Comorbidity-Oriented Primary Care and Integrated Management for Hypertension and Diabetes Mellitus
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Integrated Comorbidity Management Package, Usual Care intervention.
- Кому может быть актуально
- Состояния в реестре: Hypertension, Diabete Type 2, Comorbidities and Coexisting Conditions. Базовые параметры: 60 лет — 74 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Список центров уточняется — проверьте первичный протокол.
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Comorbidity-Oriented Primary Care and Integrated Management for Hypertension and Diabetes Mellitus: A Cluster Randomised Controlled Trial in Rural China
Обзор
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/incentive 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/DBP \<130/80 mmHg and HbA1c \<7.0%. 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.
Вмешательства
- Поведенческое Integrated Comorbidity Management Package
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, weigh - Другое Usual Care intervention
Standard primary care management for hypertension and type 2 diabetes mellitus provided according to existing national guidelines.
Первичные конечные точки
- Proportion of Participants Achieving Combined Blood Pressure and Glycemic Control Using Clinic Blood Pressure Measurement and Laboratory Glycated Hemoglobin (HbA1c) [Срок оценки: Six months]
Вторичные конечные точки (9)
- Blood Pressure Control Rate Using Standardized Clinic Systolic and Diastolic Blood Pressure Measurement [Срок оценки: Six months]
- Glycemic Control Rate Using Laboratory Glycated Hemoglobin (HbA1c) [Срок оценки: Six months]
- Change in Systolic Blood Pressure Measured in Millimeters of Mercury (mmHg) by Standardized Clinic Blood Pressure Measurement [Срок оценки: Baseline to 6 months]
- Change in Diastolic Blood Pressure Measured in Millimeters of Mercury (mmHg) by Standardized Clinic Blood Pressure Measurement [Срок оценки: Baseline to 6 months]
- Change in Laboratory Glycated Hemoglobin (HbA1c) Percentage [Срок оценки: Baseline to 6 months]
- Medication Adherence Assessed by the Adherence to Refills and Medications Scale (ARMS) [Срок оценки: 6 months]
- Physical Activity Assessed by the International Physical Activity Questionnaire (IPAQ) [Срок оценки: Baseline to 6 months]
- Incidence of Hypoglycemia Assessed by Participant Report and Medical Record Review [Срок оценки: During the 6-month intervention period]
- Incidence of Hypotension Assessed by Participant Report and Medical Record Review [Срок оценки: During the 6-month intervention period]
Критерии участия
Критерии включения
Cluster level (primary care facilities):
- Township health centers or community health service centers that provide routine primary care management services for both hypertension and diabetes.
- Agree to participate in cluster randomization and study procedures.
- Have basic capacity for chronic disease follow-up and data recording.
Individual participant level (patients):
- Aged 60 to 74 years.
- Diagnosed with hypertension and type 2 diabetes mellitus for at least 6 months.
- Received at least one chronic disease management service at the participating study site within the past 6 months.
- Able to provide written informed consent.
Критерии исключения
Cluster Level (Primary Care Facilities):
- Facilities currently participating in other intervention studies or pilot programs targeting hypertension and/or diabetes management that may interfere with the study intervention.
- Facilities with major organizational instability (e.g., restructuring, closure, or significant staff turnover) that would affect implementation or follow-up.
Individual Level:
- Severe cognitive impairment or psychiatric illness affecting participation or follow-up.
- Anticipated inability to complete 6-month follow-up.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Двойное слепое
- Основная цель
- Организация здравоохранения
Центры проведения
Список центров уточняется — проверьте первичный протокол.
Идентификаторы
NCT: NCT07528391 · 03002