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Toronto Chronic Post-SARS Cohort (Moldofsky)

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Design notes & limitations. Deliberately included as a methodologically weak but historically important study: small (22 cases, 7 controls), cross-sectional case-control with a convenience control group, but the first to characterize an ME/CFS/fibromyalgia-like chronic syndrome after a coronavirus — an early precedent for Long COVID.

Identity & trigger

Cohort id
moldofsky-post-sars
Aliases
chronic post-SARS syndrome case-control
Outbreak / event
SARS outbreak 2003 (Toronto)
Pathogen
SARS-CoV-1 (Virus)
Exposure ascertainment
clinical diagnosis

Design

Design
Case-control
Denominator defined
No
Denominator method
n/r
Recruitment
self referral
Time zero
Recovery from acute SARS (assessed 13–36 months later) (month)
Control group
Healthy convenience

Size & attrition

Enrolled
29
Analysed / enrolled
29/29 (100%)
Max follow-up (months)
36

Biospecimens

Specimens
No
Types
none
Acute-phase specimens
No
Biobank
N/A
External access
closed

Observations (1)

Symptoms

measured, not reported Proportion

Measure
Fatigue sym:fatigue
As worded
“persistent fatigue among post-SARS subjects unable to return to former occupation”
Population
whole cohort · denominator Assessed at timepoint · N=n=22
Timing
24 mo (12-24 mo) · ref Not reported
Method
Unclear
Comparator
no comparator
Comparability signature
e70533efa5 — measure sym:fatigue · Unclear · ref Not reported · denom Assessed at timepoint · 12-24 mo · Proportion
Provenance
Results (chronic fatigue, myalgia, weakness, depression, non-restorative sleep vs healthy controls) · Manual · verified OSMF research-tracker (web-verified against source) on 2026-07-20

Publications

Provenance & verification

Registration
n/r
Funders
n/r
Related cohorts
none
Symptom-inventory scope
Single domain
Last verified
2026-07-20 — OSMF research-tracker (web-verified against source)