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The Effect of Extended Yellow Fever Vaccine Information on Symptom Reports Following Vaccination

U

University of Auckland, New Zealand

Status

Completed

Conditions

Vaccination

Treatments

Behavioral: Extended information on side effects

Study type

Interventional

Funder types

Other

Identifiers

NCT00708630
KPKF001

Details and patient eligibility

About

This study aims to investigate the effect of providing additional information about possible mild side effects of the yellow fever vaccination on the reporting of physical symptoms. Additionally, the project aims to investigate the relationship between individual characteristics (trait anxiety and perceived sensitivity to medication) and the reporting of physical symptoms, as well as possible interactions between the level of information provided and individual characteristics. We hypothesize that more information about mild symptoms provided to participants will increase the number of reported symptoms after vaccination.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Receiving yellow fever vaccination
  • English speaker
  • Aged over 18

Exclusion criteria

  • No phone for follow-up

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

100 participants in 2 patient groups

1
Experimental group
Description:
Provision of extended symptom side effects information
Treatment:
Behavioral: Extended information on side effects
2
No Intervention group
Description:
Standard information on side effects

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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