HIV TestingP3NCT06785376
P3 Trial: Estimating the Impact of a Multilevel, Multicomponent Intervention to Increase Uptake of HIV Testing and Biomedical HIV Prevention
A study testing DIY (Do It Yourself), TRUST and SOC in people with HIV Testing and PrEP Uptake, run by Columbia University at 1 site in United States.
Trial summary
The major goal of this study is to evaluate a multi-component, multilevel HIV prevention intervention that targets theoretically-informed and empirically-identified barriers to and facilitators of both HIV testing and PEP/PrEP uptake by combining existing evidence-based and novel evidence-informed components and… Read more about this study
- Who is it for?
- Ages 18 to 65 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- HIV Testing, PrEP Uptake
- What is being tested?
- DIY (Do It Yourself), TRUST and SOC
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 480 participants
- Where
- 1 siteUnited States
- Study dates
- 19 Dec 2024to 28 Feb 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 18 to 65 years
- Men only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Assigned biological male sex at birth
- 18-65 years of age
- Self-identify as: Black, African-American, Afro-Caribbean, Black African, Afro-Latino or multiethnic Black
- Reside in the NYC metro area
- Not HIV-positive (tested before randomization)
- Report insertive or receptive anal intercourse with another man in the past six months
Show all 10Show fewer
- Not currently on PEP or PrEP
- Can communicate in English or Spanish
- Provide informed consent for the study
- Any sexual identity
Who cannot join
- Unable to conduct a rapid HIV-self test to confirm self-reported HIV-negative status
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site, 1 recruiting
- Recruiting
Columbia University
New York, New York, 10027
Victoria Frye, MPH, DrPH, 2128534490, vaf5@columbia.edu
Victoria Frye, MPH, DrPH
About this study
Official title: Estimating the Impact of a Multilevel, Multicomponent Intervention to Increase Uptake of HIV Testing and Biomedical HIV Prevention Among African-American/Black Gay, Bisexual and Same-gender Loving Men
The major goal of this study is to evaluate a multi-component, multilevel HIV prevention intervention that targets theoretically-informed and empirically-identified barriers to and facilitators of both HIV testing and PEP/PrEP uptake by combining existing evidence-based and novel evidence-informed components and integrating them into a community-based organization's (CBO) standard of care (SOC) PEP/PrEP navigation program. The evaluation will apply use a 2x2 factorial design to randomize and follow for 18 months 480 PrEP-eligible Black MSM (aged 18-65) living in the NYC area to one of four combinations of interventions. The impact of the social/media campaign, delivered to both geographic (print media) and Black MSM communities (social media) and launched midway through recruitment, will be assessed through assessment of timing and length of exposure as covariates in analysis.
Read the detailed description
The major goal of this study is to evaluate a multi-component, multilevel HIV prevention intervention that targets theoretically-informed and empirically-identified barriers to and facilitators of both HIV testing and PEP/PrEP uptake by combining existing evidence-based and novel evidence-informed components and integrating them into a community-based organization's (CBO) standard of care (SOC) PEP/PrEP navigation program. The existing evidence-based, individual-level component is TRUST (R01 DA-038108), a single-session peer-based HIV self-testing intervention for Black MSM. The existing, evidence-based community-level component is a social/print media campaign (CHHANGE [R21 MH-102182-01] \& PEPTALK [R21 AI-122996]) to reduce community-level HIV stigma and drive demand for HIV testing, PEP and PrEP. The novel, evidence-informed, individual-level component is "Do It Yourself (DIY)", a 3-session enhancement of the CBO SOC peer navigation program that promotes empowerment, autonomy, stigma coping/resistance and social support via a novel "sexual self-care in-a-box" and peer-to-peer training to increase HIV testing and PEP/PrEP uptake.
The Specific Aims are:
- Component test DIY, adapt social/print media campaign \& manualize full intervention. Modified intervention mapping, component testing and post-test interviews with 20 PrEP-eligible Black MSM (for DIY) and focus groups with 20 PrEP-eligible Black MSM (for media campaign adaptation) will be conducted. A 15-person community consulting group of Black MSM, community leaders, media professionals, and service providers, will provide feedback on both components and the full manualized intervention.
- Estimate main and interactive effects of components on recent HIV testing and PEP/PrEP uptake. Hypothesis 1: Exposure to TRUST, DIY, and the media campaign will each be associated with (1) higher past 3-month HIV testing; and (2) shorter time to PrEP uptake over time. Hypothesis 2: A multiplicative interaction among TRUST, DIY and length of exposure to the media campaign will emerge, such that exposure to combination of multiple interventions will be associated with the more positive outcomes compared to the impact of each intervention component individually. To test this hypotheses, this study will use a 2x2 factorial design to randomize and follow for 18 months 480 PrEP-eligible Black MSM (aged 18-65) living in NYC to one of four combinations: 1) SOC, DIY \& TRUST; 2) SOC \& TRUST (no DIY); 3) SOC \& DIY (no TRUST); 4) SOC ALONE (no TRUST and no DIY). Hypotheses will be tested via regression (GEE) and Cox proportional hazard models; impact of the social/media campaign, delivered to both geographic (print media) and Black MSM communities (social media) and launched midway through recruitment, will be assessed through assessment of timing and length of exposure as covariates in the regression models and through interrupted time series methods.
- Describe the feasibility, acceptability, and usability of intervention components and package via the Re-AIM implementation framework with an emphasis on component implementation by a CBO program.
- Conditions
- HIV Testing, PrEP Uptake
- Being tested
- DIY (Do It Yourself), TRUST, SOC
- Keywords
- HIV testing, PrEP uptake, HIV prevention, men who have sex with men
- Medical subject headings
- Homosexuality
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
DIY (Do It Yourself)Behavioural
DIY is 3-session program that promotes empowerment, autonomy, stigma coping/resistance and social support to promote sexual health and pleasure and HIV prevention.
TRUSTBehavioural
TRUST is a single-session HIV self-testing training with facilitator
SOCBehavioural
standard of care single-session, low threshold peer/near-peer navigation to PrEP.
| Study group | Role | What they receive |
|---|---|---|
| A. SOC | Active comparator | Standard of care single-session, low threshold peer/near-peer navigation to PrEP. Receives: Behavioral: SOC |
| B. SOC & TRUST | Experimental | SOC standard of care single-session, low threshold peer/near-peer navigation to PrEP; TRUST single-session HIV self-testing training with facilitator Receives: Behavioral: TRUST; Behavioral: SOC |
| C. SOC & DIY | Experimental | SOC standard of care single-session, low threshold peer/near-peer navigation to PrEP; DIY three-session sexual health promotion/HIV prevention training with facilitator Receives: Behavioral: DIY (Do It Yourself); Behavioral: SOC |
| D. SOC, TRUST & DIY | Experimental | SOC standard of care single-session, low threshold peer/near-peer navigation to PrEP; TRUST single-session HIV self-testing training with facilitator; DIY three-session sexual health promotion/HIV prevention training with facilitator Receives: Behavioral: DIY (Do It Yourself); Behavioral: TRUST; Behavioral: SOC |
What is being measured
The primary outcome is the main question the study is designed to answer.
P3M HIV testing
did the participant engage in HIV testing in the past 3 months
Measured: past 3 months
PrEP uptake
PrEP uptake (yes/no)/time to PrEP uptake (assessed via self-report, medical record)
Measured: past 3 months
Secondary outcomes (3)
consistent HIV testing
consistent HIV testing (2+ tests 3 months apart in 9 months)
Measured: over 9 months
PEP uptake
PEP uptake (self-report, medical record)
Measured: past 3 months
PrEP and PEP adherence
PrEP/PEP adherence (self-report/medical record)
Measured: past 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Jan 2025
- Study start19 Dec 2024
- Primary completion28 Feb 2028 (estimated)
- Study completion28 Feb 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for HIV TestingStudies of the same condition, open and under way.
- More trials run by Columbia UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Randomised
- Intervention model
- Factorial
- Model description
- 2x2 factorial design
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 480 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Columbia University
- Sponsor type
- University, hospital or other
- Collaborators
- National Institute of Mental Health (NIMH)
- Responsible party
- Principal investigator, Victoria Anne Frye, Columbia University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06785376
- Sponsor's protocol ID
- AAAU8754
- Other IDs
- R01MH129198
- Acronym
- P3
- Status last verified
- Aug 2026
- First submitted
- 16 Jan 2025
- Last updated
- 31 Aug 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Bond KT, Williams PM, Paige M, Lam I, Hart K, Matthews D, Smith W, Koffler E, Zhang H, Kelvin EA, Frye V, Duncan DT. Designing Pleasure-Centered, Culturally Relevant PrEP Messaging for Black Gay, Bisexual, Queer, Same-Gender-Loving, and Other Men Who have Sex with Men (SGL/MSM) in New York City. AIDS Behav. 2026 Aug;30(8):2513-2523. doi: 10.1007/s10461-026-05077-7. Epub 2026 Apr 17.
PubMed 41995922
Study at a glance
From the registry record, last updated by the sponsor on 31 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Estimating the Impact of a Multilevel, Multicomponent Intervention to Increase Uptake of HIV Testing and Biomedical HIV Prevention Among African-American/Black Gay, Bisexual and Same-gender Loving Men
- ClinicalTrials.gov ID
- NCT06785376
- Acronym / sponsor ID
- P3 / AAAU8754
- Conditions
- HIV Testing, PrEP Uptake
- Keywords
- HIV testing, PrEP uptake, HIV prevention, men who have sex with men
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 480 participants (estimated)
- Lead sponsor
- Columbia UniversityUniversity, hospital or other
- Collaborators
- National Institute of Mental Health (NIMH)
- Study start
- 19 Dec 2024 (actual)
- Primary completion
- 28 Feb 2028 (estimated)
- Study completion
- 28 Feb 2028 (estimated)
- First posted
- 21 Jan 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The major goal of this study is to evaluate a multi-component, multilevel HIV prevention intervention that targets theoretically-informed and empirically-identified barriers to and facilitators of both HIV testing and PEP/PrEP uptake by combining existing evidence-based and novel evidence-informed components and integrating them into a community-based organization's (CBO) standard of care (SOC) PEP/PrEP navigation program. The evaluation will apply use a 2x2 factorial design to randomize and follow for 18 months 480 PrEP-eligible Black MSM (aged 18-65) living in the NYC area to one of four combinations of interventions. The impact of the social/media campaign, delivered to both geographic (print media) and Black MSM communities (social media) and launched midway through recruitment, will be assessed through assessment of timing and length of exposure as covariates in analysis.
Detailed description
The major goal of this study is to evaluate a multi-component, multilevel HIV prevention intervention that targets theoretically-informed and empirically-identified barriers to and facilitators of both HIV testing and PEP/PrEP uptake by combining existing evidence-based and novel evidence-informed components and integrating them into a community-based organization's (CBO) standard of care (SOC) PEP/PrEP navigation program. The existing evidence-based, individual-level component is TRUST (R01 DA-038108), a single-session peer-based HIV self-testing intervention for Black MSM. The existing, evidence-based community-level component is a social/print media campaign (CHHANGE [R21 MH-102182-01] \& PEPTALK [R21 AI-122996]) to reduce community-level HIV stigma and drive demand for HIV testing, PEP and PrEP. The novel, evidence-informed, individual-level component is "Do It Yourself (DIY)", a 3-session enhancement of the CBO SOC peer navigation program that promotes empowerment, autonomy, stigma coping/resistance and social support via a novel "sexual self-care in-a-box" and peer-to-peer training to increase HIV testing and PEP/PrEP uptake.
The Specific Aims are:
- Component test DIY, adapt social/print media campaign \& manualize full intervention. Modified intervention mapping, component testing and post-test interviews with 20 PrEP-eligible Black MSM (for DIY) and focus groups with 20 PrEP-eligible Black MSM (for media campaign adaptation) will be conducted. A 15-person community consulting group of Black MSM, community leaders, media professionals, and service providers, will provide feedback on both components and the full manualized intervention.
- Estimate main and interactive effects of components on recent HIV testing and PEP/PrEP uptake. Hypothesis 1: Exposure to TRUST, DIY, and the media campaign will each be associated with (1) higher past 3-month HIV testing; and (2) shorter time to PrEP uptake over time. Hypothesis 2: A multiplicative interaction among TRUST, DIY and length of exposure to the media campaign will emerge, such that exposure to combination of multiple interventions will be associated with the more positive outcomes compared to the impact of each intervention component individually. To test this hypotheses, this study will use a 2x2 factorial design to randomize and follow for 18 months 480 PrEP-eligible Black MSM (aged 18-65) living in NYC to one of four combinations: 1) SOC, DIY \& TRUST; 2) SOC \& TRUST (no DIY); 3) SOC \& DIY (no TRUST); 4) SOC ALONE (no TRUST and no DIY). Hypotheses will be tested via regression (GEE) and Cox proportional hazard models; impact of the social/media campaign, delivered to both geographic (print media) and Black MSM communities (social media) and launched midway through recruitment, will be assessed through assessment of timing and length of exposure as covariates in the regression models and through interrupted time series methods.
- Describe the feasibility, acceptability, and usability of intervention components and package via the Re-AIM implementation framework with an emphasis on component implementation by a CBO program.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- Single blind (participant)
- Number of arms
- 4
- Model description
- 2x2 factorial design
| Arm | Type | Receives |
|---|---|---|
| A. SOC | Active comparator | Behavioral: SOCStandard of care single-session, low threshold peer/near-peer navigation to PrEP. |
| B. SOC & TRUST | Experimental | Behavioral: TRUST, Behavioral: SOCSOC standard of care single-session, low threshold peer/near-peer navigation to PrEP; TRUST single-session HIV self-testing training with facilitator |
| C. SOC & DIY | Experimental | Behavioral: DIY (Do It Yourself), Behavioral: SOCSOC standard of care single-session, low threshold peer/near-peer navigation to PrEP; DIY three-session sexual health promotion/HIV prevention training with facilitator |
| D. SOC, TRUST & DIY | Experimental | Behavioral: DIY (Do It Yourself), Behavioral: TRUST, Behavioral: SOCSOC standard of care single-session, low threshold peer/near-peer navigation to PrEP; TRUST single-session HIV self-testing training with facilitator; DIY three-session sexual health promotion/HIV prevention training with facilitator |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (10 listed)
- Assigned biological male sex at birth
- 18-65 years of age
- Self-identify as: Black, African-American, Afro-Caribbean, Black African, Afro-Latino or multiethnic Black
- Reside in the NYC metro area
- Not HIV-positive (tested before randomization)
Key exclusion criteria (1 listed)
- Unable to conduct a rapid HIV-self test to confirm self-reported HIV-negative status
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| DIY (Do It Yourself)DIY is 3-session program that promotes empowerment, autonomy, stigma coping/resistance and social support to promote sexual health and pleasure and HIV prevention. | Behavioural | C. SOC & DIY, D. SOC, TRUST & DIY |
| TRUSTTRUST is a single-session HIV self-testing training with facilitator | Behavioural | B. SOC & TRUST, D. SOC, TRUST & DIY |
| SOCstandard of care single-session, low threshold peer/near-peer navigation to PrEP. | Behavioural | A. SOC, B. SOC & TRUST, C. SOC & DIY, D. SOC, TRUST & DIY |
Primary outcome
P3M HIV testing
Time frame: past 3 months
did the participant engage in HIV testing in the past 3 months
PrEP uptake
Time frame: past 3 months
PrEP uptake (yes/no)/time to PrEP uptake (assessed via self-report, medical record)
3 secondary outcomes
consistent HIV testing
Time frame: over 9 months
PEP uptake
Time frame: past 3 months
PrEP and PEP adherence
Time frame: past 3 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Aug 2026.
- Derived from this study: PubMed 41995922Bond KT, Williams PM, Paige M, Lam I, Hart K, Matthews D, Smith W, Koffler E, Zhang H, Kelvin EA, Frye V, Duncan DT. Designing Pleasure-Centered, Culturally Relevant PrEP Messaging for Black Gay, Bisexual, Queer, Same-Gender-Loving, and Other Men Who have Sex with Men (SGL/MSM) in New York City. AIDS Behav. 2026 Aug;30(8):2513-2523. doi: 10.1007/s10461-026-05077-7. Epub 2026 Apr 17.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing DIY (Do It Yourself), TRUST and SOC in people with HIV Testing and PrEP Uptake, run by Columbia University 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 10 inclusion and 1 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: looking for participants now, as of the sponsor's last update on 31 Aug 2026. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Victoria Frye, MPH, DrPH (2128534490, vaf5@columbia.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
P3M HIV testing (time frame: past 3 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06785376, which also lists 1 linked publication.
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 31 Aug 2026.