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RecruitingNCT05271669Updated Mar 18, 2026

COVID-19 Immunity and Changes Over Time

An observational study in COVID-19, sponsored by Chinese University of Hong Kong. Recruiting at 1 site in China. Per ClinicalTrials.gov, last updated 2026-03-18.

Sponsored by Chinese University of Hong Kong · Observational

From the registry’s dates

  • Primary completion was expected by Jul 2026, 3 months ago, but the record still lists the study as recruiting.
  • Started Jun 2022; still recruiting 4 years 4 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,350
Sex
All
01

Study summary

The risk of household spread of SARS-CoV-2 hinges on both the transmission dynamics of the virus circulating in the community as well as the seroprotection pattern of constituent members, which can be attributed to vaccination and previous infections. This study is conceptualised to assess the dynamicity of SARS-CoV-2 risk at the household level, through monitoring the pattern of seroprotection, in conjunction with the vaccination coverage, history of infection and exposure risk in the setting of Hong Kong.

Read the detailed description

The aim of this study is to assess the SARS-CoV-2 risk at the household level, with the objectives of (a) determining the coverage of vaccination and its changes over time; (b) monitoring pattern of exposure and history of infection; and (c) evaluating the level of seroprotection and its longitudinal trend.

A cohort of households comprising 900 persons would be recruited. Invited participants would be attend the Research Centre for blood sampling and the completion of a simple questionnaire at 3 different timepoints at 12-18 months apart. A questionnaire would be administered to capture the following characteristics: (a) Socio-demographics; (b) History of SARS-CoV-2 infection; (c) adoption of precautionary measures; (d) SARS-CoV-2 testing history and (e) SARS-CoV-2 vaccination uptake.

Participants would be tested for SARS-CoV-2 serology. The main markers for measurement are nucleocapsid antibody for inferring past infection, spike antibody for the immunological responses, and seroprotection by SARS-CoV-2 surrogate virus neutralisation test.

02

Conditions studied

  • COVID-19

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Keywords

  • serology
  • cohort study
  • SARS-CoV-2 antibody
03

In context

COVID-19

7,640 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's planned enrollment of 1,350 is above the median of 261 across 3,136 observational studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

Chinese University of Hong Kong is the lead sponsor of 1,419 studies on the registry; 487 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Sampling method
Probability sample

Study population

Adults of households enrolling in a population cohort covering residents from all 18 districts in Hong Kong.

Inclusion criteria

  • adults of age 18 or above, or children under the age of 18 with informed consent of the legal guardian
  • normally residing in Hong Kong
  • could communicate in spoken and written Chinese and/or English

Exclusion criteria

Exclusion Criteria:

  • individuals with mental illness
  • prisoners
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,350 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna
06

What researchers measure

Primary outcomes

  1. Proportion of participants with COVID-19 protective immunity

    Prevalence of SARS-CoV-2 spike antibody

    Time frame: 1 year

  2. Proportion of participants with marker of past COVID-19 infection

    Prevalence of SARS-CoV-2 nucleocapsid antibody

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • Shui Shan Lee
    Hong Kong, HONG KONG 0000, China
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05271669
Lead sponsor
Chinese University of Hong Kong
Responsible party
Shui-Shan Lee, MD (Research Professor, Chinese University of Hong Kong) — Principal investigator
First posted
Mar 9, 2022
Start date
Jun 6, 2022
Primary completion
Jul 2026 (estimated)
Completion
Jan 2027 (estimated)
Last update
Mar 18, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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