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NCT05783297Completed

Midwest TXTXT Scale up of an Evidence-Based Intervention to Promote HIV Medication Adherence

Source: ClinicalTrials.gov · Last updated 4 Jun 2026

Brief summary (registry, in English)

This research study uses a cluster randomized controlled trial design to evaluate the effectiveness of Treatment Text (TXTXT) intervention on adherence and viral load suppression at 3- and 6- months post intervention initiation for youth and young adults with HIV. A total of 12 clinics will be randomized into one of the following two conditions: 1. Comparison Arm (n=6 clinics)- Clinics randomized to the comparison arm will have participants receive the standard of care for 3 months, followed by a 3-month intervention period. 2. Intervention Arm (n=6 clinics)- Clinics randomized to the intervention arm will have participants receive the TXTXT intervention for 6 months.

Status (registry)
Completed
Study type
Interventional
Enrollment
210 (actual)
First submitted
17 Jan 2023
Start date
17 Apr 2023
Primary completion date
1 Aug 2025
Lead sponsor
Amy K. Johnson, PhD, MSW
Diseases
HIV
NCT number
NCT05783297

What you commit to

  • Study type: Interventional
  • Participants enrolled: 210
  • From 17 Apr 2023 to the primary completion date, 1 Aug 2025
  • 12 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • Participant is participating in another study related to ART adherence
    • Participants outside of the age range (16-35) will be excluded from the study because this study specifically focuses on youth and young adults living with HIV as they are more likely to disengage from care, delay initiation of ART, and have lower rates of virologic suppression compared to adult populations.

Other

  • Participant is unable to give informed consent

Who the study is looking for

  • Diagnosed with HIV-infection and on ART regimen for at least one month
  • Between 16-35 years of age
  • Have a viral load ≥200c/mL and/or report poor adherence (\<90% of pills taken in the last 30 days)
  • Able to receive text messages
  • Can provide informed consent for research component
  • Current patient patient of a participating clinic

Age in the registry: 16 years to 35 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Howard Brown Health
Coordinator of this site? Confirm its status
ChicagoUnited StatesUnknown status
University of Illinois at Chicago
Coordinator of this site? Confirm its status
ChicagoUnited StatesUnknown status
University of Cincinnati
Coordinator of this site? Confirm its status
CincinnatiUnited StatesUnknown status
Corktown Health Center
Coordinator of this site? Confirm its status
DetroitUnited StatesUnknown status
Duke University
Coordinator of this site? Confirm its status
DurhamUnited StatesUnknown status
AIDS Healthcare Foundation
Coordinator of this site? Confirm its status
Fort LauderdaleUnited StatesUnknown status
Baylor College of Medicine
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
Eskenazi Health
Coordinator of this site? Confirm its status
IndianapolisUnited StatesUnknown status
Indiana University
Coordinator of this site? Confirm its status
IndianapolisUnited StatesUnknown status
KC CARE Health Center
Coordinator of this site? Confirm its status
Kansas CityUnited StatesUnknown status
Comprehensive Care Center of Southwest Louisiana
Coordinator of this site? Confirm its status
Lake CharlesUnited StatesUnknown status
Valley AIDS Council
Coordinator of this site? Confirm its status
McAllenUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.