Actively Recruiting

Phase Not Applicable
Age: 30Years - 60Years
FEMALE
ID05386628

The Effect of Myofascial Chain Release Techniques on Shoulder Joint Range of Motion Following Mastectomy Surgery in Breast Cancer Survivors

Led by Istanbul Medeniyet University · Updated on 2024-07-15

48

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the effect of myofascial chain release techniques and manual lymphatic drainage on improving shoulder joint range of motion in breast cancer survivors who have undergone mastectomy surgery. After breast surgery, patients often experience shoulder movement limitations due to fascia damage on the pectoralis major muscle. These complications can reduce quality of life and interfere with treatments like radiotherapy, making it important to prevent and address shoulder joint limitations early. Participants will be randomly assigned to one of four groups: a conventional physiotherapy program alone, physiotherapy plus manual lymphatic drainage, physiotherapy plus myofascial chain releasing techniques, or physiotherapy combined with both manual lymphatic drainage and myofascial releasing techniques. The physiotherapy program includes shoulder exercises and stretching, while manual lymphatic drainage targets lymphatic collectors in the arm and axillary areas, and myofascial releasing involves targeted pressure and vibration on arm myofascial points. Treatments are given twice a week for six weeks. Participants will undergo detailed physical assessments of the shoulder region three times: before treatment, after six weeks of treatment, and one month post-treatment. Evaluations include measuring tissue stiffness, muscle tone, tissue creep, shoulder joint motion range, daily activity ability, and mental health changes. Additional measures track skin temperature, pain levels, pain pressure threshold, and grip strength. These assessments help researchers understand how the treatments affect shoulder mobility and related symptoms over time.

CONDITIONS

Brief Title

The Effect of Myofascial Chain Release Techniques on Shoulder Joint Range of Motion in Breast Cancer Survivors

Who Can Participate

Age: 30Years - 60Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women between the ages of 30 and 60
  • Breast surgery performed within the last 2 years
  • No conservative shoulder rehabilitation treatment in the last 6 months
  • Presence of shoulder joint movement limitation due to breast surgery
Not Eligible

You will not qualify if you...

  • Declined to participate in the study
  • Underwent radical mastectomy surgery
  • Have connective tissue diseases
  • Presence of brachial plexus paresis or plegia
  • Presence of radiogenic fibrosis
  • Additional orthopedic, neurological, or rheumatological diseases affecting upper limb function
  • Active cancer metastases
  • Underwent reconstruction surgery
  • Ongoing radiotherapy or chemotherapy (must have ended at least 3 months ago)
  • Bilateral mastectomy history
  • Development of lymphedema in the arm or trunk
  • Use of muscle relaxants
  • Severe chemotherapy side effects such as hyperesthesia, nausea, skin changes, or weakness

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants receive conventional physiotherapy exercises twice a week for 6 weeks. Depending on their group assignment, they may also receive manual lymphatic drainage and/or myofascial chain releasing techniques to improve shoulder joint mobility and reduce complications after breast surgery.

Twice weekly visits for 6 weeks

Follow-up

Duration - 1 month post treatment

Participants undergo physical evaluations of the shoulder region to assess improvements and lasting effects one month after completing treatment.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

İstanbul Medeniyet University

Istanbul, Turkey (Türkiye)

Actively Recruiting

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Research Team

N

Nilüfer Kablan, PhD

G

Gülser Cinbaz, MSc

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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