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Utilizing Electronic Modules to Educate on Sexual Health Practices During Pregnancy
Who can join
Ages 18 and older · Women
Full eligibility criteria
Inclusion Criteria: * Pregnant individuals at or beyond 12 weeks gestation * Age 18 years or older * English speaking with English reading proficiency * Experiencing a low risk pregnancy with no major complications * Not currently followed by Maternal-Fetal Medicine (MFM) for high risk pregnancy management Exclusion Criteria: * Pregnancy complications requiring management by Maternal-Fetal Medicine (MFM) * Placed on pelvic rest * Advised by their provider to abstain from sexual intercourse
About the study
This study looks at whether an interactive online education module can improve knowledge, comfort, and communication about sexual health during pregnancy. Many pregnant individuals experience changes in sexual function and intimacy but may feel uncomfortable discussing these topics or may have misconceptions about what is safe during pregnancy.
Participants who are pregnant and receiving routine prenatal care will be randomly assigned to one of two groups. One group will complete an interactive, evidence-based educational module focused on sexual health and intimacy during pregnancy. The other group will review a standard educational article from the American College of Obstetricians and Gynecologists (ACOG) about sexual activity during pregnancy.
Participants will complete surveys before and after reviewing the educational material, as well as a follow-up survey two weeks later. These surveys will measure knowledge about sexual health during pregnancy, comfort discussing sexual concerns with healthcare providers, and sexual function. The goal of this study is to determine whether an interactive educational approach can better support pregnant individuals' understanding of sexual health and encourage open communication with healthcare providers during pregnancy.
What is being tested
- Standard ACOG Educational Article (behavioral)
- Interactive Sexual Health Educational Module (behavioral)
Sponsor: Loyola University · Participants: 100 · Started: Feb 28, 2026
Contact the study team
- Mary Lynn, DO · Phone: 708-327-1450
Official record on ClinicalTrials.gov — NCT07497971
Locations in the U.S.
| Illinois | Loyola University Medical Center, Maywood |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.