[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"social-media\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:social-media":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,48,77,102,129,156],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100639610","testing-and-evaluating-an-interactive-media-use-journal-for-adolescents-100639610",false,"NCT07620964","Testing and Evaluating an Interactive Media Use Journal for Adolescents","Inclusion Criteria:\n\n* English speaking\n* has internet access\n* in the United States\n\nExclusion Criteria:\n\n* youth under the age of 13 years\n* over the age of 18 years",true,"ALL","13 Years","18 Years",{"count":20,"type":21},50,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this study is to test the feasibility and acceptability of an Interactive Media Use Journal (IMUJ) co-developed with youth.\n\nThis study is part of a larger effort using Intervention Mapping to co-develop this resource, test it for feasibility and acceptability via this proposed protocol, and then eventually disseminate the resource in partnership with the American Academy of Pediatrics.\n\n50 participants between the ages of 13-18 will be recruited for this study",[27,28],"Social Media","Adolescent Behavior",[30,31,32,33,34],"social media engagement","health","behavior change","habit","intervention mapping","NOT_YET_RECRUITING","2026-06-29",{"date":38,"type":39},"2026-07-01","ACTUAL",{"date":41,"type":21},"2026-07",{"date":43,"type":21},"2026-08",{"name":45,"class":46},"University of Wisconsin, Madison","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":15,"sex":16,"minAge":18,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":58,"conditions":59,"keywords":62,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":47},"100635243","dental-communication-and-social-media-legal-and-ethical-framework-100635243","NCT07550153","Dental Communication and Social Media: Legal and Ethical Framework","Legal Considerations on Dental Communication Via Social Media: Liability, Ethics, and Regulatory Evolution","Inclusion Criteria:\n\n* For Group 1 (Dental Professionals): Registered Dentists or Dental Hygienists currently practicing in Italy.\n* For Group 2 (Patients): Individuals who use social media platforms and have accessed or are interested in dental healthcare information online.\n* For Group 3 (General Healthcare Professionals): Medical doctors and health practitioners from various specialties interested in digital communication ethics.\n* Age: Minimum 18 years of age.\n* Consent: Participants must be willing to provide informed consent for data collection and analysis.\n* Language: Ability to understand and read Italian.\n\nExclusion Criteria:\n\n* Individuals under 18 years of age.\n* Individuals who do not use social media platforms.\n* Incomplete survey submissions where the primary data points are missing.\n* Healthcare professionals not registered with their respective Italian professional orders.",{"count":56,"type":21},300,"OBSERVATIONAL","This observational study explores the legal and ethical boundaries of dental communication on social media, analyzing Italian regulatory evolution. Through surveys involving dental professionals and patients, it assesses awareness of advertising regulations and the impact of digital communication on the patient-practitioner relationship. The research identifies knowledge gaps regarding deceptive advertising and highlights the need for transparent, deontologically compliant digital practices to protect public health.",[60,61,27],"Professional Ethics","Health Communication",[63,60,64,65,66],"Healthcare Communication","Medical Jurisprudence","Social Media in Health","Health Advertising Regulations","RECRUITING","2026-04-23",{"date":70,"type":39},"2026-04-29",{"date":72,"type":39},"2025-01-01",{"date":74,"type":21},"2027-01-01",{"name":76,"class":46},"University of Roma La Sapienza",{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":16,"minAge":85,"maxAge":86,"enrollmentInfo":87,"targetDuration":4,"studyType":22,"phases":89,"briefSummary":90,"conditions":91,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":47},"100625955","the-rewire-behaviour-study-100625955","NCT07429357","The REWIRE Behaviour Study","Research on Education With Individualized REwarding Behaviour (REWIRE): A Comparison of Two Youth Mental Health Programs","REWIRE","Inclusion Criteria:\n\n* Own a smartphone.\n* Use social media for \\>3 hours\u002Fday.\n* Are aged 12-17 years.\n* Are experiencing feelings of anxiety or depression.\n* Have a caregiver who is able and willing to participate in the study alongside them.\n* Have the ability to communicate in English.\n* Must sign and date the informed consent form, or provide assent and have a Substitute Decision Maker provide informed consent\n\nExclusion Criteria:\n\n* Own a smartphone.\n* Use their smartphone for \\>1 hour\u002Fday.\n* Are accompanying a youth participant enrolled in the study.\n* Have the ability to communicate in English.\n* Are willing to sign informed consent forms.","12 Years","17 Years",{"count":88,"type":21},220,[24],"This two-phase, double-blind, balanced, parallel-group randomized controlled trial involves youth aged 12 to 17 years who experience symptoms of anxiety or depression and use social media for more than three hours per day.\n\nIn Phase 1, a small pilot group will participate in the REWIRE program to assess its feasibility, usability, and engagement before launching Phase 2. Results of the pilot will inform whether any modifications to the intervention are required and identify ways to increase adherence and reduce barriers.\n\nIn Phase 2, approximately 100 youth and their caregivers will be randomly assigned to one of two groups to evaluate the REWIRE program on anxiety and depression symptoms. One group will participate in the REWIRE program, which aims to reduce social media use to about half of usual levels while encouraging participation in positive offline activities such as spending time with friends, hobbies, physical activity, or time outdoors. The comparison group will receive psychoeducation about social media and health, but will not be asked to change their social media use. Both youth and caregivers will attend weekly group sessions over 12-weeks. Participants will also track their physical activity, complete questionnaires about mental health, daily activities, and social media use, and will provide daily smartphone usage screenshots. Youth will additionally take part in brain imaging scans and neurocognitive assessments before and after the program to explore how changes in social media use may be related to brain function. At the end of Phase 2, 20 participants will be randomly selected for interviews to explore their experiences with the intervention.\n\nAdditional secondary outcomes in Phase 2 include social phobia, social comparison, Fear of Missing Out (FOMO), loneliness, body esteem, disordered eating, social media disorder symptoms, cyberbullying, reinforcing efficacy of social media, impulsivity, suicidal ideations, well-being, executive functioning and cognition, while further assessing the feasibility.",[92,27],"Anxiety Depression","2026-02-20",{"date":95,"type":39},"2026-02-24",{"date":97,"type":21},"2026-03",{"date":99,"type":21},"2029-12",{"name":101,"class":46},"Gary Goldfield",{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":16,"minAge":18,"maxAge":109,"enrollmentInfo":110,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":112,"conditions":113,"keywords":116,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":47},"100600924","social-media-use-food-craving-and-ultra-processed-food-consumption-in-students-100600924","NCT07103811","Social Media Use, Food Craving and Ultra Processed Food Consumption in Students","The Relationship Between Social Media Use, Food Craving and Ultra-Processed Food Consumption in University Students","Inclusion Criteria:\n\n* To be between the ages of 18-25\n* To reside in Ankara\n* Being a university student\n* Volunteering\n* No communication problems\n\nExclusion Criteria:\n\n* Under 18 years of age and over 25 years of age\n* Persons who are not university students\n* Those who do not reside in Ankara\n* Those with communication problems\n* Having any psychological disorder","25 Years",{"count":111,"type":21},150,"Social media can increase unhealthy eating habits by influencing individuals' desire to eat, especially through images and advertisements of ultra-processed foods. One of the groups most affected by this situation is university students who use social media intensively. Therefore, examining the relationship between social media use and ultra-processed food consumption is important in terms of developing healthy eating awareness.",[114,115,27],"Food Craving","Ultra Processed Food",[117,118,119],"Food craving","Ultra processed food","Social media","2025-07-29",{"date":122,"type":39},"2025-08-05",{"date":124,"type":39},"2025-04-01",{"date":126,"type":21},"2025-08-15",{"name":128,"class":46},"Atılım University",{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":11,"sex":16,"minAge":18,"maxAge":4,"enrollmentInfo":136,"targetDuration":4,"studyType":22,"phases":138,"briefSummary":139,"conditions":140,"keywords":143,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":147,"lastUpdatePostDateStruct":148,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":47},"100576923","the-impact-of-social-media-delivered-chemotherapy-side-effects-education-for-breast-cancer-patients-receiving-chemotherapy-100576923","NCT06791603","The Impact of Social Media-delivered Chemotherapy Side Effects Education for Breast Cancer Patients Receiving Chemotherapy","The Impact of Social Media-delivered Chemotherapy-related Side Effects Education for Breast Cancer Patients Receiving First Time Chemotherapy","Inclusion Criteria:\n\n* Breast cancer patients aged 18 or older undergoing their first chemotherapy.\n* Possess a smartphone and are able to watch videos on it.\n\nExclusion Criteria:\n\n* Unable to read or complete questionnaires in Chinese.\n* Cognitive impairments.\n* Pregnant women.",{"count":137,"type":21},100,[24],"The goal of this clinical trial is to learn if a standardized pharmacists-provided education module by social media can improve patients' knowledge of chemotherapy-related side effects. The main questions it aims to answer is:\n\n• Do patients who received a standardized pharmacists-provided education module by social media improve their knowledge of chemotherapy-related side effects? Researchers will compare standardized chemotherapy education +video (experimental group) versus chemotherapy handouts (control group).\n\nParticipants will:\n\n* Received standardized chemotherapy education + video or chemotherapy handouts at the first and second chemotherapy section.\n* Fill out a questionnaire for outcomes assessment.",[141,27,142],"Chemotherapy Side Effects","Education of Patients",[144,145,146],"pharmacist","chemotherapy education","social media","2025-01-22",{"date":149,"type":39},"2025-01-24",{"date":151,"type":39},"2025-01-06",{"date":153,"type":21},"2026-01-31",{"name":155,"class":46},"Taipei Medical University Shuang Ho Hospital",{"id":157,"slug":158,"hasResults":11,"nctId":159,"briefTitle":160,"officialTitle":161,"acronym":4,"eligibilityCriteria":162,"healthyVolunteers":15,"sex":16,"minAge":18,"maxAge":163,"enrollmentInfo":164,"targetDuration":4,"studyType":22,"phases":166,"briefSummary":167,"conditions":168,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":173,"lastUpdatePostDateStruct":174,"startDateStruct":176,"completionDateStruct":178,"leadSponsor":180,"locationsCount":47},"100548593","smart-mhealth-strategy-for-physical-activity-and-health-promotion-100548593","NCT06423014","Smart mHealth Strategy for Physical Activity and Health Promotion","Smart mHealth Strategy in the Delivery of Behavior Change Techniques for Physical Activity and Health Promotion","Inclusion Criteria:\n\nAdults who is the age of majority, with insufficient physical activity, and a sedentary lifestyle who have smartphones\n\nExclusion Criteria:\n\n* Individuals' health conditions may affect physical activity in daily living and the experiment, such as disability, serious health problems\n\n  * There are unconventional life plans during the experiment, such as going abroad for vacation, pregnancy, and surgery.\n\n    * Individuals have using experiences in any wearable physical activity trackers in the past six months ④ People who have ever had severe allergies to any wearable device ⑤ Professional athletes or student-athletes","70 Years",{"count":165,"type":21},360,[24],"The purpose of this study is to develop a Smart mHealth Strategy that delivers behavior change techniques through wearable physical activity trackers and social media chatbots, including self-monitoring, real-time feedback and reminders, goal-setting, competition and rewards, social support, and health coaching. This study also aims to explore the effect of the Smart mHealth Strategy on the behavioral outcomes and psychological factors of physical activity, and physical and mental health. The study design is a three-stage randomized controlled trial. In each stage, 120 are recruited and randomly assigned to control and experimental groups. Participants are adults with insufficient physical activity and a sedentary lifestyle. The Smart mHealth Strategy uses smartwatches and self-developed chatbots. The constrained dialogue content is designed to finally deliver the six behavior change techniques. Data are collected in the pre-, mid-, and post-tests. The measurement includes self-administered questionnaires, Actigraphy GT9X, Inbody 270S, OMRON HEM-7130, and heart rate variability monitors.",[169,170,171,27,172],"Health Behavior Change","Wearable Technology","Chatbot","Sedentary Lifestyle","2024-05-15",{"date":175,"type":39},"2024-05-21",{"date":177,"type":39},"2023-05-01",{"date":179,"type":21},"2026-12",{"name":181,"class":46},"Taipei Medical University"]