This study is not yet accepting patients

Acupressure for COVID-19 Related Quality of Life and Stress

a study on Quality of Life Stress COVID-19

Summary

Eligibility
for people ages 18 years and up (full criteria)
Healthy Volunteers
healthy people welcome
Dates
study started
estimated completion
Principal Investigator
by Kakit P. Hui, MD (ucla)

Description

Summary

This study is being conducted to evaluate the efficacy of acupressure in promoting health and well-being among healthcare workers during the COVID-19 pandemic. The investigators hypothesize that providing participants with a remote and standardized self-acupressure training program will improve HRQOL and the perception of stress. In the event that the study demonstrates acupressure to be safe and effective for this indication, the training could be scaled up and deployed at low-cost nationally and internationally.

Official Title

Randomized Controlled Trial of Acupressure for Health-Related Quality of Life and Perception of Stress Among Health Care Providers During the COVID-19 Pandemic

Keywords

Quality of Life Stress Self-acupressure

Eligibility

You can join if…

Open to people ages 18 years and up

  • All adult patients (18 years of age and over) who are health care providers according to self-report will be eligible for participation with the exception of subjects meeting

You CAN'T join if...

as below.

Exclusion Criteria:

  • Exclusion criteria includes subjects who are physically unable to participate (e.g., from severe arthritis) or cognitively unable to participate (e.g., from dementia) will be excluded. Patients unable to provide their own informed consent will be excluded. Patients under the age of 18 years will be excluded. Pregnant women will be excluded. Patients who have previous training in acupressure will be excluded.

Lead Scientist at UC Health

  • Kakit P. Hui, MD (ucla)
    Professor of Clinical , Medicine. Authored (or co-authored) 5 research publications.

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, Los Angeles
ID
NCT04472559
Study Type
Interventional
Last Updated