Digital Intervention for HIV, STIs, and Hepatitis C

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Overseen ByAlissa Davis, PhD
Age: 18+
Sex: Female
Trial Phase: Academic
Sponsor: Columbia University
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 digital program, designed by survivors of sex trafficking, to increase testing for HIV, STIs, and hepatitis C, as well as the use of overdose prevention kits. It compares messages created by survivors with standard information to determine which is more effective. The trial seeks women in New York City who have survived sex trafficking, have recently used illicit substances, and feel safe participating. The goal is to make accessing vital health services easier for these women. As an unphased trial, this study offers a unique opportunity to contribute to innovative solutions tailored by survivors for survivors.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your healthcare provider.

What prior data suggests that this digital intervention is safe for survivors of sex trafficking?

Research shows that digital tools can safely and effectively promote healthy habits. This trial focuses on a digital program created by sex trafficking survivors. Similar studies have found that such programs do not harm participants. Instead, they encourage actions like getting tested for HIV, STIs, and Hepatitis C, and using overdose prevention kits.

Because this study uses digital messages, it poses no physical risk. The main goal is to assess how well these messages encourage testing and the use of prevention kits. Previous research suggests that digital programs are usually safe, as they primarily involve sharing information and offering support.

This trial does not test a new drug or treatment. It aims to find new ways to share important health information, so safety concerns are generally minimal.12345

Why are researchers excited about this trial?

Researchers are excited about this digital crowdsourced intervention because it offers a fresh approach to preventing and managing HIV, STIs, and Hepatitis C. Unlike traditional methods that rely on standard informational materials, this intervention is developed by sex trafficking survivors, which means it is uniquely tailored and potentially more relatable to at-risk populations. By leveraging digital platforms, it promises to be more engaging and accessible, potentially leading to greater awareness and behavior change. This innovative method could transform how we approach education and prevention in vulnerable communities.

What evidence suggests that this digital intervention is effective for increasing HIV/STI/HCV testing and overdose prevention among sex trafficking survivors?

This trial will compare a digital crowdsourced intervention, developed with input from sex trafficking survivors, to standard informational materials. Research has shown that digital tools created with survivors' input can increase their use of health services. This method involves collaborating with survivors to develop health messages tailored to their specific needs. Consequently, it may lead to more testing for HIV, STIs, and Hepatitis C, and greater use of overdose prevention kits. Survivors often face challenges like insufficient information or funds, so these personalized and accessible digital tools can help. Early results suggest that when survivors contribute to the content, it resonates better with them and improves health outcomes. This approach appears to be a promising, affordable way to enhance access to essential healthcare services.12367

Who Is on the Research Team?

AD

Alissa Davis, PhD

Principal Investigator

Columbia University

Are You a Good Fit for This Trial?

This trial is for survivors of sex trafficking living in New York City who have high rates of HIV/STIs/HCV and substance use disorder. The study aims to help them overcome barriers to care by using a digital intervention developed through crowdsourcing.

Inclusion Criteria

Living in New York City
Is a survivor of sex trafficking as defined by specific criteria
I am 18 years old or older.
See 3 more

Exclusion Criteria

Not willing to provide consent or not able to understand study procedures

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Intervention Development

Development of crowdsourced digital messages to promote HIV/STI/HCV testing and overdose prevention services

8 weeks

Randomized Controlled Trial

Comparison of the survivor-crowdsourced intervention to existing public health messaging

6 months
Ongoing virtual engagement

Follow-up

Participants are monitored for linkage to care and service utilization

6 months

What Are the Treatments Tested in This Trial?

Interventions

  • Sex Trafficking Survivor-Developed Digital Crowdsourced Intervention

Trial Overview

The trial tests if a digital, survivor-developed intervention can increase testing for HIV/STI/HCV and the use of overdose prevention kits. Participants will be randomly assigned to receive either this new intervention or existing public health messages.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Crowdsourced Messaging InterventionExperimental Treatment1 Intervention
Group II: Standard of CareActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Columbia University

Lead Sponsor

Trials
1,529
Recruited
2,832,000+

Citations

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