Actively Recruiting
Leveraging Health Information Technology to Reduce Health Disparities in Adolescent Health Outcomes: A Patient-Centered Approach
Led by Children's National Research Institute · Updated on 2026-03-18
18500
Participants Needed
1
Research Sites
2 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating whether using an electronic clinical decision support (CDS) tool based on a sexual health survey (SHS) can improve detection rates of sexually transmitted infections (STIs) among adolescents aged 15 to 21 years who visit the emergency department. The study aims to compare STI detection rates between adolescents receiving SHS-derived CDS and those receiving usual care without CDS. Additional analyses will assess detection differences by sexual risk level and race or ethnicity. The study includes two groups: one where eligible adolescents complete the SHS and receive electronic CDS if identified at risk, and a comparison group receiving usual care before the CDS tool was implemented. The intervention is behavioral, focusing on using health information technology to support clinical decisions during emergency visits. Participants will be adolescents aged 15 to 21 years visiting the emergency department. Researchers will measure detection rates of Chlamydia trachomatis and Neisseria gonorrhoeae within 3 to 7 days after the visit. Data on STI rates will also be analyzed by race and ethnicity. The study involves following participants during and after their emergency visit to evaluate the impact of the CDS tool on STI detection. The trial is sponsored by the Children's National Research Institute and plans to continue until early 2027.
CONDITIONS
Brief Title
Health Information Technology to Reduce Disparities in Adolescent Health Outcomes: A Pragmatic Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adolescents aged 15-21 years seeking care in the emergency department
You will not qualify if you...
- Unable to understand English
- Critically ill
- Cognitively impaired
- Unable to provide consent for completion of the sexual health survey and STI screening
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 3 to 7 days after emergency department visit
Participants who undergo routine care are observed to assess health outcomes related to sexual health risks.
1 follow-up visit (in-person or remote)
Trial Site Locations
Total: 1 location
1
Children's National Hospital
Washington D.C., District of Columbia, United States, 20010
Actively Recruiting
Research Team
M
Meleah Boyle
M
Monika Goyal, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SEQUENTIAL
Primary Purpose
SCREENING
Number of Arms
2
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