[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"energy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:energy":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,72],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":32,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100613801",false,"NCT07271316","Alii Supplement Study","Birth Control Supplement Study","Inclusion Criteria:\n\n* Participants must be on the hormonal birth control pill as the investigators are testing the effectiveness of a supplement for women who take the hormonal birth control pill\n* Participants must be willing to complete a follow up survey as this study will be multiple parts\n* Participants must be willing to take a daily supplement as this study is testing how a supplement influences a variety of psychological outcomes\n* Participants must be on the hormonal birth control pill for at least six months as participants who have been on the pill for less than 6 months may not be experiencing nutritional depletion yet\n* If the investigators are able to do so, the investigators will only recruit participants who take the one-month hormonal birth control pill rather than the three month hormonal birth control pill, as the investigators are going to have participants come in after 28 days (day 2 of pack 1 and day 2 of pack 2) and participants on the three-month HBC pill may be on a 21 day cycle.\n* Participants must have no food or medication allergies that will prevent the participants from safely taking the supplement\n* Participants must not be taking any vitamins or participant must report willingness to abstain from taking vitamins during the study as individuals who are already taking vitamins may not be experiencing nutritional depletion associated with hormonal birth control\n* If the investigators have the ability to do so, the investigators will only recruit participants who are not taking medications. Participants on various medications (e.g., SSRIs, ADHD medications, etc.) may report differing psychological states due to their medications, rather than the supplement. Therefore, it would be best to exclude those individuals if possible.\n\nExclusion Criteria:\n\n* Participants cannot be naturally cycling as the investigators are testing a supplement for women on hormonal birth control\n* Participants cannot be unwilling to complete a follow up study because this is a multi-part study\n* Participants cannot be unwilling to take a supplement because the study centers around taking a supplement\n* Participants cannot be on the hormonal birth control pill for less than 6 months as participants who have been on the pill for less than 6 months may not be experiencing nutritional depletion yet\n* If the investigators are able to do so, participants cannot take the three month hormonal birth control pill, as the investigators are going to have participants come in after 28 days (day 2 of pack 1 and day 2 of pack 2) and participants on the three-month HBC pill may be on a 21 day cycle.\n* Participants cannot have any food or medication allergies that will prevent the participants from safely taking the supplement\n* Participants must not be taking any vitamins or participants must report willingness to abstain from taking vitamins during the study as individuals who are already taking vitamins may not be experiencing nutritional depletion associated with hormonal birth control\n* If the investigators have the ability to do so, the investigators will only recruit participants who are not taking medications. Participants on various medications (e.g., SSRIs, ADHD medications, etc.) may report differing psychological states due to their medications, rather than the supplement. Therefore, it would be best to exclude those individuals if possible.","FEMALE","18 Years","25 Years",{"count":19,"type":20},68,"ESTIMATED","INTERVENTIONAL",[23],"PHASE2","The goal of this clinical trial is to learn if the Alii Supplement can be used to reduce symptoms related to nutritional depletion in hormonal birth control pill users. The main questions it aims to answer are:\n\nDoes usage of the supplement increase happiness, decrease perceived vulnerability to disease, increase digestive health, decrease mood swings, and increase energy?\n\nThe investigators will compare the Alii Supplement to a placebo (a capsule that contains no drug) to see if the Alii Supplement works to reduce symptoms associated with nutritional depletion.\n\nParticipants will:\n\nTake the placebo or Alii Supplement everyday for 28 days and visit the research office twice to fill out an online survey comprising of items examining the main outcome measures.",[26,27,28,29,30,31],"Nutrient Deficiency","Happiness","Digestive Health","Vulnerability to Disease","Mood Swings","Energy",[33,34,35],"Hormonal Birth Control","Nutritional Depletion","Dietary Supplement","RECRUITING","2026-01-12",{"date":39,"type":40},"2026-01-14","ACTUAL",{"date":37,"type":40},{"date":43,"type":20},"2026-04-29",{"name":45,"class":46},"Texas Christian University","OTHER",1,{"id":49,"slug":50,"hasResults":10,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":54,"sex":55,"minAge":16,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":21,"phases":58,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":47},"100615477","evaluating-heart--soils-lifeblood-on-iron-and-energy-levels-100615477","NCT07293117","Evaluating Heart & Soil's Lifeblood on Iron and Energy Levels","Inclusion Criteria:\n\n* Can read and understand English.\n* US resident.\n* Willing and able to follow the requirements of the protocol.\n\nExclusion Criteria:\n\n* Individuals with Hemochromatosis\n* Individuals with Severe Allergies\n* Pregnant or Nursing Women\n* Individuals with Gastrointestinal Disorders\n* Individuals on Iron-Related Medications\n* Individuals with Mental Health Disorders\n* Competitive Athletes",true,"ALL",{"count":57,"type":20},100,[59],"NA","This study explores how Heart \\& Soil's Lifeblood impacts iron levels and energy.",[31],"2025-12-19",{"date":64,"type":40},"2025-12-26",{"date":66,"type":40},"2025-09-09",{"date":68,"type":20},"2026-09-09",{"name":70,"class":71},"Efforia, Inc","INDUSTRY",{"id":73,"slug":74,"hasResults":10,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":54,"sex":55,"minAge":16,"maxAge":80,"enrollmentInfo":81,"targetDuration":4,"studyType":21,"phases":82,"briefSummary":83,"conditions":84,"keywords":90,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":47},"100610548","effects-of-a-collagen-supplement-on-quality-of-life-appetite-and-glycaemic-control-100610548","NCT07229014","Effects of a Collagen Supplement on Quality of Life, Appetite and Glycaemic Control","Effects of a Collagen Supplement on Quality of Life, Appetite and Glycaemic Control: a Randomised, Double-blinded, Placebo-controlled, Crossover Trial in Overweight and Obese Adults.","GluCol","Inclusion Criteria:\n\n1. Subject is a healthy (as assessed by medical history) male or female adult, aged 18-65 years and overweight or obese (BMI 25 - 40 kg\u002Fm2).\n2. Subject has an impaired quality of life, as determined by scoring at least a total of 9 on the following questions:\n\n   1. In the past 4 weeks, did you feel you had a lot of energy? All of the time (1), most of the time (2), a good bit of the time (3), some of the time (4), a little of the time (5), and none of the time (6) (number 27 from SF-36 questionnaire) Version 3.0 \\[01\u002F10\u002F2025\\] Page 11 of 20\n   2. In the past 4 weeks, have you felt calm and peaceful? All of the time (1), most of the time (2), a good bit of the time (3), some of the time (4), a little of the time (5), and none of the time (6) (number 26 from SF-36 questionnaire)\n   3. In the past 2 weeks, did you have any difficulties with sleeping? Not at all (1), small amounts (2), moderate amounts (3), a great deal (4), an extreme amount (5), all the time (6) (number 3 from WHOQoL-100)\n3. Participant has an email address, internet access, a compatible smartphone and is willing and able to maintain internet access throughout the trial to complete virtual visits via video conference and to engage with mobile apps to answer electronic questionnaires.\n4. Subject is willing and able to comply with all study procedures, including consumption of the supplement daily, CGM use for 22 days total (2 x 11 days), complete standardised meal tests, and fill out health questionnaires.\n5. Subject is willing to take a supplement of bovine animal origin.\n6. Openness to participate in an online interview at the end of the study.\n\nExclusion Criteria:\n\n1. Participant has a history or presence of uncontrolled and\u002For clinically important pulmonary, cardiac, hepatic, renal, endocrine (including type 1 and 2 diabetes), hematologic, immunologic, neurologic (e.g., Alzheimer's or Parkinson's diseases), psychiatric (including unstable depression and\u002For anxiety disorders) or biliary disorders.\n2. Participant has a clinically important gastrointestinal (GI) condition that would potentially interfere with the evaluation of the study product \\[e.g., inflammatory bowel disease, irritable bowel syndrome, chronic constipation, severe constipation (in the opinion of the investigator), history of frequent diarrhoea, history of surgery for weight loss, gastroparesis, systemic disease that might affect gut motility according to the investigator, medication managed reflux and\u002For clinically important lactose intolerance.\n3. Participant has a history of chronic insomnia (defined as insomnia at least 3 d\u002Fweek over the past month), a diagnosed sleep disorder (e.g., OSA), or a chronic medical condition that may impact energy\u002Ffatigue levels, in the judgment of the investigator.\n4. Participant is a female who is pregnant, planning to be pregnant during the study period, lactating, or is of childbearing potential and is unwilling to commit to the use of a medically approved form of contraception throughout the study period. The method of contraception must be recorded.\n5. Participant has a known allergy, intolerance, or sensitivity to any of the ingredients in the study product, including bovine animal products.\n6. Participant has a history or presence of cancer in the prior two years, except for non-melanoma skin cancer.\n7. Participant has experienced any major trauma or any other surgical event within three months of Virtual Visit 1.\n8. Participant has unstable use of a medication or supplement that the investigator considers may affect the outcomes of the trial.\n9. Participant is currently in another biomedical research study or has been in the 30 days before screening.\n10. Participant is an employee of, or has a financial interest in Darling Ingredients Inc.\n11. The individual has a condition the investigator believes would interfere with his ability to provide informed consent and to comply with the study protocol, which might confound the interpretation of the study results, or put the participant at undue risk.\n12. Participant is a vegan or vegetarian or excludes bovine products for cultural or religious reasons.","65 Years",{"count":57,"type":20},[59],"This is a clinical trial aimed to investigate if a collagen supplement can improve quality of life, appetite and blood sugar in overweight and obese adults aged 18-65.\n\nHypothesis: Consumption of a collagen supplement for 8 days will improve quality of life and improve glycaemic control in comparison with a placebo in individuals overweight or with obesity with a perceived low quality of life.\n\nParticipants will be asked to:\n\n1. Consume a collagen peptide supplement for a total of 8 days at a time\n2. Fill in questionnaires about quality of life, appetite, mood and energy\n3. Wear continuous glucose monitors",[85,86,87,88,31,89],"Quality of Life","Appetite","Sleep","Mood","Blood Glucose Profile",[91,92,93,94,95,96],"collagen","glucose","appetite","statiety","mood","sleep","2025-11-13",{"date":99,"type":40},"2025-11-14",{"date":101,"type":20},"2025-12",{"date":103,"type":20},"2027-01",{"name":105,"class":46},"King's College London"]