[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"dietary-intake\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:dietary-intake":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,82],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100650355","advancing-female-university-students-health-through-mobile-technology-in-ethiopia-100650355",false,"NCT07746791","Advancing Female University Students' Health Through Mobile Technology in Ethiopia","Advancing Female University Students Sexual and Reproductive Health, Nutrition, and Psychosocial Well-being Through Mobile Technology Interventions in Ethiopia","EMPOWER","Inclusion Criteria:\n\n* Regular undergraduate female university student will be included in the study.\n* First year female students will be included in the study.\n\nExclusion Criteria:\n\n• Students who have no mobile phone will be excluded from the study.",true,"FEMALE",{"count":20,"type":21},880,"ESTIMATED","INTERVENTIONAL",[24],"NA","Background: Female university students in Ethiopia experience a high burden of sexual and reproductive health, nutrition, and psychosocial problems, exacerbated by limited access to essential health services and support. Mobile technology provides an opportunity to deliver accessible, evidence-based health interventions.\n\nObjective: To evaluate the effectiveness of a mobile technology-based intervention in improving SRH, nutrition, and psychosocial well-being among female university students in Ethiopia.\n\nMethods: A concurrent mixed-methods study will be conducted among first-year female university students. Baseline quantitative and qualitative assessments will identify needs, barriers, and facilitators. A randomized controlled trial will evaluate a comprehensive mobile health education intervention delivered monthly. Quantitative data will be analysed using descriptive and inferential statistics, while qualitative data will undergo thematic analysis.\n\nExpected Outcomes: Improved sexual and reproductive health, dietary practices, and psychosocial well-being among female university students.\n\nDuration and Budget: The project will be implemented over the proposed study period with a total budget of 1,208,564 Ethiopian birr.",[27,28,29],"Dietary Intake","Sexual and Reproductive Health","Psychosocial Wellbeing",[31,32,33,34],"Dietary intake","SRH","Ethiopia","Psychosocial wellbeing","NOT_YET_RECRUITING","2026-08-08",{"date":38,"type":39},"2026-08-11","ACTUAL",{"date":41,"type":21},"2026-08-01",{"date":43,"type":21},"2028-06-30",{"name":45,"class":46},"Bahir Dar University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":56,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":61,"briefSummary":62,"conditions":63,"keywords":68,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":47},"100573383","improving-sleep-decision-making-and-eating-in-adolescents-with-obesity-100573383","NCT06745570","Improving Sleep, Decision-Making, and Eating in Adolescents With Obesity","Improving Sleep as a Method for Enhancing Decision-Making and Reducing Problematic Eating Behaviors in Adolescents With Obesity","STAR","Inclusion Criteria:\n\n* Ages 14-18\n* Fluent in English\n* BMI percentile ≥ 85th percentile for sex-and-age\n* Has a parent or guardian who is willing and able to participate\n* Has at least one sleep disturbance. Eligible sleep disturbances are: a. Advanced sleep timing (sleep onset 11:00pm or later for 14-16 year-olds or 11:20pm or later for 17-18 year-olds at least 3 times per week), b. Difficulty falling asleep (taking ≥ 30 mins to get to sleep 3 or more nights per week), c. Short sleep (obtaining \\\u003C 7.5 hours of sleep per night 3 or more nights per week), and d. Sleep irregularity (having more than 2 hours of variability in sleep-wake schedule across one week\n\nExclusion Criteria:\n\n* Experience of weight loss of ≥ 5% of body weight in the past 6 months\n* Current use of insomnia medication\n* Having recently begun or changed the dosage of any medication known to affect appetite or body composition within the last 3 months\n* Currently taking weight loss medications\n* Currently taking insulin\n* Diagnosed diabetes (type 1)\n* Any condition prohibiting physical activity\n* Diagnosis of an eating disorder\n* Diagnosis of obstructive sleep apnea\n* Recent or ongoing problem with drug abuse, alcohol abuse, or addiction\n* Currently pregnant or less than 3 months postpartum\n* Anticipation of a possible pregnancy in the next year\n* Unwillingness to report possible or confirmed pregnancies promptly during the course of the trial\n* Currently participating in treatment for eating or weight concerns\n* Does not have regular access to Wi-Fi connection to participate in study interventions.","ALL","14 Years","18 Years",{"count":60,"type":21},50,[24],"This study is being performed to understand the effects of a lifestyle modification and sleep intervention on weight loss outcomes in adolescence. The main question the study aims to answer is:\n\n\\- What are the initial effects of a lifestyle modification and sleep intervention, including effects on weight, eating behaviors and dietary intake, and sleep?\n\nParticipants will:\n\n* Participate in remote, group-based, weekly weight loss and sleep coaching for 16 weeks.\n* Complete study assessments at baseline (pre-intervention), mid-intervention, and post-intervention.\n* Complete daily sleep diaries for three 7-day periods at each assessment point.",[64,65,66,67,27],"Adolescent Overweight","Adolescent Obesity","Sleep","Eating Behaviors",[69,70,71],"Adolescent Weight Loss","Adolescent Sleep","Adolescent Eating","RECRUITING","2026-07-16",{"date":75,"type":39},"2026-07-20",{"date":77,"type":39},"2024-04-18",{"date":79,"type":21},"2027-01-31",{"name":81,"class":46},"Nemours Children's Clinic",{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":86,"acronym":4,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":56,"minAge":58,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":22,"phases":90,"briefSummary":91,"conditions":92,"keywords":95,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":47},"100645617","capturing-food-intake-in-patients-undergoing-radiation-therapy-for-cancer-100645617","NCT07682714","Capturing Food Intake in Patients Undergoing Radiation Therapy for Cancer","Inclusion Criteria:\n\n* Patients age ≥18 starting a new course of radiation therapy for cancer treatment\n* Written informed consent obtained from participant and ability for participant to comply with the requirements of the study.\n* Stated willingness to comply with all study procedures and availability for the duration of the study\n* Own a smartphone or smart device\n* Able to read and speak English\n\nExclusion Criteria:\n\n* Pregnant or lactating women per self report prior to starting radiation therapy",{"count":89,"type":21},20,[24],"The purpose of this study is to determine the feasibility of capturing daily dietary intake of patients undergoing radiation therapy using a mobile food record. This is a prospective single group, non-randomized, feasibility study.\n\n20 participants will be identified during routine clinical care visits with the study PI or co-investigators. Consent will be obtained in person during a clinic visit or using the e-consent process described in section 21.1. They will be asked to use the myCircadian Clock (mCC) app to document their dietary intake for the duration of their radiation treatment. No follow up data will be collected.",[93,94,27],"Cancer","Radiation Therapy",[96,97,98,99,100,101,102,103],"Mobile food record","myCircadian Clock","Radiation therapy","Cancer patients","Nutrition assessment","Feasibility study","Food logging","Smartphone application","2026-07-13",{"date":106,"type":39},"2026-07-14",{"date":108,"type":39},"2026-07-10",{"date":110,"type":21},"2027-09-01",{"name":112,"class":46},"University of Minnesota"]