SCAPE-HIV: SARS-CoV-2 (COVID-19) Antibody PrevalencE in an Adult London HIV Cohort

Sponsor
Royal Free Hospital NHS Foundation Trust (Other)
Overall Status
Recruiting
CT.gov ID
NCT05067400
Collaborator
Roche Diagnostics (Industry)
1,500
1
11.3
132.3

Study Details

Study Description

Brief Summary

Prospective, observational SARS-CoV2 serological surveillance single London HIV outpatient center study using NHS participants

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The main aim of this study is to find out how many people living with HIV (PLWH) attending a major HIV centre in London, have already been infected with SARS-CoV2 so far which will be determined through serological blood tests detecting the presence of antibodies to SARS-CoV2, or have developed antibodies in response to vaccination.

    However, it is not know whether the presence of antibodies from natural infection means anything more than a marker that someone has been exposed to SARS-CoV2 previously. It is not know whether this means someone is any less likely to be reinfected in the future or how it will affect possible future infections with SARS-CoV2. Whilst further data on natural and vaccine induced antibody responses is awaited, those with the presence of anti-SARS-CoV2 antibodies continue to be advised to take the same precautions as everyone else in terms of reducing the risk of getting COVID-19: regularly washing hands, wearing a mask and remaining socially distant where possible.

    Now that vaccination has commenced it is also unclear what markers of vaccine induced immunity will develop, including in PLWH. This study will help better determine whether HIV should be an additional 'priority' group for vaccination, and also what antibody responses exist in PLWH who have been vaccinated

    The intention is to invite the cohort in for an annual set of HIV related blood tests, covering those who are scheduled for bloods, as well as those who may have missed scheduled blood monitoring appointments during the COV19 lockdown period. In addition to these tests the study proposes offering serological testing for SARS CoV-2 as part of this surveillance study. Participation will be voluntary, and informed consent will be obtained. Participants will be informed of their result along with information about the uncertainty of its meaning, beyond indicating previous infection or vaccination.

    The study aims to test for the presence of specific antibodies that target SARS-CoV2 in people living with HIV, as a marker of whether someone has been infected before. This will help create a better understanding of whether living with HIV puts people at a higher risk of becoming infected with SARS-CoV2 compared to the general population, and which other factors or characteristics may affect this risk. This will help identify who might be more at risk of getting COVID-19 in the future and will help plan for future COVID-19 vaccine strategies.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    1500 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    SARS-CoV-2 (COVID-19) Antibody PrevalencE in an Adult London HIV Cohort
    Actual Study Start Date :
    Apr 21, 2021
    Anticipated Primary Completion Date :
    Oct 1, 2021
    Anticipated Study Completion Date :
    Apr 1, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Prevalence of SARS-CoV2 antibodies [Since 1st Jan 2020]

      The primary outcome measure is the presence of antibodies to SARS-CoV2. This is a binary outcome (present/absent)

    Secondary Outcome Measures

    1. Reporting of COVID symptoms [Since 1st Jan 2020]

      The secondary outcome measure is the reporting of previous COVID symptoms since 1st January 2020. This is a binary measure (yes/no).

    Other Outcome Measures

    1. Reporting of previous SARS-CoV2 infection (reported history) [Since 1st Jan 2020]

      Reported history of positive SARS CoV2 test since 1 Jan 2020

    2. History of SARS CoV2 vaccine [Since 1st Jan 2020]

      Reported history of receiving a SARS CoV2 vaccine (no, 1 dose, 2 dose)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Documented HIV infection

    • Registered patient at ICDC

    • Age ≥18 years at study entry

    • Able to comprehend study patient information leaflet

    Exclusion Criteria:
    • Unable to give informed consent and participant without a good understanding of verbal and written English

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Royal Free London NHS Foundation Trust London United Kingdom NW32QG

    Sponsors and Collaborators

    • Royal Free Hospital NHS Foundation Trust
    • Roche Diagnostics

    Investigators

    • Principal Investigator: Tristan Barber, MBBChir, Royal Free London NHS Foundation Trust

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Royal Free Hospital NHS Foundation Trust
    ClinicalTrials.gov Identifier:
    NCT05067400
    Other Study ID Numbers:
    • 1
    First Posted:
    Oct 5, 2021
    Last Update Posted:
    Oct 14, 2021
    Last Verified:
    Oct 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 14, 2021