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Recruiting NCT06650956

NCT06650956 Integration to Improve Adolescent Health and HPV Vaccination in Laos

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Clinical Trial Summary
NCT ID NCT06650956
Status Recruiting
Phase
Sponsor Health Poverty Action
Condition Healthy
Study Type INTERVENTIONAL
Enrollment 700 participants
Start Date 2024-11-01
Primary Completion 2025-05

Eligibility & Interventions

Sex All sexes
Min Age 10 Years
Max Age 13 Years
Study Type INTERVENTIONAL
Interventions
Integrated HPV and SRH Service PackageHuman Papillomavirus Quadrivalent (Types 6, 11, 16, and 18) Vaccine, Recombinant

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 700 participants in total. It began in 2024-11-01 with a primary completion date of 2025-05.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this study is to find out if adding HPV vaccination to adolescent health services works to increase HPV vaccine uptake in 10-13-year-old girls in Laos. The study will also look at the effects of adding HPV vaccination on the use of other health services in 10-13-year-old boys and girls. The main questions the study aims to answer are: 1. Does adding HPV vaccination to adolescent health services increase HPV vaccine uptake in girls aged 10-13 years compared to girls who only receive standard HPV vaccination services? 2. Does adding HPV vaccination to adolescent health services increase the use of other health services in 10-13-year-old adolescent boys and girls compared to adolescents who only receive standard HPV vaccination services? 3. What are the barriers and facilitators to using the combined intervention in Laos? 4. What are the opinions of adolescents, caregivers, healthcare providers, and other stakeholders on the combined intervention? 5. How much does it cost and how well it works to combine HPV vaccination with adolescent health services, as opposed to providing HPV vaccination alone? Researchers will compare a combined intervention to standard HPV vaccination services to see if the combined intervention works to increase HPV vaccination uptake and the use of other health services. The combined intervention includes HPV vaccination given at schools, health facilities, and through community outreach. It also includes education on sexual and reproductive health, counseling, and other health services. Participants in the combined intervention group will: 1. Receive the HPV vaccine at school or at a health facility. 2. Take part in group discussions about sexual and reproductive health. 3. Take part in individual counseling sessions. 4. Use other health services as needed. Participants in the comparison group will receive standard HPV vaccination services, including: • HPV vaccination given at schools, health facilities, and through community outreach.

Eligibility Criteria

Inclusion Criteria: * Female aged 10-13 years for HPV vaccination and SRH education * Male aged 10-13 years for SRH education * 10-13-year-old male and female students in randomly selected schools with at least 100 students in target classes (year-5 primary, year-1, 2 and 3 secondary) * 10-13-year-old males and females who are out-of-school and living in 2 remote villages each from four randomly selected health centers located around the selected schools Exclusion Criteria: * males and females younger than 10 years or older than 13 years

Contact & Investigator

Central Contact

Kongmany Chaleunvong, MD, PhD

✉ kchaluenvong@gmail.com

📞 +8562022200650

Principal Investigator

Thet Lynn, MD, MMedSc Global Health

PRINCIPAL INVESTIGATOR

Health Poverty Action

Frequently Asked Questions

Who can join the NCT06650956 clinical trial?

This trial is open to participants of all sexes, aged 10 Years or older, up to 13 Years, studying Healthy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06650956 currently recruiting?

Yes, NCT06650956 is actively recruiting participants. Contact the research team at kchaluenvong@gmail.com for enrollment information.

Where is the NCT06650956 trial being conducted?

This trial is being conducted at Muang Sing, Laos.

Who is sponsoring the NCT06650956 clinical trial?

NCT06650956 is sponsored by Health Poverty Action. The principal investigator is Thet Lynn, MD, MMedSc Global Health at Health Poverty Action. The trial plans to enroll 700 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology