This is a multi-morbid research project that will include patients, non-clinical populations and healthcare professionals. Clinical populations associated with this project include any condition associated with obstetrics and gynaecology, neurology, pain disorders, cardiovascular diseases and psychiatry. Not Applicable
Conditions
Interventions
The initial sub-studies associated will gather observational data to determine any mental and physical health sequelae. Diagnostic assessments and/or treatment interventions used will be identified an
Sponsors
Southern Health NHS Foundation Trust
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All participants required for each sub-study will be noted within the relevant participant information sheet/informed consent form. The sample population will include healthcare professionals, patients and the general public.
Exclusion criteria
Exclusion criteria: Under 18 years of age
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mental health impact based upon autonomic dysfunction (COVID vs long COVID) measured using a novel self-reported instrument at baseline and month 3 | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Pain outcomes associated with COVID vs long COVID measured using a novel self-reported instrument at baseline and month 3 2. Neuropsychiatric outcomes associated with COVID vs long COVID measured using a novel self-reported instrument at baseline and month 3 | — |
Countries
Canada, India, Nigeria, Pakistan, United Kingdom
Outcome results
None listed