Acupuncture and Chinese Herbal Medicine for Long COVID
This study is exploring whether acupuncture and Chinese herbal medicine can be a practical, acceptable, and helpful treatment for Long COVID. Researchers will use specific acupuncture points and herbal formulas tailored to each person's traditional Chinese medicine (TCM) diagnosis. The main goal is to see if this combined treatment approach is feasible to implement. They also want to see if people receiving these treatments over 8 weeks show improvements in their Long COVID symptoms, daily function, and overall quality of life. You can join if you are 18 years or older and have a confirmed diagnosis of COVID-19.
- Study design
- This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 10 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed from enrollment until the final follow-up at 12 weeks.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Acupuncture and Chinese Herbal Medicine for Long COVID
At a glance
Conditions
NCT07285707
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
SCUHS
Whittier, Californiano site contact published
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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Inclusion
Exclusion
What this trial measures
- Feasibility of Implementing a Combined Acupuncture and Chinese Herbal Medicine Intervention for long COVIDFrom enrollment to the final follow-up at 12 weeks
Feasibility will be measured through a feasibility assessment questionnaire which will evaluate recruitment, retention, and adherence metrics across the 12-week intervention and the final follow-up. Feasibility indicators will be summarized as proportions and descriptive statistics to evaluate the practicality of the study procedures and protocol implementation.