Table 3.
Primary outcome measures | Data source | Timepoint(s) |
Time to recovery defined as the first instance that a participant reports feeling recovered from possible COVID-19 | Patient or study partner report. | Within 28 days. |
Hospital admission or death | Patient or study partner self-report and medical record review. | Within 28 days. |
Secondary outcomes | ||
Duration of severe symptoms measured through daily diary | Self-report using online diary or telephone call/text. | Daily online diary or telephone/text at days 7, 14 and 28 if no online data received. |
Patient-reported illness severity | ||
Number of contacts with the health services | Participant of study partner report using online diary, or telephone call/text and medical record review in primary care and hospital care. | Daily online diary or telephone/text at days 7, 14 and 28 if no online data received primary care and hospital records. |
Additional antibiotic use | ||
Hospital assessment without admission | ||
Oxygen administration | ||
Intensive care unit admission | ||
Mechanical ventilation (5–8 allows for an estimation of a version of the WHO Clinical Progression Ordinal Scale) | ||
Duration of hospital admission | ||
WHO-Five Well-Being Index | WHO-Five Well-Being Index. | Baseline and days 14 and 28 either via online diary or telephone |
To determine if effects are specific who test positive for SARS-CoV-2 | Swab results and optional serology for SARS-CoV-2 to determine an ‘Intention to Treat Infected’ group within the overall cohort for sub analysis. | Swabs from enrolment and/or day 5. Convalescent serology. |
Qualitative substudy | ||
Patient experiences of consulting, being tested and taking (trial) medication for possible COVID-19 | Telephone interview with participant. | After 28 days. |
To explore healthcare professionals’ views of taking part in research during pandemics | Telephone interview with healthcare professional. | At least 2 months after practice started recruiting. |