Influenza Vaccination in Patients Living With HIV in the Northern Region

  • STATUS
    Recruiting
  • participants needed
    200
  • sponsor
    Tourcoing Hospital
Updated on 19 February 2024
HIV Infection
vaccination
influenza
immunodeficiency
influenza vaccination
trivalent influenza vaccine

Summary

Anyone living with the Human Immunodeficiency Virus (HIV) has an indication for annual influenza vaccination. (Vaccination schedule and vaccination recommendations 2019). Influenza is a viral infection that has a significant impact on the health care system. However, vaccination coverage in France is still insufficient with regard to the objectives set at 75% by the WHO and the European Commission. For the 2019-2020 seasonal influenza vaccination campaign, flu vaccination by volunteer pharmacists has become possible throughout the country. Studies that have estimated vaccination coverage among HIV-positive populations are rare and show very low rates.

Description

Cross-sectional study via a self-questionnaire given to all HIV-infected patients coming for a scheduled consultation as part of their HIV follow-up in the spring of 2020. Non-opposition letter given to the patient. Collection of data a posteriori from the medical file recorded in the eNadis patient file.

Details
Condition HIV, HIV, HIV positive, HIV infection, AIDS Vaccines
Age 18-100 years
Clinical Study IdentifierNCT04402684
SponsorTourcoing Hospital
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Any adult person living with HIV presenting for a follow-up consultation in the spring of 2020
People who do not read French may participate if they wish with the help of a medical or paramedical staff member
Patient did not object

Exclusion Criteria

Minor patients
Major under guardianship, curatorship, protected person
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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