HY-TREC: Conquering Hypertension in Vietnam: Solutions at Grassroots Level

Sponsor
Ministry of Health, Vietnam (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03590691
Collaborator
University of Massachusetts, Worcester (Other), Baylor Research Institute (Other), National Heart, Lung, and Blood Institute (NHLBI) (NIH)
671
1
2
43.7
15.3

Study Details

Study Description

Brief Summary

The objectives of the proposed project are to evaluate the implementation and effectiveness of two multi-faceted community and clinic-based strategies on the control of elevated blood pressure (BP) among adults in Vietnam via a cluster-randomized trial design.

Sixteen communities will be randomized to either an intervention (8 communities) or comparison group (8 communities). Eligible and consenting adult study participants with HTN (n = 680) will be assigned to intervention/comparison status based on the community in which they reside.

Condition or Disease Intervention/Treatment Phase
  • Other: Vietnam National Hypertension Program
  • Other: Expanded community health worker services
  • Behavioral: Storytelling intervention
  • Behavioral: Home blood pressure self-monitoring
N/A

Detailed Description

"Đương đầu với bệnh Tăng huyết áp ở Việt Nam: Giải pháp từ Y tế cơ sở (Conquering

Hypertension in Vietnam: Solutions at Grassroots level)" (Vietnam Hy-TREC) Background:

Similar to other low- and middle-income countries, Vietnam has been experiencing an epidemiologic transition with an increasing burden of non-communicable diseases (NCD). The key risk factors for cardiovascular disease (CVD) are either on the rise or at alarming levels in Vietnam, particularly hypertension (HTN). Inasmuch, the burden of CVD will continue to increase in Vietnamese men and women unless effective prevention and control measures are put in place.

Objectives: This project will be evaluating the implementation and effectiveness of two multi-faceted community and clinic-based strategies for the control of hypertension among adults residing in the rural Red River Delta region of Vietnam with uncontrolled hypertension through use of a cluster-randomized trial design.

Study population:Sixteen communities will be randomized to either an intervention (8 communities) or comparison group (8 communities). Eligible and consentingadult study participants with uncontrolled HTN (n = 680) will be assigned to intervention/comparison status based on the community in which they reside.

Methods: Both comparison and intervention groups will receive a multi-level intervention modeled after the Vietnam National Hypertension Program. Components of this program include education and practice change modules for health care providers, accessible reading materials for patients, and a community awareness multi-media program. In addition to the Vietnam National Hypertension Program, the intervention group only will receive three carefully selected enhancements integrated into routine clinical care: (1) expanded community health worker services; (2) home blood pressure self-monitoring; and (3) a "storytelling intervention," previously developed and pilot tested for feasibility and effectiveness by members of the research team. The storytelling intervention consists of interactive, literacy-appropriate, and culturally sensitive multimedia storytelling modules for motivating behavior change through the power of patients speaking in their own voice. Based on preferences that emerged during our formative work with our partnering rural communities, the storytelling intervention will be delivered by DVD, with serial installments at baseline and again at 3, 6, and 12 months after trial enrollment. Differences in changes in blood pressure and other factors will be assessed in both study groups at several follow-up time points. In conjunction with the work done being accomplished during the pilot feasibility study, current efforts by the Vietnam National Hypertension Program, and the proposed investigation, this project addresses a serious clinical and public health problem in Vietnam by implementing the first community-based study using a culturally-literacy appropriate intervention to control elevated blood pressure among the adult Vietnamese population.

Study Design

Study Type:
Interventional
Actual Enrollment :
671 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
A cluster-randomized trial designA cluster-randomized trial design
Masking:
Single (Participant)
Primary Purpose:
Supportive Care
Official Title:
Conquering Hypertension in Vietnam: Solutions at Grassroots Level
Actual Study Start Date :
Nov 7, 2019
Anticipated Primary Completion Date :
Jun 30, 2023
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Comparison group

Vietnam National Hypertension Program: a training program for health care workers and a health educational program for general public.

Other: Vietnam National Hypertension Program
A training program for health care workers including physicians and nurses and a health educational program for general public regarding hypertension management at community level will be implemented

Experimental: Intervention group

Vietnam National Hypertension Program including training program for health care workers and an health educational program for general public. PLUS Three selected enhancements integrated into routine clinical care: expanded community health worker services; home blood pressure self-monitoring; and a "storytelling intervention".

Other: Vietnam National Hypertension Program
A training program for health care workers including physicians and nurses and a health educational program for general public regarding hypertension management at community level will be implemented

Other: Expanded community health worker services
A training program will be implemented for community health workers regarding hypertension management at community level so that they can assist patients better manage their blood pressure at home.

Behavioral: Storytelling intervention
The storytelling intervention consists of interactive, literacy-appropriate, and culturally sensitive multimedia storytelling modules for motivating behavior change through the power of patients speaking in their own voice. Based on preferences that emerged during the researchers' formative work with the partnering rural communities, the storytelling intervention will be delivered by DVD, with serial installments at baseline and at 3, 6, and 12 months after trial enrollment.

Behavioral: Home blood pressure self-monitoring
Patients with hypertension will be provided blood pressure monitors and guided to self-measure their blood pressure and to record their blood pressure daily at home.

Outcome Measures

Primary Outcome Measures

  1. Change from baseline in systolic blood pressure at 12 months [At baseline and at 3, 6, and 12 months after trial enrollment]

    Changes in systolic blood pressure will be assessed in both study groups at several follow-up time points.

Secondary Outcome Measures

  1. Change from baseline in diastolic blood pressure at 12 months [At baseline and at 3, 6, and 12 months after trial enrollment]

    Changes in diastolic blood pressure will be assessed in both study groups at several follow-up time points.

  2. Change from baseline in medication adherence self-efficacy score at 12 months [At baseline and 12 months after trial enrollment]

    Patients medication adherence self-efficacy will be measured using the Medication Adherence Self-efficacy Scale (MASES) instrument.

  3. Changes from the baseline in proportions of patients with risk factors for CVD at 12 months [At baseline and 12 months after trial enrollment]

    WHO STEPs questionnaires will be used to collect data on risk factors for CVD including tobacco use, alcohol consumption, salt intake and physical activities. Proportions of patients with current smoking, excessive use of alcohol, high salt intake, and low physical activity will be calculated.

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. residence in a study commune;

  2. at least 25 years old;

  3. presence of uncontrolled HTN based on the screening process described previously and

  4. willingness to provide informed consent.

Exclusion Criteria:
  1. participation in another hypertension research study;

  2. pregnant;

  3. advanced cognitive impairment; or

  4. previous participation in developing or having exposure to the hypertension storytelling modules.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Health Strategy and Policy Institute Hanoi Vietnam 10000

Sponsors and Collaborators

  • Ministry of Health, Vietnam
  • University of Massachusetts, Worcester
  • Baylor Research Institute
  • National Heart, Lung, and Blood Institute (NHLBI)

Investigators

  • Principal Investigator: Tran Thi Mai Oanh, PhD, Health Strategy and Policy Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tran Thi Mai Oanh, Principal Investigator, Director of Health Strategy and Policy Institute, Ministry of Health, Vietnam
ClinicalTrials.gov Identifier:
NCT03590691
Other Study ID Numbers:
  • 5552338110000
  • 1U01HL138631-01
First Posted:
Jul 18, 2018
Last Update Posted:
Mar 11, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Tran Thi Mai Oanh, Principal Investigator, Director of Health Strategy and Policy Institute, Ministry of Health, Vietnam
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 11, 2022