About this trial
Long COVID is a complex condition that affects approximately 1.4 million Canadians following SARS-CoV-2 infection. Fatigue is the most common symptom of Long COVID. This feasibility trial will evaluate a new rehabilitation program called COVIDEx for treating fatigue after COVID-19, and compare its effectiveness to the standard treatment currently used. The experimental treatment group will receive an 8-week multi-modal rehabilitation program with two 50-minute sessions per week. 60 participants will be recruited, randomly assigned to the COVIDEx program or standard of care (SoC) and followed for 24 weeks.
Eligibility criteria
Qualifiers
Adults of at least 18 years of age
Able to provide informed consent
Can speak and understand English
Documented history of SARS-CoV-2 infection (positive PCR/antigen test during acute illness or clinical diagnosis by physician during or after the acute illness)
Disqualifiers
Active SARS-CoV-2 infection
Pre-existing physical, cognitive, and/or mental health conditions that make exercise contraindicated, consent unattainable, or that cause symptoms similar to those seen in post COVID-19 (e.g., major neurocognitive disorder, schizophrenia, chronic fatigue syndrome) that could affect data
Inability to follow study procedures
Pregnant and/or breastfeeding
Trial design
Treatments tested in this trial
- COVIDEx
Treatment groups
Sponsors and collaborators
Lawson Research Institute of St. Joseph's
Lead sponsor
Western University, Canada
Collaborator
Canadian Institutes of Health Research (CIHR)
Collaborator