Clinical Trials Directory

Trials / Completed

CompletedNCT05675995

Qigong for Post Acute Sequelae of COVID-19 Infection

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
University of California, Davis · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALQigong6 sessions of combined external and internal qigong delivered in a group-based format once a week.

Timeline

Start date
2023-01-04
Primary completion
2024-05-15
Completion
2024-05-15
First posted
2023-01-09
Last updated
2026-01-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05675995. Inclusion in this directory is not an endorsement.