Acupressure for Cancer-Related Fatigue
Status
Conditions
Treatments
Details and patient eligibility
About
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).
Full 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.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
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- be between ages 21 to 74
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- be first-generation immigrants
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- speak Chinese (Mandarin and/or Cantonese)
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- be diagnosed with breast cancer at stage 0, I, II III or IV
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- have completed primary treatments (including surgery, radiation, and chemotherapy) 1-5 years prior to recruitment
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- have not had recurrence
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- have moderate to severe levels of fatigue.
Exclusion criteria
- have hypothyroidism and anemia
- being using acupuncture
Trial design
Primary purpose
Allocation
Interventional model
Masking
124 participants in 2 patient groups, including a placebo group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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