IDCaPP: Implementation and Delivery of Cabotegravir Long Acting Injection for PrEP in a Community Pharmacy Setting.

Sponsor
Kelley-Ross & Associates, Inc. (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05867212
Collaborator
(none)
50
2
30
25
0.8

Study Details

Study Description

Brief Summary

The goal of this demonstration project or observational study is to evaluate the feasibility and acceptability of a pharmacist-managed cabotegravir long acting injectable for PrEP program in a community pharmacy setting.

The main question it aims to answer are:
  • Is the program feasible and acceptable at the end of 1 year of operations?

  • What are the facilitators and barriers of the program? Participants who want to start the FDA approved cabotegravir long acting injectable medication for PrEP will have the option participating in surveys and a review of their electronic health records. Medication will be administered based on FDA approved labeling guidelines and their PrEP care will be part of standard of care per CDC.

Pharmacists who want to provide the service to their patients will have the option of participating in surveys pre and post implementation.

Condition or Disease Intervention/Treatment Phase
  • Drug: Cabotegravir Injection [Apretude]

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Implementation and Delivery of Cabotegravir Long Acting Injection for PrEP in a Community Pharmacy Setting.
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Nov 30, 2025
Anticipated Study Completion Date :
Nov 30, 2025

Outcome Measures

Primary Outcome Measures

  1. Percentage of participants recruited in PrEP care [initiation]

    Percentage of participants recruited into PrEP care at initiation

  2. Percentage of participants retained in PrEP care [1 year]

    Percentage of participants retained in PrEP care at the end of 1 year

  3. Adherence rate [1 year]

    Number of participants who adhered to target injection windows period by completing injection appointments versus the number of participants who missed their target injection window period by not completing injection appointments

  4. Age [initiation]

    age in years at study initiation

  5. Percentage Sex assigned at birth [initiation]

    Percentage of people who were assigned female at birth or assigned male at birth

  6. Percentage of people with Gender identity [initiation]

    Percentage of people with gender identity of male, female, trans male, trans female, genderqueer or gender nonconforming, different identity, prefer not to answer at initiation of study.

  7. Percentage of people in a certain race [initiation]

    Percentage of people who identify as American Indian or Alaska Native, Asian, Black or African American, Native Hawaiian or Pacific Islander, White, other, or prefer not to answer) race at initiation of study.

  8. Percentage of people who identify in a certain ethnicity [initiation]

    Percentage of people who identify hispanic or latino, not hispanic or latino, prefer not to answer) ethnicity at initiation of study.

  9. Percentage of people with Insurance [1 year]

    Percentage of people with Medicaid, Medicare, commercial insurance, or uninsured throughout the study.

  10. Percentage of people who have housing [1 year]

    Percentage of people who have a steady place to live, a place to live today but worried about losing it in the future, or do not have a steady place to live at initiation of study.

  11. Percentage of people who have a primary care provider [initiation of study]

    Percentage of people who have a primary care provider relationship at initiation of study.

  12. Percentage of people with more than 1 sexual partner [initiation]

    Percentage of people with more than 1 sexual partner at initiation of study.

  13. Percentage of people with HIV positive sexual partner [initiation]

    Percentage of people who have one or more sexual partner who is HIV positive at initiation.

  14. Percentage of people who have inconsistent condom use during sex [initiation]

    Percentage of people who have inconsistent condom use during sex.

  15. Percentage of people who use injection drugs [initiation]

    Percentage of people who use injection drugs

  16. Percentage of people who use HIV post exposure prophylaxis (PEP) in the last 12 months [initiation]

    Percentage of people who use HIV post exposure prophylaxis (PEP) in the last 12 months at initiation

  17. Percentage of people who have a history of sexually transmitted infection in the previous 6 months [initiation]

    Percentage of people who use HIV post exposure prophylaxis (PEP) in the last 12 months at initiation

  18. Percentage of people of certain background characteristics [initiation]

    A baseline questionnaire will be used at initiation to collect background characteristics to determine percentage of people of a race, ethnicity, gender identity, sex assigned at birth, marital status, education level, employment status, annual income, and living situation.

  19. Percentage of people with risk of acquiring HIV at initiation [1 year]

    A baseline questionnaire will be used at initiation to collection information on percentage of people who engage in sex, has sex with and partner who is living with HIV, has sex without a condom, been diagnosed with an STI in the last 6 months, have used HIV post-exposure prophylaxis in the lat 12 months,

  20. Percentage of people who are acceptable to cabotegravir long acting injectable for PrEP [initiation]

    A 27 item questionnaire that will be given at baseline that explores the reason a person would like to be on an injection for PrEP, reasons for not being able to make injection appointments, and rating their feelings around judgement for being on an injection.

  21. Percentage of people feeling satisfied with cabotegravir long acting injectable for PrEP [1 year]

    A 7 item questionnaire will be given at every follow up appointment that explores the reason someone wants to stay on an injectable for PrEP, how comfortable they feel being on the injection, reasons for not being able to make injection appointments, and rating their feelings around judgement for being on an injection.

  22. Percentage of people who discontinue long acting cabotegravir for PrEP for a particular reason [discontinuation]

    A 2 item questionnaire will be given a discontinuation that explores why a person discontinues long acting cabotegravir and what their HIV prevention strategy will be moving forward.

  23. Percentage of Pharmacist providers who have certain attitudes to providing long acting cabotegravir for PrEP [at initiation]

    A 5 point questionnaire that explores a pharmacists reasons for providing long acting injectable cabotegravir for PrEP, reasons for being able to or not being able to provide the service.

  24. Percentage of pharmacist providers who are acceptable to providing long acting cabotegravir for PrEP [6 months]

    A 6 item questionnaire that explores the reasons a pharmacist is able to or not able to provide the service

Secondary Outcome Measures

  1. Number of STI [1 year]

    number of chlamydia, syphilis, and gonorrhea infections detected during study

  2. Number of HIV seroconversions [1 year]

    Number of HIV seroconversions detected during the study, reason for patient discontinuation, pharmacist provider and patient perspectives on barriers and facilitators.

  3. Percentage of people who discontinue long acting cabotegravir for PrEP for a particular reason [1 year]

    A 2 item questionnaire will be given a discontinuation that explores why a person discontinues long acting cabotegravir and what their HIV prevention strategy will be moving forward.

  4. Percentage of pharmacists who believe in certain barriers in providing the service [1 year]

    A 6 item questionnaire that explores the reasons a pharmacist cannot provide the service

  5. Percentage of pharmacists who believe in certain facilitators in providing the service [1 year]

    A 6 item questionnaire that explores the reasons a pharmacist can provide the service

  6. Percentage of patients who believe in certain facilitators for using the service [1 year]

    A 7 item questionnaire will be given at every follow up appointment that explores the reason someone can use the service.

  7. Percentage of patients who believe in certain barriers for using the service [1 year]

    A 7 item questionnaire will be given at every follow up appointment that explores the reason someone cannot use the service.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 18 years of age or older at the time of screening

  • Weight ≥ 35 kg

  • HIV-negative status

  • Willing to provide informed consent and undergo all required study procedures.

Exclusion Criteria:
  • Unknown or positive HIV status

  • Coadministration of drugs that significantly decrease cabotegravir concentrations according to the FDA package insert.

  • Any participants that do not meet criteria for management under CDTA

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kelley-Ross Pharmacy at the Polyclinic Seattle Washington United States 98104
2 Kelley-Ross Capitol Hill Pharmacy Seattle Washington United States 98122

Sponsors and Collaborators

  • Kelley-Ross & Associates, Inc.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Elyse Tung, Director of Clinical Services, Kelley-Ross & Associates, Inc.
ClinicalTrials.gov Identifier:
NCT05867212
Other Study ID Numbers:
  • 001
First Posted:
May 19, 2023
Last Update Posted:
May 19, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Elyse Tung, Director of Clinical Services, Kelley-Ross & Associates, Inc.
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 19, 2023