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Get Connected Efficacy Trial

Primary Purpose

HIV Infections

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Get Connected
HIV Test Locator
Sponsored by
University of Pennsylvania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections focused on measuring Prevention & Control, Internet, Adolescents, Young adults

Eligibility Criteria

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

Inclusion Criteria:

  • Assigned male sex at birth and currently identifies as male
  • Aged 15 to 24 years (inclusive) at time of screening
  • Self-report as HIV-negative or sero-status unaware
  • Speak and read English
  • Not be on PrEP at time of enrollment
  • Report having consensual anal sex with a male partner in the prior 6 months
  • Reside in Philadelphia, Houston, or Atlanta
  • Access to internet

Exclusion Criteria:

  • Assigned female sex at birth
  • Assigned male sex at birth but identifies as transgender or gender non-conforming
  • Aged 14 years or younger or 25 years or older at time of screening
  • HIV-positive
  • Does not speak or read English
  • Currently taking PrEP
  • Did not have consensual anal sex with a male partner in the prior 6 months
  • Does not reside in Philadelphia, Houston, or Atlanta
  • Currently incarcerated
  • Planning to move out of the region in next 12 months

Sites / Locations

  • Emory University
  • Children's Hospital of Philadelphia
  • Texas Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Get Connected

Non-tailored HIV Test Locator

Arm Description

Get Connected is a brief intervention focused on resolving ambivalence about HIV prevention behaviors, increasing self-efficacy for change, and enhancing motivation moving toward action.

Participants randomized to the control condition will be directed to a testing site locator. Given the availability of search engines to locate HIV/STI testing sites, the test locator condition may be considered usual care.

Outcomes

Primary Outcome Measures

Percent of Participants reporting changes in their HIV Testing Behavior using self-report questionnaires
The investigators will estimate the proportion of participants who test for HIV by intervention group and by time on study.

Secondary Outcome Measures

Percent of participants reporting changes in PrEP uptake using self-report questionnaires
The investigators will test the proportion of the sample that begins PrEP during the 12-month follow-ups.
Mean Change in motivations to engage in HIV prevention behaviors using self-report questionnaires
The investigators will measure the change in HIV prevention attitudes, norms, and self-efficacy using the NIH Adolescent Trials Network's Harmonized Questionnaire by intervention group and by time on study.
Mean Change in PrEP motivations using self-report questionnaires
The investigators will measure the change in PrEP awareness and willingness over time using the NIH Adolescent Trials Network's Harmonized Questionnaire.
Percent of Participants reporting changes in their STI Testing Behavior using self-report questionnaires
The investigators will estimate the proportion of participants who test for STIs at least once over the trial period.

Full Information

First Posted
April 24, 2017
Last Updated
January 6, 2022
Sponsor
University of Pennsylvania
Collaborators
University of North Carolina, University of Michigan, University of Minnesota, Emory University, Children's Hospital of Philadelphia, Baylor College of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT03132415
Brief Title
Get Connected Efficacy Trial
Official Title
Get Connected: Linking YMSM to Adequate Care Through a Multilevel, Tailored WebApp Intervention
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 1, 2017 (Actual)
Primary Completion Date
December 15, 2021 (Actual)
Study Completion Date
June 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Pennsylvania
Collaborators
University of North Carolina, University of Michigan, University of Minnesota, Emory University, Children's Hospital of Philadelphia, Baylor College of Medicine

4. Oversight

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

5. Study Description

Brief Summary
Get Connected (GC) is an online brief intervention that employs individual and systems-level tailoring technology to reduce barriers to HIV prevention care (e.g., HIV/STI testing, PrEP) for YMSM. The deployment of GC through a mobile-friendly WebApp seeks to optimize online interventions' acceptability, accessibility, availability, long-term affordability among youth. The investigators will enroll 480 self-reported HIV-negative or sero-status unaware, sexually active YMSM (ages 15-24) across three cities and randomize them into the GC intervention condition or to an attention-control condition. Assessments will be collected at 30 days and at 3, 6, 9 and 12 month follow-up.
Detailed Description
The number of HIV infections among men who have sex with men aged 15-24 (YMSM) has grown significantly in the past decade. For YMSM to successfully engage in HIV prevention and care services requires that they navigate a series of multilevel barriers operating at the individual (e.g., risk awareness, self-efficacy to get tested), systems (e.g., costs, medical mistrust, lack of culturally competent care), and structural (e.g., homelessness, costs, stigma) levels. The investigators developed Get Connected (GC) as an online brief intervention that employs individual and systems-level tailoring technology to reduce barriers to linkage to competent prevention care (e.g., HIV/STI testing, PrEP) for YMSM (ages 15-24). After a formative phase comprised of assessing HIV testing sites' performance via a mystery shopping procedure, the investigators will test the efficacy of GC for increasing YMSM's successful engagement in locally appropriate HIV prevention and care using a two-arm randomized controlled trial. The trial will compare GC (N=240) to an existing online HIV test locator (N=240). Participants will be recruited from three cities (Houston, Philadelphia and Atlanta) characterized by high HIV incidence, and followed over 12 months. Assessments will be collected at 30 days and at 3, 6, 9 and 12 month follow-up. Specific Aims include: Aim 1: Examine the quality of HIV test counseling and PrEP-related referrals to YMSM within local HIV/STI testing sites in 3 cities (Houston, Philadelphia & Atlanta). Aim 2: Test the efficacy of GC for increasing HIV-negative or HIV-unknown YMSM's successful uptake of HIV prevention services (e.g., routine HIV/STI testing) and PrEP awareness and willingness, as compared to the attention-control condition over a 12-month period. Aim 3: Qualitatively assess sites' satisfaction with performance assessments and their improvements in service delivery when working with YMSM across the three regions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Prevention & Control, Internet, Adolescents, Young adults

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
285 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Get Connected
Arm Type
Experimental
Arm Description
Get Connected is a brief intervention focused on resolving ambivalence about HIV prevention behaviors, increasing self-efficacy for change, and enhancing motivation moving toward action.
Arm Title
Non-tailored HIV Test Locator
Arm Type
Active Comparator
Arm Description
Participants randomized to the control condition will be directed to a testing site locator. Given the availability of search engines to locate HIV/STI testing sites, the test locator condition may be considered usual care.
Intervention Type
Behavioral
Intervention Name(s)
Get Connected
Intervention Description
The investigators designed the intervention to help participants increase their HIV risk awareness, promote self-appraisal and increase motivation for engaging in prevention services, problem solving barriers to accessing care, and locating culturally-sensitive providers. Intervention content is customized based on participants' socio-demographic characteristics, HIV/STI testing history and testing motivations, and recent sexual behaviors.
Intervention Type
Behavioral
Intervention Name(s)
HIV Test Locator
Intervention Description
The investigators will use a HIV/STI testing locator as the attention-control condition. The test locator provides a list of HIV testing sites in a city or zipcode.
Primary Outcome Measure Information:
Title
Percent of Participants reporting changes in their HIV Testing Behavior using self-report questionnaires
Description
The investigators will estimate the proportion of participants who test for HIV by intervention group and by time on study.
Time Frame
30-day, 3-month, 6-month, 9-month, and 12-month follow-up assessments
Secondary Outcome Measure Information:
Title
Percent of participants reporting changes in PrEP uptake using self-report questionnaires
Description
The investigators will test the proportion of the sample that begins PrEP during the 12-month follow-ups.
Time Frame
30-day, 3-month, 6-month, 9-month, and 12-month follow-up assessments
Title
Mean Change in motivations to engage in HIV prevention behaviors using self-report questionnaires
Description
The investigators will measure the change in HIV prevention attitudes, norms, and self-efficacy using the NIH Adolescent Trials Network's Harmonized Questionnaire by intervention group and by time on study.
Time Frame
30-day, 3-month, 6-month, 9-month, and 12-month follow-up assessments
Title
Mean Change in PrEP motivations using self-report questionnaires
Description
The investigators will measure the change in PrEP awareness and willingness over time using the NIH Adolescent Trials Network's Harmonized Questionnaire.
Time Frame
30-day, 3-month, 6-month, 9-month, and 12-month follow-up assessments
Title
Percent of Participants reporting changes in their STI Testing Behavior using self-report questionnaires
Description
The investigators will estimate the proportion of participants who test for STIs at least once over the trial period.
Time Frame
30-day, 3-month, 6-month, 9-month, and 12-month follow-up assessments

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Assigned male sex at birth and currently identifies as male Aged 15 to 24 years (inclusive) at time of screening Self-report as HIV-negative or sero-status unaware Speak and read English Not be on PrEP at time of enrollment Report having consensual anal sex with a male partner in the prior 6 months Reside in Philadelphia, Houston, or Atlanta Access to internet Exclusion Criteria: Assigned female sex at birth Assigned male sex at birth but identifies as transgender or gender non-conforming Aged 14 years or younger or 25 years or older at time of screening HIV-positive Does not speak or read English Currently taking PrEP Did not have consensual anal sex with a male partner in the prior 6 months Does not reside in Philadelphia, Houston, or Atlanta Currently incarcerated Planning to move out of the region in next 12 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa Hightow-Weidman, MD
Organizational Affiliation
University of North Carolina
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jose A Bauermeister, PhD
Organizational Affiliation
University of Pennsylvania
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rob B Stephenson, PhD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Patrick S Sullivan, PhD
Organizational Affiliation
Emory University
Official's Role
Study Chair
Facility Information:
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Facility Name
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
Yes
IPD Sharing Plan Description
The investigators will assure the timely release and sharing of data two years after the publication of the main trial findings from the final dataset. Study variables will be available; however, the investigators will protect the rights and privacy of human subjects by redacting all identifiers from the dataset. The de-identified data from this project will be available through individual requests directed to the Principal Investigator.
Citations:
PubMed Identifier
25638038
Citation
Bauermeister JA, Pingel ES, Jadwin-Cakmak L, Harper GW, Horvath K, Weiss G, Dittus P. Acceptability and preliminary efficacy of a tailored online HIV/STI testing intervention for young men who have sex with men: the Get Connected! program. AIDS Behav. 2015 Oct;19(10):1860-74. doi: 10.1007/s10461-015-1009-y.
Results Reference
background
PubMed Identifier
26303197
Citation
Bauermeister JA, Pingel ES, Jadwin-Cakmak L, Meanley S, Alapati D, Moore M, Lowther M, Wade R, Harper GW. The use of mystery shopping for quality assurance evaluations of HIV/STI testing sites offering services to young gay and bisexual men. AIDS Behav. 2015 Oct;19(10):1919-27. doi: 10.1007/s10461-015-1174-z.
Results Reference
background
PubMed Identifier
28195779
Citation
Horvath KJ, Bauermeister JA. eHealth Literacy and Intervention Tailoring Impacts the Acceptability of a HIV/STI Testing Intervention and Sexual Decision Making Among Young Gay and Bisexual Men. AIDS Educ Prev. 2017 Feb;29(1):14-23. doi: 10.1521/aeap.2017.29.1.14.
Results Reference
background
PubMed Identifier
31658201
Citation
Bauermeister JA, Golinkoff JM, Lin WY, Claude KF, Horvath KJ, Dowshen N, Schlupp A, Vickroy WJ, Desir K, Lopez AV, Castillo M, Tanney M, Wimbly TA, Leung K, Sullivan PS, Santiago DL, Hernandez R, Paul ME, Hightow-Weidman L, Lee S, Stephenson R. Testing the Testers: Are Young Men Who Have Sex With Men Receiving Adequate HIV Testing and Counseling Services? J Acquir Immune Defic Syndr. 2019 Dec 1;82 Suppl 2(2):S133-S141. doi: 10.1097/QAI.0000000000002173.
Results Reference
result
PubMed Identifier
30072358
Citation
Bauermeister JA, Golinkoff JM, Horvath KJ, Hightow-Weidman LB, Sullivan PS, Stephenson R. A Multilevel Tailored Web App-Based Intervention for Linking Young Men Who Have Sex With Men to Quality Care (Get Connected): Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2018 Aug 2;7(8):e10444. doi: 10.2196/10444.
Results Reference
derived

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Get Connected Efficacy Trial

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