Ignite Creation Date:
2024-05-06 @ 6:28 PM
Last Modification Date:
2024-10-26 @ 2:48 PM
Study NCT ID:
NCT05675995
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2024-04-09
First Post:
2023-01-04
Brief Title:
Qigong for Post Acute Sequelae of COVID-19 Infection
Sponsor:
University of California Davis
Organization:
University of California Davis
Study Overview
Official Title:
Qigong for Post Acute Sequelae of COVID-19 Infection
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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
Detailed Description:
The purpose of this study is to determine whether external 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
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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None