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HivNCT04233931

Mhealth for Pre-exposure Prophylaxis Adherence by Young Adult MSM

A study testing PrEP medication adherence mobile app in people with Hiv, run by Environment and Health Group, Inc. at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The proposed project involves the development and testing of an mhealth intervention to increase adherence to PrEP treatment using texts providing tailored pill reminders, motivational messages, and health education messages. Read more about this study

Who is it for?
Ages 20 to 29 years, men onlyHealthy volunteers can take part
Conditions the study is for
Hiv
What is being tested?
PrEP medication adherence mobile app
Could I receive a placebo?
No, everyone receives an active treatment
How many people
54 participants
Where
1 siteUnited States
Study dates
21 Jun 2017to 20 May 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 29 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Male
  • Age 20-29
  • Currently taking PrEP
  • Own smartphone

Who cannot join

  • Current participation in PrEP or other HIV-related study
  • Uncomfortable with potential privacy loss risks

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Environment and Health Group

    Cambridge, Massachusetts, 02138

Other trials in United States

About this study

The proposed project involves the development and testing of an mhealth intervention to increase adherence to PrEP treatment using texts providing tailored pill reminders, motivational messages, and health education messages. The intervention targets culturally-diverse young adult men who have sex with men (YMSM), who are at high risk for both HIV and non-adherence to PrEP medication. Supporting PrEP adherence would help reduce new HIV infections in this group.

Read the detailed description

Specific Aims: Pre-exposure prophylaxis (PrEP) treatment greatly reduces HIV risk. When the PrEP pill (Truvada) is taken daily, it can reduce HIV risk up to 92%. NIH has designated reducing HIV/AIDS as a high-priority topic for research support using AIDS-designated funds. Among other groups, the CDC recommends PrEP for men who have sex with men (MSM) who are HIV-negative and in a relationship with an HIV+ partner, and MSM who have had anal sex without a condom or have been diagnosed with an STD in the past 6 months; about 1 in 4 MSM meet these criteria. Young people, age 13-29, accounted for 27% of new HIV cases in 2009. The highest concentration of new cases was among 20-29-year olds; 70% of these were MSM. Disparities are pronounced: 57% of new HIV cases reported in 2008-2010 were among African American MSM; 21% of cases were young Latino MSM. In PrEP trials to date, adherence has been generally low. Across these trials, younger age was the most consistent factor associated with lower PrEP adherence. Medication adherence can be difficult for young people. While young adults better comprehend benefits of prevention than teens, decision-making maturity is still developing through the 20s. It is not until the late 20s that two brain systems, one that spurs sensation-seeking and one that undergirds self-regulation and planning ahead, become integrated. Males may lag behind females in this regard. Furthermore, this developmental process can be hampered for those who have experienced the stress of victimization as have many MSM. PrEP adherence interventions for young adult MSM (YMSM) must take into account developmental factors that can affect decision-making. CDC strongly encourages PrEP prescribers to offer adherence support; foundational to that support is patient education. CDC also suggests adherence plans: 1) individually tailor dosing time 2) use pill reminders 3) use supports to address changes in routine and 4) consider disclosure issues, i.e. help patients identify social network members who can support adherence or ways to overcome adherence barriers due to lack of social disclosure. To date, no PrEP adherence intervention has been developed specifically for YMSM, despite increasing HIV rates in this group and their increased risk for non-adherence. High rates of texting by young adults, coupled with strong evidence base that text reminders can improve adherence, point to mobile health (mhealth) as an ideal way to support PrEP adherence among YMSM.

The goal of the proposed SBIR is to develop and test the feasibility and short-term effectiveness of an individually-tailored, developmentally- and culturally-sensitive mhealth PrEP adherence intervention for culturally-diverse YMSM. Its scientific premise rests on three large well-conducted adherence follow-up studies to PrEP efficacy trials, i.e. VOICE, FEM-PrEP, and iPrEx, which identified adherence facilitators/barriers being targeted in the proposed study, and on meta-analyses of a large and growing literature pointing to the effectiveness of mhealth for medication adherence across chronic conditions, including HIV. The intervention will be modeled on Dr Patricia Weitzman's (proposed PI) SBIR Phase 1 and 2 mhealth anti-retroviral therapy (ART) adherence intervention for HIV+ African Americans. That intervention employed a three-pronged approach of tailored pill reminders with age- and culturally-sensitive motivational and educational texts. Texts were designed to increase ART self-efficacy, and based on principles from social learning theory and positive psychology. Using a similar approach, formative research will be conducted to create motivational and educational texts that are culturally- and developmentally-sensitive for diverse YMSM. Moreover, formative research will allow us to identify and target unique PrEP adherence barriers and facilitators among culturally-diverse YMSM. Findings will be used to create and pilot a 6-week randomized mhealth PrEP adherence intervention addressing adherence barriers and facilitators identified in PrEP RCTs, and our formative research, as well as CDC PrEP adherence recommendations. Our long-term goal is to reduce HIV infection rates among culturally-diverse YMSM by supporting PrEP adherence.

Specific Aim 1: Develop a individually-tailored, culturally- and developmentally-sensitive mhealth intervention to promote adherence to PrEP among YMSM, ages 20-29. Aim 2: Implement 6-week pilot randomized controlled trial to evaluate short-term effectiveness (did it improve PrEP adherence, PrEP knowledge and PrEP treatment self- efficacy). CONSORT guidelines for the RCT will be followed in order to ensure scientific rigor. Primary Hypothesis: Young adult MSM who receive tailored daily pill reminder plus motivational/ educational texts for 6 weeks will show greater PrEP adherence compared to controls. Secondary Hypothesis: Young adult MSM who receive tailored daily pill reminder plus motivational/educational texts for 6 weeks will show greater PrEP knowledge and PrEP treatment self-efficacy compared to controls. Aim 3: Evaluate feasibility of the intervention, e.g. implementation fidelity (to what extent was intervention delivered as planned), program appeal (how well did participants like the intervention) and program reach (how well did it reach participants). CDC estimates PrEP is appropriate for the roughly 500,000 MSM in the US. Impact models show even modest adherence to PrEP could reduce new HIV infections among MSM by 29% over 20 years. An mhealth PrEP adherence tool targeting young adult MSM, a group experiencing increased HIV incidence, could not only support that reduction but-due to easy access and low cost-actually improve upon it.

Conditions
Hiv
Being tested
PrEP medication adherence mobile app
Medical subject headings
Acquired Immunodeficiency Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PrEP medication adherence mobile appBehavioural

    Participants use a PrEP medication adherence mobile app for six weeks.

Study groups in NCT04233931
Study groupRoleWhat they receive
participantExperimentalall participants in the study receive the mobile app.
Receives: Behavioral: PrEP medication adherence mobile app

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. PrEP medication adherence tool

    A 3-item HIV medication adherence tool developed by Segeral was adapted for use with PrEP/Truvada to assess PrEP adherence

    Measured: 6 weeks

Secondary outcomes (3)
  1. PrEP treatment self-efficacy scale

    The Adherence Self-Efficacy Scale developed by Johnson was adapted to assess participants' confidence to carry out PrEP treatment-related behaviors

    Measured: 6 weeks

  2. PrEP knowledge Tool

    PrEP knowledge Tool was developed by Weitzman and Kogelman to assess participants' knowledge of PrEP through questions about medication purpose, side effects, concomitant condom use, HIV testing

    Measured: 6 weeks

  3. Intention to practice safe sex and adhere to 3-month follow-up HIV testing Tool

    This tool was developed by Weitzman and Kogelman to assess participants' intention to practice safe sex and adhere to 3-month follow-up HIV testing recommendations for individuals on PrEP

    Measured: 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Jan 2020
  2. Study start21 Jun 2017
  3. Primary completion20 May 2019
  4. Study completion20 May 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Model description
pre-post test evaluation of the impact of a mobile app on PrEP treatment adherence
Masking
None (open label)
Enrolment
54 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04233931
Sponsor's protocol ID
1R43MH112221-01A1
Status last verified
Jan 2020
First submitted
15 Jan 2020
Last updated
18 Jan 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: We have no plan to make data available.

Questions about this trial

What is this clinical trial studying?

A study testing PrEP medication adherence mobile app in people with Hiv, run by Environment and Health Group, Inc. at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Jan 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

PrEP medication adherence tool (time frame: 6 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Jan 2020.

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