Sero-prevalence of Anti-pertussis Antibodies and Disease Awareness Among Spanish Healthcare Professionals

NCT ID: NCT01706224

Last Updated: 2014-01-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

757 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-11-30

Study Completion Date

2013-05-31

Brief Summary

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This study aims to determine the sero-prevalence of anti-pertussis antibodies among healthcare professionals at hospital centres in Spain.

Detailed Description

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Conditions

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Pertussis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Group A

Subjects in this group will be all physicians actively working at hospital centres in Spain.

Blood sample

Intervention Type PROCEDURE

Samples will be tested to determine the presence of anti-pertussis antibodies.

Data collection

Intervention Type OTHER

Electronic Case Report Forms (eCRF)

Data collection

Intervention Type OTHER

Questionnaires, active questioning.

Group B

Subjects in this group will be all nurses actively working at hospital centres in Spain.

Blood sample

Intervention Type PROCEDURE

Samples will be tested to determine the presence of anti-pertussis antibodies.

Data collection

Intervention Type OTHER

Electronic Case Report Forms (eCRF)

Data collection

Intervention Type OTHER

Questionnaires, active questioning.

Group C

Subjects in this group will be all ancillary nursing professionals actively working at hospital centres in Spain.

Blood sample

Intervention Type PROCEDURE

Samples will be tested to determine the presence of anti-pertussis antibodies.

Data collection

Intervention Type OTHER

Electronic Case Report Forms (eCRF)

Data collection

Intervention Type OTHER

Questionnaires, active questioning.

Group D

Subjects in this group will be all midwives actively working at hospital centres in Spain.

Blood sample

Intervention Type PROCEDURE

Samples will be tested to determine the presence of anti-pertussis antibodies.

Data collection

Intervention Type OTHER

Electronic Case Report Forms (eCRF)

Data collection

Intervention Type OTHER

Questionnaires, active questioning.

Interventions

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Blood sample

Samples will be tested to determine the presence of anti-pertussis antibodies.

Intervention Type PROCEDURE

Data collection

Electronic Case Report Forms (eCRF)

Intervention Type OTHER

Data collection

Questionnaires, active questioning.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Written informed consent obtained from the subject.
* Subjects who the investigator believes that they can and will comply with the requirements of the protocol.
* Male and female healthcare professionals aged ≥18 years from selected hospitals.
* Healthcare professionals in frequent contact with patients in the hospitals.
* Agreeing for collection of a blood sample for the study.

Exclusion Criteria

• Medical students working as healthcare professionals.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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GlaxoSmithKline

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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GSK Clinical Trials

Role: STUDY_DIRECTOR

GlaxoSmithKline

Locations

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GSK Investigational Site

A Coruña, , Spain

Site Status

GSK Investigational Site

L'Hospitalet de Llobregat, , Spain

Site Status

GSK Investigational Site

Majadahonda, , Spain

Site Status

Countries

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Spain

References

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Rodriguez de la Pinta ML, Castro Lareo MI, Ramon Torrell JM, Garcia de Lomas J, Devadiga R, Reyes J, McCoig C, Tafalla M, Garcia-Corbeira P. Seroprevalence of pertussis amongst healthcare professionals in Spain. Vaccine. 2016 Feb 17;34(8):1109-14. doi: 10.1016/j.vaccine.2015.12.036. Epub 2015 Dec 22.

Reference Type DERIVED
PMID: 26718690 (View on PubMed)

Other Identifiers

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115539

Identifier Type: -

Identifier Source: org_study_id

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