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Acupuncture or Self-Acupuncture in Managing Cancer-Related Fatigue in Women Who Have Received Chemotherapy for Stage I, Stage II, or Stage IIIA Breast Cancer

The Efficacy of Acupuncture and Self-acupuncture in Managing Cancer-related Fatigue in Breast Cancer Patients: a Pragmatic Randomised Trial

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00957112
Enrollment
320
Registered
2009-08-12
Start date
2007-10-31
Completion date
2013-02-28
Last updated
2013-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety Disorder, Breast Cancer, Depression, Fatigue

Keywords

anxiety disorder, depression, fatigue, stage IA breast cancer, stage IB breast cancer, stage II breast cancer, stage IIIA breast cancer

Brief summary

RATIONALE: Acupuncture may help relieve fatigue caused by breast cancer. It is not yet known whether acupuncture is more effective than self-acupuncture in managing fatigue in women with breast cancer. PURPOSE: This randomized phase III trial is studying acupuncture to see how well it works compared with self-acupuncture in managing cancer-related fatigue in women who have received chemotherapy for stage I, stage II, or stage IIIA breast cancer.

Detailed description

OBJECTIVES: * Assess the efficacy of a course of acupuncture in the management of cancer-related fatigue in a homogeneous sample of women with stage I, II, or IIIA breast cancer who have completed adjuvant chemotherapy. * Assess the efficacy of self-acupuncture in comparison to therapist-administered acupuncture in sustaining, in the longer term, any effects observed with a 6-week course of acupuncture in these patients. OUTLINE: This is a multicenter study. Patients are stratified according to study center and fatigue score (low vs moderate vs severe). Patients are randomized at 3:1 ratio (arm I: arm II) to 1 of 2 treatment arms. * Arm I (experimental): Patients undergo a 20-minute acupuncture session once a week for 6 weeks. Patients also receive written information about fatigue and its possible management. * Arm II (control): Patients undergo standard care. They also receive written information about fatigue as in arm I. After 6 weeks, patients in arm I are again randomized to 1 of 3 arms. * Arm A: Patients receive treatment as in arm I for 4 more weeks. * Arm B: Patients receive treatment as in arm II for 4 more weeks. * Arm C: Patients learn to self-acupuncture and do so weekly for 4 more weeks. All patients complete questionnaires on fatigue, hospital anxiety and depression, quality of life, and use of complementary therapies at baseline and periodically during study. Patient's sociodemographic and treatment characteristic records are also reviewed. After completion of study therapy, patients are followed up periodically for 18 weeks.

Interventions

PROCEDUREacupuncture therapy

Patients undergo therapist-acupuncture with or without self-acupuncture

PROCEDUREstandard follow-up care

Patients receive standard care

Sponsors

University of Manchester
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Diagnosis of breast cancer * Stage I, II, or IIIA disease * Completed prior chemotherapy for ≥ 1 month and up to 5 years * No needling on the ipsilateral arm of patients who have undergone axillary dissection * No needling on the lymphedematous limbs * Score of ≥ 5 on a 0-10 single-item screening fatigue scale, where 0 is no fatigue at all and 10 is extremely fatigued * Hormone receptor status not specified PATIENT CHARACTERISTICS: * Life expectancy ≥ 6 months * Menopausal status not specified * Platelet count ≥ 50,000/mm\^3 * Hemoglobin ≥ 10 g/dL * Hematocrit ≥ 30% * Not pregnant * No needle phobia * No co-morbidity with any of the following: * Bleeding disorder * Thyroid dysfunction PRIOR CONCURRENT THERAPY: * See Disease Characteristics * No planned concurrent chemoradiotherapy * No concurrent steroids * No concurrent epoetin alfa or transfusion for anemia * No other concurrent complementary therapies

Design outcomes

Primary

MeasureTime frame
General fatigue as measured by the Multidimensional Fatigue Inventory

Secondary

MeasureTime frame
Mental fatigue as measured by the Multidimensional Fatigue Inventory
Anxiety as measured by the Hospital Anxiety and Depression Scale
Depression as measured by the Hospital Anxiety and Depression Scale
Quality of life as measured by the FACT-G and Breast Cancer module

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026