Limb to Standard Rehabilitation on Grip Strength and Manual Dexterity of Patients with Surgically Treated Distal Radius Fracture.","Inclusion Criteria:\n\n* Age between 30-50 years\n* Radiological diagnosis of unilateral distal radius fracture without concomitant fractures.\n* Fracture treated surgically.\n\nExclusion Criteria:\n\n* Patients with lesion of the triangular fibrocartilage.\n* Patients with distal radius fracture with consolidation disorders.\n* Patients with health conditions that cause pain or affect the motor skills of the upper limb (radiocarpal osteoarthritis, carpal tunnel syndrome, Quervain's tenosynovitis, neurodegenerative diseases, sequelae of stroke)\n* Patients with multi-site pain or chronic polyarticular diseases such as osteoarthritis or rheumatoid arthritis.\n* Unstable cardiovascular, respiratory, systemic or metabolic conditions that do not allow high-intensity physical exercise.\n* Patients who are taking nutritional supplements that interfere with the regulation of skeletal muscle strength and mass (example: whey protein, creatine, etc.)\n* Inability to understand, read and\u002For speak the Spanish language.","30 Years","50 Years",{"count":87,"type":23},52,[26],"The objective will be to determine the effectiveness of adding unilateral upper limb postoperative training to standard rehabilitation compared to standard rehabilitation on maximum grip strength and manual dexterity in patients aged 30-50 years with surgically treated distal radius fracture. It is presumed that the addition of unilateral upper limb training will significantly improve maximum grip strength and manual dexterity at the end of the intervention period compared to the group receiving only standard rehabilitation.\n\nPatients who agree to participate in this research will be randomly assigned to a control group (standard rehabilitation with unilateral training with mobility exercises) or an experimental group (standard rehabilitation with unilateral high-intensity strength training). The duration of the postoperative intervention will be 12 weeks. The primary variables are maximum grip strength and manual dexterity. Secondary variables are wrist mobility, forearm circumference, maximum voluntary isometric strength, functionality and health-related quality of life. Results will be measured at 0, 6 and 12 weeks postoperative.",[91,92],"Wrist Fractures","Distal Radius Fractures",[94,32,95,96],"Distal radius fracture","Rehabilitation","Exercise","2024-11-27",{"date":99,"type":39},"2024-12-03",{"date":101,"type":23},"2025-01",{"date":103,"type":23},"2027-08",{"name":45,"class":46},""]