[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100633569":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":29,"locations":25,"responsibleParty":35,"collaborators":39,"id":47,"slug":48,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":49,"sex":55,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":25,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":25,"overallStatus":69,"whyStopped":25,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":25},{"fullName":5,"class":6},"Nanchang University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Integrated Comorbidity Management Intervention","EXPERIMENTAL","The intervention is a multi-component, comorbidity-oriented integrated management package for patients with coexisting hypertension and type 2 diabetes mellitus delivered at the primary care level. It includes: (1) standardized assessment and risk stratification for combined cardiometabolic risk; (2) coordinated medication management and optimization for blood pressure and glycemic control, including safety monitoring; (3) integrated lifestyle modification support (diet, physical activity, weight management, and smoking cessation); (4) structured self-management education and community-based support; (5) training and capacity building for primary care providers; (6) use of standardized clinical pathways, toolkits, and digital support systems to facilitate integrated care delivery; and (7) regular follow-up, monitoring, and feedback with performance evaluation and quality improvement mechanisms.",[13],"Behavioral: Integrated Comorbidity Management Package",{"label":15,"type":16,"description":17,"interventionNames":18},"Usual Care (Standard Primary Care Management)","ACTIVE_COMPARATOR","Standard primary care management for hypertension and type 2 diabetes mellitus provided according to existing national guidelines.",[19],"Other: Usual Care intervention",[21,26],{"type":22,"name":23,"description":11,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","Integrated Comorbidity Management Package",[9],null,{"type":6,"name":27,"description":17,"armGroupLabels":28,"otherNames":25},"Usual Care intervention",[15],[30],{"name":31,"role":32,"phone":33,"phoneExt":25,"email":34},"Xuejun Yin, PhD","CONTACT","18600988138","xuejun.yin@ncu.edu.cn",{"type":36,"investigatorFullName":37,"investigatorTitle":38,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"PRINCIPAL_INVESTIGATOR","Xuejun Yin","Professor",[40,43,45],{"name":41,"class":42},"Xiangdong District General Hospital","UNKNOWN",{"name":44,"class":42},"Xinfeng County Center for Disease Control and Prevention",{"name":46,"class":42},"Health Commission of Wuyuan County","100633569","comorbidity-oriented-primary-care-and-integrated-management-for-hypertension-and-diabetes-mellitus-100633569",false,"NCT07528391","Comorbidity-Oriented Primary Care and Integrated Management for Hypertension and Diabetes Mellitus","Comorbidity-Oriented Primary Care and Integrated Management for Hypertension and Diabetes Mellitus: A Cluster Randomised Controlled Trial in Rural China","COMPACT-HTDM","Inclusion Criteria:\n\nCluster level (primary care facilities):\n\n* Township health centers or community health service centers that provide routine primary care management services for both hypertension and diabetes.\n* Agree to participate in cluster randomization and study procedures.\n* Have basic capacity for chronic disease follow-up and data recording.\n\nIndividual participant level (patients):\n\n* Aged 60 to 74 years.\n* Diagnosed with hypertension and type 2 diabetes mellitus for at least 6 months.\n* Received at least one chronic disease management service at the participating study site within the past 6 months.\n* Able to provide written informed consent.\n\nExclusion Criteria:\n\nCluster Level (Primary Care Facilities):\n\n* Facilities currently participating in other intervention studies or pilot programs targeting hypertension and\u002For diabetes management that may interfere with the study intervention.\n* Facilities with major organizational instability (e.g., restructuring, closure, or significant staff turnover) that would affect implementation or follow-up.\n\nIndividual Level:\n\n* Severe cognitive impairment or psychiatric illness affecting participation or follow-up.\n* Anticipated inability to complete 6-month follow-up.","ALL","60 Years","74 Years",{"count":59,"type":60},960,"ESTIMATED","INTERVENTIONAL",[63],"NA","The COMPACT-HTDM study is a parallel, two-arm cluster randomized controlled trial designed to evaluate a comorbidity-oriented integrated primary care management model for elderly patients with coexisting hypertension and type 2 diabetes mellitus in community health centers and township health centers. The trial aims to determine whether an integrated comorbidity management package can improve metabolic control and cardiovascular risk management compared with usual disease-specific care in routine primary care settings. Clusters are primary care facilities randomized 1:1 to intervention or control by an independent statistician using a computer-generated random sequence. Patients aged 60-74 years with diagnosed hypertension and type 2 diabetes for at least six months and recent use of chronic disease management services at the study site will be recruited through chronic disease registries. The intervention includes comorbidity-focused medication optimization and safety management, integrated lifestyle management, self-management and community support, training for primary care staff, standardized toolkits and workflow embedding, an integrated comorbidity management platform, and feedback\u002Fincentive mechanisms. The control group will continue current standard primary care management for hypertension and diabetes under existing national guidelines. Participants will be followed for six months, with possible extension to 12 months for longer-term outcomes. The primary outcome is the proportion of participants achieving both blood pressure and glycemic control targets, defined as SBP\u002FDBP \\\u003C130\u002F80 mmHg and HbA1c \\\u003C7.0%. Secondary outcomes include BMI, blood lipids, medication adherence, lifestyle behaviors, follow-up completion, referral rate, and safety events such as hypoglycemia and hypotension; implementation outcomes include acceptability, fidelity, and feasibility.",[66,67,68],"Hypertension","Diabete Type 2","Comorbidities and Coexisting Conditions","NOT_YET_RECRUITING","2026-04-07",{"date":72,"type":73},"2026-04-14","ACTUAL",{"date":75,"type":60},"2026-05-01",{"date":77,"type":60},"2028-12-31",{"name":5,"class":6}]