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Clinical Trials/NCT02428075
NCT02428075
Completed
Not Applicable

Protocol for Community-based Intervention for Blood Pressure Reduction in Nepal: a Community-based Cluster Randomized Controlled Trial

University of Aarhus1 site in 1 country1,638 target enrollmentNovember 2015
ConditionsHypertension

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
University of Aarhus
Enrollment
1638
Locations
1
Primary Endpoint
Change in mean systolic blood pressure in normotensive, pre-hypertensive and hypertensive populations
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Hypertension contributes to significant burden of cardiovascular diseases (CVDs) in low and middle-income countries; however responses to CVDs are inadequate particularly due to lack of conclusive evidence on population based approach to hypertension control. This is a community based cluster randomized trial involving family based health education through female community health volunteers in Nepal. People ≥25 years of age and who are listed in the voter list 2006 of Electoral Commission of Nepal who were either hypertensive, pre-hypertensive or normotensive are eligible for eligible for participation in the study. A computer generated random codes will be used to divide clusters into treatment and control arm. FCHVs will conduct family based health education and blood pressure measurements in the treatment arm vs not any interventions in control arm. Independent assessors will conduct the baseline and end line assessment of the intervention. Intention to treat analysis and per protocol analysis will be used in analysis to detect significant differences between treatment and control group participants at baseline and follow up. Student t-tests for normally distributed variables and chi-squared tests for categorical variables will be used. In the event that randomization do not control for differences between the treatment and control groups on baseline characteristics, the investigators will statistically control for those differences in subsequent analysis of program effects. The final outcome will be modeled by using multiple linear regressions analysis. The investigators hope that if the intervention outcomes shows positive effects in treatment arm, this approach can be adopted into the existing health care delivery system in Nepal. Assessing the FCHVs' ability may further contribute to developing a policy that can be scaled-up to a national level. The lessons learned from this project may also be replicated in rural areas and similar settings elsewhere in the world.

Registry
clinicaltrials.gov
Start Date
November 2015
End Date
February 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dinesh Neupane

PhD Fellow

University of Aarhus

Eligibility Criteria

Inclusion Criteria

  • People ≥25 years of age and who are listed in the voter list of 2006 and those participated in our prevalence study are eligible for inclusion in the baseline survey. - Person who give consent to participate in our intervention study,
  • does not have any plan to migrate from Lekhnath Municipality for at least 1 year,
  • non-pregnant women and
  • personal who are not severely ill will be included as eligible participants.

Exclusion Criteria

  • No consent
  • Pregnant women
  • Severely Il
  • Plan for migration for the study municipality within 1 year

Outcomes

Primary Outcomes

Change in mean systolic blood pressure in normotensive, pre-hypertensive and hypertensive populations

Time Frame: 1 year

Study Sites (1)

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