Myofascial Massage for Pain and Immobility Following Breast Cancer Surgery
Primary Purpose
Breast Cancer, Mastectomy; Lymphedema, Pain, Shoulder
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Myofascial Massage
Light Touch
Sponsored by
About this trial
This is an interventional treatment trial for Breast Cancer focused on measuring breast cancer, breast surgery, myofascial massage, shoulder immobility
Eligibility Criteria
Inclusion Criteria:
- 18 years or older
- Female
- Undergone breast cancer surgery 3-18 months ago
- Completed all treatment for breast cancer within the last 18 months (i.e. radiation, IV chemotherapy, surgery)
- Not expected to have any additional surgery (i.e. planning for reconstruction)
- Self reported chronic pain or immobility since surgery
Exclusion Criteria:
- Under age 18
- Not female
- Surgery < 3 months ago
- End all cancer treatments (surgery, radiation, chemotherapy) > 18 months ago
- Presence of lymphedema
- Open wounds or sores
- Currently on anticoagulants
- Currently receiving massage treatments
Sites / Locations
- MetroHealth Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Myofascial Massage
Light Touch
Arm Description
Participants randomized to this group will receive 30 minutes of myofascial massage to their affected breast, chest, and shoulder areas twice a week for 2 months. Therapists will follow a detailed 8 week protocol developed with a massage therapy consultant and the study team.
Participants randomized to this group will receive 30 minutes of light touch to their affected breast, chest, and shoulder areas twice a week for 2 months.
Outcomes
Primary Outcome Measures
Change in self reported pain scores
Shoulder Pain and Disability Index "SPADI", 5 pain items rated on a 10 point likert scale, where 0 is no pain at all and 10 is the worst pain imaginable
Change in self reported mobility scores
Shoulder Pain and Disability Index "SPADI", 8 mobility items rated on a 10 point likert scale, where 0 means no issues with mobility and 10 means they are unable to complete the task
Secondary Outcome Measures
Range of Motion
Shoulder range of motion measured by goniometer and objective functional tasks
Pressure/Pain Threshold
Pressure to pain threshold as measured by algometer
Grip Strength
Hand grip strength measured by dynamometer
Tissue Flexibility
Change in tissue flexibility as measured by adherometer
Quality of Life Survey-Functional Assessment of Cancer Therapy - Breast (FACT-B)
44-item questionnaire designed to measure physical well-being, social/family well-being, emotional well-being, functional well-being, and additional breast cancer-specific concerns
Full Information
NCT ID
NCT04233385
First Posted
January 14, 2020
Last Updated
June 28, 2023
Sponsor
MetroHealth Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT04233385
Brief Title
Myofascial Massage for Pain and Immobility Following Breast Cancer Surgery
Official Title
Pain and Immobility After Breast Cancer Surgery: A Community-Based Randomized Controlled Trial of Myofascial Massage Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 4, 2020 (Actual)
Primary Completion Date
April 30, 2024 (Anticipated)
Study Completion Date
April 30, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
MetroHealth Medical Center
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
About 25-50% of women who undergo breast cancer surgery develop persistent chest wall pain and shoulder mobility limitations following surgery. The pain and mobility limitations adversely affect quality of life, sleep, and body image. Unfortunately, current treatments for pain and mobility limitations have variable efficacy. Based on a review of relevant pre-, intra-, and post-operative factors, investigators reasoned that myofascial massage may address contributors to pain and mobility limitations following breast cancer surgery. Investigators propose a randomized controlled trial looking at myofascial massage compared to a light touch group to look at the effects on pain and immobility following breast cancer surgery.
Detailed Description
Myofascial massage is a deep tissue massage that focuses on muscles as well as the connective tissue that surrounds muscles, bones, and ligaments. The study team subsequently conducted a pilot randomized controlled trial involving 21 women with persistent pain and mobility limitations many months after surgery. They found that women who received myofascial massage to the affected breast/chest/shoulder had marked reductions in pain and mobility limitations and significant improvements in quality of life compared to a control group who received relaxation massage. They also established a practice-based research network of over 50 northeast Ohio massage therapists to guide future work.
The study team now proposes a full scale randomized controlled trial involving 202 women with persistent pain and mobility limitations at 2 participating sites. To help differentiate between the specific effects of myofascial massage and non-specific effects due to prolonged touch and attention from a massage therapist, the study will include an active control group that will receive light touch. Participants in each group will receive 30 minutes of treatment twice weekly for 2 months. Primary analyses will determine the impact of myofascial massage on pain and mobility limitations. Secondary analyses will examine the impact of myofascial massage on a number of secondary outcomes, including range of motion, quality of life, sleep, and body image.
Innovative features of the proposed project include a rigorous randomized controlled trial design, inclusion of an active control group, direct targeting of the affected breast/chest/shoulder, assessment of multiple mechanistic and patient-centered outcomes, and involvement of a massage practice-based research network. Investigators anticipate that the project will lead to a new and effective approach for addressing a major source of morbidity for women with breast cancer. Furthermore, the project may serve as a model for future trials of manual therapy among individuals with chronic medical conditions.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Mastectomy; Lymphedema, Pain, Shoulder, Mobility Limitation
Keywords
breast cancer, breast surgery, myofascial massage, shoulder immobility
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized Controlled Trial
Masking
ParticipantOutcomes Assessor
Masking Description
A blinded research assistant will perform all outcomes assessments of objective functional measures. Participants will be told they are being randomized into two different types of massage, however, we will not refer to they myofascial massage as "intervention" or the light touch as "active control"
Allocation
Randomized
Enrollment
202 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Myofascial Massage
Arm Type
Experimental
Arm Description
Participants randomized to this group will receive 30 minutes of myofascial massage to their affected breast, chest, and shoulder areas twice a week for 2 months. Therapists will follow a detailed 8 week protocol developed with a massage therapy consultant and the study team.
Arm Title
Light Touch
Arm Type
Active Comparator
Arm Description
Participants randomized to this group will receive 30 minutes of light touch to their affected breast, chest, and shoulder areas twice a week for 2 months.
Intervention Type
Other
Intervention Name(s)
Myofascial Massage
Intervention Description
The myofascial protocol outlines techniques, areas of the body, as well as time to be spent for each technique for a total of 25 minutes. The remaining 5 minutes of the massage are for the massage therapist to tailor myofascial massage to the needs and circumstances of each participant. In order to provide some level of customization, the therapist will determine the impact of massage on the participant's pre-existing pain and/or mobility limitations. Second, the therapist will assess the soft tissues around the affected breast, chest, and shoulder to determine the locations of pain, tissue firmness, and restricted mobility. Third, the therapist will use effleurage and petrissage techniques to gently massage the identified locations to soften and release the tissues. Techniques used will include deep friction of muscles, sustained compression, and fascial stretch.
Intervention Type
Other
Intervention Name(s)
Light Touch
Intervention Description
Participants randomized to this group will receive 30 minutes of light touch to their affected breast, chest, and shoulder areas twice a week for 2 months. Therapists will follow a detailed light touch protocol for each of the 16 sessions. In addition, the therapist will inquire about the participant's response to the previous light touch treatment. Second, the therapist will assess the soft tissues around the affected breast, chest, and shoulder to determine the locations of pain, tissue firmness, and restricted mobility. Third, the therapist will place both hands on the participant for 3 minutes at each identified location. Pressure will be very light and consistent, with no side-to-side movement.
Primary Outcome Measure Information:
Title
Change in self reported pain scores
Description
Shoulder Pain and Disability Index "SPADI", 5 pain items rated on a 10 point likert scale, where 0 is no pain at all and 10 is the worst pain imaginable
Time Frame
Baseline, 1 month, 2 months, 8 months, and 14 months
Title
Change in self reported mobility scores
Description
Shoulder Pain and Disability Index "SPADI", 8 mobility items rated on a 10 point likert scale, where 0 means no issues with mobility and 10 means they are unable to complete the task
Time Frame
Baseline, 1 month, 2 months, 8 months, and 14 months
Secondary Outcome Measure Information:
Title
Range of Motion
Description
Shoulder range of motion measured by goniometer and objective functional tasks
Time Frame
Baseline, 2 months, 14 months
Title
Pressure/Pain Threshold
Description
Pressure to pain threshold as measured by algometer
Time Frame
Baseline, 2 months, 14 months
Title
Grip Strength
Description
Hand grip strength measured by dynamometer
Time Frame
Baseline, 2 months, 14 months
Title
Tissue Flexibility
Description
Change in tissue flexibility as measured by adherometer
Time Frame
Baseline, 2 months, 14 months
Title
Quality of Life Survey-Functional Assessment of Cancer Therapy - Breast (FACT-B)
Description
44-item questionnaire designed to measure physical well-being, social/family well-being, emotional well-being, functional well-being, and additional breast cancer-specific concerns
Time Frame
Baseline, 2 months, 14 months
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
This study is limited to females who have undergone breast cancer surgery.
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
18 years or older
Female
Undergone breast cancer surgery 3-18 months ago
Completed all treatment for breast cancer within the last 18 months (i.e. radiation, IV chemotherapy, surgery)
Not expected to have any additional surgery (i.e. planning for reconstruction)
Self reported chronic pain or immobility since surgery
Exclusion Criteria:
Under age 18
Not female
Surgery < 3 months ago
End all cancer treatments (surgery, radiation, chemotherapy) > 18 months ago
Presence of lymphedema
Open wounds or sores
Currently on anticoagulants
Currently receiving massage treatments
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jacqueline Dolata, MBA
Phone
2167781792
Email
jdolata@metrohealth.org
Facility Information:
Facility Name
MetroHealth Medical Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44109
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jacqueline Dolata, MBA
Phone
216-778-1792
Email
jdolata@metrohealth.org
First Name & Middle Initial & Last Name & Degree
Darerian Schueller, MPH
Phone
216-778-8456
Email
dschueller@metrohealth.org
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
21435953
Citation
Andersen KG, Kehlet H. Persistent pain after breast cancer treatment: a critical review of risk factors and strategies for prevention. J Pain. 2011 Jul;12(7):725-46. doi: 10.1016/j.jpain.2010.12.005. Epub 2011 Mar 24.
Results Reference
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PubMed Identifier
21231780
Citation
Ewertz M, Jensen AB. Late effects of breast cancer treatment and potentials for rehabilitation. Acta Oncol. 2011 Feb;50(2):187-93. doi: 10.3109/0284186X.2010.533190.
Results Reference
background
PubMed Identifier
22488698
Citation
Hayes SC, Johansson K, Stout NL, Prosnitz R, Armer JM, Gabram S, Schmitz KH. Upper-body morbidity after breast cancer: incidence and evidence for evaluation, prevention, and management within a prospective surveillance model of care. Cancer. 2012 Apr 15;118(8 Suppl):2237-49. doi: 10.1002/cncr.27467.
Results Reference
background
PubMed Identifier
24816774
Citation
Hidding JT, Beurskens CH, van der Wees PJ, van Laarhoven HW, Nijhuis-van der Sanden MW. Treatment related impairments in arm and shoulder in patients with breast cancer: a systematic review. PLoS One. 2014 May 9;9(5):e96748. doi: 10.1371/journal.pone.0096748. eCollection 2014.
Results Reference
background
PubMed Identifier
18192154
Citation
Thomas-Maclean RL, Hack T, Kwan W, Towers A, Miedema B, Tilley A. Arm morbidity and disability after breast cancer: new directions for care. Oncol Nurs Forum. 2008 Jan;35(1):65-71. doi: 10.1188/08.ONF.65-71.
Results Reference
background
PubMed Identifier
24495044
Citation
Johansen S, Fossa K, Nesvold IL, Malinen E, Fossa SD. Arm and shoulder morbidity following surgery and radiotherapy for breast cancer. Acta Oncol. 2014 Apr;53(4):521-9. doi: 10.3109/0284186X.2014.880512. Epub 2014 Feb 5.
Results Reference
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PubMed Identifier
24381969
Citation
Meretoja TJ, Leidenius MHK, Tasmuth T, Sipila R, Kalso E. Pain at 12 months after surgery for breast cancer. JAMA. 2014 Jan 1;311(1):90-92. doi: 10.1001/jama.2013.278795. No abstract available. Erratum In: JAMA. 2017 Apr 25;317(16):1693.
Results Reference
background
PubMed Identifier
21620648
Citation
Colagiuri B, Christensen S, Jensen AB, Price MA, Butow PN, Zachariae R. Prevalence and predictors of sleep difficulty in a national cohort of women with primary breast cancer three to four months postsurgery. J Pain Symptom Manage. 2011 Nov;42(5):710-20. doi: 10.1016/j.jpainsymman.2011.02.012. Epub 2011 May 26.
Results Reference
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PubMed Identifier
8880841
Citation
Wallace MS, Wallace AM, Lee J, Dobke MK. Pain after breast surgery: a survey of 282 women. Pain. 1996 Aug;66(2-3):195-205. doi: 10.1016/0304-3959(96)03064-3.
Results Reference
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Myofascial Massage for Pain and Immobility Following Breast Cancer Surgery
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