LYPS Intervention for HIV Prevention

(LYPS Trial)

Not yet recruiting at 3 trial locations
ER
NL
Overseen ByNancy Liu
Age: < 65
Sex: Any
Trial Phase: Academic
Sponsor: Westat
Must be taking: PrEP
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new approach to prevent HIV using PrEP (pre-exposure prophylaxis), a medication that reduces the risk of contracting HIV. The study examines delivering PrEP through community health professionals in familiar settings, such as homes or mobile clinics, and incorporates a mobile app for support. This new method is called LYPS. Participants will receive either this new method or standard care with some app features. The trial suits individuals aged 13-24 who have had sex in the past year, do not have HIV, are willing to try PrEP, and have a smartphone. As an unphased trial, it offers a unique opportunity to explore innovative ways to access HIV prevention.

Do I have to stop taking my current medications for the trial?

The trial information does not specify if you need to stop taking your current medications. However, if you have any significant health conditions or are participating in another trial with HIV medications, you may not be eligible.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that the LYPS program, which includes PrEP (a medication to prevent HIV) and support through a mobile app, is under evaluation for safety and effectiveness. Although this specific study lacks detailed safety data, the FDA has already approved PrEP for preventing HIV, indicating the medication's general safety. Other studies have demonstrated that PrEP can be safe and effective when used properly. However, the LYPS program also incorporates a mobile app to help individuals adhere to their treatment plan, and the app's safety is still under evaluation. The LYPS program aims to make PrEP more accessible and support its use, which is already recognized as a safe method to prevent HIV.12345

Why are researchers excited about this trial?

Researchers are excited about the LYPS Intervention for HIV prevention because it offers a fresh approach to delivering PrEP (pre-exposure prophylaxis) care. Unlike traditional clinic-based models, LYPS takes PrEP directly to young people in their communities via a Community Health Professional, which could be a nurse or another healthcare expert. This is supplemented by a mobile app that provides real-time support between visits, making the intervention more accessible and personalized. This method could potentially enhance adherence to PrEP by meeting youth where they are, both physically and digitally, and providing continuous, tailored support.

What evidence suggests that the LYPS intervention could be effective for HIV prevention?

Research has shown that PrEP (pre-exposure prophylaxis) effectively prevents HIV when taken as directed, reducing the risk of HIV from sex by about 99%. However, real-life effectiveness can vary due to challenges like accessing the medication and maintaining regular use. The LYPS program in this trial aims to address these challenges by providing PrEP through community health workers and supporting users with a mobile app to enhance adherence. This approach seeks to simplify consistent PrEP use, potentially increasing its effectiveness in preventing HIV. Participants in the LYPS Intervention arm will receive this community-based PrEP care, while those in the Enhanced Standard of Care (eSOC) Control Condition will receive usual clinic-based PrEP care, enhanced with limited access to the LYPS app.12678

Who Is on the Research Team?

KH

Keith Horvath

Principal Investigator

San Diego State University

AP

Audrey Pettifor

Principal Investigator

UNC Chapel Hill

LH

Lisa Hightow-Weidman, MD, MPH

Principal Investigator

Florida State University

SH

Sybil Hosek, PhD

Principal Investigator

University of Illinois at Chicago

KM

Kate Muessig

Principal Investigator

Florida State University

Are You a Good Fit for This Trial?

This trial is for youth ages 13-24 who are HIV-negative, have had anal or vaginal sex in the past year, can speak English, weigh at least 77 pounds, and own a smartphone. They must be willing to get PrEP care from participating providers and not have serious health issues or be part of other similar studies.

Inclusion Criteria

Is not living with HIV
Willing to receive PrEP care from a provider at a participating SC either in the clinic or at one of the designated places in the community being offered by the SC SC
Willing to provide informed consent to participate in the study
See 5 more

Exclusion Criteria

Any other medical, behavioral, or other conditions that, in the opinion of the SC project lead or designee, could interfere with adherence to study procedures or compromise interpretation of study results
I am currently in another HIV medication or prevention study.
Is currently incarcerated or pending incarceration
See 2 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Enrollment

Participants are enrolled and randomized into either the LYPS intervention or enhanced standard of care (eSOC) control condition

1 week
1 visit (in-person)

Treatment

Participants receive PrEP and PrEP care through community delivery or clinic-based care, supplemented by a mobile app for adherence support

36 weeks
Quarterly visits for oral PrEP, bi-monthly for injectable PrEP

Follow-up

Participants are monitored for PrEP adherence and persistence, including blood collection and self-interviews

9 months
4 visits (in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • LYPS

Trial Overview

The study compares standard PrEP care with an enhanced program (LYPS) that offers community-based delivery by a health professional plus a mobile app to help young people stick with their PrEP medication.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: LYPS InterventionExperimental Treatment1 Intervention
Group II: Enhanced Standard of Care (eSOC) Control ConditionActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Westat

Lead Sponsor

Trials
49
Recruited
39,700+

National Institute on Drug Abuse (NIDA)

Collaborator

Trials
2,658
Recruited
3,409,000+

National Institute of Mental Health (NIMH)

Collaborator

Trials
3,007
Recruited
2,852,000+

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborator

Trials
2,103
Recruited
2,760,000+

National Institutes of Health (NIH)

Collaborator

Trials
2,896
Recruited
8,053,000+

The Emmes Company, LLC

Industry Sponsor

Trials
149
Recruited
1,052,000+
Peter Ronco profile image

Peter Ronco

The Emmes Company, LLC

Chief Executive Officer since 2023

BSc from Nottingham University

Dr. Joe Sliman profile image

Dr. Joe Sliman

The Emmes Company, LLC

Chief Medical Officer since 2020

MD from Uniformed Services University of the Health Sciences, MPH from Johns Hopkins University, BSc in Molecular and Cell Biology from Pennsylvania State University

Florida State University

Collaborator

Trials
234
Recruited
41,100+

Citations

1.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/38054579/

a modelling study of surveillance and survey data

Over 2015-2021, PrEP averted an estimated 20% (90% CrI: 11%-30%) of cumulative HIV acquisitions. The hypothetical scenarios modelled showed that, at the same ...

Linking Youth to Pre-Exposure Prophylaxis (PrEP) ...

LYPS is a two-arm randomized controlled trial (RCT) to assess the efficacy of the LYPS intervention. Up to 272 participants will be randomized in a 1:1 ...

Effectiveness of Pre-exposure Prophylaxis (PrEP) in the ... - PMC

Pre-exposure prophylaxis (PrEP) has high biological efficacy, but real-world effectiveness varies due to adherence, access, and delivery barriers. This review ...

LYPS Intervention for HIV Prevention · Info for Participants

The LYPS medical study, being run by Westat, needs participants to evaluate whether LYPS will have tolerable side effects & efficacy for ...

First efficacy results from England's PrEP IMPACT Trial

Gay and bisexual men enrolled in IMPACT had 87% fewer HIV infections than a comparable group of sexual health clinic attendees who did not take PrEP.

6.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/16511407/

Do prevention interventions reduce HIV risk behaviours ...

Results: Interventions significantly reduced unprotected sex [odds ratio (OR), 0.57; 95% confidence interval (CI) 0.40-0.82] and decreased acquisition of ...

Antiretroviral Postexposure Prophylaxis After Sexual .. ...

This effective intervention uses antiretroviral (ARV) medications to reduce the likelihood of HIV acquisition after high-risk exposures. PEP can ...

Using Registries to Monitor HIV Pre-Exposure Prophylaxis ...

Registries provide an essential element of an overall strategy to understand the safety and safe use of new medications following marketing, and they will ...