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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01233401
Other study ID # 1005006837
Secondary ID
Status Completed
Phase N/A
First received November 1, 2010
Last updated July 26, 2011
Start date June 2010
Est. completion date June 2011

Study information

Verified date July 2011
Source Yale University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This study evaluates whether offering Tetanus, diphteria and acellular pertussis (Tdap) vaccine to caregivers of newborn infants during pediatric well child visits increase the caregivers' vaccination rates.


Recruitment information / eligibility

Status Completed
Enrollment 102
Est. completion date June 2011
Est. primary completion date December 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 64 Years
Eligibility Inclusion Criteria:

- 18-64 years old

- English or Spanish speaking

Exclusion Criteria:

- Do not speak English or Spanish

Study Design

Observational Model: Case-Only, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Intervention

Other:
Survey
Mothers and Other infant caregivers are surveyed at the end of the 2 week newborn well child visit about whether they chose to receive the Tdap vaccine at the pediatrician's office.

Locations

Country Name City State
United States Hospital of St. Raphael New Haven Connecticut

Sponsors (2)

Lead Sponsor Collaborator
Yale University Saint Raphael Healthcare System

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maternal Tdap Vaccination Rate At 2 week well child visit No
Secondary Other Infant Caregiver Tdap Vaccination Rate At 2 week well child visit No
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