Immediate for Long COVID

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
Long COVIDExternal Qigong - Behavioral
Eligibility
18+
All Sexes
What conditions do you have?
Select

Study Summary

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

Eligible Conditions
  • Long COVID

Treatment Effectiveness

Effectiveness Progress

1 of 3

Study Objectives

1 Primary · 0 Secondary · Reporting Duration: 8 weeks

8 weeks
Change in physical health

Trial Safety

Trial Design

1 Treatment Group

Immediate
1 of 1

Experimental Treatment

48 Total Participants · 1 Treatment Group

Primary Treatment: Immediate · No Placebo Group · N/A

Immediate
Behavioral
Experimental Group · 1 Intervention: External Qigong · Intervention Types: Behavioral

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: 8 weeks

Who is running the clinical trial?

University of California, DavisLead Sponsor
843 Previous Clinical Trials
5,012,303 Total Patients Enrolled

Eligibility Criteria

Age 18+ · All Participants · 4 Total Inclusion Criteria

Mark “Yes” if the following statements are true for you:
You are an adult aged 18 or over who speaks English.
You have experienced a prolonged case of COVID-19 with symptoms persisting for more than three months.
You have the capability to access the web and fill out surveys.
You are able and willing to journey to the qigong sessions.