[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"feasibility-studies\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:feasibility-studies":31},{"pageToken":4,"total":5,"offset":6,"count":7,"results":8},null,26,0,25,[9,46,71,106,136,156,189,218,241,265,289,318,352,374,399,437,474,495,510,542,573,599,623,645,686],{"id":10,"slug":11,"hasResults":12,"nctId":13,"briefTitle":14,"officialTitle":15,"acronym":16,"eligibilityCriteria":17,"healthyVolunteers":18,"sex":19,"minAge":20,"maxAge":21,"enrollmentInfo":22,"targetDuration":4,"studyType":25,"phases":26,"briefSummary":28,"conditions":29,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"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":23,"type":24},40,"ESTIMATED","INTERVENTIONAL",[27],"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.",[30,31,32],"Healthy Participants","Feasibility Studies","Acceptability","RECRUITING","2026-07-09",{"date":36,"type":37},"2026-07-13","ACTUAL",{"date":39,"type":37},"2025-09-30",{"date":41,"type":24},"2027-08-06",{"name":43,"class":44},"Florida State University","OTHER",1,{"id":47,"slug":48,"hasResults":12,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":12,"sex":19,"minAge":20,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":25,"phases":56,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":45},"100642066","pilot-study-of-a-behavioral-program-for-resident-depression-in-skilled-nursing-facilities-100642066","NCT07655232","Pilot Study of a Behavioral Program for Resident Depression in Skilled Nursing Facilities","Building Resilience in Skilled Nursing Care: Open Pilot for a Behavioral Health Intervention","BRISK-I","Inclusion Criteria:\n\n* Psychological distress, as indicated by a score Patient Health Questionnaire- 2 ≥ 2 OR Patient Health Questionnaire-9 ≥ 5\n* 5+ chronic conditions based on Elixhauser Comorbidity Index\n* Aged ≥ 18 years\n* Able and willing to participate in the study\n\nExclusion Criteria:\n\n* Intended length of SNF stay \\\u003C 7 days\n* More than mild cognitive impairment, as indicted by Brief Interview for Mental Status (BIMS) \\\u003C13\n* Participant's roommate is already enrolled in study\u002Fintervention\n* High risk of suicide\u002Factive documented SI per the PHQ-9, item 9 or otherwise\n* Participation in newly initiated psychotherapy",{"count":55,"type":24},20,[27],"The goal of this clinical trial is to test a behavioral health program (Interventions for Stressful Transitions in Later Life, InSTILL, for Individuals) for skilled nursing facility residents. The main questions it aims to answer is whether the program is program is feasible, satisfactory, and helpful. Participants will join 6 bi-weekly sessions of the InSTILL program. Participants will complete assessments at three timepoints (all) and a brief-exit interview.",[59,60,61,31],"Nursing Home Resident","Skilled Nursing Facility","Depression","2026-06-15",{"date":64,"type":37},"2026-06-17",{"date":66,"type":37},"2025-11-17",{"date":68,"type":24},"2026-12-31",{"name":70,"class":44},"Massachusetts General Hospital",{"id":72,"slug":73,"hasResults":12,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":77,"eligibilityCriteria":78,"healthyVolunteers":18,"sex":19,"minAge":79,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":25,"phases":82,"briefSummary":83,"conditions":84,"keywords":86,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":101,"completionDateStruct":102,"leadSponsor":104,"locationsCount":45},"100641910","physical-activity-intervention-for-older-family-carers-100641910","NCT07653061","Physical Activity Intervention for Older Family Carers","Supporting Physical Activity and Functional Capacity Among Older Family Caregivers (CAREFIT): A Six-month, Randomised Controlled Pilot Trial","CAREFIT","Inclusion Criteria:\n\n* Aged 65 years or older\n* Spousal family caregiver living in the same household as the care recipient (a formal caregiving agreement is not required)\n* Participating in moderate- or vigorous-intensity physical activity fewer than two times per week\n* Able to safely engage in light-to-moderate physical activity based on self-report and health screening conducted by the study nurse, with consultation from the study physician if required\n* Able to understand study procedures and provide written informed consent\n\nExclusion Criteria:\n\n* Diagnosed dementia, substantial cognitive impairment, or other significant neurological disease that would interfere with participation in the study\n* Inability to provide informed consent or complete study assessments, as determined by study personnel\n* Medical conditions that may compromise safe participation in physical activity, including but not limited to active malignant disease, severe major depression, symptomatic cardiovascular disease, or coronary or vascular revascularization within the previous 12 months\n* Severe visual, hearing, speech, or other sensory or communication impairments that would prevent meaningful participation in the intervention, as determined by the study nurse\n* Concurrent participation in another interventional clinical trial","65 Years",{"count":81,"type":24},50,[27],"The goal of this pilot trial is to learn whether a six-month physical activity program tailored for older family caregivers can be successfully delivered and whether participants are willing and able to take part in it. The study will also explore possible effects of the programme on physical activity, physical function, health, and well-being.\n\nThe main questions it aims to answer are:\n\n* Can enough participants be recruited to the study?\n* Do participants adhere to the study and complete follow-up assessments?\n* How often do participants take part in the program activities?\n* How acceptable and useful do participants find the program?\n* What are the possible effects of the programme on physical activity, health, and wellbeing.\n\nResearchers will compare the physical activity program with a control group that receives health information and education about healthy ageing.\n\nParticipants will:\n\n* Complete health, physical functioning, and questionnaire assessments at the beginning of the study, after 6 months, and after 12 months\n* Wear an activity monitor on their wrist for 7 days and nights at the beginning of the study and after 6 months\n* Will be randomly assigned to either a six-month physical activity program designed for older family caregivers, or a control group that receives health information and education about healthy ageing.\n* If assigned to the physical activity program, participants will take part in weekly group-based and remote exercise sessions for 6 months.\n* Provide feedback about their experiences of the program",[31,85],"Physical Activity and Wellbeing",[87,88,89,90,91,92,93,94,95,96,97],"family caregivers","older adults","physical activity","exercise","physical functioning","feasibility","pilot study","health behavior","positive mental health","cognition","stress","NOT_YET_RECRUITING","2026-06-11",{"date":64,"type":37},{"date":62,"type":24},{"date":103,"type":24},"2027-08-31",{"name":105,"class":44},"Tampere University",{"id":107,"slug":108,"hasResults":12,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":112,"eligibilityCriteria":113,"healthyVolunteers":12,"sex":19,"minAge":20,"maxAge":4,"enrollmentInfo":114,"targetDuration":4,"studyType":25,"phases":116,"briefSummary":117,"conditions":118,"keywords":122,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":45},"100615381","central-venous-catheter-placement-with-thoracic-ultrasound-and-intracavity-ecg-positioning-100615381","NCT07291869","Central Venous Catheter Placement With Thoracic Ultrasound and Intracavity ECG Positioning","A Randomised Feasibility Study of Real-time Intracavity ECG and Thoracic Ultrasound for Central Venous Catheter Tip Confirmation in Critical Care","CVC-TIP","Inclusion Criteria:\n\n* Adult (aged ≥ 18 years)\n* Admitted, or planned for admission, to critical care\n* Requiring central venous catheter insertion as a part of their usual care\n* Suitable for both right or left internal jugular vein insertion\n\nExclusion Criteria:\n\n* Previously randomised into CVC-TIP\n* Atrial fibrillation on 12-lead ECG\n* Cardiovascular instability, defined as\n* Noradrenaline dose \\> 0.5mcg\u002Fkg\u002Fmin\n* Rapidly escalating doses of vasopressors \u002F inotropes\n* Difficulty in obtaining thoracic ultrasound images due to either\n* Weight \\> 120kg\n* Existing pneumothorax (either side)\n* Subcutaneous emphysema\n* Wounds \u002F dressing over anterior chest wall\n* Existing pacemaker\n* Non-English speaking participants\n* Death perceived as imminent\n* Any other reason as determined by treating clinician",{"count":115,"type":24},75,[27],"The goal of this interventional study is to assess the feasibility of two bedside techniques for confirming central venous catheter (CVC) placement and detecting complications:\n\n* Intracavity ECG monitoring to confirm internal jugular vein CVC tip position.\n* Thoracic point-of-care ultrasound (POCUS) to rule out pneumothorax following CVC insertion.\n\nParticipants who require an internal jugular CVC as part of their routine care and meet all inclusion and no exclusion criteria will be randomised to receive either:\n\n* Standard care, or\n* The intervention, consisting of intracavity ECG guidance and thoracic POCUS. The CVC will be inserted either on the left or right side of the neck.\n\nAll participants will undergo a post-procedure chest X-ray regardless of study arm, to allow comparison of the intervention methods with standard care.",[119,120,121,31],"Central Venous Catheter","Point of Care Ultrasound (POCUS)","Intracavitary Electrocardiogram Guiding",[123,124,125,126],"Intracavity ECG","POCUS","IC-ECG","Thoracic point of care ultrasound","2026-05-28",{"date":129,"type":37},"2026-06-02",{"date":131,"type":37},"2026-05-15",{"date":133,"type":24},"2027-10",{"name":135,"class":44},"York Teaching Hospitals NHS Foundation Trust",{"id":137,"slug":138,"hasResults":12,"nctId":139,"briefTitle":140,"officialTitle":141,"acronym":4,"eligibilityCriteria":142,"healthyVolunteers":12,"sex":19,"minAge":20,"maxAge":143,"enrollmentInfo":144,"targetDuration":4,"studyType":25,"phases":145,"briefSummary":146,"conditions":147,"keywords":4,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":148,"lastUpdatePostDateStruct":149,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":45},"100637227","the-aim-of-this-study-is-to-assess-the-feasibility-of-the-study-protocol-and-the-acceptability-of-the-mobile-application-based-intervention-the-results-will-guide-the-design-and-evaluation-of-a-definitive-larger-scale-study-to-further-examine-the-efficacy-of-the-refined-intervention-100637227","NCT07589803","The Aim of This Study is to Assess the Feasibility of the Study Protocol and the Acceptability of the Mobile Application-Based Intervention. The Results Will Guide the Design and Evaluation of a Definitive, Larger-scale Study to Further Examine the Efficacy of the Refined Intervention.","A Mobile Application Intervention Under the Guidance of a Patient Undergoing Total Joint Replacement Surgery- a Pilot Randomized Controlled Trial.","Inclusion Criteria:\n\nPrimary knee or hip joint replacement surgery No previous visits to Coxa Age 18-75 years Proficiency in the Finnish language Body mass index (BMI) below 40 Moderate alcohol consumption (AUDIT \\\u003C 20) Ability to use a mobile application (access to a compatible smartphone) The patient may have a mild systemic disease that does not significantly limit functional capacity (ASA I-II) The patient may also have a somewhat more severe condition, provided that underlying diseases are well controlled (ASA III) Medication use is moderate, consisting of 1-5 medications in addition to pain medication No use of anticoagulant medication No previously identified anesthetic complications\n\nExclusion Criteria:\n\nPrevious joint surgery Functional impairment \u002F disability Insufficient proficiency in the Finnish language No possibility to use a mobile application (no mobile phone) Patient with multiple comorbidities (multimorbid patient) The patient does not proceed to the surgical waiting list","75 Years",{"count":23,"type":24},[27],"This study is a pilot study for a larger future research project aimed at examining the effects of patient education delivered via a mobile application on patients' self-reported receipt of information in relation to their information needs, as well as on patient-reported quality of life, pain, and functional capacity, compared with traditional patient education provided during in-person appointments or by telephone. The primary objective of this pilot study is to assess the feasibility of conducting the forthcoming larger-scale study.\n\nResearch questions:\n\n1. How does patient education delivered via a mobile application meet the information needs of patients undergoing joint replacement surgery, and is the intervention feasible to implement in a larger research setting?\n2. How do the instruments used in the pilot study (EKhp\u002FRKhp, EQ-5D-5L, NRS, and OKS\u002FOHS) and the study design function when delivered via a mobile application for the intervention group and in conjunction with traditional patient education for the control group, and are the instruments and study design suitable for conducting a larger-scale study.\n\nThe study will be conducted as a randomized controlled trial (RCT). Patients will be allocated into two groups:\n\nIntervention group: receives patient education via a mobile application. Control group: receives traditional patient education during face-to-face clinic visits or by telephone.\n\nData will be collected using questionnaires before surgery (three measurement points) and after surgery (two measurement points).",[31],"2026-05-11",{"date":131,"type":37},{"date":151,"type":24},"2026-04",{"date":153,"type":24},"2027-12",{"name":155,"class":44},"Coxa, Hospital for Joint Replacement",{"id":157,"slug":158,"hasResults":12,"nctId":159,"briefTitle":160,"officialTitle":160,"acronym":4,"eligibilityCriteria":161,"healthyVolunteers":18,"sex":19,"minAge":162,"maxAge":20,"enrollmentInfo":163,"targetDuration":4,"studyType":25,"phases":165,"briefSummary":166,"conditions":167,"keywords":174,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":180,"lastUpdatePostDateStruct":181,"startDateStruct":183,"completionDateStruct":185,"leadSponsor":187,"locationsCount":45},"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":164,"type":24},100,[27],"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.",[168,169,170,171,31,32,172,173],"Pediatric Pain","Anxiety","Mood","Stress","Health Promotion","Online Mental Health Program",[175,176,177,171,178,169,170,179],"Cognitive-behavioral","School","Pediatrics","Pain","Substance use","2026-05-05",{"date":182,"type":37},"2026-05-07",{"date":184,"type":24},"2026-05-01",{"date":186,"type":24},"2026-10",{"name":188,"class":44},"Michigan State University",{"id":190,"slug":191,"hasResults":12,"nctId":192,"briefTitle":193,"officialTitle":194,"acronym":195,"eligibilityCriteria":196,"healthyVolunteers":18,"sex":19,"minAge":20,"maxAge":4,"enrollmentInfo":197,"targetDuration":4,"studyType":25,"phases":198,"briefSummary":199,"conditions":200,"keywords":203,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":208,"lastUpdatePostDateStruct":209,"startDateStruct":211,"completionDateStruct":213,"leadSponsor":215,"locationsCount":217},"100570174","protective-ventilation-with-flow-controlled-ventilation-100570174","NCT06703814","PROtective Ventilation With FLOW-Controlled Ventilation","PROtective Ventilation With FLOW-Controlled Ventilation to Improve Postoperative Pulmonary Outcome After ROBOT-Assisted Laparoscopic Surgery - an International Multicenter Pilot Randomized Clinical Trial.","PROFLOW","Inclusion Criteria:\n\n* undergoing elective robot-assisted laparoscopic surgery in supine or Trendelenburg position (either abdominal, urologic or gynecologic surgery);\n* AND increased risk of PPCs according to the ARISCAT risk score (≥ 26 points);\n* OR the combination of age \\> 40 years, scheduled surgery lasting \\> 2 hours and planned to receive an intra-arterial catheter for blood pressure monitoring during the surgery;\n* aged ≥ 18 years; and\n* able to give written informed consent to participate in the study and agree to comply with the study protocol prior to initiation of any study-mandated procedure and study intervention.\n\nExclusion Criteria:\n\n* ideal body weight \\\u003C 40 kg;\n* ASA Physical Status Classification System score IV - VI;\n* previous enrolment into the current study;\n* being the study investigator, his\u002Fher family members, employees and other dependent persons;\n* if female and of childbearing potential, known pregnancy or a positive urine pregnancy test (confirmed by a positive serum pregnancy test), or lactating; or\n* No informed consent",{"count":164,"type":24},[27],"The investigators want to investigate in patients undergoing robot-assisted laparoscopic surgery (a minimally invasive procedure) how applicable flow-controlled ventilation is, and whether it might also be safer than the current ventilation techniques, as well as its impact on potentially reducing the risk of lung-specific complications.\n\nFlow-controlled ventilation has already been tested in several studies on animals and humans and has proven to be a safe form of ventilation for patients undergoing surgery under general anesthesia.\n\nWhen patients undergo major surgery, general anesthesia is required and, as a result, mechanical ventilation of the lungs. Especially in long and complex surgeries, ventilation can become more difficult or lead to complications postoperatively. These patients may then experience shortness of breath, coughing, or require medication to improve lung function. In some cases, reintubation or additional mechanical ventilation may be necessary for support.\n\nPrevious human studies have shown that flow-controlled ventilation is less stressful and, therefore, potentially safer for the lungs compared to traditional ventilation techniques, and that less supplemental oxygen is required. This effect and the safety of flow-controlled ventilation have been demonstrated in several studies.\n\nTherefore, in this study, the investigators aim to explore whether flow-controlled ventilation is potentially safer and easier to apply than traditional ventilation techniques and whether it can reduce the risk of lung-specific complications following robot-assisted surgeries, thereby improving the recovery process postoperatively.",[201,31,202],"Postoperative Pulmonary Complications (PPCs)","Pilot Study",[204,205,206,207],"flow-controlled ventilation","postoperative pulmonary complications","mechanical ventilation","intraoperative ventilation","2026-04-16",{"date":210,"type":37},"2026-04-21",{"date":212,"type":37},"2025-08-02",{"date":214,"type":24},"2026-05-31",{"name":216,"class":44},"Cantonal Hospital of St. Gallen",3,{"id":219,"slug":220,"hasResults":12,"nctId":221,"briefTitle":222,"officialTitle":223,"acronym":224,"eligibilityCriteria":225,"healthyVolunteers":12,"sex":19,"minAge":226,"maxAge":4,"enrollmentInfo":227,"targetDuration":4,"studyType":25,"phases":229,"briefSummary":230,"conditions":231,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":232,"lastUpdatePostDateStruct":233,"startDateStruct":235,"completionDateStruct":237,"leadSponsor":239,"locationsCount":45},"100607494","preserving-ability-through-virtual-exercise-pave-100607494","NCT07189286","Preserving Ability Through Virtual Exercise (PAVE)","Preserving Ability Through Virtual Exercise (PAVE): An Intervention to Increase the Physical Activity of Hospitalized Older Adults","PAVE","Inclusion Criteria:\n\n1. in the last 72 hours, they were admitted to the medical floor that is the setting of the study,\n2. are 55 years or older,\n3. their bedside nurse approves their physical activity participation in this study\n\nExclusion Criteria:\n\n1. they are unable to pass the Evaluation to Sign Consent Measure,\n2. they score 20 or lower on the Montreal Cognitive Assessment Basic,\n3. they have an admitting diagnosis that could be worsened through virtual reality exercise,\n4. they have an attached medical device that decreases the safety of physical activity such as a nasogastric tube or continuous fluids running through a PICC line that cannot be paused,\n5. they are unable to follow commands or move their extremities against gravity during the UMove Mobility Assessment,\n6. they are unable to wear the virtual reality headset,\n7. they received the education control intervention or PAVE intervention during a prior admission,\n8. there is an active plan to discharge this patient during day of recruitment or the following day,\n9. they are on airborne or droplet precautions","55 Years",{"count":228,"type":24},140,[27],"Each day in the hospital leads to functional decline and loss of muscle mass, which older adults can find difficult or impossible to restore in the post-acute period. The overall objective of this proposed project is to explore the feasibility and preliminary efficacy of a virtual reality physical activity intervention at helping older adults engage in physical activity and maintain physical function and mental health during their hospital stay. As virtual reality technology becomes more affordable and ubiquitously available across the world, this study will demonstrate how this technology could be leveraged to maintain the function of older adults in the hospital.",[31],"2026-04-13",{"date":234,"type":37},"2026-04-14",{"date":236,"type":37},"2026-02-01",{"date":238,"type":24},"2030-01-01",{"name":240,"class":44},"University of Maryland, Baltimore",{"id":242,"slug":243,"hasResults":12,"nctId":244,"briefTitle":245,"officialTitle":245,"acronym":246,"eligibilityCriteria":247,"healthyVolunteers":12,"sex":19,"minAge":248,"maxAge":4,"enrollmentInfo":249,"targetDuration":4,"studyType":25,"phases":251,"briefSummary":252,"conditions":253,"keywords":4,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":256,"lastUpdatePostDateStruct":257,"startDateStruct":259,"completionDateStruct":261,"leadSponsor":263,"locationsCount":45},"100633088","home-based-self-exercise-in-patients-with-parkinsons-disease-a-feasibility-study-100633088","NCT07522138","Home-based Self-exercise in Patients With Parkinson's Disease: A Feasibility Study","SelfExPD","Inclusion Criteria:\n\n* Adults aged 19 years or older, clinically diagnosed with Idiopathic Parkinson's Disease (PD) according to the Movement Disorder Society (MDS) clinical diagnostic criteria\n* Patients at Hoehn and Yahr stage 1-2.5\n* Patients on stable dopaminergic therapy with no changes in the past 1 month\n* Patients receiving Lee Silverman Voice Treatment (LSVT) rehabilitation therapy once weekly as outpatients\n* Patients who have voluntarily provided informed consent to participate in the study\n\nExclusion Criteria:\n\n* Patients diagnosed with atypical parkinsonism\n* Patients with musculoskeletal problems that make participation in rehabilitation difficult\n* Patients who have limited access to the video-based home exercise feedback program","19 Years",{"count":250,"type":24},15,[27],"This study aims to test whether patients with Parkinson's disease can safely and effectively use a home-based exercise program guided by videos. Participants will follow video instructions for exercises at home while their movements are monitored by a camera, which provides real-time feedback. The study will check how well participants complete the exercises, their satisfaction with the program, and any changes in clinical function. The goal is to see if this type of home exercise can help patients increase their activity levels without significant side effects.",[254,255,31],"Home Exercise Program","PD - Parkinson's Disease","2026-04-12",{"date":258,"type":37},"2026-04-15",{"date":260,"type":24},"2026-04-20",{"date":262,"type":24},"2027-02-28",{"name":264,"class":44},"Seoul National University Hospital",{"id":266,"slug":267,"hasResults":12,"nctId":268,"briefTitle":269,"officialTitle":270,"acronym":4,"eligibilityCriteria":271,"healthyVolunteers":12,"sex":19,"minAge":162,"maxAge":272,"enrollmentInfo":273,"targetDuration":4,"studyType":25,"phases":274,"briefSummary":275,"conditions":276,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":279,"lastUpdatePostDateStruct":280,"startDateStruct":282,"completionDateStruct":284,"leadSponsor":286,"locationsCount":288},"100607337","feasibility-of-the-reality-paws-program-for-children-in-isolation-100607337","NCT07187245","Feasibility of the Reality PAWS Program for Children in Isolation","Reality PAWS: Examining the Feasibility of a Mixed Reality Dog Visitation Program for Hospitalized Children in Isolation","Inclusion Criteria:\n\n* Children 8 to 21 years old admitted to Children's Hospital Colorado or Children's Hospital Los Angeles\n* Children who are English-speaking (legal guardian may be English-speaking or Spanish-speaking)\n* Children within the normal range of development will be recruited for this study.\n\nExclusion Criteria:\n\n* Traumatic brain injury, neurological disorders, neurodevelopmental issues, or other neurological disorders and comorbidities that may confound study outcomes and administration of the study protocol and metrics (e.g., visual field disturbances, frequent nausea\u002F vomiting, not medically stable, intellectual disability)\n* Children with visual, auditory, or tactile deficits that would interfere with the ability to complete the experimental tasks\n* Children with a history of seizure disorder\n* Children currently sick with flu-like symptoms or experiencing a headache or earache\n* Children with known or suspected motion sickness\n* Children with cochlear implants or pace makers","21 Years",{"count":81,"type":24},[27],"The goal of this clinical trial is to learn if a mixed reality program, Reality PAWS, delivered on a Meta Quest 3 VR headset, is a feasible intervention for pediatric patients in isolation. It will also evaluate the safety of the program and its effect on pain, anxiety, and loneliness. The main questions the study aims to answer are:\n\nWhat is the feasibility of utilizing Reality PAWS MR as a substitute for in-person dog therapy for children under isolation precautions? Are patients compliant with using Reality PAWS MR? What are the interventional outcomes of Reality PAWS MR?\n\nParticipants will:\n\nWear a Meta Quest 3 VR headset with the Reality PAWS program. Interact with the program. Answer surveys regarding demographics, anxiety, pain, loneliness, sickness, perceived exertion, and immersion in the program.",[277,278,31],"Inpatient Pediatric Care","Isolation","2026-04-03",{"date":281,"type":37},"2026-04-08",{"date":283,"type":37},"2026-01-29",{"date":285,"type":24},"2026-07-01",{"name":287,"class":44},"Children's Hospital Colorado",2,{"id":290,"slug":291,"hasResults":12,"nctId":292,"briefTitle":293,"officialTitle":293,"acronym":294,"eligibilityCriteria":295,"healthyVolunteers":12,"sex":19,"minAge":248,"maxAge":4,"enrollmentInfo":296,"targetDuration":4,"studyType":25,"phases":298,"briefSummary":299,"conditions":300,"keywords":303,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":309,"lastUpdatePostDateStruct":310,"startDateStruct":312,"completionDateStruct":314,"leadSponsor":316,"locationsCount":45},"100615635","help-study---towards-high-throughput-and-efficient-long-axial-pet-with-oral-18ffdg-100615635","NCT07295171","HELP Study - Towards High Throughput and Efficient Long-axial PET With Oral [18F]FDG","HELP","Inclusion Criteria:\n\n* Age ≥19 years\n* Participants who have received a standard of care \\[18F\\]FDG PET\u002FCT and are willing to undergo a study specific oral \\[18F\\]FDG PET\u002FCT within 2 weeks.\n\nExclusion Criteria:\n\nParticipant Inclusion Criteria\n\n* Age ≥19 years\n* Participants who have received a standard of care \\[18F\\]FDG PET\u002FCT and are willing to undergo a study specific oral \\[18F\\]FDG PET\u002FCT within 2 weeks.\n\nParticipant Exclusion Criteria\n\n* Pregnant or breast-feeding\n* Medically unstable (e.g., acute illness, unstable vital signs)\n* Urinary incontinence\u002Fcatheter.\n* Immobile, frail or vulnerable patients who cannot leave the department and would require an uptake room in any case.\n* Patients whose fasting blood sugar at the SOC PET was \\>11.0 mmol\u002Fl\n* Unable to swallow.\n* Patients with nasogastric tubes, percutaneous gastrostomy or other non-anatomical routes for nutrition.\n* Unable to lie flat for 1h (subset of participants - first 5 participants only).\n* Claustrophobia requiring medication.\n* Undergoing active treatment or assessment of an upper digestive tract tumor (stomach\u002Fesophagus)\n* Unable to provide written consent\n* Patients receiving biguanide anti-hyperglycemic agents (e.g. Metformin).\n* Insulin dependent diabetics.",{"count":297,"type":24},27,[27],"Typically, PET scans involve an IV injection of 18F-FDG that helps identify cancer. Patients are scanned 60 minutes after injecting 18F-FDG. This study aims to assess the feasibility of a different method of administration - oral ingestion (rather than IV) of 18F-FDG through delayed imaging to identify the optimal time for scanning after consuming the drug. The study will aim to recruit 15-24 individuals who will receive two PET scans - one using delayed oral 18F-FDG imaging and a second regular 18F-FDG. The analysis will focus on establishing a suitable protocol for this administration route while considering patient preference and image quality.",[301,302,31],"Multiple Cancers","Multiple Indications Cancer",[304,305,306,307,308],"Oral FDG","LAFOV","Long-axial Field-of-view Scanner","Quadra","Low-dose Oral Radiopharmaceuticals","2026-03-26",{"date":311,"type":37},"2026-03-31",{"date":313,"type":37},"2026-02-18",{"date":315,"type":24},"2027-02-18",{"name":317,"class":44},"British Columbia Cancer Agency",{"id":319,"slug":320,"hasResults":12,"nctId":321,"briefTitle":322,"officialTitle":323,"acronym":324,"eligibilityCriteria":325,"healthyVolunteers":12,"sex":19,"minAge":20,"maxAge":4,"enrollmentInfo":326,"targetDuration":4,"studyType":25,"phases":328,"briefSummary":329,"conditions":330,"keywords":335,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":343,"lastUpdatePostDateStruct":344,"startDateStruct":346,"completionDateStruct":348,"leadSponsor":350,"locationsCount":45},"100588092","virtual-ward-for-early-discharge-in-patients-receiving-inpatient-care-100588092","NCT06936891","Virtual Ward for Early Discharge in Patients Receiving Inpatient Care","Virtual Ward for Early Discharge in Patients Receiving Inpatient Care: A Prospective Feasibility Study on Home Monitoring for the Early Discharge of Eligible Hospitalized Patients in an Outpatient Setting","VIP care","Inclusion Criteria:\n\n* Adult patients (≥18 years old).\n* Currently hospitalized and eligible for early discharge according to clinical judgment.\n* Ability to provide written informed consent.\n* Access to a smartphone or tablet with internet connection.\n* Patient is capable of using the Digizorg app or has support from a caregiver who can assist.\n* Suitable home situation for Virtual Ward care (e.g., safe environment, necessary utilities available).\n* Enrollment in one of the predefined Virtual Ward care pathways\n\nExclusion Criteria:\n\n* Patients requiring continuous hospital-based monitoring or interventions that cannot be safely delivered at home.\n* Patients who are hemodynamically unstable or require oxygen therapy \\>5 liters\u002Fminute at the time of discharge.\n* Patients unable or unwilling to comply with home monitoring procedures.\n* Patients with significant cognitive impairment without adequate caregiver support.\n* Patients with a life expectancy less than 30 days, as assessed by the treating physician.\n* Patients participating in another interventional clinical trial that could interfere with the Virtual Ward protocol.\n* Any other condition that, in the opinion of the treating physician, would make participation unsafe or infeasible.",{"count":327,"type":24},306,[27],"This study evaluates the feasibility of providing hospital-level care at home for eligible patients through a Virtual Ward. Patients are discharged early from the hospital and monitored remotely using digital vital sign monitoring and anamnesis questionnaires. The primary aim is to determine if at least 30% of eligible patients can be safely and successfully transferred to the Virtual Ward under current Dutch healthcare conditions.",[331,332,333,334,31],"Early Discharge","Telemedicine","Virtual Clinic","Hospital at Home",[336,337,338,339,340,341,342],"early discharge","telemedicine","virtual ward","virtual clinic","hospital at home","feasability","telemonitoring","2026-02-15",{"date":345,"type":37},"2026-02-17",{"date":347,"type":37},"2025-04-16",{"date":349,"type":24},"2028-12-31",{"name":351,"class":44},"Erasmus Medical Center",{"id":353,"slug":354,"hasResults":12,"nctId":355,"briefTitle":356,"officialTitle":357,"acronym":4,"eligibilityCriteria":358,"healthyVolunteers":18,"sex":19,"minAge":359,"maxAge":4,"enrollmentInfo":360,"targetDuration":4,"studyType":25,"phases":361,"briefSummary":362,"conditions":363,"keywords":4,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":365,"lastUpdatePostDateStruct":366,"startDateStruct":368,"completionDateStruct":370,"leadSponsor":371,"locationsCount":45},"100603913","feasibility-of-adding-a-plant-based-protein-pudding-to-the-diet-of-older-adults-who-attend-a-medically-managed-fitness-facility-100603913","NCT07142694","Feasibility of Adding a Plant-Based Protein Pudding to the Diet of Older Adults Who Attend a Medically Managed Fitness Facility","Evaluation of a Plant-based Protein Pudding In Older Adults Attending a Medically Managed Fitness Facility","Inclusion Criteria:\n\n* Participant is willing and able to give informed consent for participation in the trial\n* Male or female aged ≥60 years\n* Actively attend the Wellness Institute (≥8 times in the past 28 days),\n\nExclusion Criteria:\n\n* Allergy to ingredients in the study treatment\n* Inability to consume treatment product\n* Inability to obtain written informed consent\n* Apart of any physical rehab program at WI (cardiac rehab, kidney fit, etc. )","60 Years",{"count":23,"type":24},[27],"The goal of this a 12-week randomized controlled parallel arm feasibility trial is to evaluate the feasibility and acceptability of incorporating a plant-based protein pudding into the diets of older adults who attend a medically managed fitness facility. The primary participant population includes older adults, aged 60 years and above, who are generally healthy and engaged in structured fitness programs.\n\nThe main questions it aims to answer are:\n\nIs a plant-based protein pudding acceptable and well-tolerated by older adults? Does regular consumption of the pudding support muscle health and overall well-being in this population?\n\nParticipants will:\n\nConsume a plant-based protein pudding as one arm daily for 7 days per week (experimental) and the other will continue their current lifestyle (control).\n\nThe experimental group will complete surveys or questionnaires to assess acceptability, taste, and ease of integration into daily meals.\n\nUndergo basic physical or health assessments (e.g., muscle function or strength evaluations) to evaluate potential effects.",[31,364],"Nutrition Intervention","2026-02-03",{"date":367,"type":37},"2026-02-05",{"date":369,"type":24},"2026-01-15",{"date":184,"type":24},{"name":372,"class":373},"Seven Oaks Hospital Chronic Disease Innovation Centre","NETWORK",{"id":375,"slug":376,"hasResults":12,"nctId":377,"briefTitle":378,"officialTitle":378,"acronym":4,"eligibilityCriteria":379,"healthyVolunteers":12,"sex":19,"minAge":20,"maxAge":4,"enrollmentInfo":380,"targetDuration":4,"studyType":25,"phases":382,"briefSummary":383,"conditions":384,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":390,"lastUpdatePostDateStruct":391,"startDateStruct":393,"completionDateStruct":395,"leadSponsor":397,"locationsCount":45},"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":381,"type":24},150,[27],"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.",[385,386,387,32,388,389,31],"Adult Spinal Deformity","Wireless Continuous Vital Signs Monitoring","Wireless Vital Signs Monitoring System","ASD Surgery","Remote Monitoring","2026-01-06",{"date":392,"type":37},"2026-01-08",{"date":394,"type":37},"2025-12-10",{"date":396,"type":24},"2026-08-30",{"name":398,"class":44},"Rigshospitalet, Denmark",{"id":400,"slug":401,"hasResults":12,"nctId":402,"briefTitle":403,"officialTitle":404,"acronym":405,"eligibilityCriteria":406,"healthyVolunteers":18,"sex":19,"minAge":407,"maxAge":408,"enrollmentInfo":409,"targetDuration":4,"studyType":25,"phases":411,"briefSummary":412,"conditions":413,"keywords":426,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":429,"lastUpdatePostDateStruct":430,"startDateStruct":432,"completionDateStruct":434,"leadSponsor":435,"locationsCount":45},"100567397","a-mobile-app-to-improve-24-hour-movement-guideline-adherence-in-preschoolers-100567397","NCT06667661","A Mobile App to Improve 24-Hour Movement Guideline Adherence in Preschoolers","A Home-Based Intervention to Improve Adherence to the 24-Hour Movement Guidelines in Young Children","Shining Star","Inclusion (Child):\n\n* Ages 3-4 years.\n* Parent report that they meet 0 or 1 recommendation for physical activity, sleep, and screen-time as defined by the 24-hour movement guidelines. The physical activity recommendation is defined as greater than or equal to 3 hours\u002Fday of total physical activity, including 1 hour of moderate-to-vigorous physical activity. The sleep recommendation is defined as 10-13 hours\u002Fday. The sedentary behavior recommendation is defined as less than or equal to 1 hour\u002Fday of sedentary screen-time.\n\nInclusion (Parents):\n\n* Parents must agree to use their mobile phone for the duration of the study (\\~12 weeks) and download the mobile app onto their phone.\n* The parent\u002Fcaregiver is fluent in English to participate in testing the mobile app.\n* The parent\u002Fcaregiver must be willing to travel to KUMC to complete study visits.\n\nExclusion (child):\n\n* Mobility limitations as reported by the parent.\n* Meeting two or more recommendations for physical activity, sleep, and screen-time.\n* Sibling or household member is participating or participated in the study.","3 Years","4 Years",{"count":410,"type":24},80,[27],"The goal of this clinical trial is to evaluate whether a home-based mHealth intervention can improve adherence to the 24-Hour Movement Guidelines in preschool-aged children (3-4 years old) who currently meet 0 or 1 of the guidelines for physical activity, sedentary behavior, and sleep. The main questions it aims to answer are:\n\n* Can the intervention increase the proportion of children meeting all three 24-Hour Movement Guidelines (physical activity, screen-time, and sleep)?\n* Is the intervention feasible for parents to implement, as measured by a parent feedback survey?\n\nResearchers will compare an intervention group to a waitlist control group to assess whether the intervention leads to increased guideline adherence.\n\nParents and Participants:\n\n* Children will wear an accelerometer to track physical activity and sleep patterns.\n* Parents will use a mobile app that delivers weekly lessons and behavior-related goals to encourage healthy movement behaviors in their children.\n* Parents will complete questionnaires on their child's movement behaviors and development at baseline, 6 weeks, and 12 weeks.\n* Additionally, children will undergo motor skills assessments, and parents will provide feedback on cognitive development and behavioral changes.",[414,415,31,416,417,418,419,420,421,422,423,424,425],"Healthy","24-Hour Movement Guidelines","Sleep","Physical Activity","Screen Time","Sedentary Behaviors","Motor Skills","Cognition","Parent-Child Relations","Mobile Application","Health Education","Child Development",[417,427,416,425,420,428,414,415,418,419,421,422,423,424],"Sedentary Behavior","Behavioral problems","2025-12-03",{"date":431,"type":37},"2025-12-11",{"date":433,"type":37},"2025-01-29",{"date":68,"type":24},{"name":436,"class":44},"University of Kansas Medical Center",{"id":438,"slug":439,"hasResults":12,"nctId":440,"briefTitle":441,"officialTitle":442,"acronym":443,"eligibilityCriteria":444,"healthyVolunteers":12,"sex":19,"minAge":20,"maxAge":445,"enrollmentInfo":446,"targetDuration":4,"studyType":25,"phases":448,"briefSummary":449,"conditions":450,"keywords":460,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":466,"lastUpdatePostDateStruct":467,"startDateStruct":469,"completionDateStruct":471,"leadSponsor":472,"locationsCount":45},"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":447,"type":24},30,[27],"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)",[451,31,452,453,454,455,456,32,457,458,459],"Dietary Quality","College Student","Dietary Guidelines for Americans","Gut Microbiome","Lipid Profiles","Herbs and Spices","Inflammation Biomarkers","Body Composition","Anthropometrics",[461,462,463,464,465],"dietary quality","dietary guidelines for americans","college students","cardiometabolic health","gut microbiome","2025-11-18",{"date":468,"type":37},"2025-11-24",{"date":470,"type":37},"2025-07-03",{"date":68,"type":24},{"name":473,"class":44},"University of Nevada, Las Vegas",{"id":475,"slug":476,"hasResults":12,"nctId":477,"briefTitle":478,"officialTitle":479,"acronym":480,"eligibilityCriteria":481,"healthyVolunteers":12,"sex":19,"minAge":20,"maxAge":4,"enrollmentInfo":482,"targetDuration":4,"studyType":25,"phases":483,"briefSummary":484,"conditions":485,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":487,"lastUpdatePostDateStruct":488,"startDateStruct":490,"completionDateStruct":492,"leadSponsor":494,"locationsCount":45},"100609892","behavioral-health-program-for-short-stay-nursing-facility-residents--care-partners-100609892","NCT07220486","Behavioral Health Program for Short-Stay Nursing Facility Residents & Care Partners","Building Resilience in Skilled Nursing Care: A Behavioral Health Intervention for Residents & Care Partners","BRISK","Inclusion Criteria:\n\n* Patient and care partner both aged ≥ 18 years\n* Patient with care partner (known person providing regular health-related, socioemotional, or practical support) willing to participate\n* Patient reporting depression symptoms on a screening tool (Patient Health Questionnaire)\n\nExclusion Criteria:\n\n* Patient intended length of nursing facility stay \\\u003C 7 days\n* Patient evidencing more than mild impairment on a cognitive screen (Brief Interview for Mental Status)\n* Patient's roommate in skilled nursing facility already enrolled in study\u002Fintervention\n* Either patient or care partner reporting high risk of suicidality, based on a standardized safety assessment tool\n* Either patient or care partner participating in newly initiated psychotherapy",{"count":164,"type":24},[27],"The goal of this clinical trial is to test a behavioral health program (Interventions for Stressful Transitions in Later Life, InSTILL) for skilled nursing facility residents and their primary support person. The main questions it aims to answer is whether the program is program is feasible, satisfactory, and helpful. The researchers will compare the InSTILL program to minimally enhanced usual care. Participants will be randomly assigned to receive either the InSTILL program or minimally enhanced usual care. Participants will complete assessments at three timepoints (all) and a brief-exit interview.",[59,60,61,31,486],"Caregiver","2025-11-07",{"date":489,"type":37},"2025-11-10",{"date":491,"type":37},"2025-11-05",{"date":493,"type":24},"2028-05",{"name":70,"class":44},{"id":496,"slug":4,"hasResults":12,"nctId":13,"briefTitle":14,"officialTitle":497,"acronym":16,"eligibilityCriteria":498,"healthyVolunteers":18,"sex":499,"minAge":20,"maxAge":21,"enrollmentInfo":500,"targetDuration":4,"studyType":25,"phases":501,"briefSummary":28,"conditions":502,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":503,"lastUpdatePostDateStruct":504,"startDateStruct":506,"completionDateStruct":507,"leadSponsor":509,"locationsCount":45},"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":23,"type":24},[27],[30,31,32],"2025-10-01",{"date":505,"type":37},"2025-10-06",{"date":39,"type":37},{"date":508,"type":24},"2027-03-01",{"name":43,"class":44},{"id":511,"slug":512,"hasResults":12,"nctId":513,"briefTitle":514,"officialTitle":515,"acronym":516,"eligibilityCriteria":517,"healthyVolunteers":12,"sex":19,"minAge":20,"maxAge":4,"enrollmentInfo":518,"targetDuration":4,"studyType":25,"phases":520,"briefSummary":521,"conditions":522,"keywords":529,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":533,"lastUpdatePostDateStruct":534,"startDateStruct":536,"completionDateStruct":538,"leadSponsor":540,"locationsCount":217},"100605436","attach-in-denmark-a-feasibility-randomized-controlled-trial-100605436","NCT07162493","ATTACH in Denmark: A Feasibility Randomized Controlled Trial","Attachment and Child Health (ATTACH) Added to Treatment As Usual Versus Treatment As Usual Alone for Parents With Psychosocial Problems: A Feasibility Randomized Controlled Trial","AiD","Inclusion criteria\n\n* Child aged 0 - 5.7 years at enrollment.\n* Speaks Danish or English sufficiently to take part in assessments and intervention without an interpreter.\n* Both parents provide consent in case of shared child custody. Parents experience psycho-social problems that have resulted in referral to the family treatment center on the basis of legislation from the Danish Child Act (\"Barnets Lov\"), under the following Sections defining support needs: Section 29: Family counselling: Includes open access to family counselling as an early preventive effort. In this context, the counselling may involve referring the family to other departments within the municipality or to other relevant authorities that can provide the appropriate guidance and support. Section 30: Early preventive intervention: Includes a variety of approaches, such as consultancy services and participation in network or discussion groups to address and prevent challenges faced by the family at an early stage. Section 32: Supportive interventions: May be initiated on the basis of a preliminary assessment or a child welfare investigation pursuant to Sections 19 and 20 of the Child Act, or concurrently with the completion of such an assessment or investigation. Support may include practical, pedagogical, or other types of support in the home; appointment of a permanent contact person for the entire family; family therapy or individual treatment for the child or young person; family placement involving residential care in a foster family, an approved child and youth residential facility, or a housing facility; supportive placement in a foster family or in an approved child and youth residential facility; other forms of assistance aimed at providing counseling, treatment, and practical and pedagogical support.\n* Parents who have their child in out-of-home placement \u002Ffoster care (with or without consent).\n* Parental psychosocial problems such as (but are not limited to) mental health problems, cognitive difficulties, substance abuse, poverty, social isolation, adverse childhood experiences, functional or somatic disorders, criminal involvement, domestic violence, having a child with emotional regulation difficulties, having a child with developmental problems, having a child with functional or somatic problems, having a child with internalizing or externalizing problems.\n\nExclusion Criteria:\n\n* Child is older than 5.7 years at enrollment.\n* Parent does not speak Danish or English sufficiently to take part in assessments and intervention without an interpreter.\n* Consent cannot be obtained from both parents in case of shared child custody.\n* The parent is known to move to a different municipality within 5 months from randomization.",{"count":519,"type":24},52,[27],"The goal of this feasibility randomized controlled pilot trial is to learn whether the trial can be done as planned, and to investigate if the 10-session parenting program \"ATTACH(TM) increases mentalizing skills (the ability to reflect on thoughts and feelings) in parents of children between 0-5 years of age, who are receiving support for psychosocial problems in their municipal family treatment center.\n\nThe main questions the trial aims to answer are:\n\n* How many eligible parents agree to participate in the random allocation to treatment?\n* How many parents allocated to receive \"ATTACH(TM) will have completed the program 5 months after allocation (at least 7 out of 10 sessions)?\n* How many parents complete the data collection 5 months after allocation on the primary exploratory clinical outcome, i.e., parental mentalizing skills?\n* Do parents who received the ATTACH(TM) program show more increase in their mentalizing skills, compared to parents, who did not receive treatment with ATTACH(TM)?\n\nResearchers will compare ATTACH, added to Treatment as Usual, with Treatment as Usual without ATTACH in three municipal family treatment centers located in the Capital Region of Denmark.\n\nParticipants will:\n\n1. Take part in baseline data collection with a survey, video observation of parent-child interaction, and an interview assessing mentalizing skills.\n2. Be randomly allocated to receive treatment in their local family center with or without ATTACH.\n3. Take part in data collection 5 months after being allocated to either group, as well as participate in an interview about their experiences with the treatment they received.\n4. After one year, the research group will follow up on the current treatment\u002Fsupport needs of the families, who were allocated to either group.",[523,524,525,526,527,528,31],"Mentalization","Recruitment of Participants","Adherence, Treatment","Drop Out","Parenting Intervention","Vulnerable Families",[530,531,532,92],"parenting","mentalizing","intervention","2025-09-17",{"date":535,"type":37},"2025-09-23",{"date":537,"type":37},"2025-09-01",{"date":539,"type":24},"2027-12-31",{"name":541,"class":44},"Johanne Smith-Nielsen",{"id":543,"slug":544,"hasResults":12,"nctId":545,"briefTitle":546,"officialTitle":547,"acronym":4,"eligibilityCriteria":548,"healthyVolunteers":12,"sex":19,"minAge":549,"maxAge":248,"enrollmentInfo":550,"targetDuration":4,"studyType":25,"phases":551,"briefSummary":552,"conditions":553,"keywords":555,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":565,"lastUpdatePostDateStruct":566,"startDateStruct":568,"completionDateStruct":570,"leadSponsor":571,"locationsCount":45},"100603750","rtms-for-youth-inpatients-with-depression-100603750","NCT07140575","rTMS for Youth Inpatients With Depression","Seamless Integration of Repetitive Transcranial Magnetic Stimulation (rTMS) for Youth Inpatients With Depression: A Feasibility Study","Inclusion Criteria:\n\n* age 14-19 years\n* primary diagnosis of major depressive disorder or of bipolar I or II disorder, current episode depressed with no psychotic or mixed features\n* current episode of depression lasting at least 4 weeks\n* failed ≥1 evidence-based psychotherapy or antidepressant\n* have a GRID-HAMD-17 (17-item Hamilton Depression Rating Scale) score of ≥16 (moderate-severe range)\n* currently an inpatient or suitable for an elective inpatient admission\n\nExclusion Criteria:\n\n* lifetime diagnosis of a psychotic disorder, anorexia nervosa, bulimia nervosa diagnosis of a substance use disorder (except caffeine and tobacco) within the past year\n* obsessive compulsive disorder or personality disorder that is the main source and driver of distress\n* active psychosis and\u002For mania\n* history of epilepsy or any other neurologic condition that includes a history of seizures\n* use of medications that lower the seizure threshold\n* pregnancy or nursing\n* history of severe headaches within the previous year\n* improvement in depressive symptom severity between screening and baseline by 25% or more\n* inability to adhere to the protocol","14 Years",{"count":447,"type":24},[27],"Youth aged 15-24 are likelier to have depression than all age groups in Canada. One-third of depressed youth do not respond to psychotherapy and\u002For antidepressant medications. A treatment called repetitive transcranial magnetic stimulation or rTMS has proven helpful in adolescents and young adults whose depressive symptoms have been difficult to treat with psychotherapy and\u002For antidepressants. Unfortunately, youth find rTMS difficult to access because it is not funded by the Ontario Health Insurance Plan, is typically only offered to adults, and the treatment schedule usually involves once-daily sessions, 5 days\u002Fweek, for 4-6 weeks, which is associated with travel and opportunity costs e.g. missing school. This project looks at the feasibility of a new treatment pathway that allows youth with difficult-to-treat depression in hospital to receive rTMS twice-daily while engaging in on-unit schooling and therapeutic support. This \"accelerated\" way of providing rTMS is safe, has equal effectiveness to once-daily rTMS, and can shorten the time needed for treatment. This pathway is for youth already staying in hospital for difficult-to-treat depression or youth outside hospital who have difficult-to-treat depression that interferes with daily function to such a degree that they would benefit from staying in hospital. The investigators anticipate integrating rTMS and inpatient care for youth will be feasible, that it will be acceptable and accessible to youth and families, and there will be sufficient demand for this new treatment pathway. If successful, this project will inform care for youth with difficult-to-treat depression in Ontario and beyond.",[554,31],"Major Depression Moderate",[556,557,558,559,560,561,562,563,564],"feasibility study","major depressive disorder","adolescent","youth","repetitive transcranial magnetic stimulation","neuromodulation","rTMS","accelerated","inpatient","2025-08-18",{"date":567,"type":37},"2025-08-24",{"date":569,"type":24},"2025-08",{"date":153,"type":24},{"name":572,"class":44},"Sunnybrook Health Sciences Centre",{"id":574,"slug":575,"hasResults":12,"nctId":576,"briefTitle":577,"officialTitle":578,"acronym":4,"eligibilityCriteria":579,"healthyVolunteers":12,"sex":19,"minAge":20,"maxAge":4,"enrollmentInfo":580,"targetDuration":4,"studyType":25,"phases":581,"briefSummary":582,"conditions":583,"keywords":589,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":591,"lastUpdatePostDateStruct":592,"startDateStruct":594,"completionDateStruct":596,"leadSponsor":598,"locationsCount":45},"100595647","cabgprehab---a-feasibility-study-protocol-100595647","NCT07035171","CABGpreHAB - a Feasibility Study Protocol","CABGpreHAB- Home-based Multimodal Prehabilitation (CABGpreHAB) for Elective Patients Awaiting CABG-surgery - a Feasibility Study Protocol","Inclusion Criteria:\n\n* Planned to have elective isolated first-time CABG surgery.\n* 18 years or older\n* Two weeks or more before surgery\n* Speaks and understands Danish.\n* Gives written informed consent.\n\nExclusion Criteria:\n\n* Patient with unstable angina pectoris and\u002F or MI during the last two weeks.\n* Left main stem stenosis \\>50%\n* Left ventricular ejection fraction \\\u003C 35%\n* Significant ventricular arrhythmia\n* Orthopedic or neurologic preconditions precluding exercise training.\n* Inability to attend the prehabilitation program due to physical limitations.\n* Patients who have cognitive deficits that would disqualify prehabilitation.\n* Severe heart failure, NYHA Class IV\n* Lack of capacity to consent",{"count":81,"type":24},[27],"Patients with ischemic heart disease (IHD) awaiting coronary artery bypass graft (CABG) surgery often face challenges like advanced age, frailty, comorbidities, and physical inactivity. These factors, combined with the physiological and psychological stress of surgery, can hinder postoperative recovery. Traditionally, strategies to improve surgical outcomes focus on the intra- and postoperative periods. However, the pre-surgery waiting period offers a \"window of opportunity\" for prehabilitation, which aims to enhance patients' functional capacity through exercise, nutrition, and psychological support.\n\nThe CABGpreHAB feasibility study evaluates the feasibility of a home-based multimodal prehabilitation intervention for patients awaiting elective CABG surgery. This randomized pilot study compares the intervention plus usual care to usual care alone, assessing feasibility outcomes like recruitment, retention, attrition, fidelity, and adherence. The study aims to optimize a subsequent full-scale randomized controlled trial (RCT) and improve patient outcomes by leveraging the pre-surgery period for prehabilitation.",[584,585,586,31,587,588],"Ischaemic Heart Disease","Prehabilitation","Coronary Artery Bypass","Multimodal Intervention","Adult",[590],"Prehabilitation, CABG surgery, adult, preoperative,homebased","2025-06-25",{"date":593,"type":37},"2025-06-29",{"date":595,"type":37},"2025-06-24",{"date":597,"type":24},"2026-07-18",{"name":398,"class":44},{"id":600,"slug":601,"hasResults":12,"nctId":602,"briefTitle":603,"officialTitle":604,"acronym":4,"eligibilityCriteria":605,"healthyVolunteers":18,"sex":19,"minAge":606,"maxAge":4,"enrollmentInfo":607,"targetDuration":4,"studyType":25,"phases":609,"briefSummary":610,"conditions":611,"keywords":612,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":615,"lastUpdatePostDateStruct":616,"startDateStruct":617,"completionDateStruct":619,"leadSponsor":621,"locationsCount":45},"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":608,"type":24},96,[27],"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.",[32,31],[613,530,614],"home practice","skills practice","2025-06-19",{"date":591,"type":37},{"date":618,"type":37},"2025-03-17",{"date":620,"type":24},"2027-07",{"name":622,"class":44},"Arizona State University",{"id":624,"slug":625,"hasResults":12,"nctId":626,"briefTitle":627,"officialTitle":627,"acronym":4,"eligibilityCriteria":628,"healthyVolunteers":12,"sex":19,"minAge":20,"maxAge":4,"enrollmentInfo":629,"targetDuration":4,"studyType":631,"phases":4,"briefSummary":632,"conditions":633,"keywords":4,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":636,"lastUpdatePostDateStruct":637,"startDateStruct":639,"completionDateStruct":641,"leadSponsor":643,"locationsCount":45},"100592484","feasibility-study-of-a-relapse-investigation-questionnaire-administered-by-an-ms-care-coordinator-nurse-in-patients-with-multiple-sclerosis-100592484","NCT06994026","Feasibility Study of a Relapse Investigation Questionnaire Administered by an MS Care Coordinator Nurse in Patients With Multiple Sclerosis","Inclusion Criteria:\n\n* Patients followed by Dr. Manchon for Relapsing-Remitting Multiple Sclerosis or active Secondary Progressive Multiple Sclerosis\n* Adult patients (aged 18 or older)\n* Patients who have provided informed consent for participation in the local task-sharing protocol\n\nExclusion Criteria:\n\n* Pregnant women\n* Minors (under 18 years old)\n* Patients with known renal failure\n* Patients who have not provided or are unable to provide consent for the local task-sharing protocol",{"count":630,"type":24},10,"OBSERVATIONAL","This study aims to evaluate a questionnaire used by a specialized nurse to help manage relapses in people with multiple sclerosis (MS). The questionnaire is completed during a phone call when the patient reports new or worsening symptoms. It helps the nurse decide whether further tests or treatments are needed, based on a protocol developed with a neurologist. The goal is to improve how quickly and effectively patients receive care during a relapse. The study will include 10 adult patients with active forms of MS over a two-month period.",[634,635,31],"Multiple Sclerosis","Disease Management","2025-05-20",{"date":638,"type":37},"2025-05-29",{"date":640,"type":24},"2025-06-15",{"date":642,"type":24},"2025-08-15",{"name":644,"class":44},"Centre Hospitalier de Gonesse",{"id":646,"slug":647,"hasResults":12,"nctId":648,"briefTitle":649,"officialTitle":650,"acronym":651,"eligibilityCriteria":652,"healthyVolunteers":12,"sex":19,"minAge":653,"maxAge":4,"enrollmentInfo":654,"targetDuration":4,"studyType":25,"phases":656,"briefSummary":658,"conditions":659,"keywords":665,"overallStatus":98,"whyStopped":4,"lastUpdateSubmitDate":677,"lastUpdatePostDateStruct":678,"startDateStruct":680,"completionDateStruct":682,"leadSponsor":684,"locationsCount":45},"100565938","phase-2-lemborexant-to-prevent-post-operative-delirium-in-cardiac-surgery-patients-100565938","NCT06648681","Lemborexant to Prevent Post-operative Delirium in Cardiac Surgery Patients","A Randomized Trial of Lemborexant for the Prevention of Delirium After Cardiac Surgery (PROTEX): A Pilot Study","PROTEX","Inclusion Criteria:\n\n* Admitted to hospital following open cardiac surgery through midline sternotomy\n\nExclusion Criteria:\n\n* ● Known severe obstructive sleep apnea diagnosed by polysomnography or STOPBANG score \\> 5\n\n  * Periodic limb movement disorder or restless legs syndrome\n  * Narcolepsy\n  * Somnolence (Pasero Opioid Sedation Scale (POSS) \\>2)\n  * Current alcohol or substance use disorder as defined by the DSM-V\n  * Patient already taking moderate or strong CYP3A inhibitors\n  * Frequent use of medications for insomnia defined as \\>4 days per week.\n  * Liver failure (Child-Pugh score B or C)\n  * Renal failure (eGFR\\\u003C30 ml\u002Fmin\u002F1.73 m2)\n  * Pre-existing delirium (ICDSC score \\>3 or CAM\u002FCAM-ICU positive) at time of consent\n  * BMI\\>40 kg\u002Fm2\n  * Known allergy or hypersensitivity to study drug\n  * Inability to communicate in English","61 Years",{"count":655,"type":24},60,[657],"PHASE2","Post-operative delirium is a common complication following cardiac surgery and is associated with increased 1 year mortality. Currently there are no drug therapies to prevent delirium. Orexin is a neuromodulator thought to play an important role in disordered sleep, one of the instigators of delirium. Lembrorexant is an orexin antagonist, originally approved for sleep, that may also reduce the incidence of delirium. The Investigators propose a pilot study to determine the feasibility of a randomized controlled trial comparing Lembrorexant to placebo in patients following cardiac surgery in reducing the incidence of delirium, and improving sleep.",[660,661,662,663,31,416,664],"Delirium - Postoperative","Cardiac Surgery","Cardiac Surgery Subjects","Orexin Antagonist","In-hospital Mortality",[666,667,668,669,670,671,672,673,674,675,676],"lemborexant","Postoperative Delirium","sleep medication","ICDSC","CAM","cardiac surgery","sleep aid","open heart surgery","delirium","sleep quality","Richards-Campbell Sleep Questionnaire","2025-04-18",{"date":679,"type":37},"2025-04-23",{"date":681,"type":24},"2025-05-01",{"date":683,"type":24},"2027-04-30",{"name":685,"class":44},"University of British Columbia",{"id":687,"slug":688,"hasResults":12,"nctId":689,"briefTitle":690,"officialTitle":691,"acronym":4,"eligibilityCriteria":692,"healthyVolunteers":18,"sex":19,"minAge":20,"maxAge":4,"enrollmentInfo":693,"targetDuration":4,"studyType":631,"phases":4,"briefSummary":694,"conditions":695,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":698,"lastUpdatePostDateStruct":699,"startDateStruct":701,"completionDateStruct":703,"leadSponsor":704,"locationsCount":45},"100584603","evaluating-an-ai-generated-health-podcast-100584603","NCT06891495","Evaluating an AI-Generated Health Podcast","Feasibility and Validity Assessment of an AI-Generated Health Podcast: A Pilot Observational Study","Expert Group\n\nInclusion Criteria:\n\n* Licensed professionals and recognized experts in relevant fields such as dentistry, public health, and health communication\n* Minimum of 5 years of professional experience in their respective fields\n* Prior involvement in healthcare education, research, or digital health communication\n* Willingness to review and provide detailed feedback on the adapted questionnaire\n* Ability to complete the survey in English\n\nExclusion Criteria:\n\n* Professionals without formal training or relevant expertise in the specified fields\n* Individuals with conflicts of interest that might compromise the objectivity of their evaluations\n* Experts who are unable to commit the necessary time to provide thorough feedback\n\nGeneral Public Group\n\nInclusion Criteria:\n\n* Adults aged 18 years or older\n* Individuals fluent in English\n* Access to a digital audio device and an internet connection to listen to the podcast and complete the survey\n* Consent to participate in the study\n\nExclusion Criteria:\n\n* Individuals with significant hearing impairments that might hinder the ability to comprehend the audio content\n* Healthcare professionals or individuals with advanced training in dentistry or health communication\n* Persons who have participated in similar educational podcast studies previously",{"count":447,"type":24},"This study aims to explore a new way of delivering health information using an AI-generated podcast. The podcast, created with Google NotebookLM, uses verified content from the American Academy of Periodontology website to provide easy-to-understand information on gum health and prevention.\n\nThe goal is to determine whether this AI-generated podcast is a useful, engaging, and clear tool for educating the general public about health topics. Traditional health podcasts often feature expert interviews and can be lengthy, which sometimes limits their appeal and accessibility. By using AI to generate the podcast, investigator hope to offer a more standardized and concise presentation that avoids technical jargon.\n\nTo evaluate the podcast, investigator developed a questionnaire based on the Questionnaire for Assessing Educational Podcasts (QAEP). This questionnaire was adapted to better suit a non-specialist audience and covers four key areas: how easy the podcast is to access and use, the design and structure of the podcast, the clarity and completeness of the content, and the podcast's value as a learning tool.\n\nBefore using this questionnaire with the general public, investigator sent it to 10 experts in dentistry, public health, and communication for their review and feedback. Their input helped us make minor modifications to ensure the questionnaire is both clear and scientifically sound. After these revisions, investigator conducted a pilot study with 30 members of the general public who listened to the podcast and completed the questionnaire.\n\nThis study will assess the feasibility and validity of using an AI-generated podcast as a health education tool. The results will help determine if this approach can effectively improve public understanding of health information and may guide the future design of digital health communication strategies.",[696,697,31],"Public Health","Artificial Intelligence","2025-03-22",{"date":700,"type":37},"2025-03-26",{"date":702,"type":37},"2025-02-07",{"date":636,"type":24},{"name":705,"class":44},"Qassim University"]