Electronic Sexual Reproductive Health CDS Tool at the Children's Hospital of Philadelphia
NCT04974086 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 190
Last updated 2025-10-03
Summary
Many studies show early detection of sexual activity in adolescents can improve their health management and that primary care pediatricians would benefit from supports to address adolescent health, including sexual and reproductive health. The primary objective of this study is to develop and evaluate the feasibility, acceptability, and usability of a sexually transmitted infection (STI) testing clinical decision support (CDS) tool within the electronic health record (EHR) among clinicians, adolescent patients, and their parents. Secondary objectives include assessment of the CDS tool's impact on clinical measures. The STI Testing CDS tool will be embedded within clinical practice and evaluated through a single-armed prospective cohort study of primary care clinicians, adolescent patients, and parents. The STI Testing CDS tool that will support pediatric clinicians by providing evidence-based sexual health-related screening, treatment, and referrals, as needed.
Conditions
- Sexual and Reproductive Health
Interventions
- OTHER
-
Sexually transmitted infection (STI) testing clinical decision support (CDS) tool
The intervention, called the STI Testing CDS tool, includes integrating STI testing guideline prompts into the electronic health record (EHR). The prompt guides clinicians to assess and broadly respond to adolescents' sexual health behaviors through EHR survey data. Through the CDS tool, clinicians will be prompted to provide comprehensive and evidence-based sexual health care for teens including, for example: providing patient-facing education about sexual preventative health topics and facilitating ordering of HIV and sexually transmitted infection (STI) laboratory tests to improve both risk-based and routine annual preventative screening.
Sponsors & Collaborators
-
National Institute of Mental Health (NIMH)
collaborator NIH -
Children's Hospital of Philadelphia
lead OTHER
Principal Investigators
-
Brian P. Jenssen, MD · Primary care pediatrician and researcher
Study Design
- Allocation
- NA
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 13 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-09-26
- Primary Completion
- 2024-02-11
- Completion
- 2024-02-11
Countries
- United States
Study Locations
More Related Trials
-
Coital Pharmacokinetics/Pharmacodynamics (PK/PD) of Tenofovir Gel
NCT01687205 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluation of EVO100 for Prevention of Urogenital Chlamydia Trachomatis and Neisseria Gonorrhoeae Infection
NCT04553068 ·Status: COMPLETED ·Phase: PHASE3
-
Accuracy and Acceptability of Self-Diagnostic Methods for Vaginitis in Adolescent Females
NCT00706368 ·Status: UNKNOWN ·Phase: NA
-
Brief Intervention and/or Distribution of Free Condoms for Travelers
NCT01056536 ·Status: COMPLETED ·Phase: NA
-
STI Care Model to Reduce Genital Inflammation and HIV Risk in South African Women
NCT03407586 ·Status: COMPLETED ·Phase: NA
-
Risk-factors for Multidrug-resistant Bacteria Colonization Among Patients at High Risk of STIs
NCT03767374 ·Status: COMPLETED
-
Safety, PK, and PD Study of a Vaginal Insert Containing TAF and EVG
NCT03762772 ·Status: COMPLETED ·Phase: PHASE1
-
A Healthcare Economic Study of the Click Sexual Health Test
NCT04099199 ·Status: COMPLETED
-
Chemoprevention of Cancer in the Lower Female Genital Tract: The Antineoplastic Activity of the Fungicide Ciclopirox.
NCT00382330 ·Status: WITHDRAWN ·Phase: NA
-
A Clinical Feasibility Study to Assess the Performance of a Latex Condom in Healthy Monogamous Couples.
NCT05073770 ·Status: UNKNOWN ·Phase: NA
-
Women's Input on Sexual Health
NCT02057419 ·Status: COMPLETED
-
Postcoital Testing Study of the SILCS Diaphragm Used With 3% N-9 Gel, ContraGel, or No Gel
NCT02309554 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Acceptability of a Vaginal Microbicide
NCT00111943 ·Status: COMPLETED ·Phase: PHASE2
-
Daily Doxycycline to Inform Sexually Transmitted Infection Prophylaxis Regimens
NCT06545656 ·Status: COMPLETED ·Phase: PHASE4
-
Testing the POWER Project: A Neighborhood Intervention Trial
NCT00164671 ·Status: COMPLETED ·Phase: NA
-
Vulvar Vestibulitis Clinical Trial: Desipramine-Lidocaine
NCT00276068 ·Status: COMPLETED ·Phase: NA
-
Evaluation of a Novel Female Hygiene Device for Postcoital Discomfort
NCT04885556 ·Status: UNKNOWN ·Phase: NA
-
Postcoital Testing of the SILCS Diaphragm
NCT00561613 ·Status: COMPLETED ·Phase: PHASE1
-
Effect of Antibiotics on Penile Microbiome and HIV Susceptibility Study in Ugandan Men
NCT03412071 ·Status: UNKNOWN ·Phase: NA
-
Rectal Safety and Acceptability Study of Tenofovir 1% Gel
NCT01232803 ·Status: COMPLETED ·Phase: PHASE1
-
Study of Dapivirine Vaginal Ring (VR) in Adolescents
NCT02028338 ·Status: COMPLETED ·Phase: PHASE2
-
Safety, Acceptability and Preliminary Effectiveness of Carraguard™ (PC-515) in Preventing HIV/STI Transmission
NCT00213018 ·Status: COMPLETED ·Phase: PHASE2
-
Pilot Trial of Novel Circumcision Device
NCT01885286 ·Status: COMPLETED ·Phase: NA
-
Botswana Study of UC-781 Vaginal Microbicide
NCT00385554 ·Status: WITHDRAWN ·Phase: PHASE1
-
A Pivotal Study to Assess the Safety and Efficacy of The PrePex System, a Male Circumcision Device and Methodology for Rapid Scale up of Painless and Bloodless National Circumcision Programs, in Urban and Remote Rural Settings
NCT01150370 ·Status: COMPLETED ·Phase: NA