Long COVID Clinical Trial
Official title:
A Practical Clinical Randomized Controlled Trial of Traditional Chinese Medicine in the Treatment of Long COVID and an Analysis of Syndrome Types and Medication Characteristics of Traditional Chinese Medicine
This is a multi-center, outcome assessor-blinded, practical randomized controlled trial, aiming to compare the actual clinical effectiveness of individualized traditional Chinese medicine and conventional Western medicine in the treatment of long COVID. Totally 162 patients with long COVID recruited into the study will be randomly assigned to the traditional Chinese medicine treatment group or the Western medicine control group. Patients in the treatment group will receive individualized TCM syndrome differentiation treatment, and patients in the control group will receive conventional Western medicine symptomatic treatment from general Western medicine practitioners for 4 weeks. All patients were followed up once a week (±2 days) during treatment period and followed up by 4 weeks (±2 days) after the treatment. Outcome measurements will be conducted at baseline, the end of treatment (week 4 ±2 days) and the follow-up visit (week 8 ±2 days).
| Status | Not yet recruiting |
| Enrollment | 162 |
| Est. completion date | February 28, 2026 |
| Est. primary completion date | November 30, 2025 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 6 Years to 80 Years |
| Eligibility | Inclusion Criteria: - Chinese subjects with age between 6 and 80 years old; - For those who have recovered from COVID-19, it has been more than 28 days since the date of diagnosis (the diagnosis is confirmed by rapid antigen test or positive nucleic acid test of deep throat saliva or nose/throat swab); - The average score of the modified COVID-19 Yorkshire Rehabilitation Scale (C19-YRSm) is above 2 (i.e. above the moderate level). Exclusion Criteria: - People who have not been infected with COVID-19; - People who are still positive for COVID-19; - Known history of some certain serious medical disease, which is in an unstable state or even affects basic survival, such as cardiovascular disease, liver or renal dysfunction, diabetes, cancer, cerebrovascular disease, blood disorders; - Known impaired hematological characteristics or impaired liver/kidney function; - People with mild cognitive impairment, that is, those whose age/education matching percentile in the score of the Hong Kong version of Montreal Cognitive Assessment (HK-MoCA) is lower than 16; or those who cannot truthfully fill out the questionnaire due to mental and psychological factors; - Have used any drugs or other treatment methods for the treatment of COVID-19 in the past week, such as acupuncture, massage, scraping, cupping, etc.; - Known history of allergy to any traditional Chinese medicine. |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Chinese University of Hong Kong |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | 5-level EQ-5D version (EQ-5D-5L) | The 5-level EQ-5D version (EQ-5D-5L) was developed by the European Society for Quality of Life (EuroQol) and has been validated [38]. The EQ-5D-5L assesses a patient's quality of life by assessing five dimensions: mobility, self-care, daily activities, pain or discomfort, and anxiety or depression. Each aspect is assessed by 5 levels, namely none, mild, moderate, heavy, and very severe. In addition, patients self-rated their overall health status using a visual analog scale (EQVAS). | 4 weeks | |
| Primary | 5-level EQ-5D version (EQ-5D-5L) | The 5-level EQ-5D version (EQ-5D-5L) was developed by the European Society for Quality of Life (EuroQol) and has been validated [38]. The EQ-5D-5L assesses a patient's quality of life by assessing five dimensions: mobility, self-care, daily activities, pain or discomfort, and anxiety or depression. Each aspect is assessed by 5 levels, namely none, mild, moderate, heavy, and very severe. In addition, patients self-rated their overall health status using a visual analog scale (EQVAS). | 8 weeks | |
| Secondary | Measure Yourself Medical Outcome Profile in Chinese version (CMYMOP2) | The Chinese version of the Measure Yourself Medical Outcome Profile has been validated [39]. This questionnaire asks respondents to name one or two symptoms of greatest concern and the daily activities that are limited by these symptoms. Respondents rate these symptoms and activities, as well as their general health status, on a scale from 0 to 6 (0 is best, 6 is worst). | 4 weeks | |
| Secondary | Measure Yourself Medical Outcome Profile in Chinese version (CMYMOP2) | The Chinese version of the Measure Yourself Medical Outcome Profile has been validated [39]. This questionnaire asks respondents to name one or two symptoms of greatest concern and the daily activities that are limited by these symptoms. Respondents rate these symptoms and activities, as well as their general health status, on a scale from 0 to 6 (0 is best, 6 is worst). | 8 weeks | |
| Secondary | Modified COVID-19 Yorkshire Rehabilitation Scale (C19-YRSm) | This improved version of the scale allows patients to self-assess the main symptoms of the COVID, the degree of functional limitation and overall health status. There are 17 items in total, including shortness of breath, cough/throat sensitivity/voice change, fatigue, changes in smell or taste, pain or discomfort, and cognition. problems, palpitations/dizziness, tiredness/exacerbation after work, anxiety/depression, sleep problems, communication, walking or moving, self-care, other daily activities, social roles), and other symptoms (such as fever, hair loss, dry eyes, tinnitus, nausea, etc.) and general health, etc. Each item is scored from 0 to 3 (0 is asymptomatic, 1 is mild and does not affect daily life, 2 is moderate and affects daily life to a certain extent, and 3 is severe or affects daily life comprehensively). | 4 weeks | |
| Secondary | Modified COVID-19 Yorkshire Rehabilitation Scale (C19-YRSm) | This improved version of the scale allows patients to self-assess the main symptoms of the COVID, the degree of functional limitation and overall health status. There are 17 items in total, including shortness of breath, cough/throat sensitivity/voice change, fatigue, changes in smell or taste, pain or discomfort, and cognition. problems, palpitations/dizziness, tiredness/exacerbation after work, anxiety/depression, sleep problems, communication, walking or moving, self-care, other daily activities, social roles), and other symptoms (such as fever, hair loss, dry eyes, tinnitus, nausea, etc.) and general health, etc. Each item is scored from 0 to 3 (0 is asymptomatic, 1 is mild and does not affect daily life, 2 is moderate and affects daily life to a certain extent, and 3 is severe or affects daily life comprehensively). | 8 weeks | |
| Secondary | Serum level change of inflammatory factors | Inflammatory markers including interferon (IFN-ß), interferon (IFN-?2/3), pentraxin 3 (PTX3) and interleukin 6 will be measured. | 4 weeks | |
| Secondary | Safety assessment | In order to evaluate the safety of the traditional Chinese medicine treatment, the patient's complete blood count (CBC) and liver and kidney function indicators will be tested before starting the study treatment and after the treatment ends. | 4 weeks | |
| Secondary | Adverse event | Subjects will be asked about the occurrence of any adverse events during the intervention period. | 4 weeks |
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