Enhancing the Role of Commune Health Workers in HIV and Drug Control: A Randomized Controlled Trial

This proposed study is an initiative for HIV prevention and care that integrates intervention efforts at multiple strata: Community Health Workers (CHWs), Injecting Drug Users (IDUs), and their Family Members (FMs). The proposed study will demonstrate the process of development, implementation, and evaluation of an intervention for CHWs, IDUs, and their FMs. One aim is to increase the CHWs' capacities to effectively interact with IDUs and FMs for HIV and drug use prevention and treatment. Using a combination of participatory action research and a randomized controlled trial design, this study has the potential to maximize PEPFAR impact in Vietnam and other PEPFAR-funded countries by identifying a sustainable mix of interventions and their implementation in different settings. The findings may benefit not only Vietnam but also a global audience by investigating enhanced methods for controlling the HIV epidemic.

Study Overview

• Status: Completed
• Conditions: Drug Dependence
• Intervention / Treatment: Behavioral: Intervention to Address Drug Use and HIV in Vietnam

Detailed Description

Vietnam is currently facing an HIV epidemic that had affected approximately 280,000 people by the end of 2009. Injecting Drug Use (IDU) is principal driver of the HIV epidemic, contributing to between 32 % and 58 % of all HIV cases in various provinces. However, it has proven difficult to address the needs of IDUs, a high-risk group, given the prevalence of stigmatization and drug use in Vietnamese society. In addition, Vietnamese people are highly family oriented and most young IDUs have daily family contact of live in their parents' homes. Thus the burden on the family is substantial, and even greater if the IDU is HIV+.

The study will be implemented in two provinces in Vietnam: Phu Tho and Vinh Phuc. A randomized controlled trial will be conducted to evaluate the impact of the intervention in 60 commune health centers. From each center we will recruit 5 Community Health Workers (CHWs), 15 Injecting Drug Users (IDUs), and 10 Family Members (FMs) (totaling 300 CHWs, 900 IDUs, and 600 FMs). The outcomes will be evaluated at 3-, 6-, 9-, and 12- month follow-up assessments. The specific aims of the study are as follows:

1. To develop and implement an integrated intervention, CHW CARE, for CHWs, IDUs, and their FMS in Vietnam
2. To evaluate the feasibility and operational procedures of the intervention with an implementation pilot, including process evalution and monitoring, and participants feedback.
3. To assess the impact of the intervention by comparing outcome measures of CHWs, IDUs, and FMs in the intervention group to those in the control group.
4. To explore the relationships between the intervention outcomes of CHWs, IDUs, and FMs.

• Study Type: Interventional
• Enrollment (Actual): 1800
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Vietnam
  • Phú Thọ, Vietnam
    • Phú Thọ commune health centers
  • Vĩnh Phúc, Vietnam
    • Vĩnh Phúc commune health centers

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (ADULT, OLDER_ADULT)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

Injecting Drug Users:

• Age 18 or over
• Having a history of drug use
• Currently residing in the selected commune, and have no plan to move to other communes in the following year
• Voluntary informed consent

Family members of Injecting Drug Users:

• Age 18 or over
• Immediate or extended family member of the Injecting Drug User.
• Previous knowledge of the drug use of the IDU.
• Voluntary informed consent
• Currently residing in the selected commune, and have no plan to move to other communes in the following year

Community Health Workers:

• Age 18 or over
• Doctor, nurse, or other care provider working at the selected commune health centers
• Informed consent

Exclusion Criteria:

Injecting Drug Users:

• Those who have psychosis or neurological damage, or cannot understand the study purposes as judged by the interviewer in consultation with a clinic supervisor, will be excluded
• Does not meet other inclusion criteria

Family members of Injecting Drug Users:

• Those who have psychosis or neurological damage, or cannot understand the study purposes as judged by the interviewer in consultation with a clinic supervisor, will be excluded
• Does not meet other inclusion criteria

Community Health Workers:

• Inability to give informed consent
• Does not meet other inclusion criteria

Study Plan

How is the study designed?

Design Details

• Primary Purpose: PREVENTION
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: NONE

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
NO_INTERVENTION: Control; Community Health Workers (CHWs) in the control group will be invited to one group lecture didactically reviewing medical ethics, and the attending CHWs will be requested to pay a home visit to participating IDUs and FMs after the lecture.
EXPERIMENTAL: Intervention; Intervention for CHWs: 3 sessions will cover the understanding stigma and its impact, self-protection and universal precaution adherence, effective communication with patients and family members, and motivational enhancement for behavioral change. Intervention for IDUs: CHWs who participate in the intervention will be required to conduct 3 individual sessions with participating IDUs covering the following topics: physical health, risk reduction behaviors, mental health, and community integration. Intervention for FMs: CHWs who participate in the intervention will be required to conduct 2 group sessions with participating FMs covering the following topics: healthy family routine, coping with caregiver burdens, enhance family relationships, support positive behavior change.	Behavioral: Intervention to Address Drug Use and HIV in Vietnam; Intervention for CHWs: 3 sessions will cover the understanding stigma and its impact, self-protection and universal precaution adherence, effective communication with patients and family members, and motivational enhancement for behavioral change. Intervention for IDUs: CHWs who participate in the intervention will be required to conduct 3 individual sessions with participating IDUs covering the following topics: physical health, risk reduction behaviors, mental health, and community integration. Intervention for FMs: CHWs who participate in the intervention will be required to conduct 2 group sessions with participating FMs covering the following topics: healthy family routine, coping with caregiver burdens, enhance family relationships, support positive behavior change.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Community Health Worker (CHW) Interaction with patients	Provider-Client interaction scale will be used.	Changes from baseline to 3-, 6-, 9- and 12- month follow-up
Injecting Drug User (IDU) drug use	Urine test results	baseline, 3-, 6-, 9- and 12- month follow-up

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Community Health Worker (CHW) job safety, support, and satisfaction	This will be assessed by perceived risk at work and institutional support. Additionally by job satisfaction using a 29-item scale.	Changes from baseline to 3-, 6-, 9-, and 12- month follow-up
Community Health Worker (CHW) knowledge and adherence to universal precautions	This will be assessed with the universal precautions knowledge scale.	Changes from baseline to 3-, 6-, 9-, and 12- month follow-up
Injecting Drug User (IDU) family and social support	This is measured by two instruments. Social Support Questionnaire (Short; SSQ6) is a 6-item assessment to measure satisfaction of social support. Number of social support providers is captured up to 9 people in various support dimensions (Sarason et al., 1983). Medical Outcomes Study- Social Support Scale (MOS-SS) is a 20-item scale that measures the strength of perceived social support available. The scale consists of five dimensions: emotional support, informational support, tangible support, positive social interaction, and affection	Changes from baseline to 3-, 6-, 9- and 12- month follow-up
Family Member (FM) social support	This is measured by two instruments. Social Support Questionnaire (Short; SSQ6) is a 6-item assessment to measure satisfaction of social support. Number of social support providers is captured up to 9 people in various support dimensions (Sarason et al., 1983). Medical Outcomes Study- Social Support Scale (MOS-SS) is a 20-item scale that measures the strength of perceived social support available. The scale consists of five dimensions: emotional support, informational support, tangible support, positive social interaction, and affection.	Changes from baseline to 3-, 6-, 9-, and 12- month follow-up
Community Health Worker (CHW) general prejudicial attitude	A scale will be used	Changes from baseline to 3-, 6-, 9- and 12- month follow-up
Family Member (FM) Caregiver burden/coping	Caregiver burden and coping scales will be used	Changes from baseline to 3-,6-,9-, and 12-month follow-up

Collaborators and Investigators

• Sponsor: University of California, Los Angeles
• Collaborators: National Institute of Hygiene and Epidemiology, Vietnam

Study record dates

Study Major Dates

• Study Start (ACTUAL): July 1, 2014
• Primary Completion (ACTUAL): May 1, 2018
• Study Completion (ACTUAL): May 1, 2018

Study Registration Dates

• First Submitted: May 1, 2014
• First Submitted That Met QC Criteria: May 5, 2014
• First Posted (ESTIMATE): May 6, 2014

Study Record Updates

• Last Update Posted (ACTUAL): October 12, 2018
• Last Update Submitted That Met QC Criteria: October 11, 2018
• Last Verified: October 1, 2018

More Information

Terms related to this study

• Keywords: HIV; Stigma; FM; CHWs; PLH; Injecting Drug Users
• Additional Relevant MeSH Terms: Mental Disorders; Chemically-Induced Disorders; Substance-Related Disorders
• Other Study ID Numbers: R01DA033609-01 (NIH)