Limits of the Social Benefit Motive Among High-risk Patients: a Field Experiment on Influenza Vaccination Behaviour
1 other identifier
interventional
244
1 country
1
Brief Summary
Influenza vaccine uptake remains low worldwide, inflicting substantial costs to public health and health systems. Messages promoting social welfare have been shown to increase vaccination intentions, and it has been recommended that health professionals communicate the socially beneficial aspects of vaccination. This study aims to provide the first test whether this prosocial vaccination hypothesis applies to the actual vaccination behaviour of high-risk patients by comparing the effects of two motivational messages for promoting vaccination at a tertiary care public hospital in Istanbul, Turkey.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2016
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 13, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 25, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
March 25, 2017
CompletedFirst Submitted
Initial submission to the registry
January 12, 2020
CompletedFirst Posted
Study publicly available on registry
January 18, 2020
CompletedJanuary 18, 2020
January 1, 2020
4 months
January 12, 2020
January 13, 2020
Conditions
Outcome Measures
Primary Outcomes (1)
Vaccine uptake following the introduction of the pamphlet
Difference in the number of patients in each arm who agree to receive influenza vaccine following the introduction of the pamphlet. The first half of the pamphlet contains information about the the influenza vaccine and the risk groups who are vulnerable to influenza-associated serious diseases. The second half introduces the self-benefit message. And the final part asks if the participant wants to receive the influenza vaccine now.
On the same day, upto 24 hours
Secondary Outcomes (1)
Vaccine uptake in high and low risk group patients following the introduction of the pamphlet
On the same day, upto 24 hours
Study Arms (2)
Self-benefit arm
EXPERIMENTALSocial-benefit arm
ACTIVE COMPARATORInterventions
A pamphlet consisting of a short text and an abstract figure. The top half of the pamphlet described the official criteria for qualifying to be in the risk group. Bottom half indicated that one can gain immunity against influenza by getting the vaccine and included a figure of one smiley face.
A pamphlet consisting of a short text and an abstract figure. The top half of the pamphlet described the official criteria for qualifying to be in the risk group. Bottom half indicated that one can gain immunity against influenza by getting the vaccine, and gaining immunity would lower the chances of transmitting the disease to others. The figure included one smiley face surrounded by three other smiley faces.
Eligibility Criteria
You may qualify if:
- Patients hospitalized at medical departments of the hospital who are on the day of discharge
You may not qualify if:
- Egg ellergy
- Previous allergic reaction to influenza vaccine
- Pregnancy
- Cognitive disability
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
SB Istanbul Training and Research Hospital
Istanbul, 34098, Turkey (Türkiye)
Related Publications (1)
Isler O, Isler B, Kopsacheilis O, Ferguson E. Limits of the social-benefit motive among high-risk patients: a field experiment on influenza vaccination behaviour. BMC Public Health. 2020 Feb 17;20(1):240. doi: 10.1186/s12889-020-8246-3.
PMID: 32066407DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- CARE PROVIDER, INVESTIGATOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
January 12, 2020
First Posted
January 18, 2020
Study Start
November 13, 2016
Primary Completion
March 25, 2017
Study Completion
March 25, 2017
Last Updated
January 18, 2020
Record last verified: 2020-01
Data Sharing
- IPD Sharing
- Will not share