Undetectable = Untransmissible in Thailand (888/64) (888/64)

A Cross-sectional Survey of HIV Healthcare Providers and People Living With HIV in Thailand, and Their Awareness, Knowledge, and Implementation of Undetectable = Untransmissible

This is a cross-sectional study to assess awareness, knowledge, and implementation of the concept of U=U among Thai PLHIV and Thai HIV healthcare providers, as well as associated factors. Data will be collected on an online survey platform called Alchemer. Questions on the survey will evaluate awareness, knowledge, and implementation of U=U among participants, as well as collect sociodemographic information of participants.

Study Overview

Status

Completed

Conditions

Detailed Description

Recruitment

Recruitment will start with the distribution of a brief description of the survey, along with the link to the questionnaire itself. This will be distributed systematically through the use of the snowball sampling method on popular social networking platforms (such as Line, Instagram, WhatsApp, Facebook and Twitter), where 'seed' distributors, who may be categorised into different groups (such as age, gender identity and treatment facility for PLHIV or healthcare facility and type of healthcare provider for HIV healthcare providers), will share out links to a number of friends. Participants will be enrolled into the study once they click on the link leading them to the survey and complete the questionnaire.

Informed consent process

Consent will be obtained by action. A brief description of the survey will be distributed, along with the online link to the survey, which will be on SurveyGizmo. All data will be collected anonymously. A digitalised consent form will be presented to participants before they start the survey, which will outline the potential risks and benefits. All participants will be equal to or over the age of 18; therefore, parental consent is not needed.

Questionnaires

The questionnaire should take no more than 15 minutes to complete. The survey will be completed on Alchemer (formerly SurveyGizmo), a flexible, cross platform online survey software, or other popular online survey platforms with similar features, with the participant giving consent through action. Questions on the survey will evaluate awareness, knowledge, and implementation of U=U among participants, as well as collect sociodemographic information of participants. All the information collected will be kept confidential and anonymous, and participants cannot be identified in any way. There will be two different questionnaires, one for PLHIV and one for HIV healthcare providers; each survey will be slightly altered to for the appropriate participant category. After the questionnaire is completed, participants can choose to be redirected to educational webpages with more information on U=U.

Data analysis

Data used for analysis will only include data that is submitted through the online portal. It will be analysed using descriptive statistics including percentage, mean and standard deviations, as well as inferential statistics such as Chi Square test or t-test depending on the characteristics of data

Study Type

Observational

Enrollment (Actual)

770

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Bangkok
      • Pathum wan, Bangkok, Thailand, 10330
        • Institute of HIV Research and Innovation

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The study population will include any HIV healthcare providers or Thai people living with HIV on antiretroviral therapy. All participants must be of Thai nationality and 18 or above years of age.

Description

Inclusion Criteria:

  1. Thai HIV healthcare providers or Thai PLHIV on ART medication
  2. ≥ 18 years of age
  3. Can read, understand, and write Thai
  4. Provide consent to participate in the study

Exclusion Criteria:

  • None

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
People Living with HIV (PLHIV)
Thai people living with HIV, aged 18 or above, who are on Antiretroviral Therapy (ART)
HIV Healthcare Providers
Thai healthcare providers, including but not limited to doctors, nurses, counsellors, lay providers, pharmacists, lab technicians, etc., who take care of any persons living with HIV. All aged 18 or above

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To study awareness, knowledge, and implementation of U=U concept among Thai HIV healthcare providers
Time Frame: 12 months
Questions on the survey will evaluate awareness, knowledge, and implementation of U=U among participants. All the information collected will be kept confidential and anonymous, and participants cannot be identified in any way. Data used for analysis will only include data that is submitted through the online portal. It will be analysed using descriptive statistics including percentage, mean and standard deviations, as well as inferential statistics such as Chi Square test or t-test depending on the characteristics of data. We hypothesised that awareness will be low among Thai HIV healthcare providers (<50%), and thereby knowledge and implementation will be equal to or lower.
12 months
To study awareness, knowledge, and implementation of U=U and its physical, mental, and sexual health impacts on Thai PLHIV.
Time Frame: 12 months
Questions on the survey will evaluate awareness, knowledge, and implementation of U=U among participants. All the information collected will be kept confidential and anonymous, and participants cannot be identified in any way. Data used for analysis will only include data that is submitted through the online portal. It will be analysed using descriptive statistics including percentage, mean and standard deviations, as well as inferential statistics such as Chi Square test or t-test depending on the characteristics of data. We hypothesised that awareness will be relatively low among Thai PLHIV (~50%); therefore, knowledge and implementation will be equal to or lower.
12 months
To explore factors associated with awareness, knowledge, and implementation of U=U concept among Thai HIV healthcare providers and Thai PLHIV.
Time Frame: 12 months
Questions on the survey will also collect sociodemographic information of participants. All the information collected will be kept confidential and anonymous, and participants cannot be identified in any way. Data used for analysis will only include data that is submitted through the online portal. It will be analysed using descriptive statistics including percentage, mean and standard deviations, as well as inferential statistics such as Chi Square test or t-test depending on the characteristics of data. We hypothesised that factors most closely relative to awareness, knowledge, and implementation of U=U among PLHIV could be duration on ART, size of treatment facility, age, and gender identity. Among HIV healthcare providers, likely factors of influence will be size of healthcare facility and type of healthcare provider.
12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Nittaya Phanuphak, MD,Ph.D, INSTITUTE OF HIV RESEARCH AND INNOVATION FOUNDATION

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2021

Primary Completion (Actual)

March 1, 2024

Study Completion (Actual)

March 1, 2024

Study Registration Dates

First Submitted

December 11, 2021

First Submitted That Met QC Criteria

January 4, 2022

First Posted (Actual)

January 18, 2022

Study Record Updates

Last Update Posted (Actual)

March 12, 2024

Last Update Submitted That Met QC Criteria

March 8, 2024

Last Verified

January 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • IHRI012

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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