MyPEEPS Mobile

Developers

Rebecca Schnall, Ph.D., M.P.H., R.N.-B.C. at Columbia University School of Nursing, New York; and Robert Garofalo, M.D., M.P.H. at Lurie Children's Hospital, Chicago.

Program Summary

MyPEEPS Mobile is a web-based app designed to reduce sexual risks related to HIV and to increase condom use among same-sex–attracted young males ages 13 to 18. MyPEEPS Mobile is adapted from the group-based curriculum, MyPEEPS. (Note: TPPER has not assessed the effectiveness of the original MyPEEPS program, just MyPEEPS Mobile.) There are 21 activities designed to be completed consecutively. The activities deliver information about sexual health, relationships, and emotional health. The app delivers content via games, quizzes, videos, and graphics. In addition, four characters called “peeps” present scenarios to open each activity. Participants need access to (1) a phone or tablet and (2) internet access or cellular data to use MyPEEPS Mobile.

Intended Population

MyPEEPS Mobile is designed for ethnically and racially diverse same-sex–attracted young males ages 13 to 18. MyPEEPS Mobile was evaluated with young Latino males ages 14 to 17 who are LGBTQ.

Program Setting

MyPEEPS Mobile can be implemented in any setting where youth have smartphones and access to the internet. In the evaluation, the sample was recruited from community-based organizations, schools, clinics, and social media and the sample accessed the program via the web-based app.

Contact and Availability Information

Professor Rebecca Schnall, Email: rb897@cumc.columbia.edu

Sample of Curriculum Available for Review Prior to Purchase
Yes
Languages Available
English
Monitoring and Evaluation Tools
Monitoring and evaluation tools available
Yes
Monitoring and evaluation tool usage required
No
Information about available monitoring and evaluation tools (if applicable)

Monitoring of the app can be done through a dashboard in which you can see which user is using the app, how much time was spent on each activity and the time stamp of when an activity was started and completed. The outcome survey used in Schnall et al. 2022 is available upon request from Rebecca Schnall (rb897@cumc.columbia.edu).

Program Components and Core Components

Last updated in 2024

The data presented on this page reflect responses from the program’s developer or distributor to a program component checklist that asked them to report on the individual components within their TPP program. The same program component checklist was sent to the developer or distributor of every active TPP program with evidence of effectiveness. The program component table provides information on seven types of program components including content, delivery mechanism, dosage, staffing, format, context, and intended population characteristics; whether the component was present or optional in the program; whether the component is considered to be core to the program; and the lesson number or activity where the component can be found in the program.

In the drop-down menu below, under “Has component,” there are four options that indicate a component as present in the program: (1) “Yes” indicates that the component is present in at least one version of the program (whether that be the program version that was evaluated, the current version, or both versions); (2) “Yes (both versions)” indicates that the component is present in both the evaluated version of the program and the current version of the program; (3) “Yes (current version)” indicates that the component is present in the current, but not the evaluated, version of the program; and (4) “Yes (evaluated version)” indicates that the component is present in the evaluated version of the program, only. Note that for dosage components, the dosage itself is described in the Notes when available.

Some of the components identified are noted as core components of the evidence-based program, but this does not necessarily mean that these components have been rigorously tested and show evidence of effectiveness. Most often developers denoted components as core based on theory or experience in the field. Click here for the list of evidence-based components.

For more details about program components, refer to the FAQ page.

Category Component Core Component Component present Lesson number(s) / activities where present
Delivery mechanism Method: Video Yes Yes (evaluated version)
Delivery mechanism Method: Other No
Delivery mechanism Method: Other No
Delivery mechanism Method: Other No
Dosage Frequency Yes Yes (evaluated version)
Dosage Intensity Yes Yes (evaluated version)
Dosage Duration Yes Yes (evaluated version)
Dosage Other No
Staffing Other
Staffing Other
Staffing Deliverer: Community health worker No
Staffing Deliverer: Faith-based individual No
Staffing Deliverer: Health educator No
Staffing Deliverer: Mental health provider No
Staffing Deliverer: Mentors No
Staffing Deliverer: Parents/family No
Staffing Deliverer: Peers No
Staffing Deliverer: Primary care provider No
Staffing Deliverer: Social worker and/or counselor No
Staffing Deliverer: Teachers No
Staffing Deliverer: Other No
Staffing Experience: Credentials No
Staffing Experience: Education No
Staffing Experience: Other No
Staffing Number of staff providing services No
Staffing Training: Additional training required No
Staffing Training: Developer-led training required No
Staffing Training: Other No
Staffing Other Yes Yes (evaluated version)
Format Group size: Full-group activity No
Format Group size: Independent/individual activity Yes Yes (evaluated version)
Format Group size: Small-group activity No
Format Group size: Other No
Format Mode: In-person No
Format Mode: Phone (audio) No
Format Mode: Phone (text) No
Format Mode: Phone (app) Yes Yes (evaluated version)
Format Mode: Online/computer (asynchronous) Yes Yes (evaluated version)
Format Mode: Online/computer (synchronous) No
Format Mode: Other No
Format Other No
Format Other No
Format Other No
Context Context: Environmental supports No
Context Context: Environmental constraints No
Context Context: Other Yes Yes (evaluated version)
Context Setting: After school No
Context Setting: Community based No
Context Setting: Correctional facility No
Context Setting: Faith based No
Program Objectives

MyPEEPS Mobile is designed to decrease engagement in sexual behaviors that can raise the risk of HIV. The program focuses on same-sex–attracted males ages 13 to 18. The program’s aim is to increase condom use and knowledge about HIV and sexually transmitted infections (STIs), and promote youths’ communication with potential partners, peers, and family members.

Program Content

MyPEEPS Mobile is based on social learning theory. There are a total of 21 activities that deliver information on goal setting, HIV and STIs, strategies to manage stigma and shame, and information on dealing with emotions and triggers, discussing influential relationships, and using condoms. The activities should be completed sequentially, and participants must complete an activity to move on to the next one.

Program Methods

The content is delivered in videos, graphics, scenarios, interactive quizzes and games, and the stories of four peeps. The peeps are animated characters who present scenarios on program topics to participants to open each session.

Program Structure and Timeline

MyPEEPS Mobile consists of 21 activities, which must be completed sequentially over the course of three months. Each activity does not need to be completed in a single sitting. Participants work through the activities asynchronously. Completing all 21 activities takes between six and nine hours.

Staffing

One staff person with a bachelor’s degree (or preferably a master’s degree) to provide access to the app and monitor technical issues.

Staff Training

MyPEEPS Mobile is largely a self-administered app. Staff should be trained on the aspects of troubleshooting any technical issues.

Program Materials and Resources

MyPEEPS Mobile is a web-based app with no additional program materials.

Additional Needs for Implementation

MyPEEPS Mobile requires participants to have access to a smartphone or tablet along with an Internet connection or cellular service.

Fidelity

Participants are expected to complete all 21 activities.

Technical Assistance and Ongoing Support

Support from the app developer would need to be negotiated.

Allowable Adaptations

There are no allowable adaptations.

Adaptation Guidelines or Kit
No
Reviewed Studies
Citation High-Quality Randomized Trial Moderate-Quality Randomized Trial Moderate-Quality Quasi-Experiment Low Study Rating Did Not Meet Eligibility Criteria

Schnall et al. 2020

Schnall 2022

Kuhns et al. 2020

Study Characteristics
Citation Setting Majority Age Group Majority Racial/Ethnic Group Gender Sample Size

Schnall et al. 2020

n.a. n.a. n.a. n.a. n.a.

Schnall 2022

Kuhns et al. 2020

Community-based organization 14 to 17 Hispanic or Latino Young male

763

Study Findings

Evidence by Outcome Domain and Study

Citation Sexual Activity Number of Sexual Partners Contraceptive Use STIs or HIV Pregnancy

Schnall et al. 2020

n.a. n.a. n.a. n.a. n.a.

Schnall 2022

Kuhns et al. 2020

n.a. Indeterminate evidence Potentially favorable evidence Indeterminate evidence n.a.
KEY
Evidence Indication
Favorable findings
Two or more favorable impacts and no unfavorable impacts, regardless of null findings
Potentially favorable findings
At least one favorable impact and no unfavorable impacts, regardless of null findings
Indeterminate findings
Uniformly null findings
Conflicting findings
At least one favorable and at least one unfavorable impact, regardless of null findings
Potentially unfavorable findings
At least one unfavorable impact and no favorable impacts, regardless of null findings
Unfavorable findings
Two or more unfavorable impacts and no favorable impacts, regardless of null findings
Note: n.a. indicates the study did not examine any outcome measures within that particular outcome domain, or the study examined outcome measures within that domain but the findings did not meet the review evidence standards.
Detailed Findings
Citation Details

Schnall et al. 2020

This study did not meet the review's screening criteria

Schnall 2022

Kuhns et al. 2020

MyPEEPS Mobile was evaluated using a randomized controlled trial involving same-sex attracted, male-identifying people ages 13 to 18 recruited through various social media sites and clinic-based recruitment events held in Birmingham, Alabama; New York, New York; Seattle, Washington; and Chicago, Illinois. Participants were randomly assigned to either an intervention group that immediately received access to the three-month, 21-module online program or a control group that received the same three-month program but administered on delay between months nine and 12 of the study period. Surveys were administered to both groups immediately at baseline and at three, six, and nine months (before the control group received the intervention). The delayed intervention group received an additional survey in month 12 following their completion of the program; the results of this survey were not included in this study.

The study found that at the three-month follow-up, young men participating in the intervention reported a statistically significant decrease in the number of condomless anal sex acts (insertive and receptive) with partners compared to the control group (effect size = -0.07). Differences in the number of condomless anal sex acts between the two groups were not significant at the six- and nine-month follow-ups.

The study also found that young men participating in the intervention and those in the control group were not significantly different in their number of sex partners and number of condomless anal sex partners at the three-, six-, and nine-month follow-ups, nor were they different in their HIV and STI testing.

The study also examined program impacts on pre-exposure prophylaxis (PrEP) uptake, post-exposure prophylaxis (PEP) use, and the number of sex acts under the influence of substances. Findings for these outcomes were not considered for the review because they fell outside the scope of the review.

Notes

Some study entries may include more than one citation because each citation examines a different follow-up period from the same study sample, or because each citation examines a different set of outcome measures on the same study sample. A blank cell indicates the study did not examine any outcome measures within the particular outcome domain or the findings for the outcome measures within that domain did not meet the review evidence standards.

Information on evidence of effectiveness is available only for studies that received a high or moderate rating. Read the description of the review process for more information on how these programs are identified.

Language directly from the program model developer or authors.