Evaluate the Efficacy of an Oral Health Behavioral Intervention in People With Diabetes
Condition(s) studied
Investigational drug(s) / intervention(s)
Diabetes Oral Health Program: All subjects will receive a behavioral intervention through text messages with links to educational pages about oral health or diabetes. Subjects will have the option of selecting in to the product intervention.
Stannous Fluoride Dentifrice: This is an opt-in product intervention, and it is expected that not all subjects will opt-in. Subjects will need to re-order the product every 3 months. All subjects who order product will receive a toothbrush, toothpaste, and mouthwash.
Cetylpyridinium Chloride (CPC) and Zinc Lactate Mouthwash: This is an opt-in product intervention, and it is expected that not all subjects will opt-in. Subjects will need to re-order the product every 3 months. All subjects who order product will receive a toothbrush, toothpaste, and mouthwash.
Study summary
The purpose of this clinical study is to evaluate the effect of a behavioral intervention on the number of preventive and treatment dental claims in a population of people with Type 2 Diabetes.
Eligibility
Primary outcome measure(s)
- Dental Claims — 12 months
Percentage of preventive dental claims compared to treatment dental claims
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Decentralized Site - Virtual/Remote (NY, USA) | Long Island City | New York |
More Colgate Palmolive trials in the USA
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07619729 on ClinicalTrials.gov ↗ ← All trials in the USA