Optimizing Implementation of Long Acting Injectable PrEP
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Plan-Do-Study-Act.
- Who it may be relevant to
- Registry conditions: HIV Infections. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
Our goal is to optimize LAI-PrEP implementation within the context of other PrEP methods. Our strategy is flexible to allow pivot to include forthcoming PrEP dosing options should they become available
Interventions
- Behavioral Plan-Do-Study-Act
Implementation strategy of conducting cyclical small tests of change using Plan-Do-Study-Act
Primary outcome measures
- LAI-PrEP prescribing [Time frame: 3 months]
Eligibility criteria
Provider/staff inclusion criteria:
- 18 years of age or older,
- affiliated with a participating clinic, and
- be involved in prescribing or supporting PrEP care delivery.
Provider/staff exclusion criteria:
- 17 years of age or younger,
- not affiliated with a participating clinic, and
- not involved in prescribing or supporting PrEP care delivery.
De-identified electronic medical record review inclusion criteria:
- 16 years of age or older, and
- had a clinical visit for any form of PrEP care during the study period at a participating clinic site.
De-identified electronic medical record review exclusion criteria:
- 15 years of age or younger, and
- no clinical visit for any form of PrEP care during the study period at a participating clinic site.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Non-randomized
- Model
- Crossover
- Masking
- Open label
- Primary purpose
- Health services research
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07649551 · R34MH135746