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UnknownNCT03091647

Acupressure for Cancer-Related Fatigue

Acupressure Intervention to Improve Fatigue and Physical Functioning of Chinese Immigrant Breast Cancer Survivors

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
124 (estimated)
Sponsor
Georgetown University · Academic / Other
Sex
Female
Age
21 Years – 74 Years
Healthy volunteers
Not accepted

Summary

This study develops and pilot tests the efficacy of a home-based, self-administered acupressure intervention in improving cancer-related fatigue (proximal outcome), and physical functioning and other quality of life outcomes (distal outcomes) of Chinese immigrant breast cancer survivors (versus usual care control group).

Detailed description

We will enroll 124 foreign-born, Chinese-speaking women from Southern California and Maryland areas with moderate to severe levels of fatigue, diagnosed with stage 0-IV breast cancer, aged 21-74, and 1-5 years post-primary treatment. Using an adaptive treatment strategy design, participants will be randomized to either the acupressure intervention or control groups. The acupressure group will learn how to press three chief energy acupoints on each side of the body through de novo 11-minute Chinese-language video and practice acupressure every day (one minute per acupoint; a total of 6 minutes per day) for an 8-week intervention period. Participants will be telephone interviewed twice: at baseline and 8-weeks post-intervention follow-up.

Conditions

Interventions

TypeNameDescription
BEHAVIORALacupressure interventionWomen in the acupressure intervention group will learn how to press three chief energy acupoints on each side of the body through an 11-minute Chinese-language video and press three acupoints (1 minute per acupoint) on both sides of the body every day for a total of 6 minutes per day for an 8-week intervention period and record their practice on daily logs. Women will be asked to return the logs every week by email or self-addressed envelopes.
BEHAVIORALusual careWomen in the usual care group will receive primary and oncology care from their doctors as usual, and complete daily logs recording their fatigue and daily functioning levels. They also need to return the logs every week by email or self-addressed envelopes.

Timeline

Start date
2016-07-01
Primary completion
2021-06-30
Completion
2021-06-30
First posted
2017-03-27
Last updated
2021-02-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03091647. Inclusion in this directory is not an endorsement.