search
Back to results

PrEP Communication Intervention for Female Clients of a Needle Exchange

Primary Purpose

HIV/AIDS

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Enhanced Intervention
Basic Intervention
Sponsored by
Temple University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV/AIDS

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • self-identifying women -HIV-
  • 18 or older
  • self-report either sharing needles or having unprotected sex in last month
  • speak and read English
  • Never used PrEP
  • have cell phone that receives text messages
  • have Medicaid/Medicare or other insurance that covers PrEP

Exclusion Criteria:

  • self-identifying other than female
  • HIV+
  • under 18 years old
  • Doesn't speak/read English
  • No HIV risk in last three months
  • Are on or previously been on PrEP
  • Do not have a cell phone that accepts text messages
  • Do not have insurance that covers PrEP
  • mental illness that interferes with cognitive understanding or ability to provide informed consent.

Sites / Locations

  • Prevention Point PhiladelphiaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Enhanced Intervention

Basic Intervention

Arm Description

Women who are eligible and randomized to the Enhanced Intervention will receive targeted PrEP counseling; targeted written/visual materials, follow up supportive text messages, and distribution of PrEP at the syringe exchange

Women who are eligible and randomized to the Basic Intervention will receive "usual care" with general messaging from medical personnel, reminder text messages, and distribution of PrEP at the syringe exchange

Outcomes

Primary Outcome Measures

Change in PrEP uptake and adherence
Asses uptake and adherence to PrEP with blood test. Blood test results will be compared to adherence benchmarks for Tenofovir-Emtricitabine and categorized as a binary variable (yes/no) based upon the mean value observed by all patients, with data at 1 month, 3 months and 3 months post intervention.
Change in PrEP adherence
medication adherence scales and prescription pick up. Self report adherence measures on how often medication is taken and compared across the three time points. Percent of prescription pick-up as proxy measure.
Change in PrEP adherence
one item Medication Adherence question (one item with six option scale). "None of the time, a little of the time, some of the time, a good bit of the time, most of the time, and all of the time

Secondary Outcome Measures

Change in Coping Self-Efficacy
Assess coping self-efficacy using the Coping Self Efficacy (CSE) scale (13 item scale; 0 to 10 scale). Zero=cannot do at all,5=moderately certain can do and 10=certain can do. An overall CSE score is created by summing the item ratings, with higher scores indicating higher coping self efficacy.
Change in PrEP attitudes/perceptions
Assess PrEP attitudes/perceptions with perceptual mapping survey items
Change in Decisional Conflict
Assess decision conflict with the Ottawa Decisional Conflict Scale - Low Literacy Version. (10 items) Three responses: Yes, No, Unsure. Yes=0, Unsure=2, No=4. 10 items are summed; divided by 10 and then multiplied by 25. Ranges from zero (no decisional conflict) to 100 (extremely high decisional conflict)

Full Information

First Posted
February 28, 2018
Last Updated
February 20, 2020
Sponsor
Temple University
search

1. Study Identification

Unique Protocol Identification Number
NCT03541642
Brief Title
PrEP Communication Intervention for Female Clients of a Needle Exchange
Official Title
Development and Pilot Testing of a PrEP Communication Intervention and Integration Into Existing HIV Testing Services for Female IV Drug Using Clients of a Needle Exchange
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
May 30, 2021 (Anticipated)
Study Completion Date
May 30, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Temple University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will identify perceptions of PrEP in women who inject drugs (WWIDs) and develop and pilot test a targeted intervention that will be embedded in a large, urban syringe exchange program through an extensive formative evaluation process. Using perceptual mapping, an innovative marketing evaluation technique, WWIDs' PrEP perceptions will be incorporated into messaging in targeted counseling, materials, and text messaging to encourage PrEP adherence. This will then be tested in a pilot Randomized Controlled Trial (RCT) by comparing it to a general PrEP intervention to assess for uptake and adherence to PrEP, as well as improved self-efficacy and lower decisional conflict.
Detailed Description
Women who inject drugs (WWIDs) are at significantly higher risk of contracting HIV due to both needle sharing and sexual behaviors, yet utilize HIV prevention resources less. Analysis of studies testing pre-exposure prophylaxis (PrEP) has not tested effectiveness in WWIDs and little research exists on their specific barriers to uptake and adherence. The result is a significant group who is highly vulnerable to HIV infection and its negative health consequences, yet is less likely to benefit from PrEP. To address this gap this study will use a rigorous formative evaluation strategy utilizing a unique and innovative marketing evaluation technique. Using perceptual mapping and vector modeling analysis, the investigators will develop 3-D maps to identify specific message strategies to embed into an intervention using targeted PrEP counseling, written materials, and text based messaging and pilot tested for promise of efficacy compared to a general PrEP intervention. The intervention will address psycho-social barriers to PrEP through perceptual mapping but also societal and structural barriers by embedding it in a trusted syringe exchange and distributing medication through its medical clinic. Specific aims of the research are: 1. Assess WWIDs' perceptions of PrEP and potential barriers to use. To accomplish this the investigators will conduct focus groups (n=30) and interviews with syringe exchange staff (n=10) and develop a perceptual mapping survey. 2. Develop a targeted communication intervention based on vector modeling findings, including print materials, PrEP counseling, and text messages, and assess feasibility and acceptability. To accomplish this the investigators will conduct perceptual mapping surveys with HIV- WWIDs (n=100), do vector modeling analysis and create sample messages, concept test messages with WWIDs and staff (n=20), create intervention materials and conduct usability testing (n=20). 3. Pilot test the intervention by integrating into a syringe exchange to assess promise of efficacy. To accomplish this the investigators will conduct a randomized pilot (n=50) and test an "enhanced" intervention using targeted messages with a "basic" intervention that provides general PrEP counseling. To assess promise of efficacy the investigators will compare PrEP adherence (blood test; self report) and differences in PrEP attitudes, self-efficacy, and decisional conflict.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV/AIDS

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Women participants will be randomized to condition upon consent based on a random numbers table. Intervention arm will get "enhanced" intervention with customized messages and counseling/text messaging; control arm will get "basic" intervention with medical counseling and text message reminders.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Enhanced Intervention
Arm Type
Experimental
Arm Description
Women who are eligible and randomized to the Enhanced Intervention will receive targeted PrEP counseling; targeted written/visual materials, follow up supportive text messages, and distribution of PrEP at the syringe exchange
Arm Title
Basic Intervention
Arm Type
Active Comparator
Arm Description
Women who are eligible and randomized to the Basic Intervention will receive "usual care" with general messaging from medical personnel, reminder text messages, and distribution of PrEP at the syringe exchange
Intervention Type
Behavioral
Intervention Name(s)
Enhanced Intervention
Intervention Description
Targeted PrEP counseling; targeted written/visual materials; follow up supportive text messages; distribution of PrEP at the syringe exchange
Intervention Type
Behavioral
Intervention Name(s)
Basic Intervention
Intervention Description
General messaging from medical personnel; reminder text messages; distribution of PrEP at the syringe exchange
Primary Outcome Measure Information:
Title
Change in PrEP uptake and adherence
Description
Asses uptake and adherence to PrEP with blood test. Blood test results will be compared to adherence benchmarks for Tenofovir-Emtricitabine and categorized as a binary variable (yes/no) based upon the mean value observed by all patients, with data at 1 month, 3 months and 3 months post intervention.
Time Frame
one month, three months, three months post intervention
Title
Change in PrEP adherence
Description
medication adherence scales and prescription pick up. Self report adherence measures on how often medication is taken and compared across the three time points. Percent of prescription pick-up as proxy measure.
Time Frame
one month, three months, three months post intervention
Title
Change in PrEP adherence
Description
one item Medication Adherence question (one item with six option scale). "None of the time, a little of the time, some of the time, a good bit of the time, most of the time, and all of the time
Time Frame
one month, three months, three months post intervention
Secondary Outcome Measure Information:
Title
Change in Coping Self-Efficacy
Description
Assess coping self-efficacy using the Coping Self Efficacy (CSE) scale (13 item scale; 0 to 10 scale). Zero=cannot do at all,5=moderately certain can do and 10=certain can do. An overall CSE score is created by summing the item ratings, with higher scores indicating higher coping self efficacy.
Time Frame
baseline, three months, 3 months post-intervention
Title
Change in PrEP attitudes/perceptions
Description
Assess PrEP attitudes/perceptions with perceptual mapping survey items
Time Frame
baseline, three months, 3 months post-intervention
Title
Change in Decisional Conflict
Description
Assess decision conflict with the Ottawa Decisional Conflict Scale - Low Literacy Version. (10 items) Three responses: Yes, No, Unsure. Yes=0, Unsure=2, No=4. 10 items are summed; divided by 10 and then multiplied by 25. Ranges from zero (no decisional conflict) to 100 (extremely high decisional conflict)
Time Frame
baseline, three months, 3 months post intervention

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Any self-reported women who injects drugs or has other HIV risk related to drug use
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: self-identifying women -HIV- 18 or older self-report either sharing needles or having unprotected sex in last month speak and read English Never used PrEP have cell phone that receives text messages have Medicaid/Medicare or other insurance that covers PrEP Exclusion Criteria: self-identifying other than female HIV+ under 18 years old Doesn't speak/read English No HIV risk in last three months Are on or previously been on PrEP Do not have a cell phone that accepts text messages Do not have insurance that covers PrEP mental illness that interferes with cognitive understanding or ability to provide informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sarah B Bass, Ph.D., MPH
Phone
215-204-5110
Email
sbass@temple.edu
Facility Information:
Facility Name
Prevention Point Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19134
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jose Benitez, MSW
Phone
215-461-1710
Email
Jose@ppponline.org
First Name & Middle Initial & Last Name & Degree
Silvana Mazzella, MSW
Phone
215-634-5272
Ext
1112
Email
silvana@ppponline.org

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All research products from the study will be made available to other qualified individuals within the scientific community, government agencies and other interested parties after publication of results. Requests for raw data from other scientists will be considered with provision of the following information: A brief description of the specific aims and/or hypotheses, data requirements, and proposed analyses, how the data will be used, timeframe for use, and Institutional Review Board (IRB) approvals. All materials developed during the study, as well as any research instruments, will also be made available upon request. In addition, qualified individuals who are interested in the PrEP messaging and the methods from which they are created, as well as the analysis methods generated by this research, will have access after publication. It is our full intention to share all findings generated by this study, and subsequent lessons learned, with others in the scientific community.
IPD Sharing Time Frame
Three months after end of intervention data collection.

Learn more about this trial

PrEP Communication Intervention for Female Clients of a Needle Exchange

We'll reach out to this number within 24 hrs