Acupressure for COVID-19 Related Quality of Life and Stress

NCT ID: NCT04472559

Last Updated: 2022-11-01

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

164 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-06-16

Study Completion Date

2022-09-01

Brief Summary

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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.

Detailed Description

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Conditions

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Quality of Life Stress

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Self-acupressure

Group Type EXPERIMENTAL

Self-acupressure

Intervention Type BEHAVIORAL

Self-acupressure

Control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Self-acupressure

Self-acupressure

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion 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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of California, Los Angeles

OTHER

Sponsor Role lead

Responsible Party

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Kakit P. Hui, MD

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status

Countries

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United States

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.

Reference Type DERIVED
PMID: 38125337 (View on PubMed)

Other Identifiers

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20-000773

Identifier Type: -

Identifier Source: org_study_id

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