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NCT05804825 · ClinicalTrials.gov registry record · NA

Testing the Persuasiveness of Pro-inoculation Arguments

A NA study of Vaccine Refusal and Human Papillomavirus Vaccination, sponsored by University of Pennsylvania.

Completed
Registry status
NA
Development phase
523
Enrollment target
1
Study location

NCT05804825 is a NA study of Vaccine Refusal and Human Papillomavirus Vaccination that has completed, run by University of Pennsylvania. The registered enrollment target is 523 participants, below the 1,213-participant average among 5 other Vaccine Refusal trials with a reported enrollment target (57% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05804825, a NA study of Vaccine Refusal and Human Papillomavirus Vaccination, has completed, sponsored by University of Pennsylvania.

COMPLETED
Registry status
NA
Development phase
523 participants
Enrollment target
1
Study location

Study Summary

The investigators will recruit a national sample of parents of 7-10-year-olds to complete an argument strength ranking for either a simple forwarding message or between 3 and 6 randomly selected arguments from an overall set of 50 to 100 messages identified from various online sources. Parents will rate each message they see on measures of perceived argument strength/PME. Parents will also answer sociodemographic questions and then rank the believability of a set of anti-vaccine messages identified in a different study. Study findings will contribute valuable information to understanding the effectiveness of different inoculation messages.

Interventions

  • BEHAVIORAL Argument inoculation messages
  • BEHAVIORAL Simple forewarning message

Study Locations (1)

Pennsylvania

  • UPenn - Philadelphia

Trial Details

FieldValue
Enrollment Target 523 participants
Start Date 2023-05-04
Est. Completion 2023-05-24
Phase NA

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT05804825

The ClinicalTrials.gov registry entry for NCT05804825 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 523 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,213-participant average among 5 other Vaccine Refusal trials with a reported enrollment target (57% lower). The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Vaccine Refusal appearing as the primary indexed condition, and to 2 interventions - of which Argument inoculation messages is the first listed.

NCT05804825 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT05804825 about?

NCT05804825 is a clinical study titled "Testing the Persuasiveness of Pro-inoculation Arguments". The investigators will recruit a national sample of parents of 7-10-year-olds to complete an argument strength ranking for either a simple forwarding message or between 3 and 6 randomly selected arguments from an overall set of 50 to 100 messages identified from various online sources. Parents will ...

What is the current status of trial NCT05804825?

This trial is currently completed. It is a NA study. The enrollment target is 523 participants. The study started on 2023-05-04. Estimated completion is 2023-05-24.

What conditions does trial NCT05804825 study?

This clinical trial studies the following conditions: Vaccine Refusal, Human Papillomavirus Vaccination, Vaccination Hesitancy.

What interventions are being tested in trial NCT05804825?

The interventions under investigation include: Argument inoculation messages (BEHAVIORAL), Simple forewarning message (BEHAVIORAL).

Who is sponsoring clinical trial NCT05804825?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05804825 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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