Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
770 participants
OBSERVATIONAL
2021-12-01
2024-03-01
Brief Summary
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Detailed Description
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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
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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People Living with HIV (PLHIV)
Thai people living with HIV, aged 18 or above, who are on Antiretroviral Therapy (ART)
No interventions assigned to this group
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
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. ≥ 18 years of age
3. Can read, understand, and write Thai
4. Provide consent to participate in the study
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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Institute of HIV Research and Innovation Foundation, Thailand
OTHER
Responsible Party
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Principal Investigators
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Nittaya Phanuphak, MD,Ph.D
Role: PRINCIPAL_INVESTIGATOR
INSTITUTE OF HIV RESEARCH AND INNOVATION FOUNDATION
Locations
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Institute of HIV Research and Innovation
Pathum Wan, Bangkok, Thailand
Countries
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Other Identifiers
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IHRI012
Identifier Type: -
Identifier Source: org_study_id
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