Intervention Study on Hypertension Management Combined With Health Promotion at Commune Level
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|ClinicalTrials.gov Identifier: NCT01560806|
Recruitment Status : Completed
First Posted : March 22, 2012
Last Update Posted : March 22, 2012
A quasi-experimental study design was chosen to compare the model of hypertension management at commune-level with conventional management for people with high blood pressure in two communes (one for intervention versus one for reference).
A intervention model included the commune-based programme on hypertension management combined with comprehensive health promotion campaigns
|Condition or disease||Intervention/treatment||Phase|
|Hypertension Cardiovascular Risk Factor Lifestyle||Other: Commune Hypertension Management||Not Applicable|
A quasi-experimental study design was chosen: two communes were purposively selected from Ba-Vi setting: Phu-Phuong for reference and Phu-Cuong for intervention communes A hypertension management programme and the nested comprehensive health promotion campaigns were implemented simultaneously in Phu-Cuong while nothing performed in Phu-Phuong except for local conventional healthcare services.
The health promotion campaigns aimed at smoking cessation, reduction of alcohol consumption, encourage of unsalted diet and physical activity, all of which targeted to every local inhabitants.
The hypertension management programme focused on monthly check-ups, drug delivery and individual lifestyle consultation, all of which targeted to hypertensives only.
Baseline cross-sectional survey was used to assess cardiovascular pattern in local community before intervention and recruit people with high blood pressure for the management programme in intervention commune Repeated cross-sectional surveys were used to evaluate the impacts of health promotion.
Cohort study on hypertensives was used to evaluate the impacts of the management programme.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||2400 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||Quasi-experimental Intervention Study on Hypertension Management Combined With Comprehensive Healthy Lifestyle Promotion at Commune Level|
|Study Start Date :||December 2006|
|Actual Primary Completion Date :||December 2009|
|Actual Study Completion Date :||December 2009|
No Intervention: Conventional Healthcare services
People with high blood pressure detected during screening survey or opportunistically during study period will be referred to receive the conventional health care services for hypertension at district hospital or local commune health station
Experimental: Commune Hypertension Management
People with high blood pressure were managed in commune-based hypertension management programme
Other: Commune Hypertension Management
People with high blood pressure will be invited to join the management programme, with monthly check-up, delivery of multi anti-hypertensive drugs and lifestyle consultation.
Antihypertensive drugs delivered to local patients included (1) low-dose hypothiazide diuresis, (2) calcium channel blocker and (3) ACEI
Other Name: Commune-based Hypertension Management
- Proportion of people with high blood pressure receiving treatment and being controlled in intervention commune [ Time Frame: Baseline and after 3-year ]Changes in proportion of treated and controlled hypertension after 3-years intervention compared to baseline
- Changes in prevalences of behavioral cardiovascular risk factors in intervention commune [ Time Frame: Baseline and after 3-year ]Changes in prevalence of behavioral cardiovascular risk factors after 3-years intervention compared to baseline
- Changes in average blood pressure in the population in intervention commune [ Time Frame: Baseline and after 3 years ]Changes in average systolic and diastolic blood pressure in the studied population after 3-year intervention
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01560806
|Vietnam National Heart Institute|
|Hanoi, Vietnam, 10000|
|Principal Investigator:||Son T. Pham, MD||Vietnam National Heart Institute|