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Pertussis Vaccination in Pregnant Women

S

St. Justine's Hospital

Status and phase

Completed
Phase 4

Conditions

Pertussis

Treatments

Biological: Boostrix administered in high volume obstetric clinic
Biological: Boostrix administered during gestational diabetes screening

Study type

Interventional

Funder types

Other

Identifiers

NCT03909126
MSSS-PERT-001

Details and patient eligibility

About

Brief Summary: The study compares four models of pertussis vaccination dispensation to pregnant women on the vaccine coverage obtained. In addition, the cost of the different models of vaccination will be evaluated.

Full description

This is a quasi-experimental study with a non-equivalent control group in pregnant women, taking place in 4 regions of Québec (Montréal, Montérégie, Capitale-Nationale, Mauricie). Four models of vaccine dispensation will be evaluated: one university hospital around gestational diabetes screening, local health and social services centres (CSLC) and a high volume clinic. 250 participants will be recruited in each of the four types of centres.

In addition, the study will also evaluate the costs incurred by all those involved in the pertussis vaccination program for pregnant women as well as the cost per woman vaccinated.

Health Professionals:

15 to 20 health professionals involved in providing immunization services to pregnant women: obsterician-gynaecologists, family doctors and nurses in participating clinics will be interviewed to evaluate their knowledge, attitudes and professional practises regarding pertussis vaccination during pregnancy.

Evaluating the Cost:

A detailed costing approach (micro-costing) will be used. Time and movement will be studied by direct observation using a grid on an electronic file in each of the 5 environments studied in order to identify the services and activities carried out as well as to determine the resources involved in the implementation of these services and activities. Three typical vaccination days will be chosen to make these observations, in each of the four study environments.

The main activities observed will be related to preparations for vaccination up to the vaccination itself (informed consent, injection, etc.), the capture of vaccination data the management of vaccines and equipment, clinical manifestations, etc. If necessary, the people observed can be interviewed directly to better understand the activities or services provided. Otherwise, some questions may be included in the interviews described above.

The major cost categories that will be evaluated for each of the delivery modalities are human resources and supplies. The cost components listed are: nursing time (immunization / training), coordination time, support staff time, office supplies, vaccine storage equipment, vaccine transportation equipment, vaccine transportation, health and safety equipment, emergency, single-use vaccination equipment and others.

With regard to the costs borne by women, the main categories of variables evaluated will be: the time spent making appointments and attending vaccination appointments, working time lost, if any, transportation, childcare and other expenses

Enrollment

946 patients

Sex

Female

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Pregnant women at least 18 years old who speak English or French
  • Signed Informed Consent

Exclusion criteria

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

946 participants in 4 patient groups

Montreal Region of Quebec
Experimental group
Description:
Vaccination with Boostrix at time of gestational diabetes screening in a hospital setting
Treatment:
Biological: Boostrix administered during gestational diabetes screening
Montérégie
No Intervention group
Description:
Vaccination with Boostrix of pregnant women receiving routine care at the CLSC or regular clinic
Maurice Region
Experimental group
Description:
Vaccination with Boostrix of pregnant women receiving routine care at high volume clinic
Treatment:
Biological: Boostrix administered in high volume obstetric clinic
National Capital
No Intervention group
Description:
Vaccination with Boostrix of pregnant women receiving routine care at the CLSC or regular clinic

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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