The First Hospital of China Medical University
Shenyang, Liaoning, 110001, China
NCT Number: NCT03527719
China Rural Hypertension Control (CRHC) Project is a cluster randomized trial that will test the effectiveness of a village doctor-led multifaceted intensive blood pressure intervention on hypertension control in 18 months (Phase 1), cardiovascular disease risk in 36 months (Phase 2), and all-cause dementia in 48 months (Phase 3) among patients with hypertension in rural China. An extended observational follow-up, the CRHCP post-intervention observational follow-up study, will be conducted at Year 7 to evaluate long-term effects.
This study is active but is not currently recruiting participants.
40 year and older
All sexes
Interventional
Not applicable
Shenyang, Liaoning, 110001, China
The overall objective of the CRHC Project is to develop an effective, adoptable, and sustainable implementation strategy to achieve more intensive blood pressure (BP) control among rural residents in China. Moreover, this effectiveness-implementation trial will test the effectiveness of a lower BP target (<130/80 mmHg) on cardiovascular disease (CVD) and all-cause dementia. Specifically, we will test the effectiveness of a village doctor-led multifaceted intervention, compared with usual care, on BP control, CVD, and dementia among rural residents with hypertension in China. This cluster randomized trial is conducted in 326 villages from three provinces in mainland China. A total of 163 villages was randomly assigned to a village doctor-led multifaceted intervention and 163 villages to usual care, stratified by provinces, counties, and townships. A total of 33,995 individuals aged ≥40 years with uncontrolled hypertension were recruited into the study. The village doctor-led multifaceted intervention is designed to overcome barriers at the healthcare system, provider, patient, and community levels. Study participants are followed every 6 months for BP, CVD, and other study outcomes. The primary outcome is BP control (<130/80 mm Hg) at 18 months in phase 1, CVD events over 36 months in phase 2, and all-cause dementia at 48 months in phase 3. In addition, an extended observational follow-up will be conducted at Year 7 without further active intervention, to evaluate long-term outcomes including major cardiovascular events, dementia or cognitive outcomes, all-cause mortality, renal outcomes, and the sustainability of implementation fidelity.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Eligibility criteria for study villages:
Eligibility criteria of study participants:
Time frame: 18 months after baseline
The proportion of participants with controlled blood pressure(< 130/80 mm Hg)
Time frame: 36 months after baseline
Record the occurrence of newly diagnosed composite cardiovascular disease
Time frame: 48 months after baseline
Record all-cause dementia
Time frame: Year 7 after baseline
Record the occurrence of newly diagnosed composite cardiovascular disease
Time frame: 18 months after baseline
Mean systolic and diastolic pressure changes of participants
Time frame: 18 months after baseline
The proportion of participants with controlled blood pressure(< 140/90 mm Hg)
Time frame: 18 months after baseline
Use questionnaires to assess the proportion of participants who adhere to antihypertensive drugs
Time frame: 36 months after baseline
Number of newly diagnosed stroke
Time frame: 36 months after baseline
Number of newly diagnosed myocardial infarction
Time frame: 36 months after baseline
Number of patients with newly diagnosed heart failure requiring hospitalization or treatment
Time frame: 36 months after baseline
Number of cardiovascular disease death
Time frame: 36 months after baseline
Number of all-cause death
Time frame: 36 months after baseline
Mean systolic and diastolic pressure changes of participants
Time frame: 48 months after baseline
Record cognitive impairment no dementia
Time frame: 48 months after baseline
Record the composite outcome of dementia and cognitive impairment no dementia
Time frame: 48 months after baseline
Record death from all causes
Time frame: 48 months after baseline
Record the composite outcome of dementia or deaths
Time frame: 48 months after baseline
Record the composite and individual cardiovascular disease (myocardial infarction, stroke, heart failure requiring hospitalization or treatment, and cardiovascular death)
Time frame: 48 months after baseline
Record changes in mean systolic and diastolic blood pressure from baseline to 48 months
Time frame: 48 months after baseline
Record the proportion of hypertension control (BP <130/80 mm Hg or <140/90 mmHg) at 48 months
Time frame: Year 7 after baseline
Record the composite outcome of dementia and cognitive impairment no dementia
Time frame: Year 7 after baseline
Number of newly diagnosed stroke
Time frame: Year 7 after baseline
Number of newly diagnosed myocardial infarction
Time frame: Year 7 after baseline
Number of patients with newly diagnosed heart failure requiring hospitalization or treatment
Time frame: Year 7 after baseline
Number of cardiovascular disease death
Time frame: Year 7 after baseline
Number of all-cause death
Time frame: Year 7 after baseline
Record all-cause dementia
Time frame: Year 7 after baseline
Record cognitive impairment no dementia
Time frame: Year 7 after baseline
Record changes in mean systolic and diastolic blood pressure
Time frame: Year 7 after baseline
Record the proportion of hypertension control (BP <130/80 mm Hg or <140/90 mmHg)
Time frame: Year 7 after baseline
Use questionnaires to assess the proportion of participants who adhere to antihypertensive drugs
First Hospital of China Medical University
Other
Effectiveness of a Standardized Protocol-based Treatment Program on Hypertension Control in Rural China
Acronym: CRHC
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