CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 6,771 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03246815
NCT03246815N/ACompleted

STD Testing in Outpatient Practices-The STOP STDs Study

University of Pittsburgh·observational·Posted Aug 11, 2017·Updated Mar 10, 2021

In Brief

An observational study for STD. Completed, enrolled 6,771 participants across 1 site.

Detailed Summary

National guidelines have recommended routine STD screening (chlamydia and gonorrhea) for sexually active young women under the age of 25. Despite these recommendations, many young women are not being screened for STDs, with some estimates that less than 50% of women receiving health care are screened for chlamydia. Untreated STDs can lead to important sequelae to women's reproductive health including pelvic inflammatory disease, infertility and ectopic pregnancy. One of the most important barriers to widespread STD screening is provider failure to recognize an opportunity for STD screening. The goal of this study is to determine whether offering STD screening (chlamydia and gonorrhea) by a non-physician member of the medical practice (who receives an automated alert indicating STD screening should be offered) will be associated with a higher rate of STD screening in young women attending primary care practices compared to usual care (where a physician offers screening with no electronic alert). This study will be performed in UPMC-affiliated primary care practices (Family Practice, Internal Medicine, OB/GYN, Pediatrics). Practices will be assigned to the intervention or usual care. The intervention will be an auto-task in the electronic medical record to the non-physician/NP/PA medical staff (medical assistants, LPNs, RNs) to offer chlamydia and gonorrhea screening via urine or self-collected vaginal sampling, in an opt-out manner, to eligible women. Practices assigned to the usual care group will not have the intervention. STD screening rates (# women undergoing STD screening/# eligible women) will be compared between the to groups (intervention practices and control practices). Results of this study may be important to guide national STD screening recommendations and will address critical barriers to widespread STD screening.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsSTD
CountriesUnited States
CollaboratorsCDC Foundation

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedAug 11, 2017
Enrollment StartJun 12, 2017
Primary CompletionNov 11, 2019
Study CompletionDec 30, 2020
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 8.9 years ago