[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"empowerment\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:empowerment":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,53,87,122,149,176],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":31,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100543973","evaluation-of-reacts-in-an-intervention-to-improve-nutrition-hygiene-and-sexual-and-reproductive-health-services-100543973",false,"NCT06362837","Evaluation of REACTS-IN, an Intervention to Improve Nutrition, Hygiene, and Sexual and Reproductive Health Services","Realizing Gender Equality, Attitudinal Change & Transformative Systems in Nutrition (REACTS-IN)","REACTS-IN","Inclusion Criteria:\n\n(i)Women:\n\n* 15-49 y of age\n* biological mother of child in the home who is 0-5.9, 6-23.9, or 24-59.9 months\n* has lived in the community for at 12 months\n\n(ii) Husbands\u002Fpartners:\n\n* no age limit\n* lives in the home with index woman\n* has lived in community for at least 12 months\n\n(iii) Adolescents:\n\n* 10-19 years\n* male or female\n* has been in target school for at least 6 months\n* lives in the target community\n\n(iv) Children:\n\n* 0-5.9, 6-23.9, or 24-59.9 months\n\nExclusion Criteria:\n\n(i) Children:\n\n* no limitation on normal diet or growth (birth defects, illnesses)","ALL",{"count":19,"type":20},13500,"ESTIMATED","INTERVENTIONAL",[23],"NA","This is an independent evaluation of World VIsion's 7-year quasi-experimental intervention to improve nutrition, nutrition-related rights and gender equality for women, adolescent girls, and children under five years of age in rural Bangladesh, Kenya, and Tanzania. The evaluation will collect baseline, midline, and end-line data from intervention communities, schools, and health facilities. Only baseline and endline will be collected on the comparison communities. The evaluation objectives are to test if the intervention improved indicators for (i) child anthropometry, (ii) maternal and child dietary practices, (iii) women's empowerment, and (iv) equitable health service access for nutrition and sexual and reproductive needs. The evaluation analysis will take into account gender differences in the indicators.",[26,27,28,29,30],"Stunting","Gender Equality","Acceptability of Health Care","Diet; Deficiency","Empowerment",[32,33,34,35,36,37,38,39],"nutrition","gender equity","health services","sexual and reproductive rights","dietary diversity","anthropometry","sexual and reproductive health services","WASH","RECRUITING","2026-04-27",{"date":43,"type":44},"2026-04-29","ACTUAL",{"date":46,"type":44},"2024-09-01",{"date":48,"type":20},"2029-12-31",{"name":50,"class":51},"McGill University","OTHER",3,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":61,"sex":17,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":4,"studyType":21,"phases":66,"briefSummary":67,"conditions":68,"keywords":71,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":86},"100626778","physical-inactivity-among-patients-with-cardiovascular-risk-100626778","NCT07440056","Physical Inactivity Among Patients With Cardiovascular Risk","Physical Inactivity Among Patients With Cardiovascular Risk: Proportion, Associated Factors, Perceived Barriers, and Effectiveness of an Intervention for Improvement at Government Primary Medical Care Institutions in Gampaha District","INSPIRE-PA","Inclusion Criteria:\n\n1. Patients permanently residing in Gampaha district for six months or more\n2. Patients registered and followed up at medical clinics in the same state sector PMCIs in Gampaha district, for a duration of three months or more\n\nExclusion Criteria:\n\n1. Pregnant mothers with any intermediate risk factor of chronic NCDs, followed up at state PMCIs in Gampaha district\n2. Patients diagnosed with atherosclerotic cardiovascular disease (ASCVD) (e.g. Coronary heart disease, Cerebrovascular disease, Peripheral artery disease, Aortic atherosclerotic disease) followed up at state sector primary medical care institutions in Gampaha district.\n3. Patients already diagnosed and on treatment for diabetes mellitus, any type of cancer and any chronic respiratory disease (e.g. Asthma, chronic obstructive pulmonary disease) followed up at state sector primary medical care institutions in Gampaha district, as their physical activity level and their knowledge on it may have changed following the diagnosis\n4. Patients with impaired cognitive functions (confirmed with medical records), as they are unable to report accurate responses independently.\n5. Patients who have undergone any surgical procedure within the last three months (confirmed by clinical documentation)\n6. Patients who have had any debilitating illness during the preceding week limiting their physical activity during the period of illness\n7. Patients who plan to change\u002Fchange their place of residence or shift their treatment follow-up from a state-sector PMCI to the private sector or any other treatment modality (e.g: Ayurveda) within the next six months",true,"35 Years","65 Years",{"count":65,"type":20},192,[23],"The goal of this clinical trial is to learn if newly developed intervention package works to improve physical activity level among patients with intermediate cardiovascular risk factors. The main questions it aims to answer are:\n\nDoes the INSPIRE-PA intervention increase the level of physical activity among participants with intermediate cardiovascular risk factors?\n\n* What changes occur in physical activity level, BMI and blood pressure following participation in the intervention?\n* Are there any challenges, barriers, or unintended effects experienced by participants during the intervention period?\n* Researchers will compare the INSPIRE-PA intervention to usual care to determine whether the empowerment-based strategy is effective in improving physical activity levels and reducing cardiovascular risk among patients attending government primary medical care Iinstitutions.\n\nParticipants will:\n\n* Participate in the INSPIRE-PA program for 6 months\n* Attend scheduled follow-up visits at the primary medical care institution (e.g., every 2-4 weeks)for counselling, evaluation of physical activity level, and assessment of cardiovascular risk indicators\n* Engage in structured physical activity as recommended in the intervention package\n* Record their daily physical activity and any challenges or barriers in a physical activity logbook or diary\n* Undergo periodic measurements such as blood pressure, weight, waist circumference, and other relevant clinical assessments",[69,70,30],"Physical Activities","Cardiovascular (CV) Risk",[72,73,74,75],"Physical activity","primary care","behavioural intervention","level of physical activity improvement","NOT_YET_RECRUITING","2026-02-24",{"date":79,"type":44},"2026-02-27",{"date":81,"type":20},"2026-04-01",{"date":83,"type":20},"2026-09-30",{"name":85,"class":51},"University of Colombo",1,{"id":88,"slug":89,"hasResults":11,"nctId":90,"briefTitle":91,"officialTitle":91,"acronym":92,"eligibilityCriteria":93,"healthyVolunteers":61,"sex":17,"minAge":94,"maxAge":95,"enrollmentInfo":96,"targetDuration":4,"studyType":21,"phases":98,"briefSummary":100,"conditions":101,"keywords":106,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":113,"lastUpdatePostDateStruct":114,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":120,"locationsCount":86},"100587883","phase-2-cultural-adaptation-of-a-web-based-app-myplan-thailand-to-empower-and-support-friends-and-family-of-intimate-partner-violence-survivors-100587883","NCT06934174","Cultural Adaptation of a Web-Based App (myPlan Thailand) to Empower and Support Friends and Family of Intimate Partner Violence Survivors","IPV","Inclusion Criteria:\n\n* being female or males who have a female friend currently (past 6 months) experiencing IPV\n* Thai speaking\u002Freading\n* At least 18 years old\n* Have access to a safe smart-phone or computer with internet\n* Have safe email address\n* Living in Thailand\n\nExclusion Criteria:\n\n* Cannot speak\u002Freading Thai\n* Less than age 18 years old\n* Cannot access to a safe smartphone or computer with internet\n* Not living in Thailand","18 Years","60 Years",{"count":97,"type":20},100,[99],"PHASE2","This research will support and empower friends\u002Ffamily (F\u002FF) of intimate partner violence (IPV) survivors in Thailand, where IPV is critical and common, and survivors first and foremost seek help for abuse from their F\u002FF. myPlan app (www.myPlanapp.org) is a free mobile evidence-based intervention app to prevent IPV. The app was first developed in the United States (US) and has been disseminated to high-income countries (e.g., New Zealand, Canada, Australia) and lowincome (Kenya). One new hope for improving survivors' psychological and well-being is adapting and introducing the myPlan app for the concerned friends\u002Ffamily who support survivors in Thailand.\n\nTherefore, the propose of this longitudinal research study, Cultural Adaptation of a Web-Based App (myPlan Thailand) to Empower and Support Friends\u002FFamily of Intimate Partner Violence Survivors in Thailand, will have two consecutive phases with three aims: 1) To tailor the myPlan app content for concerned F\u002FF members of Thai IPV survivors, 2) To integrate the adapted myPlan app content for concerned F\u002FF members of Thai IPV survivors, 3) To test the feasibility and acceptability of the adapted myPlan app with concerned F\u002FF members of Thai IPV survivors. Phase 1 (Year 1-2) will achieve aim 1-2 to tailor the myPlan app with Thai survivors and friends\u002Ffamily. The investigators will review current content and conduct in-depth interviews with survivors and concerned F\u002FF members on social norms associated with IPV, informal support systems and the role\u002Fresponsibility in helping survivors, safety strategies used by concerned F\u002FF members and negative consequences for both survivor and F\u002FF member providing support. Moreover, in phase 1, the adapted content will be pilot tested with concerned F\u002FF members of survivors by using cognitive techniques and theater-testing methodology.\n\nPhase 2 (Year 3-4) will achieve aim 3 to test the feasibility and acceptability of the adapted myPlan app with F\u002FF. The investigators will conduct a two-group RCT design with concerned F\u002FF member randomized to receive a) the myPlan app for F\u002FF member, or b) standard usual-care safety planning information. Primary outcomes for F\u002FF members include change in knowledge and attitudes towards IPV and F\u002FF empowerment to plan and take safety support survivor. Secondary outcomes will examine change in F\u002FF' distress, frustration and consequences for supporting the survivor. This phase will also collect feasibility and acceptability data to informed a planned R01 submission in Year 3 of the study. The K43 application outlines a four-year plan to support a candidate who is a nursing instructor with 15 years of work in diverse projects, settings, and disciplines; which positions her for a successful career as an independent researcher in research field of intimate partner violence. The career development plan provides a sequence of carefully selected training and mentoring experiences, including coursework to increase research capacity, leadership skills, mentored research leading to a R01 proposal, peer reviewed publications, and professional networking, that will catapult this research to the next level of research achievement. The team will be a collaboration between the Boromarajonani College of Nursing Khon Kaen (BCNKK), Khon Kaen One Stop Crisis Center (OSCC), Johns Hopkins University (JHU), Notre Dame of Maryland University (NDM), and Auckland University of Technology (AUT), New Zealand.",[102,103,30,104,105],"Intimate Partner Violence (IPV)","Social Support","mHealth","Effectiveness",[107,108,109,110,111,112],"Intimate partner violence","Friends\u002FFamily memeber","Safety","Social support","mHealth intervention","Thailand","2025-05-08",{"date":115,"type":44},"2025-05-13",{"date":117,"type":44},"2025-04-17",{"date":119,"type":20},"2026-06",{"name":121,"class":51},"Boromarajonani College of Nursing, Khon Kaen",{"id":123,"slug":124,"hasResults":11,"nctId":125,"briefTitle":126,"officialTitle":126,"acronym":127,"eligibilityCriteria":128,"healthyVolunteers":11,"sex":17,"minAge":129,"maxAge":4,"enrollmentInfo":130,"targetDuration":4,"studyType":21,"phases":132,"briefSummary":133,"conditions":134,"keywords":4,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":139,"lastUpdatePostDateStruct":140,"startDateStruct":142,"completionDateStruct":144,"leadSponsor":146,"locationsCount":148},"100340314","empowerment-and-mobile-technology-in-the-control-of-cardiovascular-risk-factors-in-patients-with-ischemic-stroke-100340314","NCT03710902","Empowerment and Mobile Technology in the Control of Cardiovascular Risk Factors in Patients With Ischemic Stroke","CARDIOSTROKE","Inclusion Criteria:\n\n* Ischemic stroke or transient ischemic attack (ABCD2 score ≥3)\n* Age ≥40 years\n* Pre-existing or newly diagnosed hypertension\n* Informed consent from the patient or legal representative\n\nExclusion Criteria:\n\n* Known high-risk source of cardioembolism\n* Known indication for anticoagulation\n* Contraindication for anticoagulation\n* Pacemaker\n* Non-compliance to study interventions as judged by the investigator\n* Serious condition hampering the study conduct","40 Years",{"count":131,"type":20},405,[23],"The CARDIOSTROKE is a randomized trial comparing mobile-device assisted control of hypertension together with screening of occult atrial fibrillation to standard care in patients with recent ischemic stroke or transient ischemic attack.",[135,136,137,138,30],"Ischemic Stroke","Transient Ischemic Attack","Atrial Fibrillation","Hypertension","2025-03-18",{"date":141,"type":44},"2025-03-20",{"date":143,"type":44},"2018-10-17",{"date":145,"type":20},"2028-09",{"name":147,"class":51},"Jukka Putaala",4,{"id":150,"slug":151,"hasResults":11,"nctId":152,"briefTitle":153,"officialTitle":154,"acronym":4,"eligibilityCriteria":155,"healthyVolunteers":61,"sex":156,"minAge":157,"maxAge":158,"enrollmentInfo":159,"targetDuration":4,"studyType":21,"phases":161,"briefSummary":162,"conditions":163,"keywords":166,"overallStatus":76,"whyStopped":4,"lastUpdateSubmitDate":168,"lastUpdatePostDateStruct":169,"startDateStruct":171,"completionDateStruct":173,"leadSponsor":174,"locationsCount":4},"100522378","strengthening-contraceptive-counseling-services-research-protocol-for-a-multi-phase-complex-intervention-in-pakistan-and-nigeria-100522378","NCT06081842","Strengthening Contraceptive Counseling Services: Research Protocol for a Multi-phase Complex Intervention in Pakistan and Nigeria","Strengthening Contraceptive Counseling Services, a Multi-country Study Trial","Inclusion Criteria:\n\n1. Client comes to the family planning clinic with the intention to 1.a. use contraception for the first time in her life (new user), or 1.b. switch from a contraceptive method to another one (switching user), or 1.c. resume a method after not using any in the prior three months (lapse user), or 1.d. discontinue a modern method (discontinuing user);\n2. Client is not coming for the resupply of a currently used method, such as pills or injectables;\n3. Client has the intention to continue her follow-up at the health center during the duration of study follow-up;\n4. Client does not participate in another study; and\n5. Client provides informed consent.\n\nExclusion Criteria:\n\nNot willing to participate in the complete duration of the trial","FEMALE","15 Years","49 Years",{"count":160,"type":20},7920,[23],"High-quality contraceptive counseling can strengthen global efforts to reduce the unmet need for and suboptimal use of modern contraceptives. This study aims to identify a package of contraceptive counseling interventions for Pakistan and Nigeria designed to strengthen existing contraceptive services and determine its effectiveness in increasing clients' level of decision-making autonomy and meeting their contraceptive needs.",[164,30,165],"Contraception","Decision Making",[167],"Family Planning, Counselling, choice","2023-10-07",{"date":170,"type":44},"2023-10-13",{"date":172,"type":20},"2023-11",{"date":119,"type":20},{"name":175,"class":51},"World Health Organization",{"id":177,"slug":178,"hasResults":11,"nctId":179,"briefTitle":180,"officialTitle":180,"acronym":181,"eligibilityCriteria":182,"healthyVolunteers":61,"sex":17,"minAge":94,"maxAge":183,"enrollmentInfo":184,"targetDuration":4,"studyType":21,"phases":186,"briefSummary":187,"conditions":188,"keywords":193,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":204,"lastUpdatePostDateStruct":205,"startDateStruct":207,"completionDateStruct":209,"leadSponsor":211,"locationsCount":86},"100297781","stop-diabetes---knowledge-based-solutions-100297781","NCT03156478","STOP DIABETES - Knowledge-based Solutions","StopDia","Inclusion Criteria:\n\n* age of 18-70 years\n* 12 points or more in the Finnish diabetes risk score or previous gestational diabetes or repeated impaired fasting glucose (IFG) (fasting plasma glucose level 6,1 - 6,9 mmol\u002Fl) or impaired glucose tolerance (2-hour glucose level 7,8 - 11,0 mmol\u002Fl in oral glucose tolerance test)\n* living in the hospital district of Northern Savo, Päijät-Häme or South Karelia\n* possibility to use computer, smartphone or tablet with internet connection\n* having own self-phone number\n* adequate Finnish language skill\n\nExclusion Criteria:\n\n* type 1 or 2 diabetes\n* pregnancy or breastfeeding\n* current cancer or less than 6 months from the end of cancer treatment","70 Years",{"count":185,"type":20},10000,[23],"The aim of the Stop Diabetes - Knowledge based solutions (StopDia) consortium project (University of Eastern Finland, National Institute for Health and Welfare, and Technical Research Centre of Finland) is to develop and test approaches to identify individuals at increased risk of type 2 diabetes and to empower them in adopting and maintaining a healthy lifestyle by combining individual and environment level strategies into a dual-process approach targeting deliberative and automatic processes of behavior. We also aim to identify barriers and facilitators of adopting a healthy lifestyle in the society, create a model for the prevention of type 2 diabetes by joint actions of health care, third sector, and other societal actors, and develop methods to monitor the cost-effectiveness of these actions. We will carry out a 1-year randomized controlled trial on the effects of among 10 000 individuals aged 18-70 years at increased risk of type 2 diabetes living in Finland. The participants will be randomized into the control group, the digital lifestyle intervention group, or the combined digital and face-to-face lifestyle intervention group. The aim of the interventions is to enhance diet quality, increase physical activity, decrease body weight, and improve glucose tolerance in individuals at increased risk of type 2 diabetes.",[189,190,191,192,30],"Type2 Diabetes","Life Style","Diet Habit","Physical Activity",[194,195,196,197,72,198,199,200,201,202,203],"Prevention","Digital solutions","Type 2 diabetes","Life style modification","Healthy diet","Health economics","Environmental choice architecture","Socio-economic facilitators","Socio-economic barriers","Wellbeing","2017-05-15",{"date":206,"type":44},"2017-05-17",{"date":208,"type":44},"2017-04-10",{"date":210,"type":20},"2037-12",{"name":212,"class":51},"University of Eastern Finland"]