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临床试验/NCT04973254
NCT04973254已完成不适用

Cabotegravir-Rilpivirine Long Acting (CAB-RPV LA) Implementation Strategies Among High-Risk Populations

Boston Medical Center2 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2022年2月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
25
试验地点
2
主要终点
Adherence to Cabenuva Injections

研究概览

简要总结

This is a hybrid implementation-effectiveness study using both qualitative and quantitative methods. The research aims to examine whether providing a new, but approved, HIV once a month injection treatment [Cabotegravir-Rilpivirine Long Acting (CAB-RPV LA)] to individuals who are living with HIV outside of the standard doctors office or clinic increases adherence to treatment. This HIV monthly injections treatment which is already being delivered within the clinic setting, will be administered to participants in community partner spaces, reducing the barriers that having to present to a traditional clinic for treatment creates.

Individuals who will receive the injection need to have a history of being unable to take their HIV oral medication, as well as other barriers to care that make it difficult to engage in a traditional clinic setting. These barriers may include, but are not limited to, homelessness, substance use, mental illness, and stigma around their diagnosis.

Data will be collected on whether it was easier for the participants to receive care in a non-traditional setting, as well as whether the injection made it easier for them to remain adherent to their HIV medication in comparison to standard oral HIV medication.

详细描述

The proposed implementation research is designed to evaluate a novel approach to engage individuals with HIV who are at the highest risk for not accessing care or adhering to treatment. The investigators are not testing CAB-RPV LA; this is an approved drug. The investigators are also not studying the drug nor studying it for a new population, new dosage or new route of administration. Rather, the investigators are conducting an implementation three-arm cohort study that uses quantitative methods and propose to test implementation of CAB-RPV LA in community-based settings. The three cohorts/groups will be:

  • cohort 1- individuals who receive CAB-RPV LA at an alternative community-based site
  • cohort 2- individuals who receive CAB-RPV LA in the HIV clinic
  • cohort 3- individuals who share characteristics of cohort 1 and are engaged in standard of care

The research is designed to answer the following implementation and clinical questions.

A. Implementation Questions

  1. Will community-based delivery of CAB-RPV LA be an acceptable and feasible delivery method to high-risk people living with HIV (PLWH) from the patient, provider and community organization perspectives? (acceptability/feasibility)
  2. Can a community-based delivery strategy lead to initiation and completion of injections for six months for at least 80% of individuals who are enrolled into cohort 1 for an initial visit in an outreach setting? (reach) See Section 11 for information on the details of the sample size calculations and Section 7.2 for how study staff will stay in contact with participants to maximize potential for longer term engagement.
  3. What are the characteristics of patients who are most likely to have an initial injection and do these characteristics differ for individuals who receive CAB-RPV LA in and outside of the HIV clinic? (equity)
  4. Are patients who are seen for CAB-RPV LA in community-based settings satisfied with their HIV care? (patient-centeredness)
  5. Will consistent delivery of CAB-RPV LA be possible in community-based (non-HIV clinic) settings? (feasibility)
  6. Will the providers at a drop-in center or community-based organization be willing to implement CAB-RPV LA within their non-traditional setting? (adoption)

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •for Cohort 1:
  • •HIV-positive
  • •English or Spanish speaking
  • •Lab values that indicate the patient is a candidate for the medication and virally suppressed
  • •Willing to complete the locator form to receive appointment reminders prior to follow-up data collection
  • •Inclusion Criteria for Cohort 2:
  • •HIV-positive
  • •English or Spanish speaking
  • •Enrolled in care and receiving CAB-RPV LA injection at Boston Medical Center Infectious Disease Clinic (HIV clinic)
  • •Willing to complete the locator form to receive appointment reminders prior to follow-up data collection
  • •Inclusion Criteria for Cohort 3:
  • •HIV-positive
  • •English or Spanish speaking
  • •Enrolled in care but NOT receiving CAB-RPV LA injection at Boston Medical Center Infectious Disease Clinic (HIV clinic)
  • •Willing to complete the locator form to receive appointment reminders prior to follow-up data collection
  • •Matched to participants demographically and in terms of other characteristics in Cohort 1 at a 2:1 ratio

排除标准

  • •(for all 3 cohorts unless stated):
  • •Not virally suppressed prior to beginning CAB-RPV LA (does not apply to cohort 3)
  • •A history of adhering fully to their antiretroviral therapy (ART)
  • •Not willing to take CAB-RPV LA after detailed discussion of what the use of CAB-RPV LA will entail (does not apply to cohort 3)
  • •Unable to undergo clinical eligibility testing to confirm eligibility (does not apply to cohort 3)
  • •A history of integrase inhibitor mutations suggesting resistance to Cabotegravir or Cabenuva
  • •A history or evidence of resistance to either integrase strand transfer inhibitor (INSTI) or non-nucleoside reverse transcriptase inhibitors (NNRTI) HIV drugs
  • •Currently pregnant or breastfeeding
  • •Currently has HIV 1 with an HIV 2 co-infection or an HIV 2 infection
  • •Taking any drugs that have known interactions with Cabenuva, including but not limited to carbamazepine, oxcarbazepine, phenobarbital, phenytoin, St Johns Wort, systemic Dexamethasone, rifabutin, rifampin and rifapentine
  • •Chronic Hepatitis B infection

研究组 & 干预措施

Cohort 1- HIV injection at a community-based site

Experimental

CAB-RPV LA administered to patients in an alternative community-based site

干预措施: CAB-RPV LA (Other)

Cohort 2- HIV injection at a HIV clinic

Active Comparator

CAB-RPV LA administered to patients in the HIV clinic

干预措施: CAB-RPV LA (Other)

Cohort 3- Standard of care for HIV

Active Comparator

Individuals who share characteristics of cohort 1 and are engaged in standard of care

干预措施: Standard treatment within an HIV clinic (Other)

结局指标

主要结局

Adherence to Cabenuva Injections

时间窗: 3 months, 6 months

The number of participants who received CAB-RPV LA injections within the treatment window.

Adherence to Primary Care Appointments

时间窗: 3 months, 6 months

The number participants who had a primary care appointment in the previous 3 months.

Adherence to Mental Health/Behavioral Appointments

时间窗: 3 months, 6 months

The number participants who had a mental health/behavioral appointment in the previous 3 months.

Adherence to Substance Abuse Appointments in Cohorts 1 and 2

时间窗: 3 months, 6 months

The number participants who had a substance abuse appointment in the previous 3 months.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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