[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"non-communicable-chronic-diseases\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:non-communicable-chronic-diseases":97},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,47,79,117,147,175,201,233,259],{"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":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100633587","behavioral-interventions-as-primary-prevention-for-non-communicable-diseases-among-young-people-100633587",false,"NCT07528625","Behavioral Interventions as Primary Prevention for Non-Communicable Diseases Among Young People","Behavioral Interventions as Primary Prevention for Non-Communicable Diseases Among Young People; a Randomized Clinical Trial","Inclusion Criteria:\n\n* Age Range: Typically 10-19 (adolescents) or 15-24 (young adults).\n* resident in Egypt\n* accept sharing and adhered for following\n* At-risk youth (e.g., sedentary, high-sugar diet)\n* Motivated to use digital tools\n* Diverse socio-economic backgrounds\n* Healthy enough for moderate exercise\n* Presence of at least one modifiable risk factor, such as:\n\nInsufficient physical activity (not meeting WHO guidelines of 60 min\u002Fday). Unhealthy dietary habits (high sugar\u002Fsalt intake, low fruit\u002Fvegetable consumption).\n\nTobacco use or exposure to second-hand smoke (including vaping). Harmful alcohol consumption patterns.\n\nExclusion Criteria:\n\n* Individuals already diagnosed with the NCDs being targeted\n* Presence of medical conditions that cause secondary obesity or hypertension\n* Current use of medications that significantly affect metabolic or behavioral outcomes\n* Individuals with active psychosis, severe clinical depression, or eating disorders\n* Severe impairments that prevent the individual from understanding the study requirements, providing informed assent, or interacting with digital intervention tools\n* Enrollment in another clinical trial or behavioral intervention that might lead to \"treatment contamination.\"\n* Unable to consent or use tech due to severe deficit\n* Temporary residents (will move before data collection ends)\n* Safety risk (e.g., severe heart condition)",true,"ALL","15 Years","25 Years",{"count":21,"type":22},2000,"ESTIMATED","INTERVENTIONAL",[25],"NA","In consistence of North Africa vision to decrease incidence of NCDs in different population type investigators decide to give more concerns to youth (young old) who are the main human power to build future. Recent data report non-communicable diseases (NCDs) are the current leading cause of mortality in Egypt, with NCDs estimated to account for 85% of all deaths. Egypt's youth population (16-25 years old) is both the country's greatest asset and one of its biggest challenges. This age group makes up a huge share of the population, and while they are more connected to technology, social media, and modern facilities than older generations, they face lifestyle barriers that affect their health and productivity. Many modifiable risk factors affect their behavior and in consequence health. These factors related strongly to their close relationship with technology, they spend more time on mobile and computer applications that affect directly on physical inactivity, sleeping time (onset and duration) and at the end cause NCDs as obesity and CVs problems. Upper Egypt as apart from North Africa region is considered as one of the low-income countries with special cultures, specifically regarding food and physical activities. Even though young people constitute a significant proportion of the population, comparatively fewer studies have examined the prevalence of health concerns and the strategies needed to promote their well-being, especially when contrasted with research focused on groups such as the elderly or pregnant and lactating women. This project aims to investigate prevalence patterns, identify contributing factors, enhance community awareness by encouraging training of healthcare providers to best act and modify youth risk factors, and implement preventive interventions that are both cost-effective and sustainable. Furthermore, it seeks to foster adherence to these measures to strengthen health literacy and reduce the burden of conditions",[28,29],"Non Communicable Diseases","Non Communicable Chronic Diseases",[31,32,33],"young adults","non communicable diseases","behaviour intervention","NOT_YET_RECRUITING","2026-04-14",{"date":37,"type":38},"2026-04-17","ACTUAL",{"date":40,"type":22},"2026-04-01",{"date":42,"type":22},"2028-01-01",{"name":44,"class":45},"Deraya University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":17,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":23,"phases":58,"briefSummary":59,"conditions":60,"keywords":64,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":46},"100600482","health-warnings-and-counseling-for-smoking-cessation-100600482","NCT07098065","Health Warnings and Counseling for Smoking Cessation","Health Warnings and Counseling at Primary Health Care Centers for Smoking Cessation and NCD Prevention: A Randomized Controlled Trial in Bangladesh and Pakistan","Inclusion Criteria:\n\n* Adults aged 18 and older\n* Adults (≥18 years) who are current smokers (daily or occasional) and regular visitors to participating pharmacies.\n* Permanent resident of the study area,\n* Access to mobile phone\n* Able to operate smartphone or tablet.\n\nExclusion Criteria:\n\n* Without pregnancy and lactation\n* Without cognitive or psychiatric conditions,\n* Without severe medical conditions,\n* Participation in other studies, and inability to consent.","18 Years","90 Years",{"count":57,"type":22},3400,[25],"Tobacco use remains persistently high across South Asia, despite numerous public health efforts, and continues to significantly contribute to the burden of non-communicable diseases (NCDs) such as cardiovascular disease, hypertension, diabetes, and stroke. Community pharmacists-widely accessible and trusted within their communities-are an underutilized resource for delivering public health interventions. Graphic health warnings (GHWs), recommended by the World Health Organization (WHO), have been shown to promote smoking cessation, but are rarely paired with personalized counseling by healthcare providers.\n\nThis study aims to evaluate both the effectiveness and cost-effectiveness of integrating GHWs with pharmacist-led personalized counseling at primary healthcare pharmacies in Bangladesh and Pakistan. A cluster randomized controlled trial (RCT) will be conducted, enrolling 3,240 adult participants in Bangladesh and \\~160 participants in Pakistan (for feasibility study) from community pharmacies. Participants will be randomly assigned to one of three groups: (1) GHW only (distribution of printed booklets); (2) GHW + counseling (pharmacist-led counselling sessions based on booklets at baseline and six months, with monthly SMS reminders); or (3) standard care (usual pharmacy services with no additional materials).\n\nThe intervention includes twice-yearly counseling sessions-delivered both in-person and digitally-supported by educational booklets and leaflets. The primary outcome is self-reported 7-day point prevalence abstinence at 12 months (validated where feasible). Secondary outcomes include reduction in cigarettes per day, quit attempts, readiness to quit, awareness of tobacco harms, diet and physical activity scores, quality of life, blood pressure control among hypertensive participants, and cost-effectiveness. Feasibility outcomes in Pakistan include recruitment rate, participant retention, intervention fidelity and acceptability. Bayesian statistical models will be used to assess efficacy, and economic evaluations will determine the cost-effectiveness of the interventions. The findings aim to inform scalable public health strategies for tobacco control and NCD prevention in resource-limited settings.",[61,62,63,29],"Tobacco Cessation","Health Warning Label","Hypertension",[65,66,67,68,69],"Tobacco cessation","Graphic health warnings (GHWs)","Non-communicable diseases (NCDs)","Cluster randomized controlled trial (RCT)","Pharmacist-led counseling","RECRUITING","2026-04-13",{"date":35,"type":38},{"date":74,"type":38},"2026-02-01",{"date":76,"type":22},"2027-04-30",{"name":78,"class":45},"Hitotsubashi University",{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":16,"sex":17,"minAge":87,"maxAge":19,"enrollmentInfo":88,"targetDuration":4,"studyType":23,"phases":90,"briefSummary":91,"conditions":92,"keywords":98,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":4},"100632486","sustainable-and-ai-enabled-adolescents-and-youth-centred-interventions-to-upgrade-food-choices-and-promote-healthy-sustainable-diets-100632486","NCT07514312","Sustainable and AI-Enabled Adolescents and Youth-Centred Interventions to Upgrade Food Choices and Promote Healthy, Sustainable Diets","AI-Supported, Context-Aware Digital Nudging Intervention to Reduce Ultra-Processed Food Consumption and Improve Dietary Sustainability Among Adolescents and Young Adults (STAY-UP)","STAY-UP","Inclusion Criteria:\n\n* Adolescents aged 12 to 25 years\n* Ownership of a smartphone or regular access to a digital device\n* Ability to use the digital intervention platform\n* Willingness to provide informed consent (and parental consent where applicable)\n* Regular consumption of ultra-processed foods at baseline\n\nExclusion Criteria:\n\n* Presence of medical conditions requiring a specific therapeutic diet\n* Participation in another dietary or behavioral intervention study\n* Severe cognitive or psychological conditions that may impair participation\n* Inability to use digital tools or applications","12 Years",{"count":89,"type":22},1000,[25],"This study aims to evaluate the effectiveness of an artificial intelligence (AI)-supported, context-aware digital nudging intervention designed to reduce ultra-processed food consumption and improve dietary sustainability among adolescents and young adults. The intervention utilizes real-time behavioral data, including image-assisted dietary logging and contextual information, to identify high-risk consumption moments and deliver personalized, non-coercive nudges. The study will assess changes in ultra-processed food intake, contextual consumption patterns, and sustainability-related dietary indicators.",[93,94,95,96,97],"Ultra-Processed Food Consumption","Obesity Prevention","Dietary Behaviour","Unhealthy Diet","Non-Communicable Chronic Diseases",[99,100,101,102,103,104,105,106,107],"Ultra-Processed Food","Digital Intervention","Artificial Intelligence","Dietary Behavior","Adolescents","Young Adults","Nutrition","Sustainability","non-communicable disease","2026-03-31",{"date":110,"type":38},"2026-04-07",{"date":112,"type":22},"2026-09-16",{"date":114,"type":22},"2028-06-30",{"name":116,"class":45},"Istanbul Gelisim University",{"id":118,"slug":119,"hasResults":11,"nctId":120,"briefTitle":121,"officialTitle":122,"acronym":123,"eligibilityCriteria":124,"healthyVolunteers":11,"sex":125,"minAge":54,"maxAge":4,"enrollmentInfo":126,"targetDuration":4,"studyType":128,"phases":4,"briefSummary":129,"conditions":130,"keywords":133,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":139,"startDateStruct":141,"completionDateStruct":143,"leadSponsor":145,"locationsCount":46},"100602105","long-term-evaluation-of-gestational-endocrine--metabolic-dynamics-100602105","NCT07119177","Long-term Evaluation of Gestational Endocrine & Metabolic Dynamics","Long-Term Effects of Gestational Diabetes Mellitus on Postpartum Chronic Non-Communicable Diseases: A Prospective Cohort Study","LEGEND","Inclusion Criteria:\n\n* Adult patients (≥18 years old) who registered for antenatal care and delivered at Peking University Firest Hospital's obstetrics department between 2007 and 2016.\n* Diagnosed with gestational diabetes mellitus (GDM) during pregnancy via an oral glucose tolerance test (OGTT).\n* Signed informed consent.\n\nExclusion Criteria:\n\n* Lack of pregnancy-related obstetric follow-up records.\n* Inability to cooperate with and complete subsequent scheduled follow-ups.","FEMALE",{"count":127,"type":22},800,"OBSERVATIONAL","Gestational diabetes mellitus (GDM) is the most common complication and metabolic disorder during pregnancy, with clear risks to both the mother and fetus. In recent years, the long-term chronic diseases and poor prognosis in GDM women after delivery, as well as the risk of obesity and metabolic disorders in their offspring, have become key research topics. However, due to the long duration of GDM's impact on both the mother and offspring and its involvement in multiple disciplines, high-quality cohort studies are scarce. As a result, there is no definitive conclusion regarding the high-risk factors, natural progression, key mediators, timing of interventions, and targets for GDM's long-term effects on mothers and their offspring. This project intends to initiate a prospective follow-up study, establish a specialized cohort for the long-term effects of GDM on both mothers and their offspring, and complete the characterization of the natural course of non-communicable chronic diseases (NCDs) in GDM women and their offspring. The study will also explore high-risk and mediator factors, and develop predictive models. The goal is to provide education, postpartum follow-up, monitoring, and possibly initiate primary prevention for GDM women to reduce the long-term NCD risks, ultimately improving their life expectancy and providing a theoretical basis for intervention.\n\nInclusion Criteria:\n\n1. Adult patients (≥18 years old) who registered for antenatal care and delivered at Peking University Firest Hospital's obstetrics department between 2007 and 2016.\n2. Diagnosed with gestational diabetes mellitus (GDM) during pregnancy via an oral glucose tolerance test (OGTT).\n3. Signed informed consent.\n\nExclusion Criteria:\n\n1. Lack of pregnancy-related obstetric follow-up records.\n2. Inability to cooperate with and complete subsequent scheduled follow-ups.",[131,132],"Gestational Diabetes Mellitus (GDM)","Non-communicable Chronic Diseases",[134,135,132,136,137],"Gestational Diabetes Mellitus","Long-term Impact","Prospective Cohort","Predictive Model","2025-08-05",{"date":140,"type":38},"2025-08-12",{"date":142,"type":38},"2025-03-29",{"date":144,"type":22},"2026-12-31",{"name":146,"class":45},"Yang ZHANG",{"id":148,"slug":149,"hasResults":11,"nctId":150,"briefTitle":151,"officialTitle":152,"acronym":4,"eligibilityCriteria":153,"healthyVolunteers":16,"sex":17,"minAge":54,"maxAge":4,"enrollmentInfo":154,"targetDuration":4,"studyType":23,"phases":156,"briefSummary":157,"conditions":158,"keywords":161,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":166,"lastUpdatePostDateStruct":167,"startDateStruct":169,"completionDateStruct":171,"leadSponsor":173,"locationsCount":46},"100586674","evaluation-of-the-warifa-app-and-its-impact-on-healthy-lifestyle-100586674","NCT06918444","Evaluation of the WARIFA App and Its Impact on Healthy Lifestyle","Effect of the WARIFA App on User-defined Objectives, Healthy Lifestyles and Management of Type 1 Diabetes: a Pilot Randomised Controlled Trial","Inclusion Criteria:\n\n* Common for both population groups:\n* Adults over 18 years of age.\n* Owners of a smartphone operating with Android and with internet access.\n* Group 1: General population:\n* Healthy or diagnosed with no more than one NCD (CVD, any type of cancer, T2D or chronic respiratory disease).\n* Group 2: T1D:\n* Treatment with multiple subcutaneous insulin injections or an insulin pump.\n* Users of a continuous glucose monitor.\n\nExclusion Criteria:\n\n* Common for both groups:\n* Pregnancy.\n* Mobile device which is incompatible with the WARIFA app (E.g. Apple devices).\n* Unable to understand any of the app languages (Spanish, English, Norwegian or Romanian).\n* Any reason which precludes follow-up, based on the researcher's criteria.\n* Group 1: General population\n* People with two or more NCDs.",{"count":155,"type":22},104,[25],"The goal of this study is to assess the effect of the WARIFA app on the adoption of healthy lifestyle behaviours related to Non-communicable diseases (NCDs), as well as in the management of Type 1 Diabetes (T1D). This is done using user-generated data analysis, artificial intelligence (AI) and risk estimation to provide personalised recommendations on lifestyle-related behaviours through a mobile app.\n\n* Primary objective: the objective of this study is to assess the impact of using the WARIFA app on a series of outcomes, related to the promotion of healthy lifestyles and prevention of NCDs, as well as on the management of T1D.\n* Secondary objectives: to assess the feasibility of implementation of a complex health app (WARIFA), and to explore which outcomes are more relevant in this context for users.\n\nThe study will evaluate the app in two different populations:\n\n* Population 1: Citizens living in Europe of either sex aged \\> 18 years diagnosed with no more than one NCD (of the following: CVD, any type of cancer, chronic respiratory disease and T2D) and current owners of a smartphone with internet access.\n* Population 2: European adult individuals of either sex aged \\>18 years with T1D currently using multiple daily insulin injections or an insulin pump and current owners of a smartphone with internet access.\n\nThe study will be carried out in three centres in three different countries: the Instituto Universitario de Investigaciones Biomédicas y Sanitarias (iUIBS) in Spain, the Norwegian Centre for E-health Research (NSE) in Norway, and in Romania.\n\nParticipants in each population will be randomised to an intervention or control arm on a 1:1 ratio:\n\n* Intervention arm: the Warifa app will be used by the participants throughout the study. The app will provide personalised risk estimations and recommendations through user-generated data analysis and artificial intelligence.\n* Control arm: The control group will use a Warifa app with the same functionalities than the intervention arm, but without artificial intelligence.\n\nAt baseline, information will be collected by questionnaires and a physical examination, including anthropometry and a lipid profile. These measurements will be repeated in 12 weeks and will be compared between the treatment arms.\n\nThe study will last 3 months in total, start of recruitment on 10 February 2025, end of study after the last visit of the last participant, on 12 May 2025. Each user will participate in the study for 12 weeks.",[159,29,160],"Lifestyle Intervention","Type 1 Diabetes (T1D)",[162,163,164,29,165,160],"AI (Artificial Intelligence)","Mobile app","Lifestyle intervention","Risk Prediction Model","2025-04-06",{"date":168,"type":38},"2025-04-09",{"date":170,"type":38},"2025-02-24",{"date":172,"type":22},"2025-05-29",{"name":174,"class":45},"Instituto Universitario de Investigaciones Biomédicas y Sanitarias (iUIBS) de la Universidad de Las",{"id":176,"slug":177,"hasResults":11,"nctId":178,"briefTitle":179,"officialTitle":179,"acronym":4,"eligibilityCriteria":180,"healthyVolunteers":11,"sex":17,"minAge":54,"maxAge":4,"enrollmentInfo":181,"targetDuration":183,"studyType":128,"phases":4,"briefSummary":184,"conditions":185,"keywords":189,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":192,"lastUpdatePostDateStruct":193,"startDateStruct":195,"completionDateStruct":197,"leadSponsor":199,"locationsCount":46},"100560793","evaluation-of-validity-and-reliability-of-the-turkish-translation-of-the-digital-health-readiness-questionaire-in-different-chronic-diseases-100560793","NCT06581770","Evaluation of Validity and Reliability of the Turkish Translation of the Digital Health Readiness Questionaire in Different Chronic Diseases","Inclusion Criteria:\n\n* The study will include people over the age of 18, native Turkish speakers, literate, obese, diabetic, cardiovascular and respiratory patients.\n\nExclusion Criteria:\n\n* Individuals with insufficient cooperation (Mini Mental Test score \\<24) and any cognitive problems that may prevent the administration of the survey will be excluded from the study.",{"count":182,"type":22},200,"2 Months","The World Health Organization (WHO) defines digital health as the field of knowledge and application related to any aspect of the adoption of digital technology in the stages of improvement. The combination of digital health with technology brings about a new transformation in digital media. This transformation allows for the development of communication and information in health services, the ability to conduct health-related research on digital media and the evaluation of this data. The ease of access to information and the provision of a timely feedback mechanism in the face of problems have enabled the spread of digital health systems, and have also enabled chronic disease management and epidemic disease monitoring.\n\nIt is recommended that the term digital readiness be used to cover the combination of digital access and use, digital literacy and digital health literacy. Digital health readiness is also defined as the main determinant of health and is thought to contribute to the improvement of health processes with the development of digital health literacy and to be a useful solution against health problems that may arise in the follow-up of chronic diseases.\n\nAlthough there are tools in the literature that evaluate digital health readiness, there is no Turkish assessment tool that facilitates the follow-up of non-communicable chronic diseases. Therefore, the aim of our study is to evaluate the translation, validity, and reliability of the Digital Health Readiness Questionaire into Turkish in individuals with chronic non-infectious diseases.",[97,186,187,188],"Survey and Questionnaire","Validation Studies","Digital Health",[190,191],"digital health","Digital Health Readiness Questionaire","2025-02-05",{"date":194,"type":38},"2025-02-10",{"date":196,"type":38},"2024-10-15",{"date":198,"type":22},"2025-09-15",{"name":200,"class":45},"Istanbul Galata University",{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":206,"acronym":207,"eligibilityCriteria":208,"healthyVolunteers":11,"sex":17,"minAge":209,"maxAge":4,"enrollmentInfo":210,"targetDuration":4,"studyType":23,"phases":212,"briefSummary":213,"conditions":214,"keywords":216,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":223,"lastUpdatePostDateStruct":224,"startDateStruct":226,"completionDateStruct":228,"leadSponsor":230,"locationsCount":232},"100533341","a-personalized-prevention-program-ppp-based-on-the-comprehensive-geriatric-assessment-cga-for-the-prevention-of-multidimensional-frailty-related-to-non-communicable-chronic-diseases-ncds-in-older-people-100533341","NCT06224556","A Personalized Prevention Program (PPP) Based on the Comprehensive Geriatric Assessment (CGA) for the Prevention of Multidimensional Frailty Related to Non-communicable Chronic Diseases (NCDs) in Older People","A Personalized Prevention Program (PPP) Based on the Comprehensive Geriatric Assessment (CGA) for the Prevention of Multidimensional Frailty Related to Non-communicable Chronic Diseases (NCDs) in Older People: a Practical Approach in Primary Care Setting","PrimaCare_P3","Inclusion Criteria:\n\n* 65 years old and over\n* At least 1 non-communicable chronic disease\n* Signed informed consent\n\nExclusion Criteria:\n\n* not willing in partecipating in the study and no signed informed consent\n* \\\u003C65 years old\n* without non-communicable chronic diseases","65 Years",{"count":211,"type":22},1216,[25],"* Non-Communicable Diseases (NCDs) can accelerated the aging process and increase the frailty condition\n* The Comprehensive Geriatric Assessment (CGA) is the gold standard in the geriatric clinical context\n* Recently, in Italy the first Guidelines about the CGA in different settings for older people has been pubblicated\n* The CGA can identify older people at high risk of frailty who can benefit from a personalized prevention program\n* No studies has been investigated the effects of a personalized prevention program (PPP) based on the CGA in a primary care setting\n* The main hypothesis is that the CGA assessment can result in personalized prevention programs for older subjects in primary care settings with an effect in reducing the hospitalization rate and can be related to the biological paramters in NCDs",[215,97],"Older People",[217,218,219,220,221,222],"Primary care setting","Comprehensive Geriatric Assessment","Older people","Non-communicable chronic diseases","Personalized Prevention Program","Saliva collection","2024-08-27",{"date":225,"type":38},"2024-08-28",{"date":227,"type":38},"2024-06-04",{"date":229,"type":22},"2025-05",{"name":231,"class":45},"Alberto Pilotto",4,{"id":234,"slug":235,"hasResults":11,"nctId":236,"briefTitle":237,"officialTitle":238,"acronym":4,"eligibilityCriteria":239,"healthyVolunteers":16,"sex":17,"minAge":54,"maxAge":4,"enrollmentInfo":240,"targetDuration":4,"studyType":128,"phases":4,"briefSummary":242,"conditions":243,"keywords":246,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":250,"lastUpdatePostDateStruct":251,"startDateStruct":253,"completionDateStruct":255,"leadSponsor":257,"locationsCount":46},"100545896","cohort-in-qianwan-new-district-ningbo-100545896","NCT06387875","Cohort in Qianwan New District, Ningbo","Prevention and Control of Chronic Noncommunicable Diseases in Natural Population in Qianwan New District, Ningbo","Inclusion Criteria:\n\n* 1\\) Local permanent residents aged 18 and above (including residents with household registration, or residents without household registration but with a permanent job);\n* 2\\) No serious physical disability, can communicate normally;\n* 3\\) Participate voluntarily and sign informed consent.\n\nExclusion Criteria:\n\n* 1\\) Temporary resident and floating population;\n* 2\\) There are serious health conditions unable to participate in the survey;\n* 3\\) Those who are unwilling to accept the follow-up inspection of the project.",{"count":241,"type":22},30000,"Our objective is to carry out research on prevention and control of noncommunicable chronic diseases, and establish a risk prediction mechanism for chronic diseases to promote early detection, early diagnosis and early treatment of chronic diseases in natural population in Qianwan District of Ningbo, significantly reduce medical costs and extend population life span.",[244,245,97],"Cardiovascular Diseases","Stroke",[247,248,249],"cohort","natural population","Non-communicable Chronic Disease","2024-04-25",{"date":252,"type":38},"2024-04-29",{"date":254,"type":38},"2023-11-01",{"date":256,"type":22},"2027-06-30",{"name":258,"class":45},"RenJi Hospital",{"id":260,"slug":261,"hasResults":11,"nctId":262,"briefTitle":263,"officialTitle":263,"acronym":264,"eligibilityCriteria":265,"healthyVolunteers":16,"sex":17,"minAge":54,"maxAge":4,"enrollmentInfo":266,"targetDuration":4,"studyType":23,"phases":268,"briefSummary":269,"conditions":270,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":275,"lastUpdatePostDateStruct":276,"startDateStruct":278,"completionDateStruct":280,"leadSponsor":282,"locationsCount":4},"100473862","the-inland-norway-healthy-life-center-study-100473862","NCT05450406","The Inland Norway Healthy Life Center Study","INHLCS","Intervention group\n\nInclusion Criteria:\n\n* \\>18 years of age\n* Receiving follow-up from the Healthy Life Center\n\nExclusion Criteria:\n\n* In average \\>1 weekly exercise training session the last three months\n\nReference group\n\nInclusion Criteria:\n\n* \\>18 years of age\n\nExclusion Criteria:\n\n* In average \\>1 weekly exercise training session the last three months\n* Receiving follow-up from the Healthy Life Center",{"count":267,"type":22},60,[25],"Healthy Life Centers (Norwegian, 'Frisklivssentralen') is a municipal service in Norway that aims to promote both physical and mental health, as well as to limit the development of non-communicable diseases. Previous research has shown that receiving follow-up from Healthy Life Centers has led to higher levels of daily physical activity, in addition to improved self-reported health and quality of life among the participants. However, there is a lack of studies that have examined what kind of physiological health effects can be expected from participating in the Healthy Life Center's follow-up.\n\nIn this study, responses to the 12-week physical activity program of the Healthy Life Center will be compared with the responses in a negative control group that does not receive such follow-up. Both the intervention group and the reference group (the negative control group) will carry out the same tests and measurements before and after the 12 week period. The tests will include measurements of anthropometric variables (body height, body weight and waist circumference), body composition, arterial stiffness, resting blood pressure and blood variables (blood glucose, long-term blood glucose, blood lipid profile and inflammation markers), in addition to physical tests of mobility, balance, maximum aerobic capacity (maximal oxygen consumption) and maximum muscle strength. Questionnaires related to adherence to the Healthy Life Center follow-up, socio-demographic variables, eating and drinking habits, activity level, perceived physical fitness, motivation for exercise, and health-related quality of life will also be included.",[97,271,272,273,274,244],"Obesity","Insulin Resistance","Musculoskeletal Diseases","Psychological Disorder","2022-08-30",{"date":277,"type":38},"2022-08-31",{"date":279,"type":22},"2022-08",{"date":281,"type":22},"2026-07",{"name":283,"class":45},"Inland Norway University of Applied Sciences"]