Skip to content

Mpox Prospective Observational Cohort Study

Monkeypox

The goal of this multicentre prospective observational cohort study is to shed light on the following unknowns:

1. The clinical manifestations of Mpox infection since the 2022 outbreak in Canada.
2. The social and psychological impacts of Mpox infection since the 2022 outbreak in Canada
3. The transmissibility of Mpox infection
4. Viral shedding over time in infected individuals

The study is divided into Part 1 (corresponding to the acute phase of illness) and Part 2 (corresponding to the convalescent phase of the illness); part 2 will be optional. Participants enrolled during the acute phase of illness will complete part 1 of the study and will be invited to participate in Part 2 as well. Part 1 of the study will include the following three core components, at baseline and weekly (±3 days) until one week after the resolution of all symptoms (i.e. one week after complete healing of skin lesions):

1. Collection of clinical data through chart review and research staff interviews with study participants
2. Participant self-administered online questionnaires at baseline and a thrice-weekly 'acute phase participant diary'
3. Specimen collection for Mpox-related testing Optional components for Part 1 include baseline-only, questionnaire-only, and frequent sampling.

Other optional components for all participants include in the Image Atlas, an online database of clinical images of mpox, designed to provide clinicians and community members of what mpox looks like in real life, and the biobank, which will store research samples for potential future studies.

null

Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    0 and up

Critères de participation

Inclusion Criteria

Part 1:

• Being investigated for Mpox infection by a clinician based on clinical (i.e. symptoms) and/or epidemiologic (i.e. exposure to confirmed case) grounds;

Part 2:

* Clinically confirmed to be in the convalescent phase (i.e. confirmed for Mpox infection previously)
* Within 12 weeks of symptom onset

Exclusion Criteria

• None

Lieu de l'étude

Unity Health Toronto
Unity Health Toronto
Toronto, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Shreya Shah

[email protected]
416-360-4000
BC Centre For Excellence
BC Centre For Excellence
Vancouver, British Columbia
Canada

Contactez l'équipe d'étude

Primary Contact

Brody Lyon

[email protected]
604-682-2344
University Health Network
University Health Network
Toronto, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Asmaa Mabrouk

[email protected]
416-340-4800
Étude parrainée par
Unity Health Toronto
Participants recherchés
Plus d'informations
ID de l'étude: NCT06291259