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Multi-level School-based Intervention to Improve HPV Vaccine Uptake and Completion in South Africa

Mass General Brigham logo

Mass General Brigham

Status

Suspended

Conditions

HPV

Treatments

Other: HPV Vaccine Communication Strategy

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05919901
2023p001246

Details and patient eligibility

About

Human Papillomavirus (HPV) is the most common sexually transmitted infection globally, and is causally linked to cervical, anogenital, and oropharyngeal cancers. HPV-associated cancers have a disproportionate impact in low-resource settings and nowhere is this evident than in South Africa, which has a uniquely vulnerable population due to the convergence of the largest HIV epidemic globally, with HPV rates of up to 85% in young women under the age of 25. For the clinical trial phase of this study, we intend to evaluate preliminary effects of a communications strategy and key criteria to advance to a full scale hybrid type 2 trial. Our systems-focused approach leverages established partnerships with area schools serving diverse populations who are not always effectively served by traditional healthcare channels.

Enrollment

600 estimated patients

Sex

All

Ages

9 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • This study will include children enrolled in Grade 5 in participating schools (ages 9-12 years old) in Gauteng province, South Africa, who have no prior history of HPV immunization. We have selected fifth graders for our target population to follow the current Provincial Guidelines. This is in line with National Cervical Guidelines aimed at reaching young people prior to their sexual debut.

We will also be recruiting parents/caregivers of these children, given their role in decision-making. All parents/caregivers will be at least 18 years old. We will also be including adults who are at least 18 years of age, who are employed at participating schools as teachers or school administrators, and others who are engaged in the planning or implementation of the school-based HPV vaccine program (e.g., representatives from the Department of Health, nurses). We have no upper age limit for this population.

Exclusion criteria

  • Children below the age of 9 years old will not be included in the study.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

600 participants in 2 patient groups

HPV Intervention
Experimental group
Treatment:
Other: HPV Vaccine Communication Strategy
Active Control
Active Comparator group
Treatment:
Other: HPV Vaccine Communication Strategy

Trial contacts and locations

1

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Central trial contact

Eliana DaCunha, BA; Ingrid T Katz, MD, BA, MHS

Data sourced from clinicaltrials.gov

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