Mpox Prospective Observational Cohort Study
MonkeypoxThe 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.
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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 TorontoToronto, Ontario
Canada
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BC Centre For Excellence
BC Centre For ExcellenceVancouver, British Columbia
Canada
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University Health Network
University Health NetworkToronto, Ontario
Canada
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- Étude parrainée par
- Unity Health Toronto
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT06291259