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NCT06476496Completed

Pain Relief With Integrative Medicine (PRIMe)?: Feasibility of Acupuncture for Long COVID

Source: ClinicalTrials.gov · Last updated 12 May 2026

Brief summary (registry, in English)

The goal of this preliminary study is to test methods and procedures to be used in a fully-powered trial to evaluate acupuncture treatment effectiveness. Specifically, we will test the feasibility of conducting a 2-arm randomized clinical trial for evaluating the effectiveness of acupuncture for pain in patients with long COVID. Researchers will compare pain intensity and impact on general activities over 5 months in those who receive acupuncture treatment compared to patients who are receiving usual long COVID care. Participants will complete 4 online surveys at weeks 0, 4, 8, and 20. These surveys include validated mental and physical health questionnaires. Participants who are randomly selected to receive the intervention will receive 8 acupuncture treatment sessions.

Status (registry)
Completed
Study type
Interventional
Enrollment
93 (actual)
First submitted
24 Jun 2024
Start date
21 Jun 2024
Primary completion date
30 Mar 2025
Lead sponsor
University of Washington
NCT number
NCT06476496

What you commit to

  • Study type: Interventional
  • Participants enrolled: 93
  • From 21 Jun 2024 to the primary completion date, 30 Mar 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Report baseline level of pain for those who have pre-existing chronic pain (i.e., chronic pain condition(s) present prior to COVID-19 illness AND chronic pain not worsened post-COVID).
  • Already received acupuncture treatment for long COVID symptoms.
  • Is receiving active cancer therapy

Other illness

  • Has seizure disorder with high risk of seizure (i.e., new diagnosis of seizure disorder and/or new medication in the last 3 months, or uncontrolled/unclear triggers for seizures).

Lab values

  • Has severe neutropenia (\<500 WBC) due to any cause within the last 6 months

Age

  • \<18 years of age at the time of consent.

Other

  • Reports absence of pain, pain for less than 12 weeks, or a pain intensity \<4 over the last 7 days.
  • Unable to travel to the UW Northgate Clinic once a week for 8 weeks for acupuncture treatments.
  • Is currently Pregnant

Who the study is looking for

  • ≥ 18 years of age at the time of consent.
  • Previous suspected, probable, or confirmed SARS-CoV-2 infection, as defined by the Pan American Health Organization
  • Report pain symptoms including musculoskeletal pain (joint, muscle, bone pain), chest pain, abdominal pain, headache, back pain, nerve pain, and pain in ear following a SARS-CoV-2 infection that has persisted for at least 12 weeks and is still present at the time of consent.
  • Report pain intensity (0-10 scale) ≥4 in the last 7 days.28
  • As of today, has been seen by a clinician in the UW Long COVID Clinic either in-person or via telehealth/virtual visit
  • Able to speak and read English and provide informed consent to complete the study requirements.

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UW Medicine Primary Care at Northgate
Coordinator of this site? Confirm its status
SeattleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.