[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sedentary-behaviour\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sedentary-behaviour":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,85],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100646224","feasibility-of-a-habit-based-intervention-to-reduce-sedentary-behaviour-in-cancer-survivors-100646224",false,"NCT07694479","Feasibility of a Habit-Based Intervention to Reduce Sedentary Behaviour in Cancer Survivors","A Habit-Based Intervention to Reduce Sedentary Behaviour in Cancer Survivors: A Feasibility Study","Inclusion Criteria:\n\n* 18 years of age or older\n* have been diagnosed with localized or asymptomatic metastatic cancer of any type\n* completed primary cancer treatment\n* self-report being sedentary for more than or equal to 8 hours per day\n* access to the internet and a device with a webcam\n* able to complete the study in English\n\nExclusion Criteria:\n\n* presence of other primary or recurrent invasive cancer\n* having experienced a fall in the last 12 months\n* not residing in Canada\n* participating in other behaviour change interventions\n* using a gait aid device","ALL","18 Years",{"count":19,"type":20},30,"ESTIMATED","INTERVENTIONAL",[23],"NA","Cancer and its treatments are associated with long-term side effects including lowered physical strength and quality of life. Decreasing sedentary behaviour improves health outcomes in cancer survivors. Habit-based programs aimed at lowering sedentary behaviour have been successful in decreasing sedentary behaviour in other populations. However, limited clinical trials aimed at lowering sedentary behaviour have recruited cancer survivors, and none are exclusively based on Habit Theory.\n\nThe primary goal of this clinical trial is to test the feasibility of an 8-week, habit-based program to lower sedentary behaviour in cancer survivors. Sedentary behaviour refers to low-energy activities performed during waking hours in a seated, reclined or laid down position. Secondarily, this clinical trial aims to examine changes in sedentary behaviour, physical strength, habit, and quality of life.\n\nEnrolled participants will be assigned to a sedentary behaviour or active control group. The sedentary behaviour group will receive 8 weekly sheets consisting of tips recommending to lower sedentary behaviour. Tips will be individualized to participants' lifestyles, and will consider their cancer-specific and other physical limitations. Participants in the sedentary behaviour group will also meet with the researcher once a week for a check-in session for more individualized tips and progressions. The active control group will receive the Canadian 24-hour Movement Guidelines, and a handout highlighting the benefits of lowering sedentary behaviour. Both groups will be provided with wearable activity monitors (Fitbits).",[26,27],"Cancer","Sedentary Behaviour",[29,30,31,32,33,34,35],"cancer survivorship","quality of life","physical function","cancer","remote delivery","feasibility","sedentary behaviour intervention","RECRUITING","2026-07-02",{"date":39,"type":40},"2026-07-10","ACTUAL",{"date":42,"type":40},"2025-12-30",{"date":44,"type":20},"2026-09",{"name":46,"class":47},"University of Toronto","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":57,"sex":16,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":21,"phases":62,"briefSummary":63,"conditions":64,"keywords":65,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":4},"100595732","reducing-and-breaking-up-school-related-sedentary-behaviour-among-adolescents-using-co-creation-100595732","NCT07036276","Reducing and Breaking up School-related Sedentary Behaviour Among Adolescents Using Co-creation","Reducing and Breaking Up School-related Sedentary Behaviour Among Adolescents Using Co-creation","G072223N","Inclusion Criteria:\n\n* Secondary schools need to have at least 150 pupils in the first two grades (Grade 7 and 8).\n\nExclusion Criteria:\n\n* None",true,"11 Years","15 Years",{"count":61,"type":20},600,[23],"Adolescents spend the majority of the day sedentary, especially at school whilst sitting in class and at home when performing school-related tasks. As high levels of sedentary time are associated with adverse health effects, effective interventions are needed. To improve effectiveness, literature recommends a co-creative approach in which adolescents and other key stakeholders (such as teachers) are actively involved in the choice and development of intervention strategies. Therefore, this project aims to co-adapt a previously co-created intervention targeting adolescents' school-related sedentary behaviour. Further, the effect of this co-adapted intervention on adolescents' sedentary behaviour and related determinants, sleep, and mental wellbeing will be evaluated via a three-arm clustered controlled trial, including a co-adaptation intervention arm, a standard intervention arm (including schools that were not involved in co-adapting the intervention) and a control arm (continuing their curriculum as usual). By comparing these three arms, the investigators can evaluate the added value of co-creation compared to not involving adolescents or stakeholders in the development of an intervention. Lastly, the investigators will conduct a process evaluation of (1) the co-adaptation approach used to adapt the co-created intervention and (2) the implementation of both the co-adapted and standard interventions. Studies that evaluate co-created interventions are scarce. However, if such interventions prove to be more effective, this approach could be promising to change adolescents' health behaviour.",[27],[66,67,68,69,70,71,72,73,74],"Adolescents","Youth","Student","School","Classroom","Sedentary behaviour","Participatory research","Co-creation","Co-adaptation","NOT_YET_RECRUITING","2025-06-23",{"date":78,"type":40},"2025-06-25",{"date":80,"type":20},"2025-09-01",{"date":82,"type":20},"2026-06-30",{"name":84,"class":47},"University Ghent",{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":91,"eligibilityCriteria":92,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":93,"targetDuration":4,"studyType":21,"phases":95,"briefSummary":96,"conditions":97,"keywords":99,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":121},"100525631","effectiveness-of-the-rise-intervention-100525631","NCT06124248","Effectiveness of the RISE Intervention","RISE Intervention: Heading to Sustainable Movement Behavioural Change in People with Stroke","RISE","Inclusion Criteria:\n\nIn order to be eligible to participate in the baseline measurement of the intervention study, a subject must meet all of the following criteria:\n\n1. Aged 18 years or older;\n2. All types of first-ever stroke diagnosed in hospital within six months before start of the RISE intervention;\n3. Able to walk independently, as defined by a Functional ambulation categories score of at least 3;\n4. Independent regarding activities of daily living pre-stroke, as defined by a Barthel Index score of \\>18;\n5. Discharged to the home-setting;\n6. Not participating in a physical rehabilitation program lasting ≥ 3 months;\n7. Given their written informed consent.\n\nExclusion Criteria:\n\nA potential subject will be excluded from participation in this study if:\n\n1. The participant has insufficient knowledge or is cognitively unable to understand the Dutch language of the intervention content;\n2. The participant has severe comorbidities that withhold that person from safely reducing and interrupting their sedentary time (e.g. sever pulmonary diseases, hart failure or malignity's) as determined with the Physical Activity Readiness Questionnaire;",{"count":94,"type":20},1000,[23],"Study aim:\n\nPrimarily, to investigate the effectiveness of the RISE blended behaviour change intervention in people with a first stroke to prevent major adverse cardiovascular events (i.e., recurrent stroke or TIA, acute coronary events and cardiovascular death, MACE) after 1 year follow-up compared to standard care, and cost-effectiveness. For this aim, 376 persons are enrolled in the experimental group and 376 in the control group. Considering loss to follow up, it is expected that around 950-1000 patients need to be included during baseline measurement in total.\n\nAdditionally, to determine the effectiveness of the RISE intervention on reducing sedentary behaviour after discharge from acute hospital care in community dwelling people with a first-ever stroke, who have a sedentary movement behavioural pattern (so called 'sedentary prolongers' and 'sedentary movers') in comparison to usual care, at the end of the intervention period (T1). For this aim, 59 persons are enrolled in the experimental group and 59 in the control group. Considering loss to follow up, it is expected that around 197 patients need to be included during baseline measurement in total.\n\nWho can participate? People aged over 18, who return home after acute care with a first-ever stroke, who are independent in walking with or without a walking aid, will be included in the RISE intervention study.\n\nWhat does the study involve? In this clinical randomized controlled trial, participants with first-ever stroke and a sedentary movement pattern will be included and randomly assigned to either the experimental group who will receive RISE intervention and usual care or the control group who will receive usual care. Primary and secondary outcome will be measured at baseline, post-treatment and six, nine and 12 months post-randomisation.",[27,98],"Stroke",[100,101,102,103,104,105,71,98,106,107,108,109,110,111],"Physical activity","Cardiovascular diseases","Sedentary time","Sitting time","Movement behaviours","Behaviour change","Secondary prevention","Costs","Cost analysis","Cost effectiveness","MACE","Prevention","2024-09-27",{"date":114,"type":40},"2024-10-01",{"date":116,"type":40},"2023-11-29",{"date":118,"type":20},"2027-04",{"name":120,"class":47},"UMC Utrecht",21]