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Acupuncture for Lymphedema Secondary to Breast Cancer Treatment

Primary Purpose

Lymphedema

Status
Withdrawn
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Acupuncture + Electrical Stimulation
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lymphedema focused on measuring Lymphoedema, Edema, Oedema, Cancer, Breast Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • >1yr following the conclusion of breast cancer treatment
  • Lymphedema of the upper limb: unilateral (one-side)

Exclusion Criteria:

  • History or evidence of hormone-receptor positive cancer
  • Previous nodal dissection or radiotherapy to other regions
  • Contraindications for acupuncture or electrical stimulation
  • Pre-cancer or bi-lateral lymphedema
  • Evidence of active cancer
  • History of contralateral cancer, radiation or surgery
  • Edema of the neck/midline/torso
  • Pregnancy
  • Allergies to nickel, chromium, or silicon
  • Seizures (epilepsy)
  • Tremors (shakiness) that may interfere with treatment
  • Infections, scarring, open wounds, or broken skin at needle sites
  • Infections, open wounds, or broken skin on the upper limbs (electrode & landmark sites)

Sites / Locations

  • McMaster University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Acupuncture + Electrical Stimulation

Control

Arm Description

Acupuncture needles are inserted beneath the skin and electrical stimulation applied for 20 minutes.

Participants who are randomized to receive no intervention will still receive physical assessment.

Outcomes

Primary Outcome Measures

Change in amount of arm tissue water determined by Bioimpedance Analysis
Bioimpedance analysis devices take readings using 8 electrode pads that are placed on top of the skin of the arms. The electrode pads are connected to a computer that transmits a small amount of electrical current between the electrode pads. The process of taking readings takes less than 1 minute and is painless (participants may not be able to feel it working).

Secondary Outcome Measures

Change in dermal concentration of red blood cells in the arm assessed using light polarization spectroscopy
A digital camera is used to 'see under the skin' and measure the amount of red blood cells in the arm. The camera is an ordinary digital camera connected to special computer software. Assessment using the camera is harmless and patients will not be able to feel it working. A series of digital photographs of a small area of the arms will be taken. The computer uses these photographs to calculate a number that represents the amount of blood contained in the skin of the arm.
Change in arm circumference
Measurements are taken of both arms using a flexible measuring tape to be used in the calculation of size and volume.
Lymphedema Questionnaire
Survey is administered to collect data pertaining to the condition of lymphedema.

Full Information

First Posted
May 14, 2014
Last Updated
August 28, 2017
Sponsor
McMaster University
Collaborators
Canadian Interdisciplinary Network Complementary & Alternative Medicine Research, Holistic Health Research Foundation of Canada
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1. Study Identification

Unique Protocol Identification Number
NCT02158832
Brief Title
Acupuncture for Lymphedema Secondary to Breast Cancer Treatment
Official Title
Rehabilitation of Breast Cancer Treatment Related Lymphedema Using Electro-acupuncture: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Withdrawn
Why Stopped
The study Principal Investigator relocated and the grant funding the trial expired.
Study Start Date
April 2014 (Anticipated)
Primary Completion Date
January 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
Canadian Interdisciplinary Network Complementary & Alternative Medicine Research, Holistic Health Research Foundation of Canada

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is being conducted to determine if electro-acupuncture can reduce swelling of the arm due to breast cancer treatment (commonly referred to as 'lymphedema'). Research conducted on animals suggests that such treatment might be used to improve circulation leading to reductions in swelling. Previous research in humans with lymphedema suggests that treatment may be safe to use, although results regarding its efficacy in the reduction of swelling have not yet been established. This research will use sophisticated, non-invasive assessment methods to determine if a single session of electro-acupuncture treatment can be effective for reducing lymphedema. Results may be used to further develop our understanding of how electro-acupuncture can be used in the management of this condition. Electro-acupuncture may provide a promising complement or alternative to conventional lymphedema treatments such as compression bandaging, massage therapy or surgery.
Detailed Description
Participants will be invited to attend a 30-60 minute screening visit to determine eligibility. This screening visit will be located at a laboratory at McMaster University's Institute of Applied Health Sciences. Eligibility will be determined using health questionnaires and non-invasive physical assessment of the upper limbs. Participants may not be eligible for further participation based on their health status and risks to health and safety. Participants meeting eligibility criteria will be invited to 1 scheduled appointment (30-60 minutes in duration). The appointment time will be scheduled according to individual symptoms, such that it will coincide with the time of day that lymphedema symptoms are predicted to be at their highest. Upon arrival at the scheduled appointment, participants will be randomized to receive 20 minutes of acupuncture+applied electrical stimulation or no treatment. Participants in both groups will be asked to provide physical assessment data over a period of 30 minutes during the scheduled appointment. Differences between groups in tissue swelling of the affected upper-limb will be determined immediately following treatment, and at 10 minutes following treatment. Participants will be asked to report any significant changes to their health state for a period of 2 weeks following treatment. A follow-up questionnaire will be made available at 2 weeks following attendance of the scheduled appointment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphedema
Keywords
Lymphoedema, Edema, Oedema, Cancer, Breast Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Acupuncture + Electrical Stimulation
Arm Type
Experimental
Arm Description
Acupuncture needles are inserted beneath the skin and electrical stimulation applied for 20 minutes.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Participants who are randomized to receive no intervention will still receive physical assessment.
Intervention Type
Device
Intervention Name(s)
Acupuncture + Electrical Stimulation
Other Intervention Name(s)
Acupuncture, Electrical Stimulation, Electro-Acupuncture
Intervention Description
2 acupuncture needles are inserted into the upper back. 10Hz, 0.5ms biphasic square wave electrical pulses are applied to needles x20 mins. Current >sensation threshold & maintained at a level that is comfortable/painless & does not elicit skeletal muscle contractions (~5mA, <10mA). Needle locations are in the vicinity of nerves that supply the affected upper limb: EX-B1': Affected hemisphere, 1.5cm lateral to C5 spinous process. Insertion angle: shallow, 'inferior-lateral', ~15⁰ perpendicular to the skin, ~15⁰ lateral to the midline. Depth: ~1.5 cm (secure anchorage). EX-HN15': Affected hemisphere, 1.5cm lateral to the C7 spinous process. Insertion angle: shallow, 'inferior-medial' ~15⁰ perpendicular to the skin, ~15⁰ medial. Depth: ~1.5 cm (secure anchorage).
Primary Outcome Measure Information:
Title
Change in amount of arm tissue water determined by Bioimpedance Analysis
Description
Bioimpedance analysis devices take readings using 8 electrode pads that are placed on top of the skin of the arms. The electrode pads are connected to a computer that transmits a small amount of electrical current between the electrode pads. The process of taking readings takes less than 1 minute and is painless (participants may not be able to feel it working).
Time Frame
Before and after a 20 minute period at a single scheduled appointment
Secondary Outcome Measure Information:
Title
Change in dermal concentration of red blood cells in the arm assessed using light polarization spectroscopy
Description
A digital camera is used to 'see under the skin' and measure the amount of red blood cells in the arm. The camera is an ordinary digital camera connected to special computer software. Assessment using the camera is harmless and patients will not be able to feel it working. A series of digital photographs of a small area of the arms will be taken. The computer uses these photographs to calculate a number that represents the amount of blood contained in the skin of the arm.
Time Frame
Repeated measures during a single scheduled appointment - once every 2 minutes for 44 minutes
Title
Change in arm circumference
Description
Measurements are taken of both arms using a flexible measuring tape to be used in the calculation of size and volume.
Time Frame
Before and after a 20 minute period at a single scheduled appointment
Title
Lymphedema Questionnaire
Description
Survey is administered to collect data pertaining to the condition of lymphedema.
Time Frame
Administered at a single screening visit and 2 week follow up
Other Pre-specified Outcome Measures:
Title
Baseline current perception threshold
Description
Small electrodes will be placed on the tips of the middle finger and a weak electrical stimulus applied. This electrical stimulus will be raised up until the point participants can feel it as a 'tingling' or 'tapping' sensation (a non-painful stimulus). Doing so is used to assess the functioning of nerves in the affected arm.
Time Frame
Readings are taken once during a 15 minute during a single screening visit
Title
Baseline arm tissue water determined by Bioimpedance Analysis
Description
Bioimpedance analysis devices take readings using 8 electrode pads that are placed on top of the skin of the arms. The electrode pads are connected to a computer that transmits a small amount of electrical current between the electrode pads. The process of taking readings takes less than 1 minute and is painless (participants may not be able to feel it working).
Time Frame
Readings are taken once during a 15 minute screening visit

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: >1yr following the conclusion of breast cancer treatment Lymphedema of the upper limb: unilateral (one-side) Exclusion Criteria: History or evidence of hormone-receptor positive cancer Previous nodal dissection or radiotherapy to other regions Contraindications for acupuncture or electrical stimulation Pre-cancer or bi-lateral lymphedema Evidence of active cancer History of contralateral cancer, radiation or surgery Edema of the neck/midline/torso Pregnancy Allergies to nickel, chromium, or silicon Seizures (epilepsy) Tremors (shakiness) that may interfere with treatment Infections, scarring, open wounds, or broken skin at needle sites Infections, open wounds, or broken skin on the upper limbs (electrode & landmark sites)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Derek Rosa, PhD(c)
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
McMaster University
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8S 4L8
Country
Canada

12. IPD Sharing Statement

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Acupuncture for Lymphedema Secondary to Breast Cancer Treatment

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