NCT07856563

Brief Summary

This study aims to investigate vaccine-related knowledge, attitude, vaccine confidence and vaccine hesitancy among MSM across multiple countries and regions.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
11mo left

Started Jan 2027

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 11, 2026

Completed
21 days until next milestone

First Posted

Study publicly available on registry

October 2, 2026

Completed
3 months until next milestone

Study Start

First participant enrolled

January 1, 2027

Expected
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2027

Last Updated

October 2, 2026

Status Verified

September 1, 2026

Enrollment Period

11 months

First QC Date

September 11, 2026

Last Update Submit

September 30, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Vaccine uptake

    Percentage(%) of participants who have received at least one dose of HPV vaccine, assessed by self-reported vaccination history

    Baseline, at enrollment in this cross-sectional study

Secondary Outcomes (4)

  • Vaccine knowledge

    Baseline, at enrollment in this cross-sectional study

  • Vaccine attitude

    Baseline, at enrollment in this cross-sectional study

  • Vaccine confidence

    Baseline, at enrollment in this cross-sectional study

  • Vaccine hesitancy

    Baseline, at enrollment in this cross-sectional study

Study Arms (2)

Men who have sex with men

Other: No Interventions

transgender women and non-binary individuals

transgender women and non-binary individuals who have sexual relations with men

Other: No Interventions

Interventions

No interventions because it is a observational cross-sectional study

Men who have sex with mentransgender women and non-binary individuals

Eligibility Criteria

Age18 Years+
Sexmale(Gender-based eligibility)
Gender Eligibility DetailsIn certain participating countries and regions potentially extended to transgender women and non-binary individuals who have sexual relations with men, using the same questionnaire. Exclusive criteria
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Self-identify as MSM, with eligibility in certain participating countries and regions potentially extended to transgender women and non-binary individuals who have sexual relations with men, using the same questionnaire.

You may qualify if:

  • Participants will be eligible for the study if they meet all of the following conditions:
  • Have resided in a participating country or region for at least six months.
  • Are aged 18 years or older.
  • Self-identify as MSM, with eligibility in certain participating countries and regions potentially extended to transgender women and non-binary individuals who have sexual relations with men, using the same questionnaire.

You may not qualify if:

  • Participants will be excluded if they meet any of the following conditions:
  • Are aged under 18 years.
  • Decline to participate in the study or fail to complete the informed consent process.
  • Have not resided, or do not currently reside, in a participating country or region.
  • Submit duplicate responses from the same IP address or device.
  • Fail data quality checks, including automated or fraudulent submissions and failure to pass human verification procedures.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 11, 2026

First Posted

October 2, 2026

Study Start (Estimated)

January 1, 2027

Primary Completion (Estimated)

December 1, 2027

Study Completion (Estimated)

December 1, 2027

Last Updated

October 2, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share