Actively Recruiting

Phase Not Applicable
Age: 30Years +
All Genders
NCT06081010

FCHV-HTN Implementation Trial in Nepal

Led by Yale University · Updated on 2026-02-06

3572

Participants Needed

1

Research Sites

160 weeks

Total Duration

On this page

Sponsors

Y

Yale University

Lead Sponsor

D

Dhulikhel Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this hybrid type III study incorporating a cluster-randomized trial is to assess the effect of a community health worker-led hypertension prevention and control program (CHPC) on the implementation outcomes and clinical outcomes among patient with hypertension in central Nepal. The main questions it aims to answer are: 1\. What is the level of implementation outcomes, including reach, adoption, implementation fidelity, and maintenance of the CHPC implementation strategy at the patient, provider, and health system levels? 2: What is the effectiveness of the CHPC implementation strategy compared to facility-based intervention on systolic BP via a cluster randomized controlled trial. 3: What is the implementation cost and cost-effectiveness of the CHPC implementation strategy? Participants will receive four follow-up group meetings or home visits every three months for a year by a community health worker. Researchers will compare if there is a significant difference in systolic blood pressure between those who receive this intervention and those who do not receive the intervention in the same community.

CONDITIONS

Official Title

FCHV-HTN Implementation Trial in Nepal

Who Can Participate

Age: 30Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • High blood pressure (BP) of 140/90 mmHg or higher.
Not Eligible

You will not qualify if you...

  • Severe illness requiring bed rest
  • Pregnant women, due to their special health needs

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Trial Site Locations

Total: 1 location

1

Dhulikhel Hospital

Dhulikhel, Nepal

Actively Recruiting

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Research Team

D

Donna Spiegelman, ScD

CONTACT

E

Eleni Mersiadis

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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