Impact of the Epidemic of COVID-19 Infection Among People Living With HIV (SARS-CoV-2)

NCT ID: NCT04581746

Last Updated: 2022-05-10

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

1800 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-11-25

Study Completion Date

2022-12-31

Brief Summary

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The non-essential and non-urgent follow-up consultations of patients living with HIV were postponed or transformed into "teleconsultation" or exchanges of e-mails between practitioners and patients during COVID-19 epidemic. This change in care can have an impact on follow-up and access to treatment for PVVIH.

Detailed Description

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On 16 March 2020, an instruction to postpone "non-urgent" consultations was given to doctors. Thus, the non-essential and non-urgent follow-up consultations of patients living with HIV were postponed or transformed into "teleconsultation" or exchanges of e-mails between practitioners and patients. This change in care can have an impact on follow-up and access to treatment for PVVIH. In addition, the epidemic itself may have consequences: PVVIH may be at greater risk because of their immunosuppression and associated co-morbidities.

Conditions

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Virus-HIV Covid19

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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experimental arm

questionnaire and follow-up visit

Group Type OTHER

questionnaire

Intervention Type OTHER

bi-monthly questionnaire and then one visit with questionnaire and covid-19 test

Interventions

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questionnaire

bi-monthly questionnaire and then one visit with questionnaire and covid-19 test

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient followed up for HIV infection in one of the COREVIH Hauts de France centres participating in the study
* Having communicated an email address
* Having given their consent to participate in this study
* Beneficiary subject affiliated or entitled to a social security scheme

Exclusion Criteria

* Minor patient
* Refusal to participate
* Patient under guardianship
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Tourcoing Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pauline THILL, MD

Role: PRINCIPAL_INVESTIGATOR

CH TOURCOING

Locations

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CHU Amiens Picardie

Amiens, , France

Site Status

CH Lens

Lens, , France

Site Status

CH Tourcoing

Tourcoing, , France

Site Status

Countries

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France

Other Identifiers

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RIPH_2020_7

Identifier Type: -

Identifier Source: org_study_id

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