[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"energy-and-vitality\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:energy-and-vitality":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":42,"overallStatus":45,"whyStopped":4,"lastUpdateSubmitDate":46,"lastUpdatePostDateStruct":47,"startDateStruct":50,"completionDateStruct":52,"leadSponsor":54,"locationsCount":4},"100552680","m4c-nutraceutical-intervention-human-health-effects-pilot-100552680",false,"NCT06476236","M4C Nutraceutical Intervention Human Health Effects Pilot","M4C Pilot","Inclusion Criteria:\n\n* Healthy adults\n\nExclusion Criteria:\n\n* amputation\n* blood clotting disorder\n* metal implants or implanted electrical device(s)\n* known acute or chronic illness; gastrointestinal, cardiac, pulmonary, liver, or kidney abnormalities, uncontrolled hypertension\n* inability to fast i.e. low blood sugar\n* pregnant or may be pregnant during the course of the study\n* amino acid metabolizing disorder i.e. phenylketonuria\n* severe edema\n* did not pass screening criteria as determined by MRI facility\n* allergies\u002Fintolerance to any nutraceutical ingredients: amino acids, vitamins, minerals, tapioca starch, sunflower lecithin, stevia, limes or fatty acids like docosahexaenoic acid",true,"ALL","18 Years","80 Years",{"count":21,"type":22},20,"ESTIMATED","INTERVENTIONAL",[25],"NA","This 3 month pilot study will be an unblinded, convenience sampling, nutraceutical intervention trial. Twenty fasted subjects will undergo a baseline health assessment via a questionnaire, baseline clinical chemistries, blood lipids, dexa and impedence testing (to identify bone mineral density and body muscle\u002Ffat\u002Fwater composition), and metabolite\u002Fnovel biomarker testing through whole capillary blood, saliva, and urine collections. Assessments will be repeated every month (3 times after initial assessment) to cover a 3 month period. All measurements from each visit will be compared with baseline using paired t-tests or Chi square testing depending on variable. Power analyses are not included due to the pilot nature of the study. This pilot study will provide the necessary variability estimates for future trials.",[28,29,30,31,32,33,34,35,36,37,38,39,40,41],"General Health and Wellness","Energy and Vitality","Cognitive Function and Mental Health","Weight Management","Digestive Health","Exercise Tolerance","Cardiovascular Health","Bone and Joint Health","Skin, Hair, and Nail Health","Immune Support","Sports Performance and Recovery","Sleep and Relaxation","Obesity","Anti Inflammatory",[28,29,30,31,32,33,34,35,36,37,38,43,40,44],"Sleep and relaxation","anti inflammatory","NOT_YET_RECRUITING","2024-06-24",{"date":48,"type":49},"2024-06-26","ACTUAL",{"date":51,"type":22},"2024-06-17",{"date":53,"type":22},"2025-06-17",{"name":55,"class":56},"Concordia University Wisconsin","OTHER"]