[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"web-based-intervention\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:web-based-intervention":102},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,53,90],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":33,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100578742","enhancing-maternal-vaccine-knowledge-and-uptake-the-introduce-programme-trial-100578742",false,"NCT06815250","Enhancing Maternal Vaccine Knowledge and Uptake: The InTroDuce-Programme Trial","Effectiveness of the Influenza and Tdap (Tetanus, Diphtheria, Acellular Pertussis) Vaccination Educational and Learning Module (InTroDuce-Programme) in Improving Knowledge and Future Uptake of Vaccination Among Pregnant Mothers in Primary Care Clinics: A Randomised Control Trial Secondary IDs","Inclusion Criteria:\n\n* Pregnant women aged 18 years and older\n* Before or equal to 32 weeks of gestation as we need to follow-up the patients again at 36 weeks of gestation before delivery occurs.\n* Able to understand and consent to participation in the study.\n\nExclusion Criteria:\n\n* Pregnant women with severe anaphylactic or allergic reactions to previous dose of influenza or Tdap vaccination.\n* Non-Malaysian",true,"FEMALE","18 Years",{"count":20,"type":21},351,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this InTroDuce-Programme interventional trial aims to test whether a web-based educational program can improve pregnant women's knowledge about Influenza and Tdap vaccinations and increase their intention to get vaccinated in the future. The main questions it aims to answer are:\n\nDoes the InTroDuce-Programme increase knowledge and future intention of pregnant mothers to get vaccinated against Influenza and Tdap? How does demographic factors, attitudes and barriers affect vaccination decisions among pregnant mothers?\n\nResearchers will compare InTroDuce-Programme to standard care (routine antenatal care) to see if InTroDuce-Programme works to improve knowledge and future intention of pregnant mothers to be vaccinated against Influenza and Tdap. Participants will:\n\nReceive the web-based educational module (InTroDuce-Programme), which covers the importance, safety, and effectiveness of vaccinations, as well as addressing common concerns.\n\nBe followed up one month after the intervention. Answer questionnaires before and after the intervention to measure changes in vaccination knowledge and future intention to get vaccinated",[27,28,29,30,31,32],"Vaccination Uptake","Knowledge","Tetanus, Diphtheria and Acellular Pertussis Vaccination","Influenza","Web Based Intervention","Vaccine Knowledge",[34,35,36,37,38,39],"Influenza vaccination","Tdap vaccination","Educational module","Pregnant mothers","Vaccine knowledge","Vaccine uptake","RECRUITING","2026-04-27",{"date":43,"type":44},"2026-05-01","ACTUAL",{"date":46,"type":44},"2026-01-13",{"date":48,"type":21},"2026-06",{"name":50,"class":51},"Universiti Putra Malaysia","OTHER",4,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":16,"sex":61,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":4,"studyType":22,"phases":66,"briefSummary":67,"conditions":68,"keywords":74,"overallStatus":80,"whyStopped":4,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":4},"100596321","effect-of-a-mobile-based-hydration-tracking-program-on-knowledge-attitudes-and-behaviors-in-older-adults-100596321","NCT07043933","Effect of a Mobile-Based Hydration Tracking Program on Knowledge, Attitudes, and Behaviors in Older Adults","The Effect of a Mobile-Compatible Web-Based Hydration Tracking Program on Hydration Knowledge, Attitudes, and Behaviors in Older Adults: A Randomized Controlled Trial","SIVI","Inclusion Criteria:\n\n* Daily water and other fluid intake below the recommended levels: less than 2.0 L\u002Fday for older adult men and less than 1.6 L\u002Fday for older adult women (ESPEN Guidelines, 2024) Aged between 65 and 84 years Having at least a primary school education Having sufficient motor skills Having the cognitive capacity, willingness, and experience necessary to use technology Willing to participate in the study Owning a mobile phone compatible with the application Having prior experience using mobile applications\n\nExclusion Criteria:\n\n* Diagnosed with moderate or severe cognitive impairment (MMSE \\\u003C 24)\n* Having vision or hearing impairments that prevent participation\n* Diagnosed with advanced stage chronic kidney disease (Stage 4-5)\n* Diagnosed with congestive heart failure (NYHA class III-IV)\n* Being on fluid restriction by medical order\n* Having a diagnosed urinary incontinence condition\n* Having a diagnosis of terminal illness or active cancer treatment\n* Participating in another hydration-related clinical study\n* Experiencing a disruption in app usage for one week or longer for any reason","ALL","65 Years","85 Years",{"count":65,"type":21},70,[24],"This randomized controlled trial aims to evaluate the impact of a mobile-friendly, web-based hydration tracking application (named \"SIVI\") on hydration-related knowledge, attitudes, and behaviors in older adults. Inadequate fluid intake is a common and modifiable risk factor for dehydration in the elderly, leading to increased morbidity, hospitalizations, and functional decline. However, many older individuals forget to drink fluids or face barriers such as fear of incontinence, mobility limitations, or cognitive challenges.\n\nThis study will include 70 community-dwelling older adults aged 65-84 years, recruited from a Family Health Center. Participants will be randomly assigned to either the intervention or control group. The intervention group will use the SIVI application for two months. The app is specially designed for older adults and includes features such as personalized fluid goals, reminders, hydration education modules, feedback, and a user-friendly interface with large fonts and high contrast. Participants will log their daily fluid intake, receive motivational messages, and access videos and information about healthy hydration habits. A water bottle will be provided to standardize measurement across groups.\n\nThe control group will receive only routine care. Both groups will complete questionnaires measuring demographics, hydration knowledge, attitudes, behaviors, and fluid consumption habits at baseline, one month, and two months.\n\nData collection will be conducted face-to-face by the researcher, and analysis will be performed using SPSS 22.0. Statistical tests will include descriptive statistics, Shapiro-Wilk for normality, chi-square for categorical data, and t-tests and ANOVA for comparisons over time.\n\nThe results are expected to show that the SIVI application improves older adults' hydration knowledge, fosters positive attitudes, and promotes healthy fluid intake behaviors, thus supporting self-management of hydration and potentially reducing dehydration-related health risks.",[69,70,71,72,73,31],"Dehydration","Older Adults (65 Years and Older)","Hydration Status","Self-management Behavior","Mobile Application",[69,75,76,77,78,79],"Aged","Hydration","Older Adults","Mobile Applications","Self-Management","NOT_YET_RECRUITING","2025-06-21",{"date":83,"type":44},"2025-06-29",{"date":85,"type":21},"2025-10-01",{"date":87,"type":21},"2026-02-01",{"name":89,"class":51},"Ezgi Atasoy",{"id":91,"slug":92,"hasResults":11,"nctId":93,"briefTitle":94,"officialTitle":95,"acronym":4,"eligibilityCriteria":96,"healthyVolunteers":11,"sex":61,"minAge":62,"maxAge":4,"enrollmentInfo":97,"targetDuration":4,"studyType":22,"phases":99,"briefSummary":100,"conditions":101,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":105,"lastUpdatePostDateStruct":106,"startDateStruct":108,"completionDateStruct":110,"leadSponsor":112,"locationsCount":114},"100531250","web-based-nursing-intervention-to-promote-physical-activity-among-older-adults-with-coronary-heart-disease-100531250","NCT06197347","Web-based Nursing Intervention to Promote Physical Activity Among Older Adults With Coronary Heart Disease","Web-based Nursing Intervention to Promote Physical Activity Among Older Adults With Coronary Heart Disease: Protocol for a Mixed Method Pilot Study","Inclusion Criteria:\n\n* aged 65 years or older\n* agreement to participate in the study about 3 months post-hospitalization for a coronary bypass graft surgery or a percutaneous coronary intervention (as motivation to change behavior would be highest during this period)\n* no concurrent involvement in an intervention designed to increase their level of physical activity (e.g., a cardiac rehabilitation program, consultation with physical activity expert) during their participation in the project\n* an interest in increasing their level of physical activity post-hospitalization\n* fluency in French, spoken and written\n* living in the greater Montreal area\n* access to a computer connected to the Internet\n* no cognitive impairments according to the patient record (i.e., decreased or impaired complex attention, executive functions, learning abilities, memory or social skills)",{"count":98,"type":21},30,[24],"The purpose of this study is to develop and evaluate a web-based nursing intervention aimed at increasing physical activity in people aged 65 years and older with coronary heart disease.\n\nThis study aims to answer the following questions:\n\n1. What are the needs of older adults living with coronary heart disease in terms of a web-based nursing intervention to help them increase their level of physical activity?\n2. What is the acceptability (content, structure, usefulness) and feasibility (recruitment, retention, adherence, fidelity) of a web-based nursing intervention to support older adults living with coronary heart disease as they increase their level of physical activity?\n3. What are the preliminary effects of the web-based nursing intervention on the physical activity level and quality of life of older adults living with coronary heart disease?\n4. What are the qualitative impacts of the web-based nursing intervention as perceived by older adults on their physical activity level, quality of life, motivation, knowledge and self-efficacy?\n5. How can the preliminary effects of a web-based nursing intervention, developed in response to the needs of older adults living with coronary heart disease, be illustrated by its impacts as perceived by older adults post-intervention?\n\nA web-based nursing intervention was developed based on the needs of seniors living with coronary heart disease. 30 older adults living with heart disease will take part in the 8-week intervention. The effects of the intervention will be evaluated on the physical activity level, quality of life, knowledge, motivation and self-efficacy of older adults.",[77,102,103,104],"Web-based Intervention","Nursing","Healthy Lifestyle Habits","2024-11-27",{"date":107,"type":44},"2024-11-29",{"date":109,"type":44},"2024-06-01",{"date":111,"type":21},"2024-12",{"name":113,"class":51},"Centre hospitalier de l'Université de Montréal (CHUM)",1]