Health Condition 1: U071- COVID 19 virus identified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: History of confirmed COVID-19 infection in last 6 months; Minimum 4 weeks after the confirmed COVID-19 report. Residual or any other clinical complaints reported to be occurring after COVID-19 like fatigue, fever (unknown reason), anxiety, joint pain, breathlessness, headache, or any other non-serious clinical illness not explained by an alternative diagnosis. Cases who have recovered clinically&/or laboratory confirmed negative. Patients agreeing to perform WHO self-care rehabilitation program under guidance of the physician. Patients willing to participate in the study and give written informed consent
Exclusion criteria
Exclusion criteria: Patients having any serious sequelae, presence of systemic complications (persistent organic damage) or specific organ dysfunction due to SARS-CoV-2 virus. Uncontrolled cases of DM, HT, Asthma, HIV, active TB, Cancer, immune compromised illness like HIV etc. Patients having severe dyspnoea with Oxygen saturation below 95%; patients requiring ventilation support Patient reporting having Psychiatric disorders, hepatic and renal dysfunction. Contra indications to physical exercise or Patient unable to do exercise in the WHO rehabilitation self-management care plan. Patients not able to give written informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in symptom severity or clinical recovery of Long COVID complaintsTimepoint: At baseline, monthly follow-up up to 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in functional status assessed using PCFS. 6-minute walk test (the distance acquired during six minutes walking) quantifying the physical performance, any dyspnoea and endurance. Changes in fatigue: Chalder Fatigue Scale (CFQ-11) scale Changes in anxiety: Hamilton Anxiety Rating Scale (HAM-A) Changes in health-related quality of life: 12-item Short Form Survey (SF12) Change in numeric rating scale (NRS) for all other complaints Timepoint: At baseline, and up to 6 months | — |
Countries
India
Contacts
Central Council for Research in Homoeopathy