[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"health-status\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:health-status":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,44,70,96],{"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":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100622465","the-impact-of-12-week-retention-of-nutrients-on-skin-and-the-perception-of-physical-health-status-100622465",false,"NCT07383974","The Impact of 12 Week Retention of Nutrients on Skin and the Perception of Physical Health Status","Inclusion Criteria:\n\n1. Chinese adults of Asian descent aged 18 and above;\n2. Daily fruit and vegetable intake \\\u003C 240g (calculated based on the fruit and vegetable section of the food frequency questionnaire);\n3. S3 measurement index \\\u003C 30000;\n4. Participants must possess basic Chinese reading comprehension and expression skills, and be able to independently complete questionnaire surveys;\n5. Voluntary participation in the test and signing of the informed consent form;\n6. Willingness to comply with all evaluation requirements.\n\nExclusion Criteria:\n\n1. Presence of open facial skin lesions, clearly visible scars, acne marks, etc.;\n2. Skin lesions, scars, or significant pigmentation on the hand measurement area;\n3. Symptoms of skin disease on the face or hand measurement areas;\n4. Having undergone medical aesthetic procedures within the last 6 months;\n5. Participation in other clinical trials involving product use within the last 3 months;\n6. Use of health supplements or nutritional supplements (e.g., vitamins, minerals) within the last 1 month;\n7. Currently planning for pregnancy, pregnant, or lactating;\n8. Presence of any disease under current treatment;\n9. Any other health issues or chronic diseases that affect behavioral or cognitive abilities;\n10. Other iatrogenic reasons identified by experts or professionals that may affect the evaluation results.\n\nThe S3 instrument refers to a Raman spectroscopy-based biophotonic scanner. The threshold for the S3 screening value is based on previously published literature, which indicated that participants with a daily fruit and vegetable intake of less than 240g had an average Raman spectroscopy biophotonic scanner score below 25,000. However, considering practical recruitment challenges, the inclusion criterion was set at \\\u003C 30,000. The S3 device measures the Skin Carotenoid Index, a non-invasive biomarker reflecting skin carotenoid levels.",true,"ALL","18 Years",{"count":19,"type":20},120,"ESTIMATED","INTERVENTIONAL",[23],"NA","This is a randomized, double-blind, placebo-controlled clinical trial exploring the effects of a 12-week dietary supplement regimen on skin condition and perceived overall health status.\n\nThe study will involve 120 healthy Chinese adults aged 18 and above with low daily fruit and vegetable intake. Participants will be randomly assigned to one of two groups: one group will take a combination of Nu Skin's Vitamin C \\& Green Tea Capsules and Multivitamin \\& Mineral Capsules, while the other group will take a matching placebo.\n\nThe primary goal is to assess if the supplement combination improves skin health after 12 weeks, measured through specialized facial imaging (assessing spots, redness, evenness) and probe measurements (assessing elasticity, moisture, gloss). Secondary goals include evaluating changes in participants' self-perceived health status (via quality of life, fatigue, and digestive health questionnaires), psychological resilience, memory, and exploring a new method for measuring skin carotenoid levels.\n\nThis study is not intended to verify the approved health functions of the products but to explore the potential combined effects of antioxidant and nutritional supplementation on skin and general well-being.",[26,27,28,29,30],"Healthy Volunteers","Dietary Supplementation","Skin Health","Health Status","Antioxidants","RECRUITING","2026-01-26",{"date":34,"type":35},"2026-02-03","ACTUAL",{"date":37,"type":35},"2025-11-03",{"date":39,"type":20},"2026-02-02",{"name":41,"class":42},"ChinaNorm","INDUSTRY",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":51,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":55,"conditions":56,"keywords":57,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":43},"100612092","cohort-of-nursing-homes-100612092","NCT07249086","Cohort of Nursing Homes","Cohort of Nursing Homes (CNH)","Inclusion Criteria:\n\n* Voluntarily participated in this study and provided signed informed consent forms.\n* Both male and female.\n* Age 60 years old and above.\n\nExclusion Criteria:\n\n* Unable to participate in physical examinations due to being bedridden or having limited mobility.\n* Unable to communicate effectively.\n* People cannot participate for other reasons.","60 Years",{"count":53,"type":20},1500,"OBSERVATIONAL","The goal of this observational study was to establish cohorts of elderly people in hospital care and elderly people in home care.",[29],[58,59],"Health status of elderly people","Elderly (people aged 60 or more)","2025-11-21",{"date":62,"type":35},"2025-11-25",{"date":64,"type":35},"2023-11-30",{"date":66,"type":20},"2030-12-31",{"name":68,"class":69},"Institute of Hematology & Blood Diseases Hospital, China","OTHER",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":79,"conditions":80,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":43},"100547595","assessment-of-overall-functioning-in-patients-with-complex-health-issues-100547595","NCT06410014","Assessment of Overall Functioning in Patients With Complex Health Issues","CPH-Func","Inclusion Criteria:\n\n* All patients referred by a municipality to the Department of Social Medicine at Bispebjerg and Frederiksberg Hospital for a clinical assessment (Klinisk Funktion) who provide written consent to participate.\n\nExclusion Criteria:\n\n* Insufficient ability to communicate either in written or oral Danish",{"count":78,"type":20},100,"The overall aim of the study is to assess whether each outcome measures the same aspect of overall functioning or contributes with different aspects. More specifically, the aim of this study is to investigate the correlation between each single instrument.\n\nDuring study period all patients presenting at our clinic will be offered to participate in the study. Patients will be included in the study when referred to the department of Social Medicine and providing written informed consent to participate in the study. Inclusion will continue until 100 patients have completed an AMPS test. All participants will, apart from standard procedure, be asked to complete:\n\n* An AMPS-test\n* ADL-Q (Questionnaire concerning Activities of Daily Living)\n* ADL-I (Interview based questionnaire concerning Activites of Daily Living)\n\nAs standard procedure all participants will also perform\u002Fcomplete:\n\n* 30 seconds chair stand test (30sCST)\n* Hand grip strength (HGS)\n* Evaluation of ambulation (Cumulated Ambulation Score \u002FCAS)\n* WORQ (Work Rehabilitation Questionnaire)\n\nTo obtain the aim of the study correlation-analysis will be performed to investigate the relationship between each included instruments.",[81,82,83,84,29,85,86],"Activities of Daily Living","Surveys and Questionnaires","ADL Motor Skills","Disability Evaluation","Muscle Strength","Physical Examination","2024-12-06",{"date":89,"type":35},"2024-12-09",{"date":91,"type":35},"2023-10-10",{"date":93,"type":20},"2025-02-01",{"name":95,"class":69},"University Hospital Bispebjerg and Frederiksberg",{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":102,"eligibilityCriteria":103,"healthyVolunteers":15,"sex":104,"minAge":17,"maxAge":105,"enrollmentInfo":106,"targetDuration":4,"studyType":21,"phases":108,"briefSummary":109,"conditions":110,"keywords":128,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":147,"completionDateStruct":149,"leadSponsor":151,"locationsCount":43},"100439987","hiit-vs-mict-during-pregnancy-and-health-and-birth-outcomes-in-mothers-and-children-100439987","NCT05009433","HIIT vs MICT During Pregnancy and Health and Birth Outcomes in Mothers and Children","The Effect of Pre- and Postnatal High Intensity Interval Training and Moderate Intensity Continuous Training on Biological, Functional and Psychological Markers of Pregnancy Disorders and Non-communicable Diseases in Mothers and Offsprings","HIIT MAMA","Inclusion Criteria:\n\nCriteria: Inclusion Criteria:\n\nFor pregnant women:\n\n1. course of pregnancy allowing participation in physical activities adapted to pregnant women\n2. consent of the obstetric care provider to participate in the study tests and exercise classes;\n3. taking part in all diagnostic and control tests to assess selected biological, functional and psychological parameters at each trimester of pregnancy, during the puerperium and one year after childbirth;\n4. participant's consent to use data from the medical documentation on the course of childbirth and the assessment of the new-born, as well as the results of preventive examinations in children aged one, two, four and six, routinely performed according to the Polish pediatric care system;\n5. availability to participate in classes three times a week until the day of delivery;\n6. declaration of participation in postpartum classes at least once a week and self-completion of the exercise program according to written instructions prepared by the exercise specialist;\n7. women can participate in the exercise programs regardless of their level of fitness or exercise capacity, as well as the level of motor skills (based on the diagnostic exercise tests, the exercise program will be tailored to the individual needs and capabilities of a woman).\n\nFor nonpregnant women:\n\n1. nulliparous;\n2. lack of diagnosed infertility and other disorders of the reproductive system;\n3. taking part in all diagnostic and control tests to assess selected biological, functional and psychological parameters at indicated time points: before and after each of the 8-week exercise program during the first 8 months of the study and once every 3 months during the following twelve months of the study\n4. declaration of availability to participate in exercise classes three times a week for the first 8 months of the program (attendance at least 80% is required);\n5. declaration of participation in classes at least once a week and self-completion of the exercise program to the required 150 minutes of physical activity per week, according to the written guidelines prepared by the instructor, for the next 12 months of the program;\n6. women can participate in the exercise program regardless of their level of fitness or exercise capacity, as well as the level of motor skills (based on the diagnostic exercise tests, the exercise program will be tailored to the individual needs and capabilities of a woman).\n\nExclusion Criteria for Pregnant and Nonpregnant Women:\n\n1. contraindications to increased physical effort or to any of the diagnostic or control tests;\n2. allergies to materials used during diagnostic and control tests (e.g. nickel present in steel plates of vaginal electrodes, disinfectants);\n3. other conditions that, according to the researchers, will threaten the health or safety of the participants or will significantly affect the quality of the collected data.","FEMALE","45 Years",{"count":107,"type":20},600,[23],"Regular exercise during pregnancy and postpartum leads to health benefits for mother and child. Inactivity during pregnancy and after delivery is now treated as risky behavior. Physically active pregnant women significantly less often suffer from, among others, gestational diabetes, excessive weight gain, lipids disorders, hypertension, preeclampsia, depressive symptoms, functional and structural disorders, including stress urinary incontinence, back pain or diastasis recti abdominis (DRA). Prenatal physical activity reduces the risk of premature delivery and miscarriage, fetal macrosomia, complications in labor or the risk of metabolic disorders in children.\n\nHigh-intensity interval training (HIIT) has become one of the most popular trends in the fitness sector. The effectiveness of HIIT on a number of health indicators has been proven in various populations but limited data are available on HIIT during pregnancy.\n\nThe first hypothesis is that the HIIT, implemented during pregnancy and after childbirth, as a stronger exercise stimulus, will have a better impact on selected biological and psychological parameters of mothers, as well as on selected health parameters of their children, compared to the MICT (moderate intensity continuous training). Therefore, it promises better preventive effects on pregnancy complications and ailments as well as non-communicable diseases occurring in these populations. In the second hypothesis, it was assumed that HIIT and MICT implemented during pregnancy and after childbirth, tailored to the specific needs of the perinatal period, will not differ in the effectiveness of maintaining normal functional parameters in women, including prevention of urinary incontinence, back pain, DRA, etc.\n\nPregnant women who apply for the study will be divided into three groups: those attending the HIIT, MICT or educational programs. During the study, the participants will be under standard obstetric care. As comparative groups, non-pregnant women will be also recruited.\n\nThe investigators will collect data on selected biological, functional and psychological parameters in the study women at each trimester of pregnancy, during the puerperium and one year after childbirth. The data from the medical documentation on the course of childbirth and the assessment of the new-born, as well as the results of preventive examinations in the study women's children aged one, two, four and six years will be also analyzed.",[111,112,113,29,114,115,116,117,118,119,120,121,122,123,124,125,126,127],"Pregnancy","Postpartum","Childbirth","Physical Fitness","Noncommunicable Diseases","Metabolism","Diabetes Mellitus, Gestational","Pregnancy Induced Hypertension","Body Composition","Back Pain","Pain Threshold","Biomechanics","Pelvic Floor Disorders","Urinary Incontinence","Cognitive Function","Depression","Anxiety",[129,130,131,132,133,134,135,136,137,138,139,29,140,113,141,142,143],"Pregnant women","Prenatal care","Postpartum women","Postnatal care","Exercise","Physical activity","Exercise intervention","Educational intervention","Exercise test","High-intensity interval training","Moderate-intensity continuous training","Physical fitness","Birth outcomes","Infant","Child","2022-11-30",{"date":146,"type":35},"2022-12-02",{"date":148,"type":35},"2021-06-24",{"date":150,"type":20},"2031-08-31",{"name":152,"class":69},"Gdansk University of Physical Education and Sport"]