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Pneumococcal ImmunizationNCT07809113

PCV21 Acceptance in Adults ≥50 Years and Caregivers in Panama

An observational study of Pneumococcal Immunization, run by Endpoints Site Network at 1 site in Panama.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial summary

This study will look at what adults age 50 years and older in Panama know, think, and do about pneumococcal vaccination, including the 21-valent pneumococcal conjugate vaccine (PCV21). Pneumococcal disease can cause pneumonia and other serious infections, and older adults may be at higher risk of severe illness. Read more about this study

Who is it for?
Ages 50 years and olderHealthy volunteers can take part
Conditions the study is for
Pneumococcal Immunization
How many people
600 participants
Where
1 sitePanama
Study dates
1 Feb 2027to 31 Dec 2027
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: The study population will include adults aged 50 years and older in Panama who receive care through public or private health care facilities. Participants will be recruited from urban, semi-urban, and rural settings to reflect the demographic, geographic, and socioeconomic diversity of the adult population in Panama.

Who may be able to join

  • Age 50 years or older.
  • Cohort A: 50-64 years.
  • Cohort B: 65 years or older.
  • Resident of Panama, including urban, semi-urban, or rural areas.
  • Has access to medical care through the public or private health care system.
  • Able and willing to provide signed informed consent.
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  • Caregivers - Cohort B only
  • Age 18 years or older.
  • Identified as the caregiver of a Cohort B older adult.
  • Has regular cohabitation or contact with the older adult, defined as at least once per week.
  • Able and willing to provide signed informed consent.

Who cannot join

  • Older adults - all cohorts
  • Cognitive impairment that prevents the participant from providing informed consent.
  • Does not speak Spanish and no interpreter is available.
  • Caregivers - Cohort B only
  • Professional caregiver with no personal relationship to the older adult.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Rodrigo DeAntonio, MD, DrPH contact

+50762059692

rodrigo.deantonio@endpoints.site

Panama1 site
  • CEVAXIN

    Panama City, Provincia de Panamá

    Gabrielle Britton, PhD, gabrielle.britton@cevaxin.com

Other trials in Panama

About this study

Official title: Intergenerational Determinants of PCV21 Acceptance in Adults ≥50 Years in Panama: Knowledge, Attitudes, and Practices in Older Adults and Their Caregivers

This study will look at what adults age 50 years and older in Panama know, think, and do about pneumococcal vaccination, including the 21-valent pneumococcal conjugate vaccine (PCV21). Pneumococcal disease can cause pneumonia and other serious infections, and older adults may be at higher risk of severe illness. The study will help researchers understand what supports or prevents vaccine acceptance in this population.

The study will include two groups. Group A will include adults 50 to 64 years of age. Group B will include adults 65 years of age or older and a caregiver chosen by the older adult. A caregiver may be a family member or another person who regularly helps or supports the older adult. Researchers will study whether the caregiver's views about vaccines are related to the older adult's intention to receive PCV21.

Read more

Participants will complete a one-time survey about pneumococcal disease, vaccines, vaccination history, health information sources, trust in vaccines, barriers to vaccination, and factors that may make vaccination easier. Surveys may be completed on paper with help from study staff or digitally using a tablet or smartphone. The survey is expected to take about 10 to 15 minutes. For older adults and caregivers in Group B, each person will complete their own survey separately so that one person's answers do not influence the other's answers.

This is an observational study. No vaccine, medicine, or study product will be given as part of the study. Taking part involves answering survey questions only. The study will recruit participants from public and private health care facilities, including at least one rural or semi-urban site, to better reflect the diversity of adults in Panama.

The information from this study may help health care providers, public health teams, and community organizations design clearer and more useful communication about pneumococcal vaccination for adults and their caregivers. The results may also support future recommendations for adult vaccination programs in Panama and similar settings.

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07809113
Study groupRoleWhat they receive
COHORT AAdults 50-64 years
COHORT BAdults ≥65 years + caregiver (dyads)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Level of knowledge, attitudes, and practices regarding PCV21 vaccination among adults aged 50 years and older in Panama

    Knowledge, attitudes, and practices regarding pneumococcal disease and PCV21 vaccination will be assessed using a structured KAP survey. Survey domains include knowledge of pneumococcal disease and available vaccines, attitudes toward vaccination and PCV21, vaccine confidence, perceived risk, prior vaccination practices, preventive care behaviors, and sources of health information. Results will be summarized overall and by cohort.

    Measured: At enrollment / single study visit

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Sep 2026
  2. Study start1 Feb 2027 (estimated)
  3. Primary completion30 Sep 2027 (estimated)
  4. Study completion31 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
600 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07809113
Sponsor's protocol ID
MISP 104141
Other IDs
MISP 104141
Status last verified
Sep 2026
First submitted
2 Sep 2026
Last updated
9 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

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