The Georgia Latino AIDS/HIV Diagnosis and Linkage in Youth (GLADLY) Project

NCT ID: NCT02562092

Last Updated: 2021-01-22

Study Results

Results pending

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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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-08-31

Study Completion Date

2017-08-31

Brief Summary

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This study aims to understand the barriers to receiving HIV testing and retention of care for at risk and HIV positive young adults. This study also seeks to determine the feasibility and acceptability of HIV testing in a non-clinical setting.

Detailed Description

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This study aims to identify factors that can facilitate or impede the use of non-clinical HIV testing venues as well as identify potential testing sites and assess acceptability of an HIV prevention intervention. In addition, the study will implement a pilot intervention to test the feasibility non-clinical HIV testing and follow up events for HIV positive youth.

Conditions

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HIV

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Focus Group

Participants will complete a questionnaire and will be involved in a group discussion regarding good sites within the community to perform HIV testing.

Group Type NO_INTERVENTION

No interventions assigned to this group

Venue Testing Group- Negative Test

Participants will perform a rapid HIV test and will be asked to answer questions about their sexual life and living situation. No followup is needed for a negative HIV test.

Group Type OTHER

Reducing Risk Behavior

Intervention Type BEHAVIORAL

A small survey will be conducted to identify risk factors and assess demographics. Participants will receive psychological support and counseling on reducing risk behavior for one year.

Venue Testing Group- Positive Test

Participants will perform a rapid HIV test and will be asked to answer questions about their sexual life and living situation. Participants with a positive HIV test will receive care from a psychologist and case manager for one year.

Group Type OTHER

Support and Guidance

Intervention Type BEHAVIORAL

A small survey will be conducted to identify risk factors and assess demographics. Participants with a positive HIV test will receive standard HIV care, support, and guidance from a psychologist and case manager including an assessment of basic needs (food, clothing, shelter), and counseling on risk taking behaviors for one year.

Interventions

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Reducing Risk Behavior

A small survey will be conducted to identify risk factors and assess demographics. Participants will receive psychological support and counseling on reducing risk behavior for one year.

Intervention Type BEHAVIORAL

Support and Guidance

A small survey will be conducted to identify risk factors and assess demographics. Participants with a positive HIV test will receive standard HIV care, support, and guidance from a psychologist and case manager including an assessment of basic needs (food, clothing, shelter), and counseling on risk taking behaviors for one year.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Sexually active
* HIV positive or negative
* Latino youth ages 18-24 years
* Residents of the state of Georgia and can understand spoken and written English or Spanish.
Minimum Eligible Age

18 Years

Maximum Eligible Age

24 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Emory University

OTHER

Sponsor Role lead

Responsible Party

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Andres Camacho-Gonzalez

Assistant Professor of Pediatrics

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Andres Camacho-Gonzalez

Role: PRINCIPAL_INVESTIGATOR

Emory University

Locations

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Grady Health System

Atlanta, Georgia, United States

Site Status

Ponce De Leon Center

Atlanta, Georgia, United States

Site Status

Countries

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United States

Other Identifiers

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IRB00080817

Identifier Type: -

Identifier Source: org_study_id

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