Predicting Vaccine Hesitancy Using Machine Learning

July 12, 2026 updated by: Emel AVÇİN, University of Yalova

Factors Influencing Vaccine Hesitancy Among Parents of Children Aged 0-48 Months: A Machine Learning Prediction

In recent years, emerging technologies such as the Internet of Things (IoT), Artificial Intelligence (AI), and Virtual Reality (VR) have rapidly become integrated into daily life. The widespread use of these applications has led to the accumulation of vast amounts of data, giving rise to what is commonly referred to as "Big Data." Due to the sheer volume, manual processing and analysis of these large datasets are not feasible. Therefore, software tools and libraries-such as Python and R libraries-have been developed to perform these analyses efficiently and to generate predictions for the future by leveraging historical data through Machine Learning (ML) algorithms.

The primary goal of machine learning algorithms is to discover patterns within existing data and use these patterns to make accurate predictions on new data. The use of machine learning in the field of healthcare has gained significant momentum in recent years. However, a review of the literature reveals that research specifically addressing childhood vaccine hesitancy remains limited.

This study aims to identify the factors contributing to vaccine hesitancy among parents of children aged 0-48 months and to develop a predictive model using machine learning techniques based on these factors. Such a model could help anticipate the likelihood of vaccine refusal among parents and thereby support the development of targeted public health strategies for at-risk populations.

Study Overview

Study Type

Observational

Enrollment (Actual)

461

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

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

No sample size calculation was performed in this study. Between June 2025 and September 2025, all parents of children aged 0-4 years who met the inclusion criteria and could be reached with the questionnaires were included in the study. Snowball sampling method will be used to reach the parents. The study population consists of parents who have children aged 0-4 years, possess proficiency in understanding and reading the Turkish language, and can be accessed via social media platforms using technological devices.

Description

Inclusion Criteria:

Parents who meet the following criteria will be included in the study:

  • Have proficiency in understanding and reading the Turkish language,
  • Are able to use technological devices such as mobile phones or computers to access social media platforms (Participants used social media platforms such as Instagram and WhatsApp to communicate) via the internet,
  • Are 18 years of age or older,
  • Have children aged 0-4 years,
  • Consent to participate in the study,
  • Have children without any absolute contraindications to vaccination.

Exclusion Criteria:

  • Parents of high-risk infants (such as those with a history of systemic illness, preterm labor, anomalies, etc.),
  • Parents who are unwilling to participate in the study will be excluded.

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
Parents of children aged 0-48 months
Parents who meet the following criteria will be included in the study: those who have proficiency in understanding and reading the Turkish language; are 18 years of age or older; have children aged 0-4 years; are able to use technological devices such as mobile phones or computers to access social media platforms (Participants used social media platforms such as Instagram and WhatsApp to communicate) via the internet; consent to participate in the study; and whose children do not have any absolute contraindications for vaccination.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Parental Vaccine Hesitancy Status
Time Frame: Day 1 (Parents will be sent the questionnaire and asked to respond promptly.)
The Vaccine Hesitancy Scale is a measurement tool designed to assess individuals' vaccine hesitancy or opposition. It consists of 21 items across 4 subscales and uses a 5-point Likert scale format. The four subscales of the scale are: Vaccine Benefit and Protective Value, Vaccine Opposition, Solutions for Avoiding Vaccination, and Justification of Vaccine Hesitancy. Higher scores on the scale indicate greater levels of vaccine hesitancy or opposition.
Day 1 (Parents will be sent the questionnaire and asked to respond promptly.)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: EMEL AVÇİN, Assist Prof, University of Yalova

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)

July 2, 2025

Primary Completion (Actual)

March 1, 2026

Study Completion (Actual)

June 1, 2026

Study Registration Dates

First Submitted

May 17, 2025

First Submitted That Met QC Criteria

May 23, 2025

First Posted (Actual)

May 25, 2025

Study Record Updates

Last Update Posted (Actual)

July 14, 2026

Last Update Submitted That Met QC Criteria

July 12, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

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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