[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"acceptability\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:acceptability":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,45,84,117,144,181,209,234,272,287],{"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":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100053624","the-increasing-mindfulness-engagement-project-100053624",false,"NCT07170202","The Increasing Mindfulness Engagement Project","Translating Behavioral Economics Strategies to Culturally Tailor a Mobile Health Mindfulness Intervention to Reduce Risky Drinking Behaviors in Emerging Adult College Student Students","TIMEProject","Inclusion Criteria:\n\n18-29 years old First-generation college student Undergraduate college student Living in the United States Meet criteria for binge drinking (5 drinks in about 2 hours) or heavy drinking (more than 14 drinks per week).",true,"ALL","18 Years","29 Years",{"count":22,"type":23},40,"ESTIMATED","INTERVENTIONAL",[26],"NA","The goal of this clinical trial is to examine the feasibility and acceptability of different types of text messages and a integrated gaming app to increase engagement in a mindfulness mobile health application.\n\n1. Does receiving text messages increase engagement in a mindfulness app?\n2. Does an integrated gaming app increase engagement in a mindfulness app?\n\nResearchers will examine whether participants engage more in a mindfulness mobile health application if they receive text messages and if they engage in additional gaming app on their smartphone. Participants will:\n\n1. Use a mindfulness and gaming mobile health application for 28-days.\n2. Complete a pre-study survey, post-study survey, follow-up interview, and 3-month follow-up survey in addition to daily brief surveys.",[29,30,31],"Healthy Participants","Feasibility Studies","Acceptability","RECRUITING","2026-07-09",{"date":35,"type":36},"2026-07-13","ACTUAL",{"date":38,"type":36},"2025-09-30",{"date":40,"type":23},"2027-08-06",{"name":42,"class":43},"Florida State University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":18,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":24,"phases":57,"briefSummary":58,"conditions":59,"keywords":69,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":44},"100604558","tag-team---trans-adolescent-group-therapy-100604558","NCT07151079","TAG TEAM - Trans Adolescent Group Therapy","Evaluation of Trans Adolescent Group ThErapy for Alleviating Minority Stress (TAG TEAM): a Randomised Controlled Trial","TAG TEAM","Participants will be enrolled into the RCT only if they meet all the inclusion criteria and none of the exclusion criteria.\n\nInclusion Criteria:\n\n* Identifies as trans, non-binary, or gender diverse\n* Is between the ages of 12 and 17 years inclusive\n* Has completed primary school at the time of enrolment into the study\n* Has current psychological stress symptomology as determined by a score of moderate or above on the DASS-Y\n* Provide informed consent: All participants and parent\u002Flegal guardians must be willing to give informed consent\n\nExclusion Criteria:\n\n* Has current acute suicidal symptomology as determined by a combination of clinical judgement and the results of the Ask Suicide-Screening Questions (ASQ) suicide screening tool (e.g., answer yes to question 5) to determine the risk of suicide (has an active plan and\u002For intent to suicide) at time of screening interview\n* Is actively having treatment with any other group psychological intervention at the time of enrolment into the study\n* Is not proficient in English (as the group Cognitive behaviour therapy (CBT) program will be delivered in English and funds aren't available for interpreters)\n* Previous participation in the feasibility trial\n* Is currently enrolled in tertiary study (e.g., undergraduate university)","12 Years","17 Years",{"count":56,"type":23},142,[26],"This project will study the effect of the TAG TEAM group CBT program on the mental health of trans and gender diverse adolescents. TAG TEAM was co-designed by researchers and clinicians with a group of trans and gender diverse young people to help trans and gender diverse adolescents understand and cope with minority stress. Minority stress includes experiences like discrimination and rejection. TAG TEAM focuses on learning and practicing skills to support mental health and wellbeing. It also includes group discussions and activities with other trans and gender diverse young people. TAG TEAM groups are run by a psychologist and a trans peer facilitator. A trans peer facilitator is a trans and gender diverse person who is there to share their experience of being trans and to support participants in the group sessions.",[60,31,61,62,63,64,65,66,67,68],"Minority Stress","Psychological Distress","Anxiety","Depression in Adolescence","Coping","Wellbeing","Pride","Internalised Stigma","Community Connection",[70,71,72,65,73,74],"Adolescent","Trans and gender diverse","Minority stress","Group Therapy","CBT","2026-06-04",{"date":77,"type":36},"2026-06-05",{"date":79,"type":36},"2026-05-21",{"date":81,"type":23},"2027-03",{"name":83,"class":43},"Murdoch Childrens Research Institute",{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":88,"acronym":4,"eligibilityCriteria":89,"healthyVolunteers":17,"sex":18,"minAge":90,"maxAge":19,"enrollmentInfo":91,"targetDuration":4,"studyType":24,"phases":93,"briefSummary":94,"conditions":95,"keywords":101,"overallStatus":107,"whyStopped":4,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":44},"100613449","pursuit-a-technologically-augmented-school-based-program-to-improve-child-coping-and-prevent-substance-use-100613449","NCT07266740","PURSUIT: A Technologically Augmented School-based Program to Improve Child Coping and Prevent Substance Use.","Inclusion Criteria:\n\n* Aged eight to 18 years\n* Enrolled in a Michigan elementary, middle, or high school\n\nExclusion Criteria:\n\n* Age under 8\n* Age over 18 years\n* Non-enrollment in A Michigan school.","8 Years",{"count":92,"type":23},100,[26],"The study investigators aim to test an online support platform for Michigan youth aged 8-18 years enrolled in elementary, middle, or high school and their parent\u002Fcaregiver. The online support platform will be hosted on the Computerized Intervention Authoring System (CIAS) 3.0 and will provide evidence-based cognitive behavioral coping skills for physical (pain) and mental (stress, mood) health symptoms, with additional substance use prevention content for youth aged 12 and older. Evaluations will occur at baseline and then a post assessment approximately 8 weeks later.",[96,62,97,98,30,31,99,100],"Pediatric Pain","Mood","Stress","Health Promotion","Online Mental Health Program",[102,103,104,98,105,62,97,106],"Cognitive-behavioral","School","Pediatrics","Pain","Substance use","NOT_YET_RECRUITING","2026-05-05",{"date":110,"type":36},"2026-05-07",{"date":112,"type":23},"2026-05-01",{"date":114,"type":23},"2026-10",{"name":116,"class":43},"Michigan State University",{"id":118,"slug":119,"hasResults":11,"nctId":120,"briefTitle":121,"officialTitle":122,"acronym":4,"eligibilityCriteria":123,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":124,"targetDuration":4,"studyType":24,"phases":126,"briefSummary":127,"conditions":128,"keywords":132,"overallStatus":107,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":4},"100631105","integration-of-a-robotic-platform-for-clinical-monitoring-of-patients-with-severe-acquired-brain-injury-in-high-intensity-care-units-100631105","NCT07496346","Integration of a Robotic Platform for Clinical Monitoring of Patients With Severe Acquired Brain Injury in High-Intensity Care Units","A Pilot Study on the Integration of the Rob-In Care Robotic Platform in High-Intensity Care Units for Monitoring Patients With Severe Acquired Brain Injury","Inclusion Criteria:\n\n* Admission to the Neurorehabilitation Unit\n* Requirement for clinical monitoring and\u002For sub-intensive care\n* Ability to provide informed consent, or availability of a legally authorized representative to provide consent\n\nExclusion Criteria:\n\n* No indication for intensive or sub-intensive clinical monitoring\n* Expected hospitalization duration insufficient to complete the study protocol\n* Participation in another clinical study that may interfere with the present study",{"count":125,"type":23},12,[26],"Frailty is not related exclusively to age, but represents a state of increased biological and clinical vulnerability characterized by reduced functional reserve and greater susceptibility to adverse events, even in response to minor stress factors. In patients with complex conditions, such as severe acquired brain injuries, early detection and prompt treatment of clinical deterioration are essential to reduce the risk of acute readmission, complications, and in-hospital mortality. Many of these events are potentially predictable and preventable, given the presence of appropriate monitoring systems.\n\nAdvanced care models, including early warning systems, have been developed to support healthcare professionals in identifying patients at risk by detecting significant changes in physiological parameters. In recent years, technological innovations-particularly in the fields of robotics and telemedicine-have created new opportunities to enhance clinical monitoring, enabling continuous data collection and more timely, proactive interventions.\n\nSocial assistive robots are emerging as promising tools in healthcare settings. These systems can support clinicians and nurses in routine monitoring activities, help reduce workload, and facilitate more efficient and personalized care. By integrating robotic assistance with digital health platforms, it is possible to improve the quality and responsiveness of patient management, especially in high-complexity environments such as neurorehabilitation units.\n\nThis study focuses on the use of an innovative robotic telemedicine system based on the integration of the MOVER-L prototype with the ROB.IN.CARE platform, promoted by Item Oxygen (Bari, Italy). The system is designed to continuously monitor patients' clinical conditions, collecting vital parameters and identifying early signs of deterioration. It supports healthcare professionals by providing real-time data and alerts, enabling earlier and more targeted interventions.\n\nThe study is a low-intensity interventional clinical trial conducted in a Neurorehabilitation Unit. Patients with varying levels of clinical severity, classified according to the Glasgow Coma Scale, are enrolled and divided into two groups: a control group receiving standard care and an experimental group monitored using the robotic system in addition to usual care.\n\nThe primary objective of the study is to evaluate the feasibility, usability, safety, and reliability of this robotic telemedicine solution in a real clinical setting. In addition, the study assesses its acceptability among both patients and healthcare professionals. These aspects are measured using validated tools, including the System Usability Scale (SUS) and the Health and Safety Executive Stress Scale (HSE), to understand the impact of the technology on user experience and workload.\n\nThe integrated MOVER-L\u002FROB.IN.CARE system combines robotic assistance with continuous monitoring of vital signs and advanced software architecture. The platform incorporates predictive algorithms designed to stratify clinical risk and assess patient severity. It utilizes established clinical scoring systems, such as the Modified Early Warning Score (MEWS) for early detection of clinical deterioration, the quick Sequential Organ Failure Assessment (qSOFA) for sepsis risk evaluation, and the Kidney Disease: Improving Global Outcomes (KDIGO) criteria for the assessment of acute kidney injury.\n\nBy enabling early identification of clinical worsening, the system aims to improve the timeliness and effectiveness of healthcare interventions, optimize clinical workflow, and reduce the risk of adverse events and complications. Ultimately, this study explores whether robotic telemedicine can represent a safe, feasible, and valuable tool to enhance the management of fragile patients in neurorehabilitation settings.",[129,130,31,131],"User Experience","Usability","Satisfaction",[133,134],"Robotic platform","Monitoring system","2026-04-17",{"date":137,"type":36},"2026-04-22",{"date":139,"type":23},"2026-05",{"date":141,"type":23},"2026-11",{"name":143,"class":43},"Ernesto Losavio",{"id":145,"slug":146,"hasResults":11,"nctId":147,"briefTitle":148,"officialTitle":149,"acronym":150,"eligibilityCriteria":151,"healthyVolunteers":11,"sex":18,"minAge":90,"maxAge":4,"enrollmentInfo":152,"targetDuration":4,"studyType":24,"phases":154,"briefSummary":155,"conditions":156,"keywords":164,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":172,"lastUpdatePostDateStruct":173,"startDateStruct":175,"completionDateStruct":177,"leadSponsor":179,"locationsCount":44},"100633658","the-new-beginnings-podcast-brief-audio-intervention-for-parents-from-divorced-and-separated-families-100633658","NCT07529548","The New Beginnings Podcast: Brief Audio Intervention for Parents From Divorced and Separated Families","\"The New Beginnings Podcast: A Small-scale Randomized Controlled Trial of a Parenting Podcast to Improve Outcomes for Children From Divorced Families\"","NBP-P","Inclusion Criteria:\n\nFor Parents, eligibility criteria are:\n\n1. divorced, separated, separated but never married, or divorcing\u002Fseparating within the last two years;\n2. one or more children between the ages of 8-18 years old;\n3. have in-person contact with their child(ren) at least three hours per week or have at least one overnight visit every other week;\n4. have access to a smartphone with internet that can play audio files;\n5. English speaking.\n\nFor children, eligibility criteria are:\n\n1. have a parent who is participating in the trial;\n2. be between the ages of 8-18 and\n3. have access to a computer to complete assessments. If a parent has more than one child aged 8-18 interested in participating, we will randomly select one child to ensure independence of responses.\n\nExclusion Criteria:\n\n\\-",{"count":153,"type":23},80,[26],"The goal of this study is to learn if the New Beginnings Podcast can help children whose parents are going through a divorce or separation. The podcast shares parenting strategies that have been shown to help in past in-person and online programs. This study will also look at how easy it is for parents to use the podcast and how helpful they find it.\n\nThe main questions it aims to answer are:\n\n1. Do parents find the podcast easy to use, helpful, and relevant?\n2. Does listening to the podcast improve children's mental health?\n3. Does the podcast help parents build stronger relationships with their children and reduce conflict between parents?\n\nResearchers will compare families who use the podcast to families on a waitlist to see if the podcast makes a difference.\n\nParticipants will:\n\n1. Listen to podcast episodes over the course of the study\n2. Answer questions about their experiences with the podcast\n3. Complete surveys about their child's well-being, their parenting, and family relationships\n\nThis study will include 80 parents and their children.",[157,158,159,160,161,31,162,163],"Parent Child Relationship","Parenting Intervention","Parenting Behaviour","Interparental Conflict","Feasibility Study","Appropriateness","Child Mental Health",[165,166,167,168,169,170,158,171,163],"Parenting","Divorce","Separation","Separated and Divorced Parents","Podcast","Prevention","New Beginnings Program","2026-04-10",{"date":174,"type":36},"2026-04-14",{"date":176,"type":36},"2025-08-15",{"date":178,"type":23},"2026-12",{"name":180,"class":43},"Charla Aubrey Rhodes",{"id":182,"slug":183,"hasResults":11,"nctId":184,"briefTitle":185,"officialTitle":186,"acronym":4,"eligibilityCriteria":187,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":188,"targetDuration":4,"studyType":24,"phases":190,"briefSummary":191,"conditions":192,"keywords":198,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":201,"lastUpdatePostDateStruct":202,"startDateStruct":204,"completionDateStruct":205,"leadSponsor":207,"locationsCount":44},"100607926","hiv-self-testing-for-partners-of-hiv-uninfected-postpartum-women-100607926","NCT07194902","HIV Self-testing for Partners of HIV-uninfected Postpartum Women","HIV Self-testing for Partners of HIV-uninfected Postpartum Women to Facilitate PrEP and Antiretroviral Therapy Uptake to Promote HIV Treatment and Prevention","Female Inclusion Criteria:\n\n* woman\n* Age ≥18\n* ≥30 weeks pregnant per medical record due date\n* non-reactive third trimester HIV test (verified from their antenatal care chart)\n* reporting at least one unknown-serostatus partner\n* fluent in English or isiZulu\n* willing to give researchers permission to contact them for repeated assessments\n* able to provide informed consent\n\nMale Inclusion Criteria: partners meeting the inclusion criteria as described above, and who complete verification questions to confirm their identity and status as the partners of the enrolled female participants. Additional inclusion criteria for men include:\n\n* man\n* Age ≥18\n* partner of enrolled women, confirmed via couples verification tool\n* fluent in English or isiZulu\n* willing to give researchers permission to contact them\n* able to provide informed consent.\n\nExclusion Criteria: Individuals with significant psychiatric illness that could interfere with participation or the ability to provide informed consent will be excluded at the discretion of the study team.",{"count":189,"type":23},120,[26],"The purpose of this study is to test the feasibility and acceptability of a combination intervention to promote HIV self-testing (HIVST) for Partners and PrEP uptake for HIV-uninfected Postpartum Women (\"H4P\"). H4P includes evidence-based cognitive behavioral therapy (CBT) strategies, such as communication skills training, motivational interviewing, and problem-solving. The investigators will conduct a randomized pilot trial of the H4P intervention to evaluate the feasibility, acceptability, and preliminary effectiveness of a multi-step PrEP uptake and HIV self-test kit intervention for postpartum HIV-uninfected women (N = 60 and their male partners) who report a partner of unknown serostatus, and their partners, in the province of KwaZulu-Natal, South Africa.",[193,194,195,196,31,197],"HIV Self-testing","Male Partners of HIV-negative Postpartum Women","PrEP Uptake","Feasibility","HIV Prevention",[197,199,200],"PrEP","HIV Self-Testing","2026-03-19",{"date":203,"type":36},"2026-03-23",{"date":201,"type":36},{"date":206,"type":23},"2026-08-28",{"name":208,"class":43},"Massachusetts General Hospital",{"id":210,"slug":211,"hasResults":11,"nctId":212,"briefTitle":213,"officialTitle":213,"acronym":4,"eligibilityCriteria":214,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":215,"targetDuration":4,"studyType":24,"phases":217,"briefSummary":218,"conditions":219,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":225,"lastUpdatePostDateStruct":226,"startDateStruct":228,"completionDateStruct":230,"leadSponsor":232,"locationsCount":44},"100601030","feasibility-of-wireless-continuous-vital-sign-monitoring-and-impact-on-patients-undergoing-adult-spinal-surgery-in-a-general-ward-100601030","NCT07105189","Feasibility of Wireless Continuous Vital Sign Monitoring and Impact on Patients Undergoing Adult Spinal Surgery in a General Ward","Inclusion Criteria:\n\n* Included are adult patients (\\>=18 years) scheduled for ASD surgery with estimated a \\>3 day expected post-operative stay. ASD-surgery is defined as a posterior instrumented fusion of at least five spinal levels including instrumentation to the pelvis, caused by a degenerative condition of the spine.\n* Registered nurses and nurses' assistants employed at the orthopedic ward during the study period will be included if they have experience working with wCVSM during the study period. The study includes both sexes, variation of level of education and years of work experience. Included nurses and nurses' assistants should be proficient in the Danish language.\n\nExclusion Criteria:\n\n* Exclusion criteria are patients who are unable to wear continuous monitoring due to a pacemaker or allergy.\n* Patients who are not proficient in the Danish language will be excluded.",{"count":216,"type":23},150,[26],"The goal of this feasibility study is to explore the use of wireless continuous vital sign monitoring in an orthopaedic setting among orthopaedic nurses and patients undergoing adult spinal deformity surgery. In addition to the standard care National Early Warning Score the participants in this study will be monitored by CPC12S a wearable sensor that is worn on the chest using electrodes measuring electrocardiography single lead (ECG), Heart rate, respiratory rate, SpO2, blood pressure and temperature.\n\nMain hypotheses:\n\nThe use of wireless continuous vital sign monitoring in daily clinical practice for patients undergoing ASD surgery is feasible in terms of increased acceptability among orthopeadic surgical nurses measured over 12 months with a response rate of at least 80% with an average score of ≥5 at the last measurement in each of the four dimensions of the USE questionnaire: Usefulness, ease of use, ease of learning and satisfaction.\n\nThe following parameters will be evaluated:\n\nPrimary outcome:\n\n1. The feasibility in terms of acceptability of the concept of wCVSM among orthopedic surgical ward nurses.\n\n   Secondary outcomes:\n2. The feasibility in terms of acceptability of the concept of wCVSM in patients undergoing ASD surgery.\n3. The technical fidelity of wCVSM, assessed by data collected of vital signs, display of alerts to staff nurses and response to the alerts.\n4. The frequency of vital sign deviations in patients after ASD surgery using wCVSM compared to NEWS2.\n5. Clinical outcomes of patients undergoing ASD surgery including surgical complications, reinterventions, ICU admissions, unplanned ward transfer, and admissions to another department.",[220,221,222,31,223,224,30],"Adult Spinal Deformity","Wireless Continuous Vital Signs Monitoring","Wireless Vital Signs Monitoring System","ASD Surgery","Remote Monitoring","2026-01-06",{"date":227,"type":36},"2026-01-08",{"date":229,"type":36},"2025-12-10",{"date":231,"type":23},"2026-08-30",{"name":233,"class":43},"Rigshospitalet, Denmark",{"id":235,"slug":236,"hasResults":11,"nctId":237,"briefTitle":238,"officialTitle":239,"acronym":240,"eligibilityCriteria":241,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":242,"enrollmentInfo":243,"targetDuration":4,"studyType":24,"phases":245,"briefSummary":246,"conditions":247,"keywords":257,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":263,"lastUpdatePostDateStruct":264,"startDateStruct":266,"completionDateStruct":268,"leadSponsor":270,"locationsCount":44},"100599273","feasibility-and-potential-efficacy-of-herbs-and-spices-for-improving-dietary-quality-in-college-students-a-pilot-study-100599273","NCT07082348","Feasibility and Potential Efficacy of Herbs and Spices for Improving Dietary Quality in College Students: A Pilot Study","Assessing the Feasibility and Potential Efficacy of Herbs and Spices for Improving Dietary Quality and Adherence to the Dietary Guidelines for Americans in College Students With Poor Dietary Quality: A Pilot Study","HerbSpicesDiet","Inclusion Criteria:\n\n* College students (undergraduate and graduate)\n* Ages 18-39 years\n* BMI 18.5-40 kg\u002Fm\n* Having poor dietary quality (a Rapid Prime Diet Quality Score of 12 or below),\n* Maintain current lifestyle habits (e.g., medications\u002F supplement use, exercise, and sleep), and avoid taking new supplements or medications throughout the study.\n\nExclusion Criteria:\n\n* Individuals diagnosed with myocardial infarction within the past 6 months\n* Uncontrolled hypertension\n* BMIs \\\u003C18.5 or \\>40 kg\u002Fm2\n* Autoimmune disease or immune compromised\n* A recent diagnosis of cancer or under current treatment for cancer\n* A history of kidney stones\n* Having pacemaker\n* Participating in a weight loss program\n* Having a history of any significant GI disease\n* Insulin use\n* Currently on dialysis\n* Currently consuming pro-\u002Fpre-biotics or antiobiotics\n* Diagnosed with unstable chronic metabolic disease\n* Have allergies to any herbs and spices\n* Are pregnant\u002Fnursing\n* Participating in another investigational study\n* Unable or unwilling to give consent","39 Years",{"count":244,"type":23},30,[26],"The goal of this single-arm feasibility, pilot study is to assess the feasibility, acceptability, and potential effectiveness of the Herbs and Spices Nutrition Education Program (HSNP-focusing on incorporating herbs and spices into the diet for adherence to the DGA's) for determining the scalability of implementing this intervention for a larger scale, more comprehensive study The main questions it aims to answer are:\n\n* What is the feasibility and acceptability of incorporating herbs and spices into the diet along with DGA-focused nutrition education through the HSNP in college students with poor dietary quality?\n* What are the preliminary effects of the HSNP on dietary intake\u002Fquality, cardiometabolic, and gut health in college students with poor dietary quality?\n* What are the barriers associated with HSNP implementation in college students with poor dietary quality?\n\nParticipants will:\n\n* Be asked to come to the study site initially for a Screening Study Visit to confirm eligibility.\n* Be asked to come the clinical study site for a Pre-HSNP and Post-HSNP Study Visit (one week prior starting the HSNP and after week 6 of completing the HSNP) for assessments of cardiometabolic and gut health.\n* Be asked to come to the Nutrition Center for weeks 0 and 3 of the HSNP, where they will receive education on the Dietary Guidelines for Americans and the health benefits of herbs and spices, have a sensory evaluation of foods, be provided budget-friendly recipes and resources, and given take-home herbs, spices, and supporting materials\n* Be asked to complete 3-Day Food Records throughout the 6 week study period for assessment of dietary quality (4 total)",[248,30,249,250,251,252,253,31,254,255,256],"Dietary Quality","College Student","Dietary Guidelines for Americans","Gut Microbiome","Lipid Profiles","Herbs and Spices","Inflammation Biomarkers","Body Composition","Anthropometrics",[258,259,260,261,262],"dietary quality","dietary guidelines for americans","college students","cardiometabolic health","gut microbiome","2025-11-18",{"date":265,"type":36},"2025-11-24",{"date":267,"type":36},"2025-07-03",{"date":269,"type":23},"2026-12-31",{"name":271,"class":43},"University of Nevada, Las Vegas",{"id":273,"slug":4,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":274,"acronym":15,"eligibilityCriteria":275,"healthyVolunteers":17,"sex":276,"minAge":19,"maxAge":20,"enrollmentInfo":277,"targetDuration":4,"studyType":24,"phases":278,"briefSummary":27,"conditions":279,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":280,"lastUpdatePostDateStruct":281,"startDateStruct":283,"completionDateStruct":284,"leadSponsor":286,"locationsCount":44},"100606027","Translating Behavioral Economics Strategies to Culturally Tailor a Mobile Health Mindfulness Intervention to Reduce Risky Drinking Behaviors in Black College Student Men","Inclusion Criteria:\n\n* US-born\n* Black\n* biological man\n* undergraduate college student\n* criteria for binge drinking (5 drinks in about 2 hours) or heavy drinking (more than 14 drinks per week).","MALE",{"count":22,"type":23},[26],[29,30,31],"2025-10-01",{"date":282,"type":36},"2025-10-06",{"date":38,"type":36},{"date":285,"type":23},"2027-03-01",{"name":42,"class":43},{"id":288,"slug":289,"hasResults":11,"nctId":290,"briefTitle":291,"officialTitle":292,"acronym":4,"eligibilityCriteria":293,"healthyVolunteers":17,"sex":18,"minAge":294,"maxAge":4,"enrollmentInfo":295,"targetDuration":4,"studyType":24,"phases":297,"briefSummary":298,"conditions":299,"keywords":300,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":304,"lastUpdatePostDateStruct":305,"startDateStruct":307,"completionDateStruct":309,"leadSponsor":311,"locationsCount":44},"100585868","digital-support-strategies-for-caregiver-home-practice-100585868","NCT06907966","Digital Support Strategies for Caregiver Home Practice","Digital Implementation Support Strategies for Caregiver Home Practice","Caregiver Inclusion Criteria:\n\n* Informed consent\n* Ownership and regular use of a smartphone\n* English or Spanish language fluency\n* Concurrent enrollment in the family-based EBI Bridges\n* Parent of a child aged 11-17 years old\n\nCaregiver Exclusion Criteria:\n\n\\- Decline to download the home practice app on their personal smartphone.\n\nChild Inclusion Criteria:\n\n* Parent\u002Fguardian consent\n* Informed assent\n* Parent is enrolled in the study\n* English reading ability at the 4th grade level or higher\n\nChild Exclusion Criteria:\n\n* No parent\u002Fguardian consent\n* Parent\u002Fguardian is not enrolled in the study concurrently","11 Years",{"count":296,"type":23},96,[26],"This project is a pilot trial of the Engaging Families home practice smartphone application (or \"app\") as an add on to a family-based prevention program. Although there are many evidence-based preventive interventions delivered to caregivers to prevent youth substance use and mental illness and promote youth positive family and youth outcomes, the impact of these interventions is often limited by low home practice of intervention skills among caregivers. The Engaging Families home practice app is a digital behavior change intervention that was developed to support caregivers in practicing intervention skills at home. Researchers will ask participants if the app was acceptable and feasible for daily use at home. Researchers may also compare how often caregivers who use the study app do home practice of intervention skills compared with caregivers who do not receive the home practice app but are encouraged to use an app to help schedule their activities.",[31,30],[301,302,303],"home practice","parenting","skills practice","2025-06-19",{"date":306,"type":36},"2025-06-25",{"date":308,"type":36},"2025-03-17",{"date":310,"type":23},"2027-07",{"name":312,"class":43},"Arizona State University"]