- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05195346
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
Study Overview
Status
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
Enrollment (Actual)
Contacts and Locations
Study Locations
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Bangkok
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Pathum wan, Bangkok, Thailand, 10330
- Institute of HIV Research and Innovation
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Thai HIV healthcare providers or Thai PLHIV on ART medication
- ≥ 18 years of age
- Can read, understand, and write Thai
- Provide consent to participate in the study
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
|---|
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People Living with HIV (PLHIV)
Thai people living with HIV, aged 18 or above, who are on Antiretroviral Therapy (ART)
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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
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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To study awareness, knowledge, and implementation of U=U concept among Thai HIV healthcare providers
Time Frame: 12 months
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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.
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12 months
|
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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
|
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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.
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12 months
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Collaborators and Investigators
Investigators
- Principal Investigator: Nittaya Phanuphak, MD,Ph.D, INSTITUTE OF HIV RESEARCH AND INNOVATION FOUNDATION
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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