CHEER Oral Health in Pregnancy Study
NCT07377344 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 160
Last updated 2026-04-07
Summary
Many pregnant people don't get the dental care they need, even though it's safe and important. The CHEER Study offers free dental check-ups, cleanings, and supplies to help participants take care of their teeth and gums during pregnancy. The purpose of this research study is to compare two types of noninvasive oral health interventions to evaluate their effectiveness. We want to learn if one method is more effective in supporting oral health and improving pregnancy outcomes. There are two aims of this study:
Aim 1: To evaluate whether a structured oral health intervention reduces periodontal inflammation during pregnancy and postpartum in pregnant people with indicators of periodontal disease.
Aim 2: To assess whether a structured oral health intervention is associated with changes in oral health behaviors or birth outcomes in pregnant people with periodontal disease.
Conditions
- Gingivitis
- Dental Health
- Pregnancy
- Pregnancy Outcomes
- Randomized Controlled Trial
- Periodontal Disease
- Gum Disease
Interventions
- BEHAVIORAL
-
Enhanced Care
All participants receive standard oral hygiene education at the baseline visit.
- BEHAVIORAL
-
Enhanced Care +
All participants receive standard oral hygiene education at the baseline visit. Test participants also receive a home oral care kit (toothbrush, toothpaste, and floss), and will start receiving weekly oral health check-ins and reminder surveys following their initial visits at one-week intervals starting the day after their baseline visit
Sponsors & Collaborators
-
Colgate Palmolive
collaborator INDUSTRY -
University of California, San Francisco
lead OTHER
Principal Investigators
-
Effie Ioannidou, DDS, MDS · University of California, San Francisco
-
Laura Jelliffe-Pawlowski, PhD · University of California, San Francisco
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-06-01
- Primary Completion
- 2028-06-01
- Completion
- 2028-06-01
Countries
- United States
Study Locations
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