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P3 (Prepared, Protected, emPowered) (P3)

Primary Purpose

Sexually Transmitted Diseases, Safe Sex, Adherence, Medication

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
P3
P3+
Control
Sponsored by
University of North Carolina, Chapel Hill
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Sexually Transmitted Diseases focused on measuring PrEP, gamification, mHealth, HIV prevention, truvada, eHealth, app, adherence, ymsm, transgender women

Eligibility Criteria

16 Years - 24 Years (Child, Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Are aged 16-24
  • Were assigned male sex at birth
  • Report sex with men or transgender women
  • Are able to speak and read English
  • Have reliable daily access to an Android or iOS smartphone with a data plan
  • Are HIV-uninfected (self-report)
  • Are not currently on PrEP but plan to initiate in the next 7 days and have an active PrEP prescription (prescription confirmed by study staff) OR on PrEP have an active PrEP prescription (prescription confirmed by study staff)
  • Recruited from one of 9 subject recruitment venues (SRV) cities (Atlanta, Georgia; Boston, Massachusetts; Bronx, New York; Chicago, Illinois; Houston, Texas; Philadelphia, Pennsylvania; Tampa, Florida; Chapel Hill, NC; Charlotte, NC)

Exclusion Criteria:

  • Aged younger than 15 years or older than 24 years
  • Not available to meet with project staff for planned study visit(s)
  • Non-English speaking
  • Living with HIV
  • Not currently prescribed PrEP (study staff unable to verify participant has an active PrEP prescription by a health provider)
  • Anticipate not having reliable access to a smartphone with a data plan for 2 or more days during field testing or 1 or more weeks during the RCT intervention period
  • Planning to move out of study area during the study period
  • Unwilling or unable to comply with protocol requirements.
  • Participated in field trial phase of P3 study
  • Unable to be consented due to active substance use or psychological condition.

Sites / Locations

  • University of South Florida Infectious Diseases
  • PRISM Health
  • The Adolescent and Young Adult Research (AYAR) at the CORE Center
  • The Fenway Institute
  • Children's Hospital at Montefiore
  • UNC-Chapel Hill
  • RAIN
  • Adolescent Initiative at Children's Hospital of Philadelphia
  • Texas Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

P3

P3+

Control

Arm Description

Participants will use P3

Participants will use P3+

Participants will receive the standard of care

Outcomes

Primary Outcome Measures

PrEP Adherence Defined by Tenofovir Diphosphate (P3 and P3+ vs Control)
PrEP adherence is measured by blood sample levels of tenofovir diphosphate (TFV-DP) with blood concentration consistent with > 4 doses/week at 3- and 6- month follow-ups. The estimation of the average treatment effect compared P3 and P3+ combined to Control.
PrEP Adherence Defined by Emtricitabine Triphosphate (P3 and P3+ vs Control)
PrEP adherence is measured by blood sample levels of emtricitabine triphosphate (FTC-TP) with blood concentration consistent with > 4 doses/week at 3- and 6- month follow-ups. The estimation of the average treatment effect compared P3 and P3+ combined to Control.

Secondary Outcome Measures

Number of Participants With Self-reported Retention in PrEP Clinical Care
The investigators define "retention in care" as at least 1 PrEP clinical visit occurring in the last 3 months.
PrEP Persistence
PrEP persistence will be measured by self-report at follow up of current PrEP use.
Insertive Condomless Anal Sex
Sexual Practices were assessed by self-reported number of insertive condomless anal sex occurrences during the past 3 months. This question is asked at the 3- and 6-month follow-up surveys.
Receptive Condomless Anal Sex
Sexual Practices were assessed by self-reported number of receptive condomless anal sex occurrences during the past 3 months. This question is asked at the 3- and 6-month follow-up surveys.
Sexually Transmitted Infections (STI) Incidence
Self-reported STIs (combined rectal and urethral gonorrhea and chlamydia, syphilis) in last 3 months. This question is asked at the 3- and 6-month follow-up surveys.
PrEP Adherence Defined by Tenofovir Diphosphate (P3 vs Control and P3+ vs Control)
PrEP adherence is measured by blood sample levels of tenofovir diphosphate (TFV-DP) with blood concentration consistent with > 4 doses/week at 3- and 6- month follow-ups. The estimation of the average treatment effect compared P3 to Control and also P3+ to Control.
PrEP Adherence Defined by Emtricitabine Triphosphate (P3 vs Control and P3+ vs Control)
PrEP adherence is measured by blood sample levels of emtricitabine triphosphate (FTC-TP) with blood concentration consistent with > 4 doses/week at 3- and 6- month follow-ups. The estimation of the average treatment effect compared P3 to Control and also P3+ to Control.
Self-Reported Weekly PrEP Use
Number of participants reported taking their PrEP medication >/= 4 days in the past week.
Self-Reported Monthly PrEP Use
Median self-reported percent of time in the past month that participants' took their PrEP as prescribed.
Mean Site-Level Intervention Cost
Information was collected on (1) time spent by study staff for training and supervision of adherence counselor(s); (2) time participants spent in the adherence counseling sessions; and (3) costs associated with the delivery of both P3 and P3+. Resources were organized into standard expenditure categories and attributed to the corresponding P3 or P3+ arm and study site as appropriate.

Full Information

First Posted
October 3, 2017
Last Updated
October 4, 2022
Sponsor
University of North Carolina, Chapel Hill
Collaborators
Emory University, Duke University, Children's Hospital of Philadelphia, The Fenway Institute, Montefiore Hospital, Baylor College of Medicine, Ruth M. Rothstein CORE Center, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), University of South Florida
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1. Study Identification

Unique Protocol Identification Number
NCT03320512
Brief Title
P3 (Prepared, Protected, emPowered)
Acronym
P3
Official Title
P3 (Prepared, Protected, emPowered): Promoting Pre-exposure Prophylaxis (PrEP) Adherence Through a Social Networking, Gamification, and Adherence Support App
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
May 15, 2019 (Actual)
Primary Completion Date
September 16, 2021 (Actual)
Study Completion Date
September 16, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
Emory University, Duke University, Children's Hospital of Philadelphia, The Fenway Institute, Montefiore Hospital, Baylor College of Medicine, Ruth M. Rothstein CORE Center, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), University of South Florida

4. Oversight

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

5. Study Description

Brief Summary
P3 (Prepared, Protected, emPowered) is an interactive smartphone app for HIV-uninfected YMSM and YTW that utilizes social networking and game-based mechanics as well as a comprehensive understanding of what constitutes "best practices" in app development to improve PrEP adherence and persistence in PrEP care.
Detailed Description
Sustainable, integrated PrEP adherence interventions are critically needed to reduce HIV incidence among YMSM and YTW. It is imperative that the investigators develop adherence interventions for YMSM and YTW initiating PrEP that are engaging, age-appropriate and take advantage of technologies that are already embedded in these individual's lives. A smartphone-delivered PrEP adherence intervention is well suited for this population, given they have a high-uptake and utilization of smartphone technology. The use of smartphones to deliver HIV prevention and care interventions has grown substantially in recent years due to: a) wide-scale adoption of smartphone technology among high-risk groups, b) the ability to deliver interventions in real-time within risk contexts, and c) low implementation costs.The accessibility, affordability, anonymity and acceptability of smartphones make them the intervention medium of choice for engaging youth and a logical platform to deliver an adherence intervention targeting PrEP. Further, smartphone interventions address can overcome issues that impede engagement with in-person interventions such as transportation logistics, stigma and confidentiality. Further youth, including YMSM and YTW are receptive to smartphone delivered interventions and these interventions can impact HIV related prevention behaviors. P3 (Prepared, Protected, emPowered) is an interactive smartphone app for HIV-uninfected YMSM and YTW that utilizes social networking and game-based mechanics as well as a comprehensive understanding of what constitutes "best practices" in app development to improve PrEP adherence and persistence in PrEP care. Built on a successful, evidence-based platform designed and tested by our collaborating technology partner, Ayogo, P3 is flexible and responsive to changes in technology. This flexibility will also allow us to quickly respond to and modify our intervention to align with emerging PrEP practice standards and guidelines. Despite the benefits of app-based interventions, maintaining engagement over time can be particularly challenging. Lack of rapport building may contribute to lower retention rates in technology-based interventions. Further, the available literature suggests that some tools, including technology based tools, may be more beneficial to patient adherence when combined with education or counseling. To investigate this possibility, the investigators will include a study arm (P3+) that includes P3 and adherence counseling delivered by a counselor through the P3 app. This study has three phases, usability testing, field testing, and a randomized-controlled trial (RCT). In usability testing the investigators will test beta versions of the app and gain feedback about the intervention from the target population, identify any technical issues, and get feedback on app content. Field testing is to ensure that the features, platform and content of P3 and P3+ are acceptable to the target population and that there are no technical challenges or user concerns with either the app, the dried blood spot (DBS), hair, or mitra sampling collection. The last phase is a three arm, RCT that will test the efficacy of P3, a novel, theory-based mobile app that utilizes game mechanics and social networking features to improve PrEP adherence, retention in PrEP clinical care, and PrEP persistence among young men who have sex with men (YMSM) and young trans women (YTW) who have sex with men, ages 16-24. The investigators will test the efficacy of P3 and P3+, which adds Next Step Counseling delivered by an adherence counselor through the app, against PrEP standard of care. Participants will be randomized to P3, P3+, or standard of care. A cost comparison between P3 and P3+ will be conducted.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sexually Transmitted Diseases, Safe Sex, Adherence, Medication
Keywords
PrEP, gamification, mHealth, HIV prevention, truvada, eHealth, app, adherence, ymsm, transgender women

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
The trial will consist of a three-arm RCT to test intervention efficacy among young men who have sex with men (YMSM) and young transgender women who have sex with men (YTWSM) who are starting PrEP or are non-adherent to PrEP. Study arms will include P3, P3+, and standard of care (SOC). Participants will be recruited from seven cities. The investigators will enroll up to 240 participants and randomize them 1:1:1 to receive P3, P3+, or SOC. Assessments will be completed at months 0, 3, and 6.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
246 (Actual)

8. Arms, Groups, and Interventions

Arm Title
P3
Arm Type
Experimental
Arm Description
Participants will use P3
Arm Title
P3+
Arm Type
Experimental
Arm Description
Participants will use P3+
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Participants will receive the standard of care
Intervention Type
Behavioral
Intervention Name(s)
P3
Other Intervention Name(s)
Prepared, Protected, emPowered
Intervention Description
P3 is an interactive smartphone app that utilizes social networking and game-based mechanics to improve PrEP adherence and persistence in PrEP care. The participant will install P3 on their phone, receive a guided tour of the app and a reminder card with the research coordinator's phone number and email address and instructed to contact the research coordinator immediately to report difficulties with any app components or to report any problems with their phone or phone service. A help link is embedded within the app that directly links to study staff if assistance is needed. P3 arm participants will have 24-hour access to all features of P3.
Intervention Type
Behavioral
Intervention Name(s)
P3+
Intervention Description
In P3+, participants receive all of P3 and the ability to text in the app with an adherence counselor, using Next Step Counseling (NSC). NSC is an interactive, client-centered motivational intervention to improve PrEP adherence. Key components of NSC include: review experiences with adherence, exploration of adherence facilitators and barriers, identification of adherence needs, identification of strategies to meet needs, and development of an adherence action plan. Participants will install P3+ on their phone. The adherence counselor feature will be unlocked for those in the P3+ arm. P3+ participants will have 24-hour access to all features of P3+.
Intervention Type
Behavioral
Intervention Name(s)
Control
Intervention Description
Control participants will receive the standard of care for receiving a prescription for PrEP.
Primary Outcome Measure Information:
Title
PrEP Adherence Defined by Tenofovir Diphosphate (P3 and P3+ vs Control)
Description
PrEP adherence is measured by blood sample levels of tenofovir diphosphate (TFV-DP) with blood concentration consistent with > 4 doses/week at 3- and 6- month follow-ups. The estimation of the average treatment effect compared P3 and P3+ combined to Control.
Time Frame
Month 3, Month 6
Title
PrEP Adherence Defined by Emtricitabine Triphosphate (P3 and P3+ vs Control)
Description
PrEP adherence is measured by blood sample levels of emtricitabine triphosphate (FTC-TP) with blood concentration consistent with > 4 doses/week at 3- and 6- month follow-ups. The estimation of the average treatment effect compared P3 and P3+ combined to Control.
Time Frame
Month 3, Month 6
Secondary Outcome Measure Information:
Title
Number of Participants With Self-reported Retention in PrEP Clinical Care
Description
The investigators define "retention in care" as at least 1 PrEP clinical visit occurring in the last 3 months.
Time Frame
Month 3, Month 6
Title
PrEP Persistence
Description
PrEP persistence will be measured by self-report at follow up of current PrEP use.
Time Frame
Month 3, Month 6
Title
Insertive Condomless Anal Sex
Description
Sexual Practices were assessed by self-reported number of insertive condomless anal sex occurrences during the past 3 months. This question is asked at the 3- and 6-month follow-up surveys.
Time Frame
Month 3, Month 6
Title
Receptive Condomless Anal Sex
Description
Sexual Practices were assessed by self-reported number of receptive condomless anal sex occurrences during the past 3 months. This question is asked at the 3- and 6-month follow-up surveys.
Time Frame
Month 3, Month 6
Title
Sexually Transmitted Infections (STI) Incidence
Description
Self-reported STIs (combined rectal and urethral gonorrhea and chlamydia, syphilis) in last 3 months. This question is asked at the 3- and 6-month follow-up surveys.
Time Frame
Month 3, Month 6
Title
PrEP Adherence Defined by Tenofovir Diphosphate (P3 vs Control and P3+ vs Control)
Description
PrEP adherence is measured by blood sample levels of tenofovir diphosphate (TFV-DP) with blood concentration consistent with > 4 doses/week at 3- and 6- month follow-ups. The estimation of the average treatment effect compared P3 to Control and also P3+ to Control.
Time Frame
Month 3, Month 6
Title
PrEP Adherence Defined by Emtricitabine Triphosphate (P3 vs Control and P3+ vs Control)
Description
PrEP adherence is measured by blood sample levels of emtricitabine triphosphate (FTC-TP) with blood concentration consistent with > 4 doses/week at 3- and 6- month follow-ups. The estimation of the average treatment effect compared P3 to Control and also P3+ to Control.
Time Frame
Month 3, Month 6
Title
Self-Reported Weekly PrEP Use
Description
Number of participants reported taking their PrEP medication >/= 4 days in the past week.
Time Frame
Month 3, Month 6
Title
Self-Reported Monthly PrEP Use
Description
Median self-reported percent of time in the past month that participants' took their PrEP as prescribed.
Time Frame
Month 3, Month 6
Title
Mean Site-Level Intervention Cost
Description
Information was collected on (1) time spent by study staff for training and supervision of adherence counselor(s); (2) time participants spent in the adherence counseling sessions; and (3) costs associated with the delivery of both P3 and P3+. Resources were organized into standard expenditure categories and attributed to the corresponding P3 or P3+ arm and study site as appropriate.
Time Frame
Throughout the duration of the study, approximately 1.5 years

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Self-identify as MSM or TW who has sex with men
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Are aged 16-24 Were assigned male sex at birth Report sex with men or transgender women Are able to speak and read English Have reliable daily access to an Android or iOS smartphone with a data plan Are HIV-uninfected (self-report) Are not currently on PrEP but plan to initiate in the next 7 days and have an active PrEP prescription (prescription confirmed by study staff) OR on PrEP have an active PrEP prescription (prescription confirmed by study staff) Recruited from one of 9 subject recruitment venues (SRV) cities (Atlanta, Georgia; Boston, Massachusetts; Bronx, New York; Chicago, Illinois; Houston, Texas; Philadelphia, Pennsylvania; Tampa, Florida; Chapel Hill, NC; Charlotte, NC) Exclusion Criteria: Aged younger than 15 years or older than 24 years Not available to meet with project staff for planned study visit(s) Non-English speaking Living with HIV Not currently prescribed PrEP (study staff unable to verify participant has an active PrEP prescription by a health provider) Anticipate not having reliable access to a smartphone with a data plan for 2 or more days during field testing or 1 or more weeks during the RCT intervention period Planning to move out of study area during the study period Unwilling or unable to comply with protocol requirements. Participated in field trial phase of P3 study Unable to be consented due to active substance use or psychological condition.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa Hightow-Weidman, MD
Organizational Affiliation
UNC Chapel Hill
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of South Florida Infectious Diseases
City
Tampa
State/Province
Florida
ZIP/Postal Code
33606
Country
United States
Facility Name
PRISM Health
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Facility Name
The Adolescent and Young Adult Research (AYAR) at the CORE Center
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States
Facility Name
The Fenway Institute
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Facility Name
Children's Hospital at Montefiore
City
Bronx
State/Province
New York
ZIP/Postal Code
10467
Country
United States
Facility Name
UNC-Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Name
RAIN
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
29202
Country
United States
Facility Name
Adolescent Initiative at Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Texas Children's Hospital
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36306520
Citation
Budhwani H, Yigit I, Maragh-Bass AC, Rainer CB, Claude K, Muessig KE, Hightow-Weidman LB. Validation of HIV Pre-Exposure Prophylaxis (PrEP) Medication Scales with Youth on PrEP: PrEP Confidence Scale and PrEP Difficulties Scale. AIDS Patient Care STDS. 2022 Nov;36(11):443-450. doi: 10.1089/apc.2022.0072. Epub 2022 Oct 27.
Results Reference
derived
PubMed Identifier
30563818
Citation
LeGrand S, Knudtson K, Benkeser D, Muessig K, Mcgee A, Sullivan PS, Hightow-Weidman L. Testing the Efficacy of a Social Networking Gamification App to Improve Pre-Exposure Prophylaxis Adherence (P3: Prepared, Protected, emPowered): Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2018 Dec 18;7(12):e10448. doi: 10.2196/10448.
Results Reference
derived

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P3 (Prepared, Protected, emPowered)

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