CompletedNot Applicable

VITAL Start: Brief Facility-based Video Intervention

Malawi800 participantsStarted 2018-10-01

Plain-language summary

This a multi-center, parallel group, randomized controlled outcome assessor blinded trial with a qualitative descriptive component that seeks to assess the effectiveness of a brief facility-based video intervention to optimize retention and adherence to ART among pregnant and breastfeeding women with HIV infection.

Who can participate

Age range16 Years

SexFEMALE

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Inclusion Criteria: * Women who are HIV positive by two antibody rapid tests approved by the Malawi Ministry of Health * Women age ≥18 years or 16-17 years if married or have a child * Women who understand chichewa * Women who are willing to provide informed consent * Women who intend to remain in the health center catchment area for at least 6 months Exclusion Criteria: * Women already on ART * Women with significant pre-existing psychiatric comorbidity at enrollment that may impact ability to provide consent according to the clinical judgment of study personnel (including cognitive impairment or known psychotic disorder) * Women who participated in the study pilot

What they're measuring

Composite of Retention in ART Clinic and Viral Suppression

Timeframe: 12 months

Trial details

NCT IDNCT03654898

SponsorBaylor College of Medicine

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-10-26

Results submitted2023-10-16

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