Feasibility of Positive Links for Youth Care Engagement Intervention

The University of Texas Health Science Center at San Antonio30 enrolled

Overview

A small pilot study to assess feasibility and acceptability of the PL4Y intervention.

After completing enrollment and informed consent, participants will be randomly assigned to PL4Y in a 2:1 fashion (intervention:control) with a target enrollment of 40 receiving the intervention and 20 in the control arm for a total of 60 participants. There is no blinding in this study protocol.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

HIV Antibody Positivity

Interventions

Mobile health appBEHAVIORAL

A mobile app provided to participants to assess effectiveness in managing HIV

Eligibility

Sex: ALLMin age: 18 YearsMax age: 29 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Confirmed HIV infection * Recent diagnosis of HIV (within the past 6 months) OR be virologically unsuppressed (\>1000 copies/ml) OR disengaged from HIV care (\< 2 visits/last 12 months \> 90 days apart) Exclusion Criteria: * Cannot consent * Unwilling to come to visits * Unwilling to be in San Antonio for a year

Locations (1)

University Health Center Downtown

San Antonio, Texas, United States

Outcomes

Primary Outcomes

Completion of Feasibility Survey

Feasibility survey completion by participants regarding usability of the PL4Y intervention

Time frame: 12 months

Viral plasma load measurement

Virologic suppression is the primary goal of HIV treatment. Virologic failure is defined as a measurement over 200 copies per mL by the Department of Health and Human Services, and is the primary determinant of successful HIV control.

Time frame: 12 months

Data from ClinicalTrials.gov

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