Biomedical HIV/AIDS Prevention Program Yunnan

HIV/AIDS Clinical Trial

— B-HAPPY  

Official title:

Yunnan-ADARC HIV Prevention Program: Developing and Testing a Model to Implement and Sustain PrEP Delivery in China

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03992274
• Other study ID #: AAAS8800
• Secondary ID: 1R01MH119884-01A
• Status: Recruiting
• Phase: N/A
• Start date: August 1, 2020
• Est. completion date: October 2024

Study information

• Verified date: April 2022
• Source: Columbia University
• Contact: Kathrine Meyers, DrPH,MPP,MSc
• Phone: 2123046110
• Email: kam2157[@]cumc.columbia.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

B-HAPPY is an implementation project to study the process by which pre-exposure prophylaxis (PrEP) is introduced and integrated into a specific international health system facing high rates of HIV incidence among men who have sex with men. The study will use a stepped wedge design to compare implementation outcomes across eight municipalities in Yunnan, China.

Description:

B-HAPPY is an implementation science project that will introduce and evaluate the implementation of PrEP among over 1000 men who have sex with men (MSM), in eight municipalities in Yunnan, China. The project aims to compare the effectiveness of two implementation strategy bundles: 1) Standard Implementation: comprising the strategies that the Yunnan Center for Disease Control and Prevention would usually use to introduce HIV prevention innovations in the absence of the proposed study; and 2) Enhanced Implementation: standard implementation enhanced by a SIC-guided approach to plan and implement PrEP. This study will use a stepped-wedge design, where sites will go through four study periods: a Pre-Baseline Period (Routine Service with no PrEP Implementation), a Baseline Period (Standard Implementation of PrEP), an Experiment Period (Enhanced Implementation of PrEP), and a Post-Experiment-Observation Period. Sites are randomized to the timing of the intervention initiation, with 2 sites moving from Standard Implementation to Enhanced Implementation every 6 months. The intervention condition changes over time and the intervention effect is the difference in outcomes between the Baseline and Experiment Periods, and the Post-Experiment and Baseline Periods. The specific aims of the proposed study are: 1. To evaluate whether the addition of SIC-guided PrEP delivery (Enhanced Implementation) to standard health system PrEP delivery improves services outcomes. Through a stepped-wedge randomized trial across eight Yunnan municipalities, within site change over time will be examined; timing of introduction of Enhanced Implementation will be randomized across four cohorts of two sites each. Client-services outcomes include progress to achieving the "Five-80s" (patient PrEP awareness, screening, offering, initiation, continuation). 2. To examine the implementation process and efficiency of the Enhanced versus Standard implementation approaches. Using the Stages of Implementation Completion (SIC) and Cost of Implementing New Strategies (COINS) tools, sites will be monitored for implementation process and resource use. Outcomes will include proportion of implementation activities completed; duration of each implementation phase; and cost and resource allocation for completion of each implementation phase.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 352
• Est. completion date: October 2024
• Est. primary completion date: April 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years and older

Eligibility

This study will recruit two types of study participants: A. MSM clients at study sites; B. study staff who will be involved in the implementation of this project. A. MSM clients: Inclusion criteria: Clients at study sites (VCT or STI [sexually transmitted infections] clinics) are eligible

for inclusion in the study if they meet all of the following criteria:

• Aged 18 years or older
• Male sex at birth
• Willing and able to provide written consent form
• Able and willing to provide finger-scan and contact information
• Not infected with HIV-1
• Any male sex partner in past 12 months Exclusion Criteria: Clients at study sites (VCT or STI clinics) will be excluded from the study if they meet

any of the following criteria:

• Diagnosed with HIV or AIDS
• Signs or symptoms of acute HIV infection
• Unable to provide inform consent
• At enrollment, has any medical, psychological, or social condition that, in the opinion of the investigator, would jeopardize the health or wellbeing of the participant during the study or the integrity of the data B. Study staff: Inclusion criteria: Staff at study sites (VCT or STI clinics) are eligible for inclusion in the study if they

meet all of the following criteria:

• Aged 18 years or older
• Employed at site for at least 3 months
• Willing and able to provide consent Exclusion criteria: Staff at study sites (VCT or STI clinics) will be excluded from the study if they meet any

of the following criteria:

• Unable to provide consent
• At enrollment, has any medical, psychological, or social condition that, in the opinion of the investigator, would jeopardize the health or wellbeing of the participant during the study or the integrity of the data

Related Conditions & MeSH terms

• Acquired Immunodeficiency Syndrome
• HIV Infections
• HIV/AIDS

Intervention

Other:
• Enhanced implementation of PrEP
During Enhanced Implementation study sites will receive Implementation Support to plan and introduce PrEP by following the eight stages of the PrEP-adapted SIC. Implementation Support specifically will involve a centralized technical assistance system developed using US-based PrEP experience focused on addressing implementation issues identified through real-time analysis of client, clinic, and implementation data.

Locations

Country	Name	City	State
China	Yunnan Center for Disease Prevention and Control	Kunming	Yunnan

Sponsors (5)

Lead Sponsor	Collaborator
Columbia University	Hunter College of The City University of New York, National Institute of Mental Health (NIMH), Oregon Social Learning Center, Yunnan Center for Disease Control and Prevention

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	PrEP awareness	Number of clients who are aware of PrEP	Up to 48 months
Primary	PrEP eligible	Number of clients who are eligible for PrEP	Up to 48 months
Primary	PrEP offer	Number of clients who are offered PrEP	Up to 48 months
Primary	PrEP initiation	Number of clients initiating PrEP	Up to 48 months
Primary	PrEP continuation	Number of PrEP initiators who remain PrEP-eligible and sustain use at six months	Up to 48 months
Primary	Proportion of PrEP implementation activities completed	The SIC is an 8-stage observational assessment tool recording organizational site completion of implementation activities that map onto the three phases of implementation (Pre-Implementation, Implementation, Sustainability). Proportion of PrEP implementation activities completed will be measured.	Up to 48 months
Primary	Time to completion for each implementation phase	The SIC is an 8-stage observational assessment tool recording organizational site completion of implementation activities that map onto the three phases of implementation (Pre-Implementation, Implementation, Sustainability). Time to completion of each implementation phase will be measured.	Up to 48 months
Primary	Cost and resource allocation for completion of each implementation phase	Costs and resource allocation for completion of each implementation phase will be measured with the Cost of Implementing New Strategies (COINS) tool.	Up to 48 months