Vaccine Hesitancy Intervention--Provider (VHIP)

Not Applicable

Completed

• Conditions: Childhood Vaccination
• Interventions: Behavioral: Academic Detailing

• Registration Number: NCT01667354
• Lead Sponsor: Kaiser Permanente

Brief Summary

The primary aim of this trial is to test the effectiveness of an intervention to train primary care physicians to determine if it leads to decreased parental vaccine hesitancy.

Detailed Description

The primary aim of this trial is to test the effectiveness of an intervention to train primary care physicians to determine if it leads to decreased parental vaccine hesitancy. The investigators will train primary care teams with an initial training followed by telephone coaching and follow-up visits, and assess the outcomes of parental vaccine hesitancy (primary) and physician self-efficacy (secondary) at baseline and 6 months.

Study Timeline

• Study Start: 2012-02
• Study First Submitted: 2012-03-06
• Study First Submitted QC: 2012-08-15
• Study First Posted: 2012-08-17
• Primary Completion: 2013-10
• Study Completion: 2014-04
• Status Verified: 2017-10
• Last Update Submitted: 2017-10-11
• Last Update Posted: 2017-10-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 491

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intervention Clinics	Academic Detailing	Providers in intervention clinics will receive a training followed by telephone coaching and follow-up visits for six months.

Primary Outcome Measures

Name	Time	Method
Parental Vaccine Hesitancy Measure	Change from Baseline in Parental Hesitancy at 6 months	The investigators will contact mothers of newborns in study practices and conduct a telephone survey at two time points: baseline and 6 months. Surveys will assess parental hesitancy, parental trust in provider, and other covariates such as perceived social norms, other sources of information about vaccines, and demographic information.

Secondary Outcome Measures

Name	Time	Method
Physician Self Efficacy Measure	Change from Baseline in Physician Attitudes at 6 months	Assessed via self-administered surveys of providers in all participating clinics at baseline and 6-months. The investigators will measure physician attitudes, perceived norms, intentions to change behavior, practice characteristics, and physician demographics.

Trial Locations

Locations (1)

Group Health Research Institute; 🇺🇸 Seattle, Washington, United States