[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"behavior-change\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:behavior-change":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,53,80,106,133,170,199,224],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100640079","motivating-activity-through-text-communications---helping-adults-increase-movement-100640079",false,"NCT07593677","Motivating Activity Through Text Communications - Helping Adults Increase Movement","Motivating Activity Through Text - Comparing Human and AI Messages (MATCH AIM) Trial","MATCH AIM","Inclusion Criteria:\n\n* Be 40 years of age or older\n* Own a smartphone running an Android or iOS operating system\n* Have proficiency with the English language\n* Be capable of providing informed consent\n* Be able to perform moderate physical activity without restrictions\n* Be willing to complete the entire 6-month protocol\n* Be willing to establish a 12-hour window - beginning no later than 9:45 am and ending no later than 9:45 pm - for receiving text messages.\n\nExclusion Criteria:\n\n* Residing outside of the continental United States\n* Self-reporting 90 minutes or more of moderate-to-vigorous intensity physical activity per week\n* contraindications to normal physical activity as identified on the Physical Activity Readiness Questionnaire (PAR-Q)\n* Mobility restrictions that interfere with unassisted physical activity\n* Being pregnant or planning to become pregnant during the study\n* Planning to undergo surgery during the course of the study protocol\n* Having a prior diagnosis of Alzheimer's disease or a related dementia\n* Evidence of mild cognitive impairment as indicated by a mini-Montreal Cognitive Assessment (MoCA) test score of 12 or higher\n* Concurrent participation in another study involving weight loss or physical activity\n* Failure to respond to at least 85% of Ecological Momentary Assessment (EMA) prompts during the 7-day qualification phase.",true,"ALL","40 Years",{"count":21,"type":22},150,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to compare the effect of different types of text messages on physical activity levels of middle-aged and older adults and to determine whether these messages are effective in adults age 40 and older who are engaging in less than 90 minutes per week of moderate or higher intensity physical activity. The main questions it aims to answer are:\n\n* Which types of motivational messages show the greatest effects on changes in daily step counts in a 3-month precision text messaging intervention?\n* What are the effects of personalized text messages on automatic affective evaluations, habit strength (experienced automaticity), exercise identity, working memory capacity, and processing speed?\n\nParticipants will:\n\n* Wear a Fitbit activity tracker continuously for 3 months and are encouraged to continue wearing it through 6 months.\n* Wear an activPAL activity monitor on their thigh for 7-day assessment periods at the beginning of the study, at 3 months, and at 6 months.\n* Complete 3 cognitive assessments (\"brain games\") per day on their smartphone during the 7-day assessment periods at baseline, 3 months, and 6 months.\n* Be asked to set goals to increase their daily steps over the first 3 months of the study.\n* Receive up to 4 motivational text messages per day for 3 months to encourage physical activity.\n* Keep study-related apps (Fitbit app, AIM app, MetricWire app) open in the background on their smartphone.\n* Complete questionnaires at the beginning of the study, at 3 months, and at 6 months",[28,29,30,31],"Physical Inactivity","Aging","Cognitive Ability","Behavior Change",[33,34,35,36,37,38,39],"physical activity","behavioral adherence","motivation","cognitive function","aging","older adults","text messaging","NOT_YET_RECRUITING","2026-05-21",{"date":43,"type":44},"2026-05-22","ACTUAL",{"date":46,"type":22},"2026-06-01",{"date":48,"type":22},"2027-08-02",{"name":50,"class":51},"University of Michigan","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":17,"sex":18,"minAge":61,"maxAge":62,"enrollmentInfo":63,"targetDuration":4,"studyType":23,"phases":65,"briefSummary":66,"conditions":67,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":52},"100613064","collaborative-opportunities-for-reducing-alcohol-and-sexual-violence-together-100613064","NCT07261722","Collaborative Opportunities for Reducing Alcohol and Sexual Violence Together","Harnessing the Power of Military Peers to Reduce Sexual Violence and Risky Drinking in Service Members","COAST","Inclusion Criteria:\n\n* Enlisted U.S. Navy service members on active duty status\n* Meet criteria for risky drinking (i.e. score of 4+ for men, 2+ for women according to the AUDIT-C)\n* Have an eligible peer and the pair must socialize together at least twice a month\n\nExclusion Criteria:\n\n* Individuals who endorse evidence of withdrawal (Item 6 on the AUDIT)","18 Years","24 Years",{"count":64,"type":22},132,[25],"The goal of this clinical trial is to test if a modified peer-based motivational intervention (the Military PAIRS; MPAIRS) is reasonable and practical for military contexts. The main questions it aims to answer are:\n\n* Does it works to reduce SV?\n* Does it works to reduce risky drinking? To test this, participants will answer questions about their SV history and risky drinking. Then they will be given MPAIRS. After 1 month, they will be asked about their SV history and risky drinking again.",[68,31,69],"Sexual Violence","Military Training","RECRUITING","2026-04-20",{"date":73,"type":44},"2026-04-23",{"date":75,"type":44},"2025-10-10",{"date":77,"type":22},"2027-04",{"name":79,"class":51},"State University of New York at Buffalo",{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":18,"minAge":87,"maxAge":88,"enrollmentInfo":89,"targetDuration":4,"studyType":23,"phases":91,"briefSummary":92,"conditions":93,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":52},"100629311","peeg-guided-anesthesia-and-behavioral-outcomes-in-children-100629311","NCT07473024","pEEG-Guided Anesthesia and Behavioral Outcomes in Children","Long-Term Behavioral Outcomes After pEEG-Guided Anesthesia in Children: A Follow-Up Study Using the Post-Hospitalization Behavior Questionnaire","Inclusion Criteria:\n\n* Children aged 3-10 years\n* Surgical duration longer than 1 hour\n* Patients undergoing urology, plastic surgery, or pediatric surgery procedures\n* Availability of early postoperative PHBQ data\n* Verbal consent from parents or legal guardians for participation in the follow-up telephone interview\n\nExclusion Criteria:\n\n* Patients with neuromotor developmental abnormalities\n* History of epilepsy or antiepileptic medication use\n* Patients requiring postoperative intensive care unit admission\n* Emergency surgical procedures\n* Inability to contact the family or refusal of verbal consent for the telephone interview\n* Patients who underwent another surgical procedure between the initial surgery and the follow-up period","3 Years","10 Years",{"count":90,"type":22},230,[25],"Post-hospitalization behavioral changes are common in children after surgery and general anesthesia and may persist for varying durations depending on individual and perioperative factors. The Post-Hospitalization Behavior Questionnaire (PHBQ) is a well-validated instrument widely used to evaluate negative postoperative behavioral changes in pediatric patients following hospitalization or surgical procedures. Although early postoperative behavioral disturbances have been extensively studied, most research has focused on short-term outcomes within the first weeks after surgery, while long-term behavioral outcomes remain insufficiently investigated.\n\nProcessed electroencephalography (pEEG) monitoring provides an objective method for assessing anesthetic depth during surgery. Parameters such as the Patient State Index (PSI) and Spectral Edge Frequency 95 (SEF95) allow dynamic evaluation of cortical activity and may help optimize anesthetic administration by preventing excessively deep or inadequate anesthesia. Improved anesthetic depth management may theoretically influence postoperative recovery and behavioral outcomes.\n\nIn the initial randomized study, early postoperative behavioral assessments were obtained within the first postoperative month using the Post-Hospitalization Behavior Questionnaire (PHBQ). In the present follow-up study, children will be contacted again 12-24 months after surgery to evaluate long-term behavioral outcomes. PHBQ scores at long-term follow-up will be compared between children who previously received EEG-guided anesthesia and those managed with standard anesthesia without processed EEG monitoring. By examining both early and long-term behavioral outcomes, this study aims to determine whether intraoperative EEG-guided anesthesia management influences postoperative behavioral changes in the pediatric population.",[94,31,95,96],"Anesthesia","Behavior Child Problems","Anesthesia Depth Monitoring","2026-03-14",{"date":99,"type":44},"2026-03-17",{"date":101,"type":44},"2026-02-02",{"date":103,"type":22},"2026-08-22",{"name":105,"class":51},"Istanbul University",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":17,"sex":18,"minAge":61,"maxAge":4,"enrollmentInfo":112,"targetDuration":4,"studyType":23,"phases":114,"briefSummary":115,"conditions":116,"keywords":117,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":4},"100561682","evaluation-of-report-back-strategies-for-long-term-and-short-term-exposure-information-in-rural-tribal-populations-100561682","NCT06593340","Evaluation of Report-Back Strategies for Long-term and Short-term Exposure Information in Rural Tribal Populations","Inclusion Criteria:\n\n* Enrolled member of the participating tribe\n\nExclusion Criteria:\n\n* Participant in one of our previous studies",{"count":113,"type":22},112,[25],"The goal of this study is to evaluate different ways to provide feedback about environmental sampling results to participants. Specifically, the study will look at exposures with long-term risk (radon) and short-term risk (indoor particulate matter, PM2.5). The hypothesis is that providing feedback in real-time will result in participants engaging in more activities to try to reduce their exposure. One of the main questions of interest is: How does the information messenger impact the effectiveness of report-back strategies in rural, tribal populations?\n\nParticipants will have radon and PM2.5 measurement equipment installed at their home and will answer questions about any actions they took to reduce exposure. Previously developed approaches to reporting back those exposures will be used to test which feedback method results in more actions to reduce exposure.",[31],[118,119,120,121,122,123],"exposure","Native American","radon","particulate matter","PM2.5","report-back","2025-12-08",{"date":126,"type":44},"2025-12-12",{"date":128,"type":22},"2026-10",{"date":130,"type":22},"2028-04",{"name":132,"class":51},"University of Utah",{"id":134,"slug":135,"hasResults":11,"nctId":136,"briefTitle":137,"officialTitle":138,"acronym":139,"eligibilityCriteria":140,"healthyVolunteers":17,"sex":18,"minAge":61,"maxAge":4,"enrollmentInfo":141,"targetDuration":4,"studyType":23,"phases":143,"briefSummary":144,"conditions":145,"keywords":153,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":160,"lastUpdatePostDateStruct":161,"startDateStruct":163,"completionDateStruct":165,"leadSponsor":167,"locationsCount":169},"100605106","optical-diagnosis-of-neoplasia-using-artificial-intelligence-100605106","NCT07158203","Optical Diagnosis of Neoplasia Using Artificial Intelligence","Assistance for Optical Diagnosis of Neoplasia Using Artificial Intelligence (FAIR Study)","FAIR","Endoscopists who meet the following inclusion\u002Fexclusion criteria Inclusion criteria\n\n* Endoscopists experienced with more than 100 colonoscopies. Exclusion criteria\n* Endoscopists who are involved in the development of the protocol of the present study.\n\nInclusion and exclusion criteria for the study videos. Inclusion criteria.\n\n* Videos with a duration of 15 seconds including both WL and NBI.\n* Videos with diminutive polyps with confirmed pathology. Exclusion criteria.\n* Videos with no clear image of the polyps.\n* Videos with more than one polyp on-screen.\n* Inflammatory bowel disease\n* Polyposis\n* Hereditary colorectal disease\n* Videos which CADx cannot provide sufficient number of outputs.",{"count":142,"type":22},70,[25],"Computer-aided diagnosis (CADx) for colonoscopy aims to enhance optical diagnosis but often underperforms when used alongside humans due to under-reliance on AI. Psychological interventions like cognitive forcing, such as delaying CADx suggestions, may improve human-AI interaction by fostering critical assessment. However, their impact on patient-important outcomes remains unexplored.\n\nThe investigators will conduct an ex-vivo randomized study with 70 endoscopists assessing 100 polyp videos (≤5 mm) using a CADx tool (GI Genius, Medtronic). Participants will be randomized to either:\n\n* Intervention group: CADx suggestions will be shown in the last 3 seconds of the 15 second polyp video.\n* Control group: CADx suggestions will be shown in real-time throughout the playback of the 15 second polyp video.\n\nThe primary endpoint is sensitivity for high-confidence neoplasia detection, with secondary endpoints assessing endoscopists' reliance on AI.\n\nCADx systems on the market function in various ways, such as real-time, delayed, or on-demand diagnosis. Our study aims to inform users and manufacturers whether cognitive forcing through delayed CADx suggestions enhances human-AI interaction, leading to improved clinical outcomes.",[146,147,148,149,150,31,151,152],"Polyps Colorectal","Colonoscopy","Optical Biopsy","Colorectal Cancer Control and Prevention","Colorectal Cancer Screening","Psychological Factors","Psychological Intervention",[154,155,156,157,158,159],"behaviour","optical biopsy","colonoscopy","CADx system","colorectal polyps","psychological intervention","2025-08-28",{"date":162,"type":44},"2025-09-05",{"date":164,"type":22},"2025-09",{"date":166,"type":22},"2025-12",{"name":168,"class":51},"Fundacin Biomedica Galicia Sur",2,{"id":171,"slug":172,"hasResults":11,"nctId":173,"briefTitle":174,"officialTitle":175,"acronym":176,"eligibilityCriteria":177,"healthyVolunteers":11,"sex":18,"minAge":61,"maxAge":178,"enrollmentInfo":179,"targetDuration":4,"studyType":23,"phases":181,"briefSummary":182,"conditions":183,"keywords":187,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":160,"lastUpdatePostDateStruct":191,"startDateStruct":193,"completionDateStruct":195,"leadSponsor":197,"locationsCount":52},"100571757","family-centered-weight-loss-for-black-adults-fam-wel-b-ing-100571757","NCT06724406","FAMily-centered WEight Loss for Black Adults (FAM WEL B-ing)","FAMily-centered WEight Loss for Black Adults (FAM WEL B-ing): Optimization and Evaluation Using Multiphase Optimization Strategy (MOST) and Social Network Analysis (SNA)","FAM WEL B-ing","Inclusion Criteria:\n\n* self-identified as Black or African American (Index participant)\n* BMI equal to greater than 30 kg\u002Fm\\^2 (Index); BMI equal to greater than 27.5 kg\u002Fm\\^2 (family partner)\n* have a partner\u002Ffamily member willing to enroll in the study and must share a mutual goal of achieving weight loss\n* English speaking\n* ages 18-75\n* any gender\n* have access to and be able to use a smartphone, tablet, or computer that has web-access (this is required for data collection and some program components being tested)\n\nExclusion Criteria:\n\n* participation in an intensive weight loss program (more than 12 visits) in the prior 6 months\n* type 1 diabetes\n* significant psychiatric illness, defined as depression or other major psychiatric illness not considered reasonably managed by counseling, medication, or both\n* had bariatric surgery (surgery for weight loss) in the last 2 years or considering bariatric surgery in the next 6 months\n* using or planning to start medications intentionally for weight loss\n* are pregnant or planning to get pregnant in the next 6 months\n* are breastfeeding and less than 2 months postpartum\n* alcohol or substance abuse, defined as alcohol or substance use that interferes with work activities and\u002For has had a major negative impact on family\u002Fsocial function, the latter defined as more than 2 episodes per month.\n* malignancy other than non-melanoma skin cancer, unless considered cured \\> 5 years ago. Exceptions include 1) men with localized prostate cancer (treated with usual modalities or managed with \"active surveillance\"), and 2) postmenopausal women receiving adjuvant endocrine therapy (e.g., aromatase inhibitor) for non-metastatic, hormone receptor-positive breast cancer\n* self-report of advanced kidney disease (estimated glomerular filtration rate (GFR) \\\u003C 30 mL\u002Fmin)","75 Years",{"count":180,"type":22},256,[25],"The goal of this clinical trial is to learn the best combination of family components that yields optimal weight loss among Black adults. The main question it aims to answer is:\n\nWhat combination of four family components in combination with a standard behavioral weight loss program yields optimal weight loss among Black adults? Researchers will compare different combinations of family skills components (communication content, cohesion content, number of sessions, and mode of delivery) to see the best weight loss.\n\nParticipants will:\n\n* Participate in a 6-month behavioral weight loss intervention\n* Attend core weight loss in-person group sessions, and dyad based family sessions\n* Keep track of weight, dietary intake and physical activity",[184,185,186,31],"Obesity and Overweight","Diabetes Mellitus","Weight Loss",[188,189,190],"weight loss program","African American or Black families","nutrition and physical activity behavior change",{"date":192,"type":44},"2025-08-29",{"date":194,"type":44},"2025-02-03",{"date":196,"type":22},"2028-12-31",{"name":198,"class":51},"University of North Carolina, Chapel Hill",{"id":200,"slug":201,"hasResults":11,"nctId":202,"briefTitle":203,"officialTitle":204,"acronym":4,"eligibilityCriteria":205,"healthyVolunteers":17,"sex":18,"minAge":206,"maxAge":207,"enrollmentInfo":208,"targetDuration":4,"studyType":23,"phases":210,"briefSummary":211,"conditions":212,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":215,"lastUpdatePostDateStruct":216,"startDateStruct":218,"completionDateStruct":220,"leadSponsor":222,"locationsCount":52},"100593972","i-recycle-i-protect-the-environment-i-leave-a-livable-world-as-a-legacy-100593972","NCT07013383","I Recycle, I Protect the Environment, I Leave a Livable World as a Legacy","The Effect of the \"I Recycle, I Protect the Environment, I Leave a Livable World as a Legacy\" Program on Recycling Behaviors of Secondary School Students","Inclusion Criteria:\n\nBeing 10-14 years old and attend the school where the study is being conducted, Voluntarily agree to take part in the research,\n\nExclusion Criteria:\n\nHaving received previous education on environmental health","9 Years","14 Years",{"count":209,"type":22},58,[25],"The research will be conducted to determine the effect of \"I Recycle, I Protect the Environment, I Leave a Livable World as a Legacy\" program on secondary school students' recycling behaviour.",[213,31,214],"Recycling","Student","2025-08-14",{"date":217,"type":44},"2025-08-19",{"date":219,"type":22},"2025-09-25",{"date":221,"type":22},"2026-05-20",{"name":223,"class":51},"Feyza Bardak",{"id":225,"slug":226,"hasResults":11,"nctId":227,"briefTitle":228,"officialTitle":229,"acronym":230,"eligibilityCriteria":231,"healthyVolunteers":11,"sex":18,"minAge":61,"maxAge":232,"enrollmentInfo":233,"targetDuration":4,"studyType":23,"phases":235,"briefSummary":236,"conditions":237,"keywords":246,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":257,"lastUpdatePostDateStruct":258,"startDateStruct":260,"completionDateStruct":262,"leadSponsor":264,"locationsCount":169},"100581602","troubled-desire--therapeutic-chat-for-reduction-of-csam-use-td-chat-100581602","NCT06852443","Troubled-Desire & Therapeutic Chat for Reduction of CSAM Use (TD-CHAT)","Troubled Desire & Therapeutic Chat for Reduction of CSAM Use","TD-CHAT","Inclusion Criteria:\n\n* Adult participant (≥18 years);\n* recent (last 2 weeks) CSAM use or past CSAM use and self-reported risk;\n* proficiency in English, German or Spanish;\n* voluntary participation and agreement to the terms of the study.\n\nExclusion Criteria:\n\n* Severe neuropsychiatric comorbidities (unstable psychotic disorder, organic brain damage, diminished intellectual functioning, untreated drug or alcohol addiction);\n* history of contact CSA perpetration (past or present);\n* ongoing criminal investigation, trial, punishment, or probation status for online or offline CSA or CSAM use;\n* current inpatient psychiatric treatment or other concurrent treatment targeting CSAM behaviours","99 Years",{"count":234,"type":22},180,[25],"The goal of this prospective multicentred, stratified, parallel-group superiority study is to prevent and reduce the usage of Child Sexual Abuse Material (CSAM) by a Therapist Chat Service (TCS) and Selfhelp Platform for Self-Referred Patients, mostly men with a sexual interest in children. The interventions are based on Cognitive Behavioral Therapy (CBT) principles and designed to treat the sexual behavioral disorder related with CSAM consumption.\n\n1. Participants in the Selfhelp modules group will show a statistically significantly higher proportion of reduction in CSAM behaviours four weeks after baseline, as compared to participants in the waitlist control group.\n2. Participants in the Selfhelp modules followed by TCS group will show a statistically significantly higher reduction of CSAM behaviours compared to participants in the Selfhelp-only and TCS-only groups, post-intervention.\n\nResearchers will compare TCS-only-, Selfhelp-only-, Selfhelp + TCS- and Waiting group to see if if the interventions decrease CSAM use and improve mental well-being.\n\nParticipants will get web based selfhelp-modules and\u002For text-based chat intervention operated by trained therapists.",[238,239,240,31,241,242,243,244,245],"Prevention","Well Being","Sexual Behavior","Behavior Problems","Behavior Change Interventions","Child Sexual Abuse Material (CSAM) Consumption","Behavioral Disorder","Online Behaviour",[247,248,249,250,251,252,253,254,255,256],"Child Sexual Abuse Material (CSAM) consumption","CSAM","Child Sexual Abuse","Digital online intervention","CSA","CBT","iCBT","Cognitive Behavioural Therapy","Pedophilia","chat Intervention","2025-05-06",{"date":259,"type":44},"2025-05-07",{"date":261,"type":44},"2025-04-01",{"date":263,"type":22},"2026-07-31",{"name":265,"class":51},"Charite University, Berlin, Germany"]