Evaluate the Efficacy of an Oral Health Behavioral Intervention in People With Diabetes

NCT07619729 · tracked via the Priya Life Science USA tracker

Sponsor

Colgate Palmolive

Phase

Phase 4

Started

2026-05-26

Last updated

2026-09-03

Condition(s) studied

Diabetes Type 2Periodontal DiseaseCaries

Investigational drug(s) / intervention(s)

Diabetes Oral Health ProgramStannous Fluoride Dentifrice →Cetylpyridinium Chloride (CPC) and Zinc Lactate Mouthwash

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

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Consented to participation in the Fidelis Care Diabetes Care program. * Aged 18 years and older * English speaking. * Willing and able to receive text messages, and participate in online activities for the duration of the program. * Diagnosis of Type 2 Diabetes. Exclusion Criteria: * Severe cognitive impairment. * General anesthesia in the past 3 months. * Type 1 diabetes. * Self-reported pregnant.

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

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Official registry record

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