Actively Recruiting

Phase Not Applicable
Age: 9Years - 110Years
All Genders
Healthy Volunteers
ID06997705

Strengthening HPV Vaccination and Adolescent Health Research Program (SHARP) in Ivory Coast

Led by Jhpiego · Updated on 2025-05-30

3384

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Cervical cancer is a major health issue worldwide, especially in sub-Saharan Africa, where it is the leading cancer among women. Vaccination against human papillomavirus (HPV) helps prevent cervical cancer and is usually given to children aged 9 to 15 years. This research evaluates how combining HPV vaccination with adolescent primary care and preventive health services affects vaccine uptake and other health services in Côte d'Ivoire. The study aims to make service delivery more convenient and effective for adolescents in schools, communities, and health facilities. The study compares an intervention group receiving an optimized integrated adolescent health service package, including HPV vaccination, with a comparison group receiving routine adolescent health services. The intervention includes expanded availability of services through schools, communities, and health facilities, as well as community awareness activities. The comparison group receives the standard Systematic Medical Visit program for adolescents. The research uses a quasi-experimental design with data collected over time in two regions, each with intervention and comparison districts. Participants will be adolescents aged 9 to 15 and their parents or caregivers living in the study regions. The study involves surveys of households, parents, and adolescents at the beginning and end of the study, as well as interviews with program managers and community members. Researchers will measure HPV vaccination rates, intentions to vaccinate, knowledge about HPV, and attitudes towards integrated services. Service coverage data will be collected monthly during the intervention. The study will assess the feasibility, acceptability, effectiveness, and sustainability of the integrated adolescent health package over several months.

CONDITIONS

Brief Title

Integrated HPV Vaccination and Adolescent Health in Ivory Coast

Who Can Participate

Age: 9Years - 110Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adolescents aged 9 to 15 years
  • Reside in the study regions
  • Have parental or guardian permission
  • Provide assent and agree to participate
  • Parents or caregivers must be legal guardians of adolescents aged 9 to 15
  • Parents or caregivers must reside in the study regions
  • Parents or caregivers provide informed consent and agree to participate
Not Eligible

You will not qualify if you...

  • People with time constraints
  • Those who do not speak French or local dialects used in the study regions
  • Those unable to participate due to illness, intoxication, or psychological impairment
  • Those residing outside the study health regions
  • Those who do not provide consent or assent to participate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Up to 8 months

Participants receive an optimized integrated adolescent health service package including HPV vaccination through school, health facility, and community settings. The intervention also includes community sensitization activities.

Monthly visits during intervention

Follow-up

Duration - Up to 2 months after intervention

Participants' vaccination status, HPV knowledge, and attitudes towards integrated services are assessed at the end of the intervention period.

1 visit (in-person) at endline

Trial Site Locations

Total: 1 location

1

École Nationale Supérieure de Statistique et d'Économie Appliquée (ENSEA)

Abidjan, Côte d’Ivoire

Actively Recruiting

Loading map...

Research Team

S

Shana Kagan, MN, MSc

P

Pooja Sripad, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

Similar Trials

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here