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临床试验/NCT07619729
NCT07619729Enrolling By Invitation4 期

Clinical Study to Evaluate the Efficacy of an Oral Health Behavioral Intervention on Medical and Dental Claims in People With Diabetes

Colgate Palmolive1 个研究点 分布在 1 个国家目标入组 10,000 人开始时间: 2026年5月26日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
Enrolling By Invitation
入组人数
10,000
试验地点
1

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • Severe cognitive impairment.
  • General anesthesia in the past 3 months.
  • Type 1 diabetes.
  • Self-reported pregnant.

研究组 & 干预措施

Type 2 Diabetes

Experimental

This is a single-group study. All subjects will be enrolled in the experimental group.

干预措施: Stannous Fluoride Dentifrice (Drug)

Type 2 Diabetes

Experimental

This is a single-group study. All subjects will be enrolled in the experimental group.

干预措施: Cetylpyridinium Chloride (CPC) and Zinc Lactate Mouthwash (Drug)

Type 2 Diabetes

Experimental

This is a single-group study. All subjects will be enrolled in the experimental group.

干预措施: Diabetes Oral Health Program (Behavioral)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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