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Diagnosis and Management of Myofascial Pain Syndrome in Women With Mastectomies

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02181166
Enrollment
60
Registered
2014-07-03
Start date
2014-08-31
Completion date
2016-12-31
Last updated
2014-07-03

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

Conditions

Breast Cancer, Myofascial Trigger Point

Keywords

Breast Neoplasms, Mastectomy, Myofascial pain syndromes, Physical Therapy Modalities

Brief summary

Myofascial pain considerably affects women undergoing treatment for breast cancer, is characterized by the presence of myofascial taut bands and trigger points. This study aims to evaluate the effects of ischemic compression, high-voltage electrical stimulation and rehabilitation of kinesio in women with myofascial pain following treatment of breast cancer. This is a randomized blind controlled study. For this, we invited 60 volunteers undergoing treatment for breast cancer, randomized and allocated into three groups: G1 (cinesioterapia), G2 (ischemic compression cinesioterapia +) and G3 (high voltage electrical stimulation cinesioterapia +). The stance, the plantar pressure distribution and the balance will be assessed by means of photogrammetry and baropodometry respectively. Myofascial trigger points will be assessed with the use of infrared thermography, algometry and numerical rating scale of pain (END). Moreover, the quality of life of the volunteers will be assessed by the Functional Assessment of Cancer Therapy-Breast (FACT-B +4). The volunteers will undergo 10 sessions of treatment, and reassessed at the end of treatment and after thirty days. Normality test is used to verify data distribution and consistent statistical test for proper intra and comparisons between groups, being thus considered two factors in the comparisons, time and group. A significance level of 5% is assumed.

Interventions

OTHERIsquemic compression
OTHERHigh voltage electrical stimulation

Sponsors

University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
35 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* mastectomy * aged between 35 and 70 years * myofascial trigger point in the upper trapezius muscle

Exclusion criteria

* metastasis or recurrence of breast cancer * bilateral mastectomy * in physiotherapy treatment * degenerative diseases of the spine * use of muscle relaxants or anti-inflammatory analgesics in the last week * report of fibromyalgia

Design outcomes

Primary

MeasureTime frameDescription
Pain2 yearsWill be apply the following assessment tools: algometry (evaluates pressure pain threshold), and numerical scale of pain assessment (assesses pain intensity).

Secondary

MeasureTime frameDescription
Quality of life2 yearsThrough a Functional Assessment of Cancer Therapy- Breast (FACT B + 4).
Skin Temperature2 yearsThrough of thermograph will be evaluated skin temperature on myofascial trigger points.
Posture2 yearsThrough computerized photogrammetry postural assessment.

Countries

Brazil

Contacts

Primary ContactVânia Ferreira, PT
vaniatie@hotmail.com+551636020215

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026