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OpenTrials
Completed

NCT Number: NCT05675995

Qigong for Post Acute Sequelae of COVID-19 Infection

The purpose of this study is to conduct a pilot feasibility study of a combination of external and internal qigong on health-related quality of life in individuals with prolonged symptoms following COVID-19 infection.

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Key information

About this study

The purpose of this study is to determine whether a combination of external and internal qigong, a traditional Chinese medicine healing practice, improves quality of life and symptoms for individuals with prolonged symptoms following a COVID-19 infection (sometimes called "long COVID"). The study involves completing questionnaires and participating in 6 weekly in person small group qigong sessions with an experienced qigong practitioner.

Participants will be randomized to participate in either an immediate or waitlist control group that will receive the qigong sessions starting 8 weeks later. Participants will complete 3 sets of questionnaires, each about 8 weeks apart and an interview about their experiences with qigong after completing the 6 sessions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • English-speaking adults age 18 or greater
  • History of a COVID-19 infection with lingering symptoms lasting longer than 12 weeks
  • Willing and able to access the internet to complete questionnaires
  • Willing and able to travel to the qigong sessions to participate in person in Sacramento, CA.

Exclusion criteria

  • Lung scarring secondary to COVID-19 infection as evidenced by signs of parenchymal lung damage on imaging or FVC < 80% (any patient with post COVID-related shortness of breath must have PFTs to be considered for enrollment).
  • Dementia
  • Any other condition that makes it difficult for the individual to complete questionnaires or attend the qigong sessions.

Treatment and study plan

Qigong

Behavioral

6 sessions of combined external and internal qigong delivered in a group-based format once a week.

Primary outcomes

  1. Changes in physical and mental health

    Time frame: 8 weeks

    Changes in PROMIS-29 summary scores from before to after intervention in all participants

Sponsors and collaborators

Lead sponsor

University of California, Davis

Other

Registry information

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Jan 9, 2023
Registry last updated
Jan 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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