Enhancing Oral Cancer Awareness

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorVirginia Commonwealth University

About this trial

To evaluate the impact of AI-powered chatbot interactions versus traditional educational handouts on increasing participants' knowledge of oral cancer and its prevention

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Identify as African American as defined by the US Census

Participants must be able to read, speak, and write in English

Disqualifiers

Individuals who cannot physically or mentally participate in the research project will be excluded

Adults unable to consent

Individuals who are not yet adults (infants, children, teenagers)

Prisoners

Trial design

Design model

Parallel

Treatments tested in this trial

  • Traditional Education

    Behavioral

    Participants will receive traditional educational handouts focusing on increasing awareness of oral cancer risks, preventive strategies, and the importance of regular dental check-ups. Participants will be provided time to read the handouts based on calculated reading time.

  • AI-powered Chatbox

    Behavioral

    The chatbot interaction will be initiated through a provided link, allowing participants to access information and ask questions related to oral health and cancer prevention. The chatbot is programmed to provide accurate information on oral cancer risks, symptoms, preventive measures, and the importance of regular dental check-ups. Participants will be encouraged to interact with the chatbot for a specified duration

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Traditional Educational MaterialsActive comparator 1 intervention
Group B: Engaging with an AI-powered ChatbotExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Compare participant retention rates between the AI-powered tool arm and the conventional educational material arm

Compare the percentage of participants that continued the intervention to the participants that continued using the active comparator to measure intervention feasibility.

Time frame
Baseline, and post intervention (3 months)
2

Evaluate the impact of AI-powered chatbot interactions versus traditional educational handouts on knowledge and behavior

Assess the effectiveness of the interventions by baseline and post intervention surveys assessing oral cancer knowledge, attitudes, and behaviors utilizing a questionnaire based on the Health Belief Model. The questionnaire will include scales measuring knowledge about oral cancer, its causes, risk factors, signs, preventive methods. Each question will have one correct answer, and the final score at baseline and after the intervention will be compared. Based on previous literature, a score of 60-70% can indicate adequate knowledge about a disease, but the primary goal of the outcome is to compare improvement in knowledge between control vs intervention arms.

Time frame
Baseline, and post intervention (3 months)
3

Investigate socio-demographic factors that affect oral cancer knowledge in the African American population

Pre-intervention surveys will include questions assessing socio-demographic variables of the participants. These variables will serve as covariates in the analysis to measure their effects on knowledge and attitudes. The effect of demographic factors affecting healthcare service utilization, such as education attainment and health insurance status, on knowledge about and attitude toward oral cancer will be measured through regression analysis to investigate their impact on oral cancer awareness and prevention efforts.

Time frame
Baseline, and post intervention (3 months)
4

Evaluate the acceptability of AI-powered chatbot interactions versus traditional educational handouts

Assess the acceptability of the interventions by baseline and post intervention surveys assessing satisfaction, appropriateness, ease of use, and acceptability of the interventions to improve oral cancer knowledge. Satisfaction and acceptability will be measured through a set of questions in the post-intervention questionnaire with 5 Likert scale-based responses ranging from "Strongly Disagree" to "Strongly Agree", and the final score will be compared between arms.

Time frame
Baseline, and post intervention (3 months)

Secondary outcomes

Other outcomes

Sponsors and contacts

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Virginia Commonwealth University

Lead sponsor

American Association for Cancer Education

Collaborator