[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Hiroshima University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":234},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,53,79,112,138,160,184,211],{"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":32,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100633495","procedure-manual-based-simulation-training-to-improve-operating-room-nurses-core-competencies-100633495",false,"NCT07527429","Procedure Manual-Based Simulation Training to Improve Operating Room Nurses' Core Competencies","The Impact of Procedure Manual-Based Simulation Training on Operating Room Nurses' Core Competencies in a Cambodian National Hospital: A Quasi-Experimental Study","Inclusion Criteria:\n\n* Registered nurses who are appointed to work in the intraoperative phase of Cambodia-China Friendship Preah Kossamak Hospital.\n* Registered nurses at Cambodia-China Friendship Preah Kossamak Hospital who are willing to participate in the study.\n\nExclusion Criteria:\n\n* Registered Nurses Cambodia-China Friendship Preah Kossamak Hospital who are unable to participate in intervention requirements.\n* Registered Nurses Cambodia-China Friendship Preah Kossamak Hospital who are scheduled to participate in hospital mission assignments.",true,"ALL","18 Years",{"count":20,"type":21},49,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to evaluate the effectiveness of a procedure manual-based simulation training program in improving the core competencies of operating room nurses in a Cambodian national hospital. Operating room nurses play a critical role in maintaining patient safety, assisting the surgical team, and ensuring efficient surgical workflow.\n\nThis study will use a single-group quasi-experimental pre-post design. Baseline data will be collected before the intervention to assess operating room nurses' core competencies, interprofessional collaboration, job satisfaction, and surgical procedure duration.\n\nParticipants will receive structured educational sessions and simulation-based training based on standardized surgical procedure manuals. After the training phase, nurses will implement the procedure manuals during real surgical procedures for six weeks. End-line data will be collected to evaluate improvements in competency levels, teamwork, job satisfaction, and surgical efficiency.",[27,28,29,30,31],"Core Competency","Patient Safety","Interprofessional Collaboration","Surgical Outcome","Job Satisfaction",[33,34,35,36,37,38,29,39,31],"Simulation Training","Procedure Manual","Operating Room Nurses","Cambodia","Quasi-Experimental Study","Nursing Education","Surgical Outcomes","NOT_YET_RECRUITING","2026-04-13",{"date":43,"type":44},"2026-04-16","ACTUAL",{"date":46,"type":21},"2026-04-20",{"date":48,"type":21},"2027-03-31",{"name":50,"class":51},"Hiroshima University","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":22,"phases":62,"briefSummary":63,"conditions":64,"keywords":66,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":52},"100622517","post-stroke-nurse-led-rehabilitation-to-improve-functional-activity-and-community-participation-in-bangladesh-100622517","NCT07384650","Post-stroke Nurse-led Rehabilitation to Improve Functional Activity and Community Participation in Bangladesh","Post-discharge Nurse-led Rehabilitation to Improve Functional Activity and Community Participation Among Stroke-Patients in Bangladesh: A Randomized Controlled Trial","Inclusion Criteria:\n\n1. 18 years old and above, both males \\& females,\n2. Irrespective of the type of stroke and time of stroke,\n3. mRS 2-4 with disability on upper and\u002For lower limb(s)\n4. Physician advice on rehabilitation, and who needs assistive devices for ADL,\n5. Having a phone, and\n6. Willing to provide consent \\& participate in the study.\n\nExclusion Criteria:\n\n1. Participation in other clinical trials,\n2. Planning to receive institutional rehabilitation services, and\n3. Cannot communicate (having speech difficulties).",{"count":61,"type":21},166,[24],"Stroke causes various levels of disability which decreases physical function for a prolonged period. The purpose of this study is to evaluate the effectiveness of a nurse-led rehabilitation program including a multidisciplinary team focused on improving the functional ability among post-stroke patients in Bangladesh. A prospective, open-label (1:1) randomized controlled trial (RCT) will be conducted at the National Institute of Neuroscience \\& Hospital (NINS\\&H) in Dhaka, Bangladesh from January 2026 to September 2026. Participants will be the post-stroke patients who got discharged from NINS\\&H within 2 weeks after the onset of stroke and the family caregivers of the patients and meet the inclusion criteria. The sample size will be calculated based on G-Power analysis with a medium effect size and will be 166. The intervention will be designed to provide the 6-months Nurse-led rehabilitation program including a multidisciplinary team regarding self-care and the use of assistive devices. Assessment for rehabilitation will be performed by the multidisciplinary team with research nurses (RA nurses), physiotherapists (PT) and occupational therapists (OT). The control group will receive the usual care. The primary outcome is improved activity and participation measured by the Functional Independence Measurement (FIM). The secondary outcomes are improved motor function, self-efficacy, emotional status and participation ability. The endpoints will be compared at baseline, 3rd and 6th months. We assume that patients receiving rehabilitation education and assistive device progress to achieve an optimal level of independence, with improved motor function, emotional status and participation ability to re-integrate into society.",[65],"Stroke",[65,67,68,69],"rehabilitation","functional activity","participation","RECRUITING","2026-04-01",{"date":73,"type":44},"2026-04-07",{"date":75,"type":44},"2026-02-05",{"date":77,"type":21},"2026-10-31",{"name":50,"class":51},{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":22,"phases":89,"briefSummary":90,"conditions":91,"keywords":96,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":111},"100615991","evidence-based-nursing-to-reduce-adverse-events-regarding-ventilator-associated-pneumonia-pressure-injuries-and-central-line-bloodstream-infection-in-intensive-care-unit-in-bangladesh-100615991","NCT07299799","Evidence-Based Nursing to Reduce Adverse Events Regarding Ventilator Associated Pneumonia, Pressure Injuries and Central Line Bloodstream Infection in Intensive Care Unit in Bangladesh","Evidence-Based Nursing to Reduce Adverse Events Regarding Ventilator Associated Pneumonia, Pressure Injuries and Central Line Bloodstream Infection in Intensive Care Unit: A Quasi-experimental Study in Bangladesh","EBP in Nursing","Trial 1 \\& 2-\n\nInclusion Criteria:\n\nNurse\n\n* who is a registered nurse in Bangladesh.\n* who agrees to participate in this study and the EBP training.\n* who will stay at the ICU for 6 months. Patient\n* Irrespective of age and sex, participants must be at least 18 years old\n* Legal guardian of a patient consent to participation in the study\n\nExclusion Criteria:\n\nNurse\n\n* Who will not directly involve patient care in ICU. Patient\n* No exclusion criteria",{"count":88,"type":21},272,[24],"Quality of care is crucial for preventing adverse events such as infection in the intensive care units (ICUs). The most common ICU-acquired infections include pneumonia such as Ventilator Associated Pneumonia (VAP), Pressure Ulcer (PU), Medical Device Related Pressure Ulcer (MDRPU), and Central Line-Associated Bloodstream Infection (CLABSI). VAP, PU, and MDRPU are significant indicators of the quality of care, while CLABSI is a critical marker of healthcare quality in ICUs, as it is largely preventable through strict adherence to infection control protocols.\n\nVAP is a lung infection that occurs in patients receiving mechanical ventilation for more than 48 hours. A PU is defined as localized damage to the skin or underlying tissue caused solely by pressure, while MDRPUs may also result from friction or pressure from medical devices or other objects. CLABSI is a severe infection caused by improperly inserted or maintained central venous catheters, which underscores the need for stringent catheter management protocols.",[92,93,94,95],"Ventilator Acquired Pneumonia","Central Line Associated Blood Stream Infections (CLABSI)","Pressure Ulcer (PU)","Medical Device Related Pressure Ulcer (MDRPU)",[97,98,99,100,101,102],"evidence based practice","Nurses competency","Ventilator Associated Pneumonia","Pressure Ulcer","Central Line Bloodstream Infection","Medical Device Related Pressure Ulcer","2026-02-10",{"date":105,"type":44},"2026-02-11",{"date":107,"type":21},"2026-02-15",{"date":109,"type":21},"2026-05-30",{"name":50,"class":51},2,{"id":113,"slug":114,"hasResults":11,"nctId":115,"briefTitle":116,"officialTitle":116,"acronym":117,"eligibilityCriteria":118,"healthyVolunteers":16,"sex":119,"minAge":18,"maxAge":4,"enrollmentInfo":120,"targetDuration":4,"studyType":22,"phases":122,"briefSummary":123,"conditions":124,"keywords":127,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":131,"lastUpdatePostDateStruct":132,"startDateStruct":134,"completionDateStruct":136,"leadSponsor":137,"locationsCount":52},"100616828","impact-of-mhealth-education-on-hemoglobin-level-among-pregnant-women-with-anemia-in-rural-bangladesh-100616828","NCT07310680","Impact of mHealth Education on Hemoglobin Level Among Pregnant Women With Anemia in Rural Bangladesh.","Mobile Health","Inclusion Criteria:\n\n\\- 1. Pregnant women who will be diagnosed with mild and moderate anemia (Blood hemoglobin levels are between 7g\u002FdL and 10.9 g\u002FdL).\n\n2\\. Have at least one active mobile phone in the family. 3. Those who will give written informed consent to participate in the intervention study at the time of enrollment\n\nExclusion Criteria:\n\n\\- 1. Hospitalized at the time of the study period. 2. Women with any known or suspected chronic or congenital disease, such as blood inflammation, diabetic mellitus, thalassemia, hypertension, and psychiatric illness.\n\n3\\. Those who have severe anemia. 4. Having the possibility of leaving the study area during this study period.","FEMALE",{"count":121,"type":21},132,[24],"Anemia in pregnancy can result in negative pregnancy outcomes, which are higher among pregnant women of rural Bangladesh. A cost-effective health education program is urgently needed to introduce, which will help to improve their hemoglobin level by changing their lifestyle. In many rural settings, mobile-based health (mHealth) education programs have been shown to improve hemoglobin levels effectively during the antenatal period. So, we aim to assess the impact of a mHealth education program on improving hemoglobin levels among anemic pregnant women of rural Bangladesh.\n\nThe study will be carried out in the rural settings of a district of Bangladesh named Chandpur. This study timeline is from December 2025 to May 2026.\n\nAfter this survey, a randomized controlled trial study will be conducted where 160 pregnant women who are diagnosed with mild and moderate anemia will be offered to participate. Pregnant women who will give informed consent will be randomly assigned to two arms: intervention and control. Every arm will have an equal number of anemic pregnant women. Pregnant women in the intervention arm will receive anemia management-related health education through mobile messages and calls. This intervention program will educate pregnant women about the causes, risks, and symptoms of anemia, with the prevention strategies like dietary improvement, supplementation, parasitic disease control, safe motherhood, family planning, and iron-rich food production. Additionally, they will get regular care, a booklet and reminders of ANC visits during the study period. In contrast, the pregnant women of the control arm will receive regular care during this period, but after the end-line assessment, they will also get the booklet. After 4 months of the intervention program, the end-line assessment will be done, where the hemoglobin, nutritional status, and literacy about anemia will be assessed. Multiple comparisons will be performed by two-way analysis of variance tests for the evaluation of the outcome variables. Additionally, a Generalized Estimating Equations (GEE) model will be used to analyze the effect of the mHealth education program on related factors. A p-value less than 0.5 will be considered significant in this study.\n\nIf this mHealth-based education program shows improvement in hemoglobin level, this can be utilized in low-resource settings widely to ensure safe pregnancy outcomes in the future.",[125,126],"Anemia","Pregnant Women",[125,128,129,130],"Pregnant women","mHealth","Bangladesh","2025-12-20",{"date":133,"type":44},"2025-12-30",{"date":135,"type":21},"2026-02-01",{"date":77,"type":21},{"name":50,"class":51},{"id":139,"slug":140,"hasResults":11,"nctId":141,"briefTitle":142,"officialTitle":142,"acronym":85,"eligibilityCriteria":143,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":144,"targetDuration":4,"studyType":22,"phases":145,"briefSummary":146,"conditions":147,"keywords":150,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":152,"lastUpdatePostDateStruct":153,"startDateStruct":155,"completionDateStruct":157,"leadSponsor":159,"locationsCount":111},"100564082","effect-of-implementing-evidence-based-practice-and-nurses-behavior-change-on-quality-of-care-in-intensive-care-unit-focus-on-ventilator-associated-pneumonia-in-a-tertiary-hospital-in-bangladesh-100564082","NCT06624540","Effect of Implementing Evidence-based Practice and Nurse's Behavior Change on Quality of Care in Intensive Care Unit: Focus on Ventilator Associated Pneumonia in a Tertiary Hospital in Bangladesh","Study 2:\n\nInclusion criteria:\n\n* Who will be a registered nurse in Bangladesh.\n* Who will agree to participate in this study and the EBP training.\n\nExclusion criteria:\n\n* Who will not directly involve patient care in ICU.\n\nStudy 3:\n\nInclusion Criteria:\n\n* Irrespective of age and sex, participant must be 18 years old.\n* Legal guardian of a patient consents to participation in the study\n* Intubated patients after admission.\n\nExclusion Criteria:\n\n* Who stays less than 2 days at the GICU.\n* Who dies or is extubated within 2 days after admitted in the GICU.\n* ICU readmission.",{"count":88,"type":21},[24],"Quality of care is crucial for preventing adverse events such as infection in the intensive care units (ICUs). The most common ICU-acquired infections include pneumonia such as ventilator-associated pneumonia (VAP), Central Line Bloodstream Infection (CLABSI), catheter-associated urinary tract in, Medical Device Related Pressure Ulcer (MDRPU) and Pressure Ulcer (PU). This study explores the patient outcome in ICU by examining the causes and prevalence of ICU-acquired infection. The implementation of evidence-based practice (EBP) to reduce infection and change the nurses practice (behavioral changes) to adhere with EBP based on simulation-based training.\n\nGeneral objective:\n\nTo evaluate the effect of EBP by using recent technologies-based equipment to prevent VAP and promote behavior change among nurses for better outcome of the patient in ICU.\n\nSpecific Objectives:\n\n1. To determine the incidence of adverse events (VAP rate, MDRPU rate, PU rate, CLABSI rate), length of stay and survival rate in ICU.\n2. To evaluate the effectiveness of EBP education by changing nurses' behavior and determine its impact on improving patient outcomes in the ICU.\n3. To evaluate the effectiveness of EBP including proper equipment use and changed nurses behavior acquired through the training for better patient outcome (VAP ratio) in the ICU.\n4. To examine the feasibility of evaluation process and outcomes and successful implementation of EBP in ICU.\n\nHypothesis:\n\nIt is hypothesize that implementing EBP in ICU, including new equipment use and nurses training, will improve patient outcome.\n\nThese research consist of three studies:\n\nPhase 1: Incidence of adverse events (VAP rate, MDRPU rate, PU rate, CLABSI rate), length of stay and survival rate in ICU. The patients of General ICU will be followed up after admission up to discharge or death at ICU. The investigators use the study findings for our subsequent intervention study 3 as historical data.\n\nPhase 2: A pre- and post- quasi-experimental study will be conducted for 6 months to evaluate the nurse's competency on EBP after getting 1-month EBP training. This study has 3 steps: (1) Pre-observation period to measure nurse's competency level for 2-month, (2) nurse's EBP training period with preparation for 1 month, and (3) post-implementation period to measure nurse's competency and implementation of EBP practice for 2 months. Study nurses will receive EBP training, EBP and proper equipment for patient management. The nurses will receive EBP education and training with necessary equipment, such as a close suction catheter, an endotracheal tube, a suction device, and a mouth care brush. In this study, use global standard equipment for the patients safety.\n\nPhase 3: A pre- and post- quasi-experimental study will be implemented to evaluate the efficacy of EBP implementation. The investigators use new equipment and implement EBP for patients and assess the patient outcomes. The investigators compare the findings from study 1 (as historical data) with the data from this study 3.\n\nThe investigators will compare the VAP infection prevalence and patients' outcomes related to ICU-acquired infection between pre- and post- test phase.",[148,149],"Ventilator Associated Pneumonia (VAP)","Evidence Based Practice",[97,99,151],"Nurses Knowledge","2025-12-09",{"date":154,"type":44},"2025-12-15",{"date":156,"type":44},"2024-10-10",{"date":158,"type":21},"2026-02-28",{"name":50,"class":51},{"id":161,"slug":162,"hasResults":11,"nctId":163,"briefTitle":164,"officialTitle":165,"acronym":4,"eligibilityCriteria":166,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":167,"targetDuration":4,"studyType":22,"phases":169,"briefSummary":170,"conditions":171,"keywords":172,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":176,"lastUpdatePostDateStruct":177,"startDateStruct":179,"completionDateStruct":181,"leadSponsor":183,"locationsCount":52},"100479211","reduction-of-recurrence-of-stroke-by-nurse-led-education-in-bangladesh-100479211","NCT05520034","Reduction of Recurrence of Stroke by Nurse-led Education in Bangladesh","Effectiveness of Health Education Program Among Patients & Family Caregivers on Modifiable Risk Factors mRS 0 to 4 to Reduce Recurrence of Stroke After Discharge From a Tertiary Hospital in Bangladesh","For patient\n\n1. Who was discharged from NINSH to home or who visited NINSH right after getting a stroke\n2. First-time stroke\n3. All types of strokes, except subarachnoid haemorrhage\n4. modified Rankin Scale (0 - 4)\n5. Stroke patient who is 18 years old and above\n6. Both males \\& females\n7. Who provided written consent \\& willing to participate in the study\n\nFor family caregivers\n\n1. Primary caregivers irrespective of sex and aged 18 years old and above, living with the patient who take care of an above patient and who meets all of the inclusion criteria (will be decided by one person)\n2. Who will provide written consent \\& willing to participate in the study\n\nExclusion Criteria:\n\nExclusion criteria of patient\n\n1. Who has stroke with the recurrence\n2. Stroke subtype: caused by genetic problems or injury\u002Faccident\n3. Patients with multi-organ failure or terminal stage\n4. Participation in other clinical trials\n5. Unwillingness to participate in the study\n6. Not having a mobile phone at home\n7. mRS 5\n\nExclusion criteria of caregiver\n\n1. Who is not living with the patient\n2. Who is under 18 years old\n3. Who is mentally unstable and\u002For cognitively impaired (diagnosed cases)",{"count":168,"type":21},432,[24],"Stroke is a major public issue that can be occurred a patient with severe and unbearable disability for a long time. Recurrence of stroke is increasing due to a lack of knowledge and compliance with treatment regarding the modifiable risk factors of stroke and behavioral and lifestyle changes. Nurse-led health education with (self) monitoring of modifiable risk factors and behaviors can be an effective way to create knowledge about the behavioral changes in stroke patients.\n\nThe investigators hypothesized that health education among first stroke patients and their family caregivers could reduce the stroke recurrence rate by controlling modifiable risk factors compared to the first stroke patients without health education.",[65],[65,173,174,175,130],"Caregiver","Recurrence of stroke","Health education","2025-09-08",{"date":178,"type":44},"2025-09-15",{"date":180,"type":44},"2022-10-02",{"date":182,"type":21},"2026-03-30",{"name":50,"class":51},{"id":185,"slug":186,"hasResults":11,"nctId":187,"briefTitle":188,"officialTitle":189,"acronym":4,"eligibilityCriteria":190,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":191,"targetDuration":4,"studyType":22,"phases":193,"briefSummary":194,"conditions":195,"keywords":197,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":203,"lastUpdatePostDateStruct":204,"startDateStruct":206,"completionDateStruct":208,"leadSponsor":210,"locationsCount":4},"100576535","nurse-led-rehabilitation-to-improve-self-care-among-stroke-patients-in-bangladesh-100576535","NCT06786559","Nurse-led Rehabilitation to Improve Self-care Among Stroke Patients in Bangladesh","Post Discharge Nurse-led Rehabilitation to Improve Self-care Among Stroke Patients in Bangladesh: A Pilot Randomized Controlled Trial","Inclusion Criteria:\n\n* For Patient\n\n  1. who is 18 years old and above, both males \\& females,\n  2. is irrespective of type of stroke and time of stroke,\n  3. is within 5 days to 2 weeks of onset of the current stroke\n  4. Physician advice rehabilitation, and who needs assistive devices for ADL,\n  5. has family caregivers,\n  6. lives in the study area, and\n  7. who will provide written consent \\& willing to participate in the study.\n\nFor family care giver\n\n1. Primary caregivers irrespective of sex and aged 18 years old and above, living with the patient who take care of an above patient and who meets all the inclusion criteria.\n2. Who will provide written consent \\& willing to participate in the study\n\nExclusion Criteria:\n\n* For patient\n\n  1. Participation in other clinical trials,\n  2. not having a smartphone at home, For family care giver No exclusion criteria",{"count":192,"type":21},64,[24],"Stroke causes various levels of disability, which decreases physical function for a prolonged period. The purpose of this study is to test the feasibility and efficacy of a nurse-led rehabilitation program focused on improving the activity of daily living (ADL) among post-stroke patients in Bangladesh. A feasibility study, including descriptive and randomized controlled trial (RCT), will be conducted at the National Institute of Neuroscience \\& Hospital (NINS\\&H) in Dhaka, Bangladesh, from March 2025 to August 2025. Participants will be the post-stroke patients who got discharged from NINS\\&H from 5th days to 2 weeks after the onset of stroke and the family caregivers of the patients and meet the inclusion criteria. The sample size will be calculated based on G-Power analysis with a medium effect size and will be 64. The intervention will be designed to provide the 3-month nurse-led rehabilitation program regarding self-care and the use of assistive devices. Assessment for rehabilitation will be performed by the multidisciplinary team with research nurses (RA nurses), physiotherapists (PT), and occupational therapists (OT). The control group will receive the usual care. The Functional Independence Measure (FIM) measures the primary outcome as improved self-care. The secondary outcomes are self-efficacy and participation in social activities for patients and the care burden of family caregivers. We also qualitatively describe changes and improvements of cognitive, emotional, and behavioral aspects among patients and their families. The endpoints will be compared at baseline and the 3rd month. Rehabilitation with proper assistive devices may improve self-dependence, ADL, and social participation. The caregiver's burden will decrease through the implementation of self-care education and assistive devices for daily life adjustment.",[65,196],"Disability Physical",[65,198,199,200,201,202],"Disability","Rehabilitation","Assistive device","Self-Care","Care Burden","2025-01-15",{"date":205,"type":44},"2025-01-22",{"date":207,"type":21},"2025-03-01",{"date":209,"type":21},"2025-08-30",{"name":50,"class":51},{"id":212,"slug":213,"hasResults":11,"nctId":214,"briefTitle":215,"officialTitle":216,"acronym":4,"eligibilityCriteria":217,"healthyVolunteers":16,"sex":17,"minAge":218,"maxAge":4,"enrollmentInfo":219,"targetDuration":4,"studyType":22,"phases":221,"briefSummary":222,"conditions":223,"keywords":225,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":227,"lastUpdatePostDateStruct":228,"startDateStruct":230,"completionDateStruct":231,"leadSponsor":233,"locationsCount":52},"100574609","comparing-of-different-visual-aids-like-videoinfo-graphics-and-pamphlets-in-enhancing-community-awareness-and-promoting-behavioral-change-towards-the-prevention-of-hypertension-in-basilica-of-the-most-holy-trinity-onitsha-anambra-statenigeria-100574609","NCT06761508","Comparing of Different Visual Aids Like Video,info-graphics and Pamphlets in Enhancing Community Awareness and Promoting Behavioral Change Towards the Prevention of Hypertension in Basilica of the Most Holy Trinity Onitsha Anambra State,Nigeria","Comparison of Different Visual Aids in Enhancing Community Awareness and Promoting Behavioral Change in the Prevention of Hypertension in Anambra State,Nigeria","Inclusion Criteria:\n\n* Adults age over 35 years old\n* Who does not know his\u002Fher blood pressure status within the last 6 months (The person who does not know he or she has a hypertension or not.)\n* Who agree to participate\n\nExclusion Criteria:\n\n* Who cannot come to the church 4 weeks later after the intervention.\n* Known hypertensive patients","35 Years",{"count":220,"type":21},81,[24],"The goal of this observational study is to assess different level of enhanced awareness and behavioral change of adults over the age of 35 who will be educated using video,infographic and pamphlet for the interval of one month",[224],"Hypertension",[226],"Behavioural change in hypertension prevention","2025-01-05",{"date":229,"type":44},"2025-01-07",{"date":227,"type":21},{"date":232,"type":21},"2025-04-05",{"name":50,"class":51},""]