To Validate Changes in Knowledge, Attitudes and Practices (KAPs) Related to the Know Your OQ Initiative and to Understand the Readability, Comprehension and Ease of Use of the Know Your OQ Quiz

April 13, 2026 updated by: Colgate Palmolive

Evaluation of Short-term Changes and Self-reported User Experiences Related to the Know Your OQ™ Initiative

To validate changes in knowledge, attitudes and practices (KAPs) related to the KnowYour OQ initiative and to understand the readability, comprehension and ease of use of the Know Your OQ quiz

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Quantitative analysis will be carried out for changes in knowledge, attitudes and practices(KAPs) after the exposure to the Know Your OQ™ intervention. Qualitative and quantitative analysis will becarried out for readability, comprehension and ease of use of the Know Your OQ™ quiz.

Study Type

Observational

Enrollment (Actual)

176

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Kentucky
      • Lexington, Kentucky, United States, 40507
        • National Association of Hispanic Nurses

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Nurses attending NAHN conference

Description

Inclusion Criteria:

  • Signed Informed Consent Form.
  • Male and female subjects aged 18-65+ years old
  • Availability for the duration of the study
  • English or Spanish fluency
  • Access to laptop, tablet or computer with internet/data connection

Exclusion Criteria:

  • Not present at NAHn Convention

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Cohort of Nurses from NAHN
Prospective nurses candidates will be screened to identify those subjects who meet the inclusion/exclusion characteristics. The first 100 subjects who meet the inclusion/exclusion characteristics, sign an Informed Consent Form will be entered into the study.
Other: Oral health education
The participants will receive oral health education from multiple different sources, including the Know Your OQ website (https://www.knowyouroq.com/).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knowledge, attitudes and practices towards oral health questionnaire intervention
Time Frame: 1 year
Once subjects navigate the Know Your OQ webpage, read the provided information on oral health and complete the Know Your OQ survey, they will immediately receive a survey which explores comprehension/readability and general feedback on both the webpage and the Know Your OQ survey. Subjects who indicate negative feedback towards the intervention, including difficulties in understanding the questions of the survey and the material on the webpage, will be invited for a brief follow-up telephone interview and your participation that is optional.
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Qualitative Interviews
Time Frame: 1 year
N=30 nurses who participated in the oral health education intervention and the NAHN community programming will participate in semi-structured qualitative interviews to gain information around oral health practices in their communities, access to oral health care and education, and the community programming.
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Colgate Palmolive

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 3, 2024

Primary Completion (Actual)

July 18, 2025

Study Completion (Actual)

August 15, 2025

Study Registration Dates

First Submitted

January 6, 2025

First Submitted That Met QC Criteria

March 11, 2025

First Posted (Actual)

March 17, 2025

Study Record Updates

Last Update Posted (Actual)

April 15, 2026

Last Update Submitted That Met QC Criteria

April 13, 2026

Last Verified

January 1, 2025

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CRO-2024-06 KYOQ-MH

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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