[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"behavior-change-interventions\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:behavior-change-interventions":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,48,79,113,135,177],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":4},"100637231","unconscious-mind-training-100637231",false,"NCT07597603","Unconscious Mind Training","H22 - Unconscious Mind Training and Memory Encoding","Inclusion Criteria:\n\n* Can read and write\n* Willing and able to follow the requirements of the protocol\n\nExclusion Criteria:\n\n\\- Medical instability, restlessness, or other factors that would compromise data acquisition",true,"ALL","10 Years","75 Years",{"count":21,"type":22},100,"ESTIMATED","INTERVENTIONAL",[25],"NA","H22 - Unconscious Mind Training and Memory Encoding\n\nPhase I\n\nThe core problem this clinical trial, H22, seeks to address is the pervasive challenge of modifying deeply ingrained, often unconscious, unwanted behaviors within the general population. Many individuals struggle with habits or actions that negatively impact quality of life, productivity, or well-being, yet conventional methods often fall short due to the unconscious nature of these behaviors.\n\nSpecifically, the trial aims to investigate the efficacy of H22, a novel intervention designed to engage and train the unconscious mind, in mitigating these unwanted behaviors. The central hypothesis guiding this research is that H22 training will empower volunteers to significantly reduce the frequency and intensity of identified unwanted behaviors.",[28,29,30,31],"Memory Encoding","Memory","Behavior Change Interventions","Habits",[33,34,35],"Behavior","Cognitive ability","Unconscious mind","NOT_YET_RECRUITING","2026-05-31",{"date":39,"type":40},"2026-06-03","ACTUAL",{"date":42,"type":22},"2027-01",{"date":44,"type":22},"2028-01",{"name":46,"class":47},"Dream Video LLC","OTHER",{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":23,"phases":57,"briefSummary":58,"conditions":59,"keywords":63,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":74,"leadSponsor":76,"locationsCount":78},"100632391","prevention-of-noise-induced-hearing-loss-in-primary-education-100632391","NCT07513077","Prevention of Noise-Induced Hearing Loss in Primary Education","Effectiveness of an Educational Program in Primary Schools to Prevent Noise-induced Hearing Loss","Inclusion Criteria:\n\nFor schools: None.\n\nFor children:\n\n* Dutch primary school children in group 7 (corresponding to Year 6 in the UK).\n* Informed consent from legally authorized parent(s) or guardian(s).\n\nParents:\n\n• Child is participating.\n\nExclusion Criteria:\n\nFor schools:\n\n• HoorToren package has been taught at group 6 in the previous school year.\n\nFor children:\n\n* Children without informed consent from legally authorized parent(s) or guardian(s).\n* Children who cannot read and write Dutch.\n\nFor parents:\n\n• Parents who cannot read and write Dutch",{"count":56,"type":22},600,[25],"The goal of this randomized controlled trial is to evaluate the effectiveness of the educational program the HoorToren in promoting recreational safe listening behavior among Dutch primary school children in group 7 (aged 10-11 years) and thereby contribute to preventing noise-induced hearing loss. The main objectives are:\n\n* To evaluate the HoorToren's effects on promoting the child's safe listening behavior when using headphones or earbuds. Both safe listening and its psychological determinants will be measured.\n* To evaluate the HoorToren's effects on parents' perception of their child's safe listening behaviors. The effects on parental behavior promoting or facilitating their child's safe listening behavior, including its psychological determinants, will also be evaluated.\n\nResearchers will compare children who receive lessons from the HoorToren educational program, and their parents (intervention group) with children and their parents who do not receive the lessons (control group) to evaluate the effectiveness of the HoorToren. Outcomes will be assessed using newly developed and validated self-report questionnaires for both children and their parents. Additionally, the child's listening behavior will be measured via a smartphone application installed on the child's phone. Measurements will take place at four time points during the school year.",[60,61,30,62],"Effectiveness of Application Education Intervention","Noise Induced Hearing Loss","Primary School Children",[64,65,66,67,68],"Noise-induced hearing loss","Prevention","Primary school","Randomized controlled trial","Effectiveness","RECRUITING","2026-03-30",{"date":72,"type":40},"2026-04-06",{"date":70,"type":40},{"date":75,"type":22},"2027-08",{"name":77,"class":47},"Erasmus Medical Center",1,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":87,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":23,"phases":90,"briefSummary":91,"conditions":92,"keywords":95,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":112},"100543695","sustaining-physical-activity-after-cancer-exercise-sessions-100543695","NCT06359210","Sustaining Physical Activity After Cancer Exercise Sessions","An Adaptive Physical Activity Maintenance Intervention","SPAACES","Inclusion Criteria:\n\n* ≥18 years old,\n* Able to speak\u002Fread English,\n* Diagnosed with any type of cancer,\n* Completed primary or adjuvant treatment (i.e., chemotherapy, radiation therapy, surgery) within the previous five years, with no planned treatment within the next nine months. This does not include long-term or chronic therapies such as anti-hormone or targeted therapies (e.g., aromatase inhibitor, androgen deprivation therapy),\n* Participant is registered\u002Fenrolled to participate in one of three community-based exercise programs.\n\nExclusion Criteria:\n\n* Existing participation in ≥90 minutes per week of at least moderate intensity aerobic exercise AND two or more days per week of resistance exercise or known contraindications for exercise.\n* Known contraindications for non-medically supervised moderate or greater intensity exercise (e.g., uncontrolled hypertension, inability to walk without an assistive device)\n* Current or planned participation in another exercise oncology program (not one of the three community partner exercise programs), or previous participation in another or one of the three community partner exercise programs in the past 12-months.","18 Years",{"count":89,"type":22},105,[25],"The goal of this clinical trial is to develop and test an adaptive physical activity (PA) maintenance intervention for cancer survivors, after participating in a community-based exercise oncology program. The main questions it aims to answer are:\n\n* Aim 1: Examine the feasibility and acceptability of the intervention among cancer survivors and community partners. The researchers will utilize quantitative surveys, focus groups, and semi-structured interviews to collect information about feasibility, implementation, adaptation, and sustainability.\n* Aim 2: Examine the effects of the intervention among cancer survivors. The researchers will compare the proportion of participants achieving the exercise guidelines for cancer survivors six-months following completion of the initial exercise program.\n\nParticipants will participate in a community-based exercise oncology program and then return to three months of free living. Based on the PA measured at the three-month follow-up, participants will be categorized as a \"Responder\" or \"Incomplete Responder\", and then randomized to the PA maintenance intervention. Researchers will compare those that are classified as Responders (meeting exercise guidelines for cancer survivors) and Incomplete Responders (not meeting guidelines for cancer survivors) to see what level of intervention is needed to influence sustainable behavior change in this population.",[93,94,30],"Exercise Oncology","Physical Activity Behavior",[96,97,98,99,100,101,102],"exercise oncology","physical activity","behavior change","adaptive intervention","cancer survivors","physical activity maintenance","community partnerships","2026-03-17",{"date":105,"type":40},"2026-03-19",{"date":107,"type":40},"2024-03-04",{"date":109,"type":22},"2026-12-31",{"name":111,"class":47},"Colorado State University",3,{"id":114,"slug":115,"hasResults":11,"nctId":116,"briefTitle":117,"officialTitle":118,"acronym":4,"eligibilityCriteria":119,"healthyVolunteers":11,"sex":17,"minAge":87,"maxAge":4,"enrollmentInfo":120,"targetDuration":4,"studyType":23,"phases":122,"briefSummary":123,"conditions":124,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":78},"100607228","informing-low-acuity-emergency-department-patients-of-non-emergent-resources-2-100607228","NCT07185828","Informing Low-acuity Emergency Department Patients of Non-emergent Resources (2)","Informing Low-acuity Emergency Department Patients of Non-emergent Healthcare Resources Following Discharge to Decrease Emergency Department Utilization (2)","Inclusion Criteria:\n\n* \\>= 18 years of age\n* Geisinger ED visit rated as low acuity (L4 or L5)\n* Discharged from Geisinger ED in past 24 hours\n\nExclusion Criteria:\n\n* Cannot be contacted via the communication modality being used in the study (i.e., SMS), due to insufficient\u002Fmissing contact information in the EHR or because the patient opted out\n* Admitted to hospital\n* Already included in intervention in past 365 days",{"count":121,"type":22},8286,[25],"The goal of this campaign is to reduce unnecessary visits to a Geisinger emergency department (ED). In this campaign, patients will be assigned to receive or not receive outreach following ED discharge with a low-acuity visit designation. Outreach will occur via a text message the day after discharge from the ED as well as information added to the patient's after visit summary (AVS). Depending on the assigned condition, it will include calls to see their primary care provider (PCP) or use an Intelligent Triage tool. The study will assess whether ED use within the following 120 days differs across patients in different outreach conditions (current standard practice vs contact your PCP vs use Intelligent Triage). It will also examine whether patients follow through on the message-specific calls to action differently across conditions.",[125,30],"Emergency Service, Hospital","2026-03-12",{"date":128,"type":40},"2026-03-13",{"date":130,"type":40},"2025-04-15",{"date":132,"type":22},"2026-08",{"name":134,"class":47},"Geisinger Clinic",{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":141,"eligibilityCriteria":142,"healthyVolunteers":11,"sex":17,"minAge":87,"maxAge":143,"enrollmentInfo":144,"targetDuration":4,"studyType":23,"phases":146,"briefSummary":147,"conditions":148,"keywords":156,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":170,"completionDateStruct":172,"leadSponsor":174,"locationsCount":176},"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":145,"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.",[65,149,150,151,152,30,153,154,155],"Well Being","Sexual Behavior","Behavior Change","Behavior Problems","Child Sexual Abuse Material (CSAM) Consumption","Behavioral Disorder","Online Behaviour",[157,158,159,160,161,162,163,164,165,166],"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":169,"type":40},"2025-05-07",{"date":171,"type":40},"2025-04-01",{"date":173,"type":22},"2026-07-31",{"name":175,"class":47},"Charite University, Berlin, Germany",2,{"id":178,"slug":179,"hasResults":11,"nctId":180,"briefTitle":181,"officialTitle":181,"acronym":4,"eligibilityCriteria":182,"healthyVolunteers":16,"sex":17,"minAge":183,"maxAge":4,"enrollmentInfo":184,"targetDuration":4,"studyType":23,"phases":186,"briefSummary":187,"conditions":188,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":189,"lastUpdatePostDateStruct":190,"startDateStruct":192,"completionDateStruct":194,"leadSponsor":196,"locationsCount":4},"100568317","acceptability-usability-and-preliminary-effectiveness-of-chatgpt-in-increasing-seasonal-influenza-vaccination-uptake-among-older-adults-in-hong-kong-100568317","NCT06679647","Acceptability, Usability and Preliminary Effectiveness of ChatGPT in Increasing Seasonal Influenza Vaccination Uptake Among Older Adults in Hong Kong","Inclusion Criteria:\n\n* Aged ≥65 years;\n* Possession of a Hong Kong ID;\n* Able to speak and comprehend Cantonese;\n* Have a smartphone with internet access;\n* Have not taken SIV for the approaching flu season.\n\nExclusion Criteria:\n\n* With diagnosis of cognitive impairment or dementia;\n* Either blindness or deafness;\n* With known contraindications to the SIV as indicated by the Hong Kong Centre for Health Protection","65 Years",{"count":185,"type":22},50,[25],"In this project, we will train a ChatGPT to provide real-time answers to questions related to the SIV for older adults in Hong Kong.\n\nThis study aims to evaluate the usability, acceptability, and preliminary effectiveness of the ChatGPT among 50 community-living people aged 65 years and above in Hong Kong.\n\nThe primary objectives are to evaluate the usability and acceptability (including the extent of usage and subjective experiences of behavioural, cognitive, and affective engagement) of the ChatGPT at the end of the 4-week intervention period (T1).\n\nThe secondary objectives are to evaluate the following conditions measured at T1, as compared to those measured at baseline (T0):\n\n1. Self-reported uptake of SIV in the past month.\n2. Changes in behavioural intention to receive SIV for the approaching flu season.\n3. Changes in knowledge and attitudes related to SIV.",[30],"2024-11-06",{"date":191,"type":40},"2024-11-07",{"date":193,"type":22},"2024-12-01",{"date":195,"type":22},"2025-03-31",{"name":197,"class":47},"Chinese University of Hong Kong"]