ACTIVE_NOT_RECRUITING

Let's K-Talk - HPV Study for Ethnic Koreans

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to test the feasibility, acceptability, and preliminary efficacy of a storytelling video-based intervention using AI chatbot technology (K-Talk) to promote HPV vaccination behavior among Korean Americans aged 18 to 45. The main questions this study aims to answer are: * Is the K-Talk intervention feasible for use among Korean Americans aged 18 to 45? * Is the K-Talk intervention acceptable to the target population? * What is the preliminary efficacy of the K-Talk intervention in promoting HPV vaccination uptake? Participants will be Korean Americans aged 18 to 45 who are at risk for HPV infection. Participants will be asked to complete a baseline survey and then will be "randomized" into one of four groups: Group 1 (chatbot + storytelling intervention), Group 2 (chatbot only), Group 3 (storytelling only), and Group 4 will be only exposed to written didactic HPV education materials. All groups will receive written didactic HPV education materials. Researchers will compare how Group 1, a combination of AI Chatbot and storytelling intervention is more effective than other intervention groups in promoting HPV vaccination uptake among underserved, hard-to-reach Korean Americans.

Official Title

Let's K-Talk: A Storytelling Intervention Leveraging Chatbot Technology to Prevent HPV and HPV Associated Cancers for Ethnic Koreans Living in the U.S.

Quick Facts

Study Start:2023-05-10
Study Completion:2026-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05884697

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.

Ages Eligible for Study:18 Years to 45 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Identify as a Korean ethnic person
  2. 2. Reside in the U.S.
  3. 3. between the ages of 18 and 45
  4. 4. be able to speak or read English
  5. 5. not have been vaccinated against HPV
  6. 6. use a mobile device.
  1. 1. Participants who do not identify as a Korean ethnic person
  2. 2. Participants who do not reside in the U.S.
  3. 3. Participants who are not between the ages of 18 and 45.
  4. 4. Participants who cannot speak or read English.
  5. 5. Participants who have been vaccinated against HPV.
  6. 6. Participants who do not use a mobile device.

Contacts and Locations

Principal Investigator

Minjin Kim, PhD., RN
PRINCIPAL_INVESTIGATOR
UC College of Nursing

Study Locations (Sites)

Minjin Kim
Cincinnati, Ohio, 45221-0038
United States

Collaborators and Investigators

Sponsor: University of Cincinnati

  • Minjin Kim, PhD., RN, PRINCIPAL_INVESTIGATOR, UC College of Nursing

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 Registration Dates

Study Start Date2023-05-10
Study Completion Date2026-07-31

Study Record Updates

Study Start Date2023-05-10
Study Completion Date2026-07-31

Terms related to this study

Keywords Provided by Researchers

  • Korean immigrants
  • HPV Vaccines
  • Storytelling Intervention
  • Korean Americans
  • Artificial Intelligence Chatbot

Additional Relevant MeSH Terms

  • Human Papillomavirus Viruses
  • Papillomavirus Vaccines