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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04581746
Acronym
coVIHd-19
Enrollment
1800
Registered
2020-10-09
Start date
2020-11-25
Completion date
2022-12-31
Last updated
2022-05-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19, Virus-HIV

Brief summary

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

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.

Interventions

OTHERquestionnaire

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

Sponsors

Tourcoing Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of SARS CoV2 infection in PVVIH in Hauts de FranceInclusionDetermination of the number of patients with microbiologically or clinically-biologically proven SARS CoV2 infection at inclusion in the study

Secondary

MeasureTime frameDescription
Prevalence of SARS CoV2 infection in PVVIH in Hauts de Francethrough study completion, an average of 19 monthsDetermination of the number of patients with microbiologically or clinically-biologically proven SARS CoV2 infection at the end of the study
Determine the incidence rate of COVID 19 among PVVIH discontinuing antiretroviral treatmentthrough study completion, an average of 19 monthsReason for discontinuing antiretroviral treatment
Determine the incidence rate of COVID 19 among PVVIH antiretroviral treatmentthrough study completion, an average of 19 monthsPercentage of patients who stopped their antiretroviral treatment
Psychological consequences of this epidemic among PVVIH : HADthrough study completion, an average of 19 monthsEvaluation of the psychological scales HAD on PVVIH
Psychological consequences of this epidemic among PVVIH : PROQOL-HIVthrough study completion, an average of 19 monthsEvaluation of the psychological scales PROQOL-HIV on PVVIH
Determine the incidence rate of COVID 19 among PVVIH who stopped all follow-upthrough study completion, an average of 19 monthsPercentage of patients who stopped all follow-up by an infectious disease specialist

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026