Acupressure for COVID-19 Related Quality of Life and Stress
NCT ID: NCT04472559
Last Updated: 2022-11-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
164 participants
INTERVENTIONAL
2021-06-16
2022-09-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Self-acupressure
Self-acupressure
Self-acupressure
Control
No interventions assigned to this group
Interventions
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Self-acupressure
Self-acupressure
Eligibility Criteria
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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.
18 Years
ALL
Yes
Sponsors
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University of California, Los Angeles
OTHER
Responsible Party
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Kakit P. Hui, MD
Professor
Principal Investigators
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Ka-Kit Hui, MD
Role: PRINCIPAL_INVESTIGATOR
University of California, Los Angeles
Locations
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UCLA
Los Angeles, California, United States
Countries
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References
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Abbott R, Hui EK, Kao L, Tse V, Grogan T, Chang BL, Hui KK. Randomized Controlled Trial of Acupressure for Perception of Stress and Health-Related Quality of Life Among Health Care Providers During the COVID-19 Pandemic: The Self-Acupressure for Stress (SAS) Trial. Am J Med Open. 2023 Dec;10:100056. doi: 10.1016/j.ajmo.2023.100056. Epub 2023 Aug 25.
Other Identifiers
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20-000773
Identifier Type: -
Identifier Source: org_study_id
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