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OpenTrials
Completed

NCT Number: NCT01009645

The Effect of Fact Versus Myth Messages on Receipt of Influenza Vaccination

The purpose of this study is to evaluate whether message design of educational materials increases vaccination rates among participants.

Completed

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Northwestern Medical Faculty Foundation General Internal Medicine and Geriatric Clinics

Chicago, Illinois, 60611, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participant must have a scheduled appointment at least 6 weeks in advance in either the GIM or Geriatrics clinics at NMFF.
  • Participant must be a patient of Northwestern Medical Faculty Foundation.
  • Participant does not intend to receive the influenza vaccine.

Exclusion criteria

  • Participant has a diagnosis of Alzheimer's Disease or Dementia
  • Participant has received an influenza vaccination during either the last influenza season or the current.
  • The scheduled visit is the participant's first time being seen by this doctor (appointment is to establish care in the clinic).

Treatment and study plan

Fact Only Education Message

Behavioral

Participants randomized to this intervention will receive an educational brochure listing the facts of the influenza vaccine.

Other names: Fact Only

Fact and Myth Educational Message

Behavioral

Participants randomized to this intervention will receive an educational brochure listing the facts and myths of the influenza vaccine.

Other names: Fact & Myth

Fact, Myth, Why Educational Message

Behavioral

Participants randomized to this intervention will receive an educational brochure listing the facts, myths, and refutation of the myths of the influenza vaccine.

Other names: Fact, Myth, Why

Control Educational Message

Behavioral

Participants randomized to this intervention will receive an educational brochure created and used by the CDC in a previous influenza season.

Other names: Control

Primary outcomes

  1. Influenza Vaccination

    Time frame: 1 week following randomization

    The primary outcome is receipt of influenza vaccination at appointment directly following the post-test. A pre-test was completed by participants during a telephone interview that occurred approximately two weeks prior to a scheduled clinic appointment. The post-test was completed via an in-person interview by participants immediately prior to their scheduled appointment. That is, the participants met with the Research Assistant, completed the post-test, and then proceeded to see their physician for a previously scheduled office visit.

Secondary outcomes

  1. Recall Accuracy

    Time frame: 1 week following receipt of message

    Participants were given 8 statements about the flu/flu shot and asked to recall if they had seen the statement on the message they received via FedEx. Participants responded that statement had been "presented as a fact," "presented as a myth," "presented, but I don't recall if it was a fact or a myth," or "not presented." Participants scored 1 for each correct answer; 0 for each incorrect answer or for response "I don't recall." Recall accuracy was calculated among each message format, range for recall accuracy was 0 - 8 with 0 indicating no correct answers and 8 representing 100% accuracy. Thus units of measurement are "units on a scale" to represent participant scores out of 8 on the recall items.

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Nov 9, 2009
Registry last updated
Oct 30, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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