ACTIVE_NOT_RECRUITING

Information Seeking About Pre-exposure Prophylaxis

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of these two intervention studies is to test promising health communication messaging strategies most likely to enhance Black, Hispanic, and non-Hispanic White YMSM's (young men who have sex with men's) engagement with online content about injectable and oral PrEP (pre-exposure prophylaxis). Participants will be asked to browse a mock Google results page featuring various kinds of PrEP information, and their browsing behavior will be unobtrusively logged. In Study 1, participants will be randomly assigned to browse for information about oral PrEP or browse for information about injectable PrEP. The design of Study 2 will be identical to Study 1 but will focus only on injectable PrEP content. In addition to browsing behavior, visual behavior data will also be collected in Study 2 with eye-trackers.

Official Title

Information Seeking About Pre-exposure Prophylaxis Among Men Who Have Sex With Men

Quick Facts

Study Start:2023-05-30
Study Completion:2025-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05728034

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 34 Years
Sexes Eligible for Study:MALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Have an Internet-connectable device (Study 1 only)
  2. * Be 18-34 years of age
  3. * Identify as cisgender male
  4. * Identify as gay or bisexual
  5. * Be HIV negative
  6. * Have had anal sex in the past 6 months
  7. * Meet one of the following criteria: a. Have a sexual partner with HIV, b. Have inconsistent condom use, c. Have received an STI diagnosis in the last 6 months.
  1. * Does not meet all of the criteria above

Contacts and Locations

Principal Investigator

Christofer J Skurka, PhD
PRINCIPAL_INVESTIGATOR
Penn State University

Study Locations (Sites)

Pennsylvania State University
University Park, Pennsylvania, 16802
United States

Collaborators and Investigators

Sponsor: Penn State University

  • Christofer J Skurka, PhD, PRINCIPAL_INVESTIGATOR, Penn State University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-05-30
Study Completion Date2025-07

Study Record Updates

Study Start Date2023-05-30
Study Completion Date2025-07

Terms related to this study

Additional Relevant MeSH Terms

  • Pre-exposure Prophylaxis