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
Brief 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.

Completed
Quality of Life
Stress

Behavioral: Self-acupressure

Self-acupressure

Eligibility Criteria

Inclusion Criteria:

- 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 exclusion criteria 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.

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
United States
Locations

UCLA
Los Angeles, California, United States

Ka-Kit Hui, MD, Principal Investigator
University of California, Los Angeles

University of California, Los Angeles
NCT Number