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A Waiting Room-Delivered Video to Enhance Clinical Outcomes Among Persons Living With HIV

NCT03508310 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 4003

Last updated 2025-09-17

No results posted yet for this study

Summary

The purpose of this project is to beta-test a brief waiting room video intervention that promotes early initiation of antiretroviral treatment among treatment-naïve HIV-positive patients, adherence to antiretroviral treatment and retention in care among HIV-positive patients currently on therapy, sexual risk reduction tailored to HIV-positive persons, and patient-initiated discussion of these topics with their health providers. The video is currently being created, and will be ready for beta-testing by June 1, 2016. Results of the beta-testing will be used to refine and improve the video before dissemination to HIV/AIDS treatment facilities nationally. This video project is being funded by the Centers for Disease Control and Prevention, Division of HIV/AIDS Prevention (DHAP).

Conditions

  • HIV Infections

Interventions

OTHER

Taking Care of Me Video

The video's conceptual framework incorporates Social Cognitive Theory, Information-Motivation-Behavioral Skills model, and Social Action Theory, which together address cognitive and behavioral factors related to study outcomes. Storylines embedded prevention messages aimed at increasing treatment initiation (n=9), medication adherence (n=35), retention in care (n=22), partner protection (n=12), and communication with health care providers (n=7).

Sponsors & Collaborators

  • Sentient Research

    collaborator INDUSTRY

  • UCLA David Geffen School of Medicine and Fielding School of Public Health

    collaborator UNKNOWN

  • Denver STD Prevention Training Center, Denver Public Health Department

    collaborator UNKNOWN

  • California State University, Long Beach

    collaborator OTHER

  • Education Development Center, Inc.

    collaborator INDUSTRY

  • Centers for Disease Control and Prevention

    lead FED

Principal Investigators

  • Mary S. Neumann, PhD · Centers for Disease Control and Prevention

  • Aaron Plant, MPH · Sentient Research

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
87 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-01
Primary Completion
2017-03-30
Completion
2017-05-17

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03508310 on ClinicalTrials.gov