Acupuncture for Aromatase Inhibitor Induced Joint Pain
Primary Purpose
Breast Cancer
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Acupuncture
Sham Acupuncture
Sponsored by
About this trial
This is an interventional supportive care trial for Breast Cancer focused on measuring Aromatase Inhibitors, Joint Pain, Symptoms Control, Acupuncture
Eligibility Criteria
INCLUSION CRITERIA:
- Age>45 years
- Postmenopausal status defined as cessation of menses for >1 year or follicle- stimulating hormone (FSH)>20 mIU/mL
- History of stage I or II, hormone receptor-positive breast cancer
- Currently taking a third-generation aromatase inhibitor (anastrazole, letrozole or exemestane)
- Ongoing musculoskeletal pain in one or more joints (baseline BPI worst pain score > 3 points on a scale of 0 to 10)
- English-speaking
- Signed informed consent
EXCLUSION CRITERIA:
- Previous treatment with acupuncture
- Inflammatory, metabolic or neuropathic arthropathies
- Bone fracture or surgery of the afflicted extremity during the past six months
- Current narcotic use, corticosteroid therapy or cortisone injections
- Severe concomitant illnesses or metastatic disease
- Severe coagulopathy or bleeding disorder
- Dermatological disease within the acupuncture area
Sites / Locations
- Columbia University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Acupuncture Arm
Control Arm
Arm Description
Patients in the treatment arm will receive acupuncture administered twice weekly for six weeks and will be allowed to take pain medication as necessary.
The control patients will receive a form of sham acupuncture, which will consist of superficial needling at nonspecific body points, administered twice weekly for six weeks.
Outcomes
Primary Outcome Measures
Change in Joint Pain
This is defined as the difference in the Brief Pain Inventory - Short Form (BPI-SF) scale at six weeks versus baseline.
Secondary Outcome Measures
Change in Joint Stiffness and Function
The Western Ontario and McMaster Universities Osteoarthritis (WOMAC) index Version 3.1 will be used and consists of 24 questions related to three subscales: pain (0-20), stiffness (0-8) and physical function (0-68).
Safety and Tolerability measured by Frequency of Adverse Events
Reporting of the severity and frequency of adverse events (NCI Common Terminology Criteria Version 3.0) (40) related to the interventions will be conducted every two weeks during telephone interviews. All treatment-related adverse events will be reported for both treatment arms.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00826397
Brief Title
Acupuncture for Aromatase Inhibitor Induced Joint Pain
Official Title
Pilot Study on the Effect of Acupuncture on Joint Pain Induced by Aromatase Inhibitors in Breast Cancer Patients
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
June 2005 (Actual)
Primary Completion Date
October 2008 (Actual)
Study Completion Date
September 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a randomized, controlled, pilot study to determine the safety and efficacy of acupuncture as an adjunct to pharmacological treatment compared to pharmacological intervention alone for the treatment of musculoskeletal pain related to aromatase inhibitors (AI) in postmenopausal breast cancer patients. Twenty participants (20 in each arm) will be enrolled at the Breast Oncology clinic at Columbia University Medical Center (CUMC). Patients in the treatment arm will receive acupuncture administered twice weekly for six weeks and will be allowed to take pain medication as necessary. The control patients will initially receive pain medication alone, then will cross-over to the acupuncture arm after six weeks. The investigators hypothesize that acupuncture will reduce AI induced joint symptoms.
The study will enroll a total of 40 patients, half of whom will be randomized to one of the two arms to receive acupuncture plus pharmacological treatment (arm A) or pharmacological treatment alone (arm B). Joint pain will be assessed by the BPI-SF score at baseline and six weeks. All patients will have a baseline BPI worst pain item (#2) ≥3 points on a scale of 0-10.
Detailed Description
The purpose of this study is to determine the safety and efficacy of acupuncture as a complementary therapy to pain medication for joint pain associated with aromatase inhibitors for breast cancer treatment. Breast cancer patients are living longer largely due to the benefits of hormonal therapy. Aromatase inhibitors (AIs) are a new class of hormonal agents which block estrogen synthesis in postmenopausal women. However, musculoskeletal pain occurs in up to 50% of patients treated with AIs and often does not respond to conventional pain medications. AI-induced joint pain interferes with patient compliance and may cause major disability. Therefore, safe and effective treatments are needed to alleviate AI-induced musculoskeletal pain.
Acupuncture is a traditional Chinese method of medical treatment and a popular modality for treating musculoskeletal pain. Acupuncture involves the use of thin needles to stimulate specific points of the body and leads to pain control through the release of endorphin in the central nervous system. Clinical trials have found a benefit of acupuncture for the treatment of knee and back pain. Given the lack of effective treatments for AI-induced joint pain and the safety and efficacy of acupuncture, it is therefore reasonable to evaluate whether acupuncture is effective in breast cancer patients who experience musculoskeletal pain related to AIs.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
Aromatase Inhibitors, Joint Pain, Symptoms Control, Acupuncture
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Acupuncture Arm
Arm Type
Experimental
Arm Description
Patients in the treatment arm will receive acupuncture administered twice weekly for six weeks and will be allowed to take pain medication as necessary.
Arm Title
Control Arm
Arm Type
Sham Comparator
Arm Description
The control patients will receive a form of sham acupuncture, which will consist of superficial needling at nonspecific body points, administered twice weekly for six weeks.
Intervention Type
Procedure
Intervention Name(s)
Acupuncture
Intervention Description
Each acupuncture session will last approximately 45 minutes and includes standardized body treatment with an emphasis on affected joints.
Intervention Type
Procedure
Intervention Name(s)
Sham Acupuncture
Intervention Description
The sham acupuncture session will consist of superficial needling at nonspecific body points, administered twice weekly for six weeks, and will last approximately 45 minutes and includes standardized body treatment with an emphasis on affected joints.
Primary Outcome Measure Information:
Title
Change in Joint Pain
Description
This is defined as the difference in the Brief Pain Inventory - Short Form (BPI-SF) scale at six weeks versus baseline.
Time Frame
Baseline and 6 weeks
Secondary Outcome Measure Information:
Title
Change in Joint Stiffness and Function
Description
The Western Ontario and McMaster Universities Osteoarthritis (WOMAC) index Version 3.1 will be used and consists of 24 questions related to three subscales: pain (0-20), stiffness (0-8) and physical function (0-68).
Time Frame
Baseline and 6 weeks
Title
Safety and Tolerability measured by Frequency of Adverse Events
Description
Reporting of the severity and frequency of adverse events (NCI Common Terminology Criteria Version 3.0) (40) related to the interventions will be conducted every two weeks during telephone interviews. All treatment-related adverse events will be reported for both treatment arms.
Time Frame
6 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA:
Age>45 years
Postmenopausal status defined as cessation of menses for >1 year or follicle- stimulating hormone (FSH)>20 mIU/mL
History of stage I or II, hormone receptor-positive breast cancer
Currently taking a third-generation aromatase inhibitor (anastrazole, letrozole or exemestane)
Ongoing musculoskeletal pain in one or more joints (baseline BPI worst pain score > 3 points on a scale of 0 to 10)
English-speaking
Signed informed consent
EXCLUSION CRITERIA:
Previous treatment with acupuncture
Inflammatory, metabolic or neuropathic arthropathies
Bone fracture or surgery of the afflicted extremity during the past six months
Current narcotic use, corticosteroid therapy or cortisone injections
Severe concomitant illnesses or metastatic disease
Severe coagulopathy or bleeding disorder
Dermatological disease within the acupuncture area
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dawn Hershman, MD
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Acupuncture for Aromatase Inhibitor Induced Joint Pain
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