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Article: Randomized, waitlist-controlled trial of Cordyceps sinensis mycelium culture extract (Cs4) for long COVID patients in Hong Kong

TitleRandomized, waitlist-controlled trial of Cordyceps sinensis mycelium culture extract (Cs4) for long COVID patients in Hong Kong
Authors
KeywordsCordyceps sinensis (Berk) Sacc
Cs4
Long COVID
modified COVID-19 Yorkshire Rehabilitation Scale (C19-YRSm)
randomized trial
Issue Date2025
Citation
Acta Materia Medica, 2025, v. 4, n. 2, p. 250-261 How to Cite?
AbstractWe assessed Cordyceps sinensis mycelium culture extract (Cs4) for alleviating long COVID symptoms. In this randomized trial 110 participants were assigned to receive Cs4 (55 participants) or were waitlisted (55 participants) for 12 weeks. The primary outcome was the change in long COVID symptom severity at 12 weeks, as measured by the modified COVID-19 Yorkshire Rehabilitation Scale. The secondary outcomes included changes in the Brief Fatigue Inventory Form, Insomnia Severity Index, Hospital Anxiety and Depression Scale, St. George’s Respiratory Questionnaire, and the Short Form 12 health survey at 12 weeks. Participants receiving Cs4 showed improvement in long COVID symptoms compared to the waitlist control group (MD, −10.1; 95% CI, −14.1 to −6.1; P < 0.001) at 12 weeks. Cs4 recipients also experienced improvement in fatigue (MD, −8.1; 95% CI, −14.2 to −2.0; P = 0.011), insomnia (MD, −2.9; 95% CI, −4.6 to −1.2; P = 0.001), and respiratory symptoms (MD, −6.3; 95% CI, −11.4 to −1.2; P = 0.018). Cs4 also improved the quality of life (physical component MD, 7.0; 95% CI, 4.2–9.8; P < 0.001; mental component MD, 6.8; 95% CI, 2.9–10.7; P < 0.001). No severe adverse events were reported. Cs4 may be a beneficial treatment for patients with long COVID symptoms.
Persistent Identifierhttp://hdl.handle.net/10722/360380

 

DC FieldValueLanguage
dc.contributor.authorChen, Yuanyuan-
dc.contributor.authorChen, Guang-
dc.contributor.authorZhang, Cheng-
dc.contributor.authorTang, Guoyi-
dc.contributor.authorChan, Yautuen-
dc.contributor.authorWang, Ning-
dc.contributor.authorFeng, Yibin-
dc.date.accessioned2025-09-10T09:06:32Z-
dc.date.available2025-09-10T09:06:32Z-
dc.date.issued2025-
dc.identifier.citationActa Materia Medica, 2025, v. 4, n. 2, p. 250-261-
dc.identifier.urihttp://hdl.handle.net/10722/360380-
dc.description.abstractWe assessed Cordyceps sinensis mycelium culture extract (Cs4) for alleviating long COVID symptoms. In this randomized trial 110 participants were assigned to receive Cs4 (55 participants) or were waitlisted (55 participants) for 12 weeks. The primary outcome was the change in long COVID symptom severity at 12 weeks, as measured by the modified COVID-19 Yorkshire Rehabilitation Scale. The secondary outcomes included changes in the Brief Fatigue Inventory Form, Insomnia Severity Index, Hospital Anxiety and Depression Scale, St. George’s Respiratory Questionnaire, and the Short Form 12 health survey at 12 weeks. Participants receiving Cs4 showed improvement in long COVID symptoms compared to the waitlist control group (MD, −10.1; 95% CI, −14.1 to −6.1; P < 0.001) at 12 weeks. Cs4 recipients also experienced improvement in fatigue (MD, −8.1; 95% CI, −14.2 to −2.0; P = 0.011), insomnia (MD, −2.9; 95% CI, −4.6 to −1.2; P = 0.001), and respiratory symptoms (MD, −6.3; 95% CI, −11.4 to −1.2; P = 0.018). Cs4 also improved the quality of life (physical component MD, 7.0; 95% CI, 4.2–9.8; P < 0.001; mental component MD, 6.8; 95% CI, 2.9–10.7; P < 0.001). No severe adverse events were reported. Cs4 may be a beneficial treatment for patients with long COVID symptoms.-
dc.languageeng-
dc.relation.ispartofActa Materia Medica-
dc.subjectCordyceps sinensis (Berk) Sacc-
dc.subjectCs4-
dc.subjectLong COVID-
dc.subjectmodified COVID-19 Yorkshire Rehabilitation Scale (C19-YRSm)-
dc.subjectrandomized trial-
dc.titleRandomized, waitlist-controlled trial of Cordyceps sinensis mycelium culture extract (Cs4) for long COVID patients in Hong Kong-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.15212/AMM-2024-0089-
dc.identifier.scopuseid_2-s2.0-105008347557-
dc.identifier.volume4-
dc.identifier.issue2-
dc.identifier.spage250-
dc.identifier.epage261-
dc.identifier.eissn2737-7946-

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