- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03403114
Vaccine Attitudes and Practices of Hospital Specialists (SPECIVAC)
April 16, 2021 updated by: Assistance Publique - Hôpitaux de Paris
This study aims to evaluate the perceptions and knowledge of hospital specialists regarding vaccine recommendations targeting their patients, to study their behavior with respect to these recommendations and to quantify their vaccine hesitancy.
Study Overview
Study Type
Observational
Enrollment (Actual)
1851
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
-
-
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Annecy, France, 74370
- CRC Annecy
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Besançon, France, 25030
- CIC Besançon
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Clermont-Ferrand, France, 63003
- CIC Clermont-Ferrand
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Dijon, France, 21079
- CIC Dijon
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Lille, France, 59045
- CIC Lille
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Limoges, France, 87042
- CIC Limoges
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Lyon, France, 69437
- Service d'Hygiène, Epidémiologie et Prévention, Groupement Hospitalier Edouard Herriot et Unité de recherche clinique ne Immunologie du centre hospitalier Lyon Sud
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Montpellier, France, 34295
- CIC Montpellier
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Nancy, France, 54511
- Service de maladies infectieuses Nancy
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Nîmes, France, 30029
- Service de maladies infectieuses Nîmes
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Rennes, France, 35033
- CIC Rennes
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Strasbourg, France, 67000
- CIC Strasbourg
-
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Ile De France
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Paris, Ile De France, France, 75014
- CIC Cochin Pasteur
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Paris, Ile De France, France, 75877
- CIC Bichat
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
- Physicians with a frequent activity of practice and advice vaccines, called "vaccinators" (most medical specialties): 100% of those meeting the inclusion criteria will be contacted for inclusion
- Physicians "no or weak vaccinators" (anesthesiologists, surgeons, psychiatrists…): 30% of those meeting the inclusion criteria will be chosen by drawing lots
Description
Inclusion Criteria:
- To be a physician in one of the participating institutions
- Or to be a contract physician in participating institutions
Exclusion Criteria:
- Interns
- Attached practitioners
- Emergency physicians
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Proportions of Hospital Specialists (HS) with knowledge of vaccine recommendations targeting their patients
Time Frame: 15 minutes
|
15 minutes
|
Proportions of HS regularly recommending recommended vaccines to their patients
Time Frame: 15 minutes
|
15 minutes
|
Proportions of HS with doubts about recommended vaccines
Time Frame: 15 minutes
|
15 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Link between perception of benefits and risks of vaccines, knowledge of vaccine-preventable diseases, trust in different sources of information and vaccine hesitancy will be measured by questionnaire (measure by multiple logistic regressions)
Time Frame: 15 minutes
|
15 minutes
|
|
Measure of attitudes and practices of HS vis-a-vis to vaccination and their specialty by questionnaire
Time Frame: 15 minutes
|
number of HS vaccinator or not by specialty in connection with their attitudes and practices
|
15 minutes
|
Percentages of HS feeling sufficiently trained or confident to explain to patients about vaccines
Time Frame: 15 minutes
|
15 minutes
|
|
Percentages of HS claiming to be vaccinated, by type of vaccine
Time Frame: 15 minutes
|
15 minutes
|
|
Percentages of HS children reported vaccinated by type of vaccine
Time Frame: 15 minutes
|
15 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Odile LAUNAY, Professor, CIC 1417 Centre d'investigation clinique
- Study Chair: Pierre VERGER, MD, ORS PACA UMR 912 SESSTIM
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)
February 1, 2018
Primary Completion (Actual)
October 4, 2019
Study Completion (Actual)
October 4, 2019
Study Registration Dates
First Submitted
December 11, 2017
First Submitted That Met QC Criteria
January 10, 2018
First Posted (Actual)
January 18, 2018
Study Record Updates
Last Update Posted (Actual)
April 19, 2021
Last Update Submitted That Met QC Criteria
April 16, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- NI16019
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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