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mLab App Plus: A Randomized Controlled Trial of a Mobile Health (mHealth) Intervention

Primary Purpose

HIV Infections, Sexually Transmitted Diseases, Viral, Syphilis

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
mLab App Plus
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for HIV Infections

Eligibility Criteria

18 Years - 35 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria: 18-35 years of age Assigned male sex at birth and identify as (1) a man or (2) a trans woman Understand and read English Self-identify as any race or ethnicity Substantial risk for acquiring HIV infection per CDC (Centers for Disease Control) guidance All participants must report having sex with a man/men Smart phone ownership Self-report being HIV-negative or unknown status Self-report being negative for syphilis or unknown status Not having been tested for HIV or syphilis in the past 6 months Not currently taking Pre-Exposure Prophylaxis (PrEP) Understand the limitations of the duplex lateral flow test and the mLab App Plus (e.g., a confirmatory test is needed and self-test must be performed in the presence of a qualified clinician)

Sites / Locations

  • Columbia University Irving Medical CenterRecruiting
  • Vanderbilt University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

mLab App Plus

Standard of Care

Arm Description

Participants randomized to intervention will receive standard of care counseling, complete online surveys, be provided with the mLab App Plus, and a box of condoms. The intervention arm will also complete two HIV/Syphilis Ab Combo Rapid Tests (DPP® HIV-Syphilis Test) at their baseline (first test) and 3-month follow- up (second test) appointments.

Participants randomized to standard care will receive standard of care counseling, complete online surveys and be sent an email with links to mobile-optimized online prevention information, including PrEP and HIV/STI testing information found on the Centers for Disease Control (CDC) website, and a box of condoms.

Outcomes

Primary Outcome Measures

The number of participants who are able to self-administer the DPP® HIV-Syphilis test with mLab App Plus
A successful self-test is defined as having completed the DPP® HIV-Syphilis test by themselves and having accurately identified and interpreted their HIV and Syphilis statuses as determined by the supervising clinician. In the event that the clinician, rather than the participant administers the DPP® HIV-Syphilis test, the test is not recorded as a successful self-test.

Secondary Outcome Measures

The number of negative/positive results
The number of negative/positive results
The number of Young Men who have sex with men/ Young transgender women referred for HIV/STI services (participants with HIV and/or syphilis only)
Using count of referral
The number of Young Men who have sex with men/ Young transgender women linked to (attend one appointment) HIV/STI prevention or care services
Using count of appointments attended

Full Information

First Posted
September 22, 2023
Last Updated
September 22, 2023
Sponsor
Columbia University
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1. Study Identification

Unique Protocol Identification Number
NCT06059443
Brief Title
mLab App Plus: A Randomized Controlled Trial of a Mobile Health (mHealth) Intervention
Official Title
mLab App Plus: A Randomized Controlled Trial of an mHealth Intervention for Increasing Access to HIV and Syphilis Testing and Care Among Young Men
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 25, 2023 (Anticipated)
Primary Completion Date
September 24, 2024 (Anticipated)
Study Completion Date
September 24, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University

4. Oversight

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

5. Study Description

Brief Summary
Men who have sex with men (MSM), especially young men who have sex with men (YMSM), and transgender women (TGW) have some of the highest rates of HIV and syphilis diagnoses in the United States. The goal of this study is to pilot the mobile Lab (mLab) App Plus to assess YMSM's and YTGW's abilities to perform and interpret self-tests for HIV and syphilis and consequently increase the number of YMSM and young transgender woman (YTGW) who initiate self-testing for HIV and syphilis.
Detailed Description
From 2018 to 2019, the rate of syphilis increased by 11.2%. It has increased steadily since 2000 especially among men, in which MSM bear a disproportionate majority of cases (47% of all cases were among MSM in 2019). HIV and syphilis rates continue to rise among YMSM. While MSM account for only about 2% of the US population, they are most affected by HIV, constituting 56% of people living with HIV (PLWH). Moreover, the rate of syphilis among MSM is profoundly elevated, at least 100 times higher than that in men who have sex with women and even higher among YMSM. Importantly, syphilis makes it easier to both acquire and transmit HIV, and about half of MSM who have syphilis are co-infected with HIV. The risk of syphilis and HIV continues to rise in YMSM in New York City, the study site. Given these epidemiologic risk factors for HIV and syphilis, there is a strong scientific premise for this pilot study that proposes to test innovative and effective HIV and sexually transmitted infection (STI) testing, prevention, and treatment models. Given that approximately 17% of MSM living with HIV in the U.S. are unaware of their status and significant comorbid syphilis in that population, both pathogens may be simultaneously transmitted. The increasing number of syphilis diagnosed in MSM highlights the importance of STI control in this population, not just for the health of the patient, but also for prevention of HIV and syphilis in uninfected persons. YMSM and YTGW, and specifically Blacks and Latinos, are disproportionately infected with HIV. In response to the need for interventions to increase HIV testing in youth, our study team developed the mLab App, which affords advantages over existing self-test options to support the potential for higher uptake of the HIV self-test. The app provides HIV prevention information, push notification reminders for testing, step-by-step instructions for using the OraQuick HIV tests (OraQuick), and an image upload function so individuals can send an image of their OraQuick HIV test to the study team. In response to the mLab App study and the scientific evidence of need for at-home syphilis point of care (POC) testing among YMSM and YTGW, we propose to implement the mLab App Plus to assess YMSM's and YTGW's abilities to perform and interpret self-tests for HIV and syphilis and consequently increase the number of YMSM and YTGW who initiate self-testing for HIV and syphilis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Sexually Transmitted Diseases, Viral, Syphilis

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
Participants will be randomly assigned to one of two trial arms using the randomization module in REDCap. We will use block randomization with randomly permutated blocks to reduce opportunities for selection bias
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
mLab App Plus
Arm Type
Experimental
Arm Description
Participants randomized to intervention will receive standard of care counseling, complete online surveys, be provided with the mLab App Plus, and a box of condoms. The intervention arm will also complete two HIV/Syphilis Ab Combo Rapid Tests (DPP® HIV-Syphilis Test) at their baseline (first test) and 3-month follow- up (second test) appointments.
Arm Title
Standard of Care
Arm Type
No Intervention
Arm Description
Participants randomized to standard care will receive standard of care counseling, complete online surveys and be sent an email with links to mobile-optimized online prevention information, including PrEP and HIV/STI testing information found on the Centers for Disease Control (CDC) website, and a box of condoms.
Intervention Type
Behavioral
Intervention Name(s)
mLab App Plus
Intervention Description
Participants will use the mLab Plus app to test for Syphilis and HIV using the DPP HIV/Syphilis Test
Primary Outcome Measure Information:
Title
The number of participants who are able to self-administer the DPP® HIV-Syphilis test with mLab App Plus
Description
A successful self-test is defined as having completed the DPP® HIV-Syphilis test by themselves and having accurately identified and interpreted their HIV and Syphilis statuses as determined by the supervising clinician. In the event that the clinician, rather than the participant administers the DPP® HIV-Syphilis test, the test is not recorded as a successful self-test.
Time Frame
Baseline and 3-Month Follow-up
Secondary Outcome Measure Information:
Title
The number of negative/positive results
Description
The number of negative/positive results
Time Frame
Baseline and 3-Month Follow-up
Title
The number of Young Men who have sex with men/ Young transgender women referred for HIV/STI services (participants with HIV and/or syphilis only)
Description
Using count of referral
Time Frame
Baseline and 3-Month Follow-up
Title
The number of Young Men who have sex with men/ Young transgender women linked to (attend one appointment) HIV/STI prevention or care services
Description
Using count of appointments attended
Time Frame
Baseline and 3-Month Follow-up

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Assigned male sex at birth and identify as (1) a man or (2) a trans woman
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18-35 years of age Assigned male sex at birth and identify as (1) a man or (2) a trans woman Understand and read English Self-identify as any race or ethnicity Substantial risk for acquiring HIV infection per CDC (Centers for Disease Control) guidance All participants must report having sex with a man/men Smart phone ownership Self-report being HIV-negative or unknown status Self-report being negative for syphilis or unknown status Not having been tested for HIV or syphilis in the past 6 months Not currently taking Pre-Exposure Prophylaxis (PrEP) Understand the limitations of the duplex lateral flow test and the mLab App Plus (e.g., a confirmatory test is needed and self-test must be performed in the presence of a qualified clinician)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rebecca Schnall, PhD, MPH
Phone
212-342-6886
Email
rb897@columbia.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Ian Esliker
Phone
212-305-0904
Email
ie2204@cumc.columbia.edu
Facility Information:
Facility Name
Columbia University Irving Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rebecca Schnall, PhD, MPH
Phone
212-342-6886
Email
rb897@columbia.edu
First Name & Middle Initial & Last Name & Degree
Ian Esliker
Phone
212-305-0904
Email
ie2204@cumc.columbia.edu
Facility Name
Vanderbilt University
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37235
Country
United States
Individual Site Status
Active, not recruiting

12. IPD Sharing Statement

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mLab App Plus: A Randomized Controlled Trial of a Mobile Health (mHealth) Intervention

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