Evaluation of the Know Your OQ™ Oral Health Literacy Tool in an Indian Population (KYOQIN)

August 23, 2024 updated by: Colgate Palmolive

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

This was a research study to evaluate the effectiveness of the questionnaire "Know Your OQ™" (Know Your Oral Health Quotient™) in changing people's level of knowledge about oral health in India and to evaluate the readability, understanding and ease of completion of the questionnaire "Know Your OQ™".

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

150

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

  • India
      • Mumbai, India
        • IPSOS Research Private Limited

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

Non-Probability Sample

Study Population

A total of 150 male and female adults were split into two groups: 100 regular subjects and 50 nurses. These groups were further stratified by educational qualification (Completed High School, Pursuing Graduation, Completed Graduation, Completed Post Graduation), sex (male and female), age group (18-24, 25-35, 36-45, 46-55, 56-65, >65), experience with oral health problems (yes and no), and the cities they reside in (Mumbai, Delhi, Chennai, Kolkata, Bengaluru).

Description

Inclusion Criteria:

  • Sign Informed Consent Form
  • Male and female subjects aged ≥18 years old
  • Availability of 10 days for completing the study
  • Belong to NCCS (National Consumer Classification System) A,B
  • Access to a cell phone, laptop, tablet or computer with internet/data connection
  • Fluent in English

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
Nurses
Regular Consumers

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Knowledge, Attitude, Practice (KAP)
Time Frame: Baseline, Intervention, Immediate Follow-Up, 1 week Follow-Up
Change in Knowledge, Attitude, and Practice before and after exposure to the Know Your OQ™ tool. Day minus 3: Pretest Knowledge, Attitude, Practice (KAP) & Demographics, Day 0: Know Your OQ, Day 0 Immediate follow up: Post-test Comprehension Questionnaire, Week 1 follow up: Post test Knowledge, Attitudes and Practices Questionnaire
Baseline, Intervention, Immediate Follow-Up, 1 week Follow-Up

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)

May 20, 2024

Primary Completion (Actual)

June 8, 2024

Study Completion (Actual)

June 8, 2024

Study Registration Dates

First Submitted

July 30, 2024

First Submitted That Met QC Criteria

July 30, 2024

First Posted (Actual)

August 2, 2024

Study Record Updates

Last Update Posted (Actual)

August 26, 2024

Last Update Submitted That Met QC Criteria

August 23, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • CRO-2024-03-KYOQ-BG

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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