[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"habits\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:habits":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,48,81,109],{"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":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":23,"phases":59,"briefSummary":60,"conditions":61,"keywords":64,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":80},"100583431","mobile-cued-adherence-therapy-mcat-for-blood-pressure-medication-100583431","NCT06876233","Mobile Cued Adherence Therapy (mCAT) for Blood Pressure Medication","Mobile Cued Adherence Therapy (mCAT): A Scalable Habit Formation Intervention to Improve Blood Pressure Medication Adherence Based on a Widely Used Smartphone App","mCAT","Eligibility Criteria:\n\n* Aged 18 years or older\n* Currently diagnosed with hypertension (either stage I or stage II hypertension)\n* Able to read\u002Fwrite\u002Funderstand English\n* Have daily access to a smartphone\n* Engaged in hypertension care: Already been prescribed hypertension medication for a minimum of 6 months at the time of study enrollment\n* Demonstrated AH medication nonadherence by having over 73 days without documented AH medication prescription coverage (observable in Arizona Health Care Cost Containment System (AHCCCS) prescription drugs claims) in the past 12 months (i.e. \\\u003C80% mean adherence)","18 Years",{"count":58,"type":22},600,[25],"The goal of this clinical trial is to determine the effectiveness of a novel mobile health-based habit formation intervention for increasing and maintaining adherence to anti-hypertensive (AH) medication among people living with hypertension and indicate medication nonadherence. The main questions it aims to answer are:\n\n* Can daily incentives for AH pill taking increase and maintain AH medication adherence, control blood pressure, and reduce healthcare utilization and costs?\n* Can daily incentives for AH pill taking, combined with action planning (e.g., \"After I drink my morning coffee, I will take my medication.\") increase and maintain medication adherence, control blood pressure, and reduce healthcare utilization and costs?\n* What aspects of daily incentives and\u002For action planning do participants find most helpful or effective for AH medication adherence?\n* What barriers exist for participants who receive daily incentives and\u002For action planning?\n\nResearchers will compare three study groups: those who only receive daily incentives for the AH pill taking, those who receive daily incentives for AH pill taking combined with action planning, and a control group (who do not receive daily incentives for AH pill taking or action planning). By comparing these three groups, the researchers will be able to determine the effectiveness of the daily incentives with or without action planning for promoting long-term AH medication adherence, reduce healthcare costs, and improve blood pressure.\n\nParticipants will:\n\n* Complete 5 online surveys over the course of 2 years (baseline, month 4, month 8, month 12, month 24).\n* Submit blood pressure reading for 7 consecutive days after each survey timepoint.\n* Submit photo evidence of their AH pill taking for 4 months (intervention groups only).\n\nThe highest- and lowest-performing participants in each intervention group will also be invited to complete a 30-minute interview to identify additional factors that contributed to either successful or unsuccessful completion of the intervention.",[62,63,31],"Medication Adherence","Hypertension",[65,66,67,68,69],"habits","medication adherence","hypertension","blood pressure","mobile app","RECRUITING","2026-03-12",{"date":73,"type":40},"2026-03-16",{"date":75,"type":40},"2025-09-01",{"date":77,"type":22},"2029-03-30",{"name":79,"class":47},"Chad Stecher@asu.edu",1,{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":87,"eligibilityCriteria":88,"healthyVolunteers":16,"sex":17,"minAge":89,"maxAge":4,"enrollmentInfo":90,"targetDuration":4,"studyType":23,"phases":92,"briefSummary":93,"conditions":94,"keywords":97,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":105,"leadSponsor":107,"locationsCount":80},"100627343","planning-actions-for-consistent-engagement-100627343","NCT07447401","Planning Actions for Consistent Engagement","Manipulating Action Plans to Improve Physical Activity Behavior and Cognitive Health in Older Adults","PACE","Inclusion Criteria:\n\n* age 60 years or older\n* own a smartphone\n* willingness to download an app onto their personal smartphone and complete the cognitive assessments and questionnaires on their smartphone, wear the accelerometer, and undergo randomization\n* insufficient PA (i.e., not meeting current PA guidelines) but report intentions to increase their PA over the next 6 months\n* self-reported ability to ambulate without assistance\n* English as a primary language\n\nExclusion Criteria:\n\n* Individuals that are unwilling or unable to obtain medical clearance (if needed)\n* have received a diagnosis of mild cognitive impairment or ADRD\n* concurrently participating in another study involving PA or weight loss\n* planning to have surgery or relocate within the next 9 months","60 Years",{"count":91,"type":22},148,[25],"The goal of this clinical trial is to evaluate whether different approaches to action planning can promote physical activity (PA) habits, increase PA behavior, and improve cognitive functioning in older adults who are currently inactive or insufficiently active.\n\nThe main questions it aims to answer are:\n\n1. Does a trial-and-error approach to PA action planning lead to greater improvements in PA habits, PA behavior, and cognitive functioning compared to standard PA planning or non-PA planning?\n2. Does greater consistency and successful enactment of action plans result in more substantial changes in PA habits, behavior, and cognitive functioning?\n\nResearchers will compare three groups to determine which planning approach yields superior outcomes.:\n\n1. Non-PA planning (generic weekly planning)\n2. PA planning (weekly planning for PA)\n3. PA trial-and-error planning (weekly PA plans followed by preferred plan adoption)\n\nParticipants will:\n\n1. Wear Fitbit monitors continuously for 9 months to track PA behavior\n2. Complete mobile cognitive assessments daily for 7 days before the intervention, monthly during the intervention, and at follow-up\n3. Create action plans and report on PA habits, intentions, and plan enactment weekly during the intervention and at follow-up",[95,96,31],"Physical Activity","Cognition",[98,95,96,99,100],"Action Planning","Habit","Older Adults","2026-03-09",{"date":103,"type":40},"2026-03-11",{"date":42,"type":22},{"date":106,"type":22},"2028-07",{"name":108,"class":47},"University of North Carolina, Greensboro",{"id":110,"slug":111,"hasResults":11,"nctId":112,"briefTitle":113,"officialTitle":114,"acronym":115,"eligibilityCriteria":116,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":23,"phases":119,"briefSummary":120,"conditions":121,"keywords":123,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":80},"100589081","incentives-and-reminders-to-improve-long-term-medication-adherence-inmind-100589081","NCT06949774","INcentives and ReMINDers to Improve Long-term Medication Adherence (INMIND)","INcentives and ReMINDers to Improve Long-term Medication Adherence","INMIND","Inclusion Criteria:\n\n* Male and female clients age 18 and older.\n* Started ART at Mildmay or another clinic within the preceding 2 months\n* Able to speak and understand either English or Luganda.\n* Have their own cell phone or have consistent access to someone else's phone.\n* Willing to receive daily text messages for the 6 months of intervention duration.\n* Willing and able to use the WisePill device distributed for adherence verification for the duration of the study.\n\nExclusion Criteria:\n\n* Not mentally fit to consent.\n* Language other than Luganda or English.\n* Not willing to consistently use the Wisepill device for adherence measurement.",{"count":118,"type":22},550,[25],"Low medication adherence when initiating antiretroviral treatment (ART) is a key barrier to HIV virologic suppression, resulting in avoidable cases of drug resistance, death, and viral transmission. Routinized pill-taking can lead to successful long-term ART adherence, and short-term behavioral economics-based supports are a novel way to overcome the limited success of existing routinization interventions. This study proposes to test this combined approach for promoting long-term ART adherence using a Stage III Sequential, Multiple Assignment, Randomized Trial (SMART) design in one of the largest HIV clinics in Uganda to identify the most cost-effective adaptive intervention that if found effective is generalizable to other settings and other chronic diseases.",[122,62,31],"HIV\u002FAIDS",[124,125],"Behavioral: Daily Text Messages","Behavioral: Incentivization based on","2025-09-04",{"date":128,"type":40},"2025-09-11",{"date":130,"type":40},"2025-04-02",{"date":132,"type":22},"2029-10-31",{"name":134,"class":47},"RAND"]