Acupressure for Cancer-Related Fatigue

Georgetown University124 enrolled

Overview

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).

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

124

Conditions

Breast Cancer

Interventions

acupressure interventionBEHAVIORAL

Women 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.

usual careBEHAVIORAL

Women 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.

Eligibility

Sex: FEMALEMin age: 21 YearsMax age: 74 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 1\) be between ages 21 to 74 * 2\) be first-generation immigrants * 3\) speak Chinese (Mandarin and/or Cantonese) * 4\) be diagnosed with breast cancer at stage 0, I, II III or IV * 5\) have completed primary treatments (including surgery, radiation, and chemotherapy) 1-5 years prior to recruitment * 6\) have not had recurrence * 7\) have moderate to severe levels of fatigue. Exclusion Criteria: * have hypothyroidism and anemia * being using acupuncture

Locations (1)

Georgetown University

Washington D.C., District of Columbia, United States

Outcomes

Primary Outcomes

Cancer-related fatigue (proximal outcome)

The primary outcome will be measured by 6-item PROMIS (Patient-Reported Outcomes Measurement Information System) (e.g., felt tired, exhausted, limited at work).