Pertussis Vaccination in Pregnant Women

Sponsor
St. Justine's Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03909126
Collaborator
Ministere de la Sante et des Services Sociaux (Other)
946
3
4
24
315.3
13.2

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Biological: Boostrix administered during gestational diabetes screening
  • Biological: Boostrix administered in high volume obstetric clinic
Phase 4

Detailed 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

Study Design

Study Type:
Interventional
Actual Enrollment :
946 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Pertussis Vaccination in Pregnant Women: Implementation and Evaluation of Different Models of Vaccination Dispensation
Actual Study Start Date :
Jun 1, 2019
Actual Primary Completion Date :
May 30, 2021
Actual Study Completion Date :
May 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Montreal Region of Quebec

Vaccination with Boostrix at time of gestational diabetes screening in a hospital setting

Biological: Boostrix administered during gestational diabetes screening
Boostrix administered during gestational diabetes screening

No Intervention: Montérégie

Vaccination with Boostrix of pregnant women receiving routine care at the CLSC or regular clinic

Experimental: Maurice Region

Vaccination with Boostrix of pregnant women receiving routine care at high volume clinic

Biological: Boostrix administered in high volume obstetric clinic
Boostrix administered in high volume obstetric clinic

No Intervention: National Capital

Vaccination with Boostrix of pregnant women receiving routine care at the CLSC or regular clinic

Outcome Measures

Primary Outcome Measures

  1. Proportion of pregnant women vaccinated against pertussis [11 months, May 2019 o March 2020]

    Proportion of pregnant women vaccinated against pertussis will be evaluated in 5 Quebec regions

  2. Proportion of pregnant women who consider pertussis as serious risk for infant [12 months, May 2019 to April 2020]

    Understanding of pertussis risk

  3. Proportion of pregnant women who consider pertussis vaccination during pregnancy as safe. [12 months, May 2019 to April 2020]

    Understanding of vaccine risk perception in pregnant women

  4. Costs for each vaccinated woman [12 months, January to December 2019]

    The cost of vaccination will be evaluated and compared between the four vaccination models.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Pregnant women at least 18 years old who speak English or French

  • Signed Informed Consent

Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 CLSC Montérégie Longueuil Quebec Canada
2 CHU Sainte-Justine Montréal Quebec Canada H3T 1C5
3 CLSC Capitale Nationale Québec Quebec Canada

Sponsors and Collaborators

  • St. Justine's Hospital
  • Ministere de la Sante et des Services Sociaux

Investigators

  • Principal Investigator: Caroline Quach, MD, St. Justine's Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Caroline Quach, MD, Medical Lead Infection Prevention and Control, St. Justine's Hospital
ClinicalTrials.gov Identifier:
NCT03909126
Other Study ID Numbers:
  • MSSS-PERT-001
First Posted:
Apr 9, 2019
Last Update Posted:
Sep 24, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Caroline Quach, MD, Medical Lead Infection Prevention and Control, St. Justine's Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 24, 2021