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Active, Not Recruiting

NCT Number: NCT03527719

China Rural Hypertension Control Project

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The First Hospital of China Medical University

Shenyang, Liaoning, 110001, China

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Eligibility criteria for study villages:

  • The village has a regular village doctor who is willing to participate in the hypertension control project
  • The village does not plan to merge with other villages within 3 years
  • The village is at least 2 kilometers away from other participating villages
  • The village participates in the China New Rural Cooperative Medical Scheme

Eligibility criteria of study participants:

  • Men or women aged ≥40 years
  • Mean untreated systolic BP ≥140 mm Hg and/or diastolic BP ≥90 mm Hg or mean treated systolic BP ≥130 mm Hg and/or diastolic BP ≥80 mm Hg for individuals without a history of clinical CVD; or mean treated/untreated systolic BP ≥130 mm Hg and/or diastolic BP ≥80 mm Hg for individuals with a history of clinical coronary heart disease, heart failure, stroke, diabetes, or chronic kidney disease
  • Have lived in a participating village for at least 6 months
  • No intention to migrate within next 3 years
  • Taking part in the New Rural Cooperative Medical Scheme
  • Not pregnant or planning to become pregnant
  • No malignant tumors and life expectancy ≥3 years
  • Willing to participate and able to sign informed consent

Treatment and study plan

Village-doctor-led multifaceted intervention

Other
  • Establishing a network including hypertension specialists at city/county hospitals, primary care physicians at township hospitals, and village doctors to collaboratively manage hypertension
  • Using hypertension control rate as one of the metrics for incentive supplements to village doctors
  • Providing discounted or free antihypertensive medications to patients with hypertension
  • Training village doctors to measure blood pressure according to a standard protocol
  • Training village doctors to use a simple stepwise protocol for hypertension treatment
  • Training village doctors to conduct health coaching on lifestyle change (e.g., lowering sodium and alcohol intake) and medication adherence
  • Providing free blood-pressure monitor and training to patients for home blood pressure measurement
  • Encouraging lifestyle change and medication adherence
  • Connecting patients through WeChat or telephone for group social support

Primary outcomes

  1. Primary Outcome of Phase 1: Hypertension control rate

    Time frame: 18 months after baseline

    The proportion of participants with controlled blood pressure(< 130/80 mm Hg)

  2. Primary Outcome of Phase 2: Composite cardiovascular disease outcome

    Time frame: 36 months after baseline

    Record the occurrence of newly diagnosed composite cardiovascular disease

  3. Primary Outcome of Phase 3: All-cause dementia

    Time frame: 48 months after baseline

    Record all-cause dementia

  4. Primary Outcome of Extension Study: Composite cardiovascular disease outcome

    Time frame: Year 7 after baseline

    Record the occurrence of newly diagnosed composite cardiovascular disease

Secondary outcomes

  1. Secondary Outcome of Phase 1: Mean systolic and diastolic pressure changes

    Time frame: 18 months after baseline

    Mean systolic and diastolic pressure changes of participants

  2. Secondary Outcome of Phase 1: Hypertension control rate(<140/90 mm)

    Time frame: 18 months after baseline

    The proportion of participants with controlled blood pressure(< 140/90 mm Hg)

  3. Secondary Outcome of Phase 1: Adherence to antihypertensive medication rate

    Time frame: 18 months after baseline

    Use questionnaires to assess the proportion of participants who adhere to antihypertensive drugs

  4. Secondary Outcome of Phase 2: Stroke

    Time frame: 36 months after baseline

    Number of newly diagnosed stroke

  5. Secondary Outcome of Phase 2: Myocardial infarction

    Time frame: 36 months after baseline

    Number of newly diagnosed myocardial infarction

  6. Secondary Outcome of Phase 2: Heart failure requiring hospitalization or treatment

    Time frame: 36 months after baseline

    Number of patients with newly diagnosed heart failure requiring hospitalization or treatment

  7. Secondary Outcome of Phase 2: Cardiovascular disease death

    Time frame: 36 months after baseline

    Number of cardiovascular disease death

  8. Secondary Outcome of Phase 2: All-cause death

    Time frame: 36 months after baseline

    Number of all-cause death

  9. Secondary Outcome of Phase 2: Mean systolic and diastolic pressure changes

    Time frame: 36 months after baseline

    Mean systolic and diastolic pressure changes of participants

  10. Secondary Outcome of Phase 3: Cognitive impairment no dementia

    Time frame: 48 months after baseline

    Record cognitive impairment no dementia

  11. Secondary Outcome of Phase 3: Composite outcome of dementia and cognitive impairment no dementia

    Time frame: 48 months after baseline

    Record the composite outcome of dementia and cognitive impairment no dementia

  12. Secondary Outcome of Phase 3: Death from all causes

    Time frame: 48 months after baseline

    Record death from all causes

  13. Secondary Outcome of Phase 3: Composite outcome of dementia or deaths

    Time frame: 48 months after baseline

    Record the composite outcome of dementia or deaths

  14. Secondary Outcome of Phase 3: Composite and individual cardiovascular disease (myocardial infarction, stroke, heart failure requiring hospitalization or treatment, and cardiovascular death)

    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)

  15. Secondary Outcome of Phase 3: Changes in mean systolic and diastolic blood pressure from baseline to 48 months

    Time frame: 48 months after baseline

    Record changes in mean systolic and diastolic blood pressure from baseline to 48 months

  16. Secondary Outcome of Phase 3: Proportion of hypertension control (BP <130/80 mm Hg or <140/90 mmHg) at 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

  17. Secondary Outcome of Extension Study: Composite outcome of dementia and cognitive impairment no dementia

    Time frame: Year 7 after baseline

    Record the composite outcome of dementia and cognitive impairment no dementia

  18. Secondary Outcome of Extension Study: Stroke

    Time frame: Year 7 after baseline

    Number of newly diagnosed stroke

  19. Secondary Outcome of Extension Study: Myocardial infarction

    Time frame: Year 7 after baseline

    Number of newly diagnosed myocardial infarction

  20. Secondary Outcome of Extension Study: Heart failure requiring hospitalization or treatment

    Time frame: Year 7 after baseline

    Number of patients with newly diagnosed heart failure requiring hospitalization or treatment

  21. Secondary Outcome of Extension Study: Cardiovascular disease death

    Time frame: Year 7 after baseline

    Number of cardiovascular disease death

  22. Secondary Outcome of Extension Study: All-cause death

    Time frame: Year 7 after baseline

    Number of all-cause death

  23. Secondary Outcome of Extension Study: All-cause dementia

    Time frame: Year 7 after baseline

    Record all-cause dementia

  24. Secondary Outcome of Extension Study: Cognitive impairment no dementia

    Time frame: Year 7 after baseline

    Record cognitive impairment no dementia

  25. Secondary Outcome of Extension Study: Mean systolic and diastolic pressure changes

    Time frame: Year 7 after baseline

    Record changes in mean systolic and diastolic blood pressure

  26. Secondary Outcome of Extension Study: Proportion of hypertension control (BP <130/80 mm Hg or <140/90 mmHg)

    Time frame: Year 7 after baseline

    Record the proportion of hypertension control (BP <130/80 mm Hg or <140/90 mmHg)

  27. Secondary Outcome of Extension Study: Adherence to antihypertensive medication rate

    Time frame: Year 7 after baseline

    Use questionnaires to assess the proportion of participants who adhere to antihypertensive drugs

Sponsors and collaborators

Lead sponsor

First Hospital of China Medical University

Other

Collaborators

  • Chaoyang Central Hospital
  • Disease Control and Prevention Centre of Chaoyang City
  • Disease Control and Prevention Centre of Liaoning Province
  • First Affiliated Hospital Xi'an Jiaotong University
  • Hanzhong People's Hospital
  • Shengjing Hospital
  • Tongji Hospital
  • Tulane University

Registry information

Official study title

Effectiveness of a Standardized Protocol-based Treatment Program on Hypertension Control in Rural China

Acronym: CRHC

Important dates

Study start
2018
Primary completion
2026
Study completion
2026
First posted
May 17, 2018
Registry last updated
Dec 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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