[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Institute of Nutrition, Slovenia (Nutris)\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":131},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,49,85,109],{"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":4,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":4},"100626951","assessing-dietary-intake-of-selected-food-components-using-short-questionnaires-100626951",false,"NCT07442305","Assessing Dietary Intake of Selected Food Components Using Short Questionnaires","Validation of Short Questionnaires for Assessing Dietary Intake of Selected Food Components","NutriPlant\u002FFFQ","Inclusion criteria:\n\n* Willingness to participate in the study.\n* Signed Statement of Informed and Voluntary Consent to Participate in the Study.\n* Age between 18 and 65 years at the time of enrolment in the study.\n* Willingness to comply with all study procedures and to keep a dietary record in accordance with the provided instructions.\n\nExclusion criteria:\n\n* Pregnancy or breastfeeding.\n* Specific dietary practices followed by a small proportion of the population (veganism, LCHF, calorie-restricted diets; note: vegetarians are not excluded).\n* Diets prescribed by medical professionals.\n* Mental incapacity that prevents adequate understanding or participation.\n\nReasons for excluding a participant during the study:\n\n* Inability to participate in the study\n* Wishes to discontinue participation\n* Incomplete data provided",true,"ALL","18 Years","65 Years",{"count":22,"type":23},50,"ESTIMATED","OBSERVATIONAL","The aim of the study is to validate short questionnaires for assessing dietary intake of selected food components, with a focus on dietary fibre and iron. Two internationally developed short questionnaires (FiberScreen \\[for dietary fibre\\] and IRONQ-FFQ \\[for iron\\]) were adapted to the Slovenian context and will be compared with the standard 24-hour dietary recall method.",[27,28,29],"Nutritional Status","Iron-deficiency","Diet",[31,32,33,34,35,36],"dietary intake","nutritional status","micronutrients","iron","ffq","food recall","NOT_YET_RECRUITING","2026-02-27",{"date":40,"type":41},"2026-03-02","ACTUAL",{"date":43,"type":23},"2026-03-01",{"date":45,"type":23},"2027-12-31",{"name":47,"class":48},"Institute of Nutrition, Slovenia (Nutris)","OTHER",{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":17,"sex":18,"minAge":57,"maxAge":20,"enrollmentInfo":58,"targetDuration":4,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":67,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":84},"100608331","study-of-the-efficacy-of-dietary-supplementation-in-targeting-sleep-quality-nutrisom-01b-100608331","NCT07200167","Study of the Efficacy of Dietary Supplementation in Targeting Sleep Quality (NutriSom-01B)","Study of the Efficacy of Dietary Supplementation in Targeting Sleep Quality (NutriSom Study B)","NutriSom-01B","Inclusion criteria:\n\n* subject Informed consent form (ICF) is signed\n* aged 24-65 years at the time of the signature of ICF\n* suboptimal sleep quality according to Pittsburgh Sleep Quality Index (PSQI-SI): PSQI \\> 5\n* no clinically significant (subthreshold) insomnia according to Pittsburgh Sleep Quality Index (PSQI-SI) (Kmetec et al., 2022): PSQI \\\u003C= 9\n* a body mass index (BMI) \\\u003C= 32 kg\u002Fm2\n* stable medications for non excluded concurrent medical conditions for six weeks prior to the screening visit\n* ability to ingest oral food supplement (study product)\n* willing to follow all study procedures, including attending all site visits and use of actigraphy\n\nExclusion criteria:\n\n* diagnosed or subject to therapy due to sleep disorders\n* acute infectious disease\n* any kind of chronic pharmacological therapy with antihypertensives or antidepressants\n* any kind of other pharmacological therapy that could interact with active ingredients used in the study\n* pregnancy or planned pregnancy, lactation, menopause (with pharmacological treatment)\n* use of beta-blockers\n* chronic use of use of prostaglandin synthesis inhibitors (nonsteroidal anti-inflammatory drugs), such as acetylsalicylic acid and ibuprofen\n* supplementation with melatonin or other food supplements intendent for sleep quality during last 2 weeks\n* unwillingness to maintain caffeine abstinence after 4:00 PM during the study\n* not having a mobile upper extremity for attaching an actigraph\n* known alcohol and\u002For drug abuse\n* unwillingness to comply with the maximum limit of 2 alcoholic drinks per day, and only up to 1 alcoholic drink after 6:00 PM during the study\n* known lactose\u002Fgluten intolerances\u002Ffood allergies\n* known gastrointestinal disease\n* less than 5 years after treatment for gastrointestinal cancer (stomach, duodenum or colon)\n* have stomach or bowel resection\n* night work or work shifts with night work\n* mental incapacity that precludes adequate understanding or cooperation\n* participation in another investigational study","24 Years",{"count":59,"type":23},70,"INTERVENTIONAL",[62],"NA","single-center, randomized, cross over, double-blind, placebo controlled intervention study",[65,66],"Sleep Onset Latency","Sleep Quality",[68,69,70,71,72,73,74,75],"melatonin","supplementation","sleep","sleep onset latency","actigraphy","sleep quality","sleep efficiency","valerian","2025-09-30",{"date":78,"type":41},"2025-10-06",{"date":80,"type":23},"2025-10-01",{"date":82,"type":23},"2026-10-30",{"name":47,"class":48},1,{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":91,"eligibilityCriteria":92,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":93,"enrollmentInfo":94,"targetDuration":4,"studyType":60,"phases":96,"briefSummary":97,"conditions":98,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":84},"100576479","nutriplant---opportunities-for-increasing-consumption-of-local-fruits-and-vegetables-100576479","NCT06785831","NutriPlant - Opportunities for Increasing Consumption of Local Fruits and Vegetables","Opportunities for Increasing Consumption of Local Fruits and Vegetables in Slovenian Population (NutriPlant)","NutriPlant","1. Inclusion criteria:\n\n   * Signed informed consent of the participant to participate in the study\n   * Age between 18 and 70 years\n   * Functional constipation or irritable bowel syndrome\n   * Expressed willingness to eat the investigated food daily (sauerkraut, apples, dried apples or psyllium; period of four weeks)\n2. Exclusion criteria:\n\n   * Known allergy to the investigated foods (fresh apples, dried apples, sauerkraut or psyllium)\n   * Pregnancy or breastfeeding\n   * Previous gastrointestinal surgery with the exception of cholecystectomy and appendectomy\n   * Other gastrointestinal diseases (chronic inflammatory bowel disease, celiac disease, gastroparesis, etc.)\n   * Serious chronic diseases\n   * Introduction of extensive changes in diet or physical activity in the last 4 weeks before the inclusion examination\n   * Regular use of laxatives or inability to stop using laxatives for the duration of the study\n   * Concurrent participation in another study","70 Years",{"count":95,"type":23},120,[62],"The effects of different foods to normal bowel function in adult population will be investigated. A randomised controlled intervention trial will be conducted on about 120 (30 per group) adult (18-70 years) subjects with functional constipation and irritable bowel syndrome with constipation according to the IV. Rome criteria. At least one week before inclusion in the study, patients will stop taking laxatives and other anti-constipation medications. Subjects will be randomly selected to consume one of the test foods (fresh apples, dried apples, sauerkraut) or the active control (psyllium) in the equivalent amount of 3 g of fiber per day for 4 weeks. Subjects will be asked not to change their lifestyle habits, such as diet and physical activity level, and not to take oral laxatives during the period of participation in the study.",[99,100],"Functional Constipation","Irritable Bowel Syndrome","2025-01-14",{"date":103,"type":41},"2025-01-21",{"date":105,"type":23},"2025-01-20",{"date":107,"type":23},"2026-09-30",{"name":47,"class":48},{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":115,"eligibilityCriteria":116,"healthyVolunteers":17,"sex":18,"minAge":57,"maxAge":20,"enrollmentInfo":117,"targetDuration":4,"studyType":60,"phases":119,"briefSummary":63,"conditions":120,"keywords":121,"overallStatus":122,"whyStopped":4,"lastUpdateSubmitDate":123,"lastUpdatePostDateStruct":124,"startDateStruct":126,"completionDateStruct":128,"leadSponsor":130,"locationsCount":84},"100562243","efficacy-of-dietary-supplementation-with-melatonin-in-targeting-sleep-quality-100562243","NCT06600633","Efficacy of Dietary Supplementation With Melatonin in Targeting Sleep Quality","Study of the Efficacy of Dietary Supplementation in Targeting Sleep Quality (NutriSom Study A)","NutriSom-01A","Inclusion criteria:\n\n* subject Informed consent form (ICF) is signed\n* aged 24-65 years at the time of the signature of ICF\n* suboptimal sleep quality according to Pittsburgh Sleep Quality Index (PSQI-SI): PSQI higher than 5\n* no clinically significant (subthreshold) insomnia according to Pittsburgh Sleep Quality Index (PSQI-SI) (Kmetec et al., 2022): PSQI up to 9\n* a body mass index (BMI) up to 32 kg\u002Fm2\n* stable medications for non excluded concurrent medical conditions for six weeks prior to the screening visit\n* ability to ingest oral food supplement (study product)\n* willing to follow all study procedures, including attending all site visits and use of actigraphy\n\nExclusion criteria:\n\n* diagnosed or subject to therapy due to sleep disorders\n* acute infectious disease\n* any kind of chronic pharmacological therapy with antihypertensives or antidepressants\n* any kind of other pharmacological therapy that could interact with active ingredients used in the study\n* pregnancy or planned pregnancy, lactation, menopause (with clinically relevant symptoms\u002Ftherapy)\n* use of beta-blockers\n* chronic use of use of prostaglandin synthesis inhibitors (nonsteroidal anti-inflammatory drugs), such as acetylsalicylic acid and ibuprofen\n* supplementation with melatonin or other food supplements intendent for sleep quality during last 2 weeks\n* unwillingness to maintain caffeine abstinence after 4:00 PM during the study\n* not having a mobile upper extremity for attaching an actigraph\n* known alcohol and\u002For drug abuse\n* unwillingness to comply with the maximum limit of 2 alcoholic drinks per day, and only up to 1 alcoholic drink after 6:00 PM during the study\n* known lactose\u002Fgluten intolerances\u002Ffood allergies\n* known gastrointestinal disease\n* less than 5 years after treatment for gastrointestinal cancer (stomach, duodenum or colon)\n* have stomach or bowel resection\n* night work (including as part of shift work)\n* mental incapacity that precludes adequate understanding or cooperation\n* participation in another investigational study",{"count":118,"type":23},30,[62],[65,66],[68,69,70,71,72,73,74],"RECRUITING","2024-09-18",{"date":125,"type":41},"2024-09-20",{"date":127,"type":41},"2024-09-17",{"date":129,"type":23},"2025-09-17",{"name":47,"class":48},""]