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ENROLLING BY INVITATION
NCT06062979

Clinical Effectiveness-Implementation Hybrid Type 2 Study on Home-Delivered Cabenuva for People Living With HIV Who Are Not Retained in Care

Sponsor: Whitman-Walker Institute

View on ClinicalTrials.gov

Summary

The purpose of this study is to assess adherence to home-delivered long-acting injectable rilpivirine/cabotegravir (Cabenuva) among people living with HIV enrolled in the Mobile Outreach Retention and Engagement (MORE) program at Whitman-Walker Health due to significant barriers to being retained in care; the MORE program provides supportive services including dedicated care navigation, transportation assistance, and mobile/home-delivered care. The investigators will examine the equivalence of treatment outcomes among patients receiving injectable treatment within the MORE program as compared to those of patients receiving Cabenuva in standard care at Whitman-Walker Health.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

180

Start Date

2023-11-01

Completion Date

2025-06-30

Last Updated

2024-04-25

Healthy Volunteers

Not specified

Conditions

Interventions

DRUG

rilpivirine/cabotegravir

WWH is currently providing Cabenuva treatment as a treatment option for eligible patients. The purpose of the proposed study is to use an observational, prospective cohort design to further investigate the delivery of Cabenuva among two subpopulations of WWH patients.

Locations (2)

Whitman-Walker 1525 Clinic

Washington D.C., District of Columbia, United States

Whitman-Walker Max Robinson Center

Washington D.C., District of Columbia, United States