Repeated Cross Sectional Surveillance Study To Determine the Influenza Vaccination Rates in German Participants
NCT ID: NCT06800885
Last Updated: 2025-12-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
5000 participants
OBSERVATIONAL
2024-10-22
2026-02-02
Brief Summary
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This study aims to address the gap by assessing current influenza vaccination rates, particularly among those aged 60 and older, to inform public health interventions and encourage healthcare providers to recommend influenza vaccination more proactively.
The primary objective of this study is to determine the influenza vaccination rates in the German population during the current respiratory season. The study will focus on:
1. Assessing the vaccination rates among the two main age groups 18 years of age through and including 59 years of age and 60 years of age (inclusive) and older
2. Assessing the vaccination rate among individuals with risk-based vaccination recommendation according to Standing Committee on Vaccination (Ständige Impfkommission) (STIKO) The study will target a disproportionate sample of the German population regarding age: 30% aged 18 years of age through and including 59 year of age and 70% aged 60 years of age (inclusive) and older. Within these age groups, the study targets a representative distribution regarding gender and region.
This study is conducted as an online survey that will either be self-completed by the respondents (CAWI) or completed via an interviewer for a subgroup of respondents aged 70+ (CATI). The survey is estimated to last 10 minutes and will comprise of closed-ended questions only (i.e., respondents will not have the possibility to add any free-text). The survey will be conducted in German.
The panelists will be divided into strata based on demographic variables like gender and region. Within each stratum, participants will be randomly selected to participate in the survey.
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Detailed Description
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Conditions
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Study Design
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OTHER
CROSS_SECTIONAL
Study Groups
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Group 1: 18 Years of Age to 59 Years of age
Healthy diverse adults aged 18 years to 59 (inclusive) years of age
No interventions assigned to this group
Group 2: 60 Years of Age and Older
Healthy diverse adults aged 60 years (inclusive) of age and older
No interventions assigned to this group
Subgroup 1: Pregnant Women 18 Years of Age to 59 Years of Age
Pregnant woman aged 18 years to 59 (inclusive) years of age
No interventions assigned to this group
Subgroup 2: Patients with Chronic Illness
Diverse patients with chronic illness
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Be at least 18 years old at the time of survey completion.
* Agree with privacy policy and AE (Adverse Event) reporting requirements before proceeding with the survey.
* Read and agree to the ICF (Informed Consent Form) by ticking a box before proceeding with the survey or telephone interview.
Exclusion Criteria
* Living in nursing home Note: The above information is not intended to contain all considerations relevant to a potential participation in a clinical trial.
18 Years
ALL
Yes
Sponsors
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Sanofi Pasteur, a Sanofi Company
INDUSTRY
Responsible Party
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Locations
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Germany, , Germany
Countries
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Other Identifiers
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FLU00216
Identifier Type: -
Identifier Source: org_study_id
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