Prevention of cervical cancer Cancer
Conditions
Interventions
The randomization schedule will be done in blocks of 6 in a 50:50 ratio. Allocation will only occur once the consent will be obtained. A secured order list made by a computer generator will determine
Sponsors
Centre Hospitalier Universitaire de Sherbrooke
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Women are eligible for study enrollment if: 1. They agree to get a prescription of HPV vaccination 2. Understand French
Exclusion criteria
Exclusion criteria: Women who: 1. Do not know their HPV immunization status 2. Refuse vaccination
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of HPV vaccination at 6 months after randomisation | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Rates of vaccination measured using phone call at 6 months for high-risk patients in intervention and control groups. High-risk patients are categorized as presenting one or more of these risk factors: smoker or past smoker, more than two sexual partners in the past 12 months, low education status (high school or college), history of abnormal pap smear or had their last pap smear more than 3 years ago 2. Type and frequency of barriers to vaccination in intervention and control groups mentioned by non-vaccinated patients in a phone call at 6 months 3. Type and frequency of barriers to vaccination in intervention group mentioned in phone calls at 1 and 3 months which were overcome by recall calls | — |
Countries
Canada
Contacts
Public ContactJessica Ruel-Laliberte
Outcome results
None listed