[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Federal University of Uberlandia\",\"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,[8,46,81],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100557302","parkinson-brasil---database-on-motor-and-non-motor-aspects-of-parkinsons-disease-in-brazil-100557302",false,"NCT06536348","PARKINSON BRASIL - Database on Motor and Non-Motor Aspects of Parkinson's Disease in Brazil","Inclusion Criteria:\n\n* Experimental group: (i) present a neurological diagnosis of Parkinson's disease; (ii) be classified between stages I to IV of the Hoehn \\& Yahr Scale; (iii) have central visual acuity equal to or greater than 20\u002F40 (equivalent to 0.50) in each eye or equal to or greater than 20\u002F30 (equivalent to 0.66) in one eye according to the Snellen scale.\n* Control group: (i) not having a neurological diagnosis of Parkinson's disease or other neurological disease that resembles PD; (ii) have central visual acuity equal to or greater than 20\u002F40 (equivalent to 0.50) in each eye or equal to or greater than 20\u002F30 (equivalent to 0.66) in one eye according to the Snellen scale.\n\nExclusion Criteria:\n\nFor both groups, individuals who have other neurological or musculoskeletal diseases that interfere with the execution of the tests will be excluded.",true,"ALL","18 Years","120 Years",{"count":20,"type":21},958,"ESTIMATED","OBSERVATIONAL","This is an observational, cross-sectional study with a control group, with the general objective of developing and evaluating a national database, unprecedented in Brazil, containing clinical, epidemiological, motor, and non-motor aspects of Parkinson's disease (PD). The database will be open and accessible to national and international researchers in order to contribute to the advancement of research related to PD. The aim is to collect data, in a paired way, from a control group and an experimental group. Data collection will include the application of questionnaires, the execution of motor activities, and clinical scales. Information that can identify the participants will be removed from the database for later storage in a repository. Quantitative, qualitative, and descriptive variables from the database will be estimated in order to characterise and contrast the groups studied. The results of this study will contribute to a better characterization of the staging of PD as a function of the epidemiological, motor, and non-motor aspects evaluated, as well as to the development of technologies and methods that can be applied in clinical practice.",[25],"Parkinson Disease",[27,28,29,30,31,32],"Parkinson's disease","motor assessment","non-motor assessment","database","computer vision","inertial sensors","RECRUITING","2026-05-16",{"date":36,"type":37},"2026-05-19","ACTUAL",{"date":39,"type":37},"2025-01-01",{"date":41,"type":21},"2034-10-01",{"name":43,"class":44},"Federal University of Uberlandia","OTHER",5,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":15,"sex":53,"minAge":17,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":66,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":80},"100637032","effects-of-mindful-eating-on-female-nutrition-students-100637032","NCT07573410","Effects of Mindful Eating on Female Nutrition Students","Efficacy of a Mindful Eating Intervention on Eating Behavior, Body Image, and Mental Health in Female Nutrition Students: a Pilot Randomized Clinical Trial","Inclusion Criteria:\n\n* Female gender\n* Active enrollment in the Nutrition undergraduate program at the time of data collection\n* Agreement to participate in the study\n\nExclusion Criteria:\n\n* Diagnosis of severe cognitive or mental disorders; Regular practice (at least once a week in the last six months) of meditation, yoga, or mindfulness\n* Regular practice (at least once a week in the last six months) of meditation, yoga, or mindfulness","FEMALE",{"count":55,"type":21},88,"INTERVENTIONAL",[58],"NA","The goal of this pilot randomized clinical trial is to evaluate the efficacy of a mindful eating intervention (\"Eat for Life\") on eating behavior, body image, and mental health in female nutrition students. The main questions it aims to answer are: Does a mindful eating intervention reduce disordered eating behaviors in female nutrition students? Does the intervention improve body appreciation, mindfulness levels, and mental health?\n\nResearchers will compare an active control group receiving nutritional guidance to an intervention group participating in the \"Eat for Life\" mindful eating program to see if the mindful eating intervention reduces disordered eating behaviors and improves overall psychological well-being and body appreciation.\n\nParticipants will: Complete online questionnaires evaluating eating behavior, mindfulness, mental health, and body image at three distinct time points: before the intervention (baseline), post-intervention, and at a 3-month follow-up.\n\nIf assigned to the intervention group, attend 12 weekly face-to-face mindful eating sessions lasting approximately two hours each. If assigned to the active control group, receive weekly informative leaflets via WhatsApp with nutritional guidance based on the Dietary Guidelines for the Brazilian Population for 12 weeks",[61,62,63,64,65],"Mental Health","Body Image","Feeding Behavior","Feeding and Eating Disorders","Stress and Anxiety",[67,68,69,70],"mindful eating","feeding behavior","Students","mental health","NOT_YET_RECRUITING","2026-05-06",{"date":74,"type":37},"2026-05-11",{"date":76,"type":21},"2026-06-01",{"date":78,"type":21},"2027-12-01",{"name":43,"class":44},1,{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":87,"eligibilityCriteria":88,"healthyVolunteers":15,"sex":53,"minAge":89,"maxAge":90,"enrollmentInfo":91,"targetDuration":4,"studyType":56,"phases":93,"briefSummary":94,"conditions":95,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":80},"100505545","effects-of-omega-3-and-whey-protein-supplementation-on-lean-mass-in-older-adults-100505545","NCT05862779","Effects of Omega-3 and Whey Protein Supplementation on Lean Mass in Older Adults","Effects of Omega-3 and Whey Protein Supplementation on Lean Mass and Strength Gains in Older Adults Performing Resistance Exercise: A Randomized, Double-Blind and Placebo-Controlled Study","W-3 and Whey","Inclusion Criteria:\n\n* Postmenopausal women (at least 1 year of menstrual interruption, self-reported);\n* To be able to practice strength exercises;\n* To be able to carry out supplementation;\n* Do not present physical, orthopedic or cardiovascular complications that prevent the performance of physical exercises;\n* No history of stroke or acute myocardial infarction;\n* Not being a smoker and\u002For alcoholic;\n* Do not perform hormone replacement therapy;\n* Do not use anti-inflammatory drugs;\n* To have normal kidney function;\n* To submit a medical certificate of health that proves that the individual is able to perform exercises.\n\nExclusion Criteria:\n\n* Do not provide the necessary information for the development of the study;\n* Individuals with diseases previously diagnosed and undergoing treatment, such as type II diabetes mellitus, cancer, rheumatoid arthritis, high blood pressure, dyslipidemia, cardiovascular, and kidney and\u002For liver diseases.","60 Years","85 Years",{"count":92,"type":21},80,[58],"To evaluate the effect of omega-3 supplementation combined with whey protein intake on lean mass and strength gains in older adults performing resistance exercise. Participants will be randomized into the 4 groups. The placebo group will receive 4 g per day of corn oil and 40 g per day of maltodextrin. The omega 3 + placebo group will receive 4 g per day of fish oil and 40 g per day of maltodextrin. The whey protein + placebo group will receive 40g per day of whey and 4g per day of corn oil. The omega 3 + whey group will receive 4g per day of fish oil and 40g per day of protein. All will perform the same exercise protocol for 12 weeks",[96],"Sarcopenia","2024-10-14",{"date":99,"type":37},"2024-10-16",{"date":101,"type":37},"2024-07-30",{"date":103,"type":21},"2026-05",{"name":43,"class":44},""]