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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age30-60
SponsorIstanbul Medeniyet University

About this trial

In breast cancer patients, limitation of shoulder joint movement occurs following mastectomy surgery. Studies have reported that damage to the fascia on the pectoralis major muscle during mastectomy surgery contributes to the development of the limitation. The aim of this study is to investigate the effect of release techniques applied to the fascia on the pectoralis major muscle and the fascial chain on the incerasing of shoulder joint range of motion.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Women between the ages of 30-60

Having breast surgery within 2 years

Not have received conservative treatment for shoulder rehabilitation in the last 6 months

Having limitation of movement of the shoulder joint due to breast surgery

Disqualifiers

Not having agreed to participate in the study

Having undergone radical mastectomy surgery

Having connective tissue disease

Presence of brachial plexus paresis/plegia

Trial design

Design model

Parallel

Treatments tested in this trial

  • conventional physiotherapy

    Other intervention

    A basic physiotherapy program consisting of shoulder exercises will be applied to the participants. content of the physiotherapy program * Shoulder passive/active abduction, flexion, internal and external rotation exercises * Posture exercises * Neck stretching exercises * Pectoralis major stretching exercises * Shoulder capsule stretching exercises * Scapular Mobilization exercises

  • Manual lymphatic drainage

    Other intervention

    manual lymph drainage is a manual technique that is applied to the lymphatic system with a pressure of 40-50 mmHg and increases the working speed of lymphatic nodules/collectors. Manual lymph drainage will be made to the anterior axillar-axillar, posterior axillar-axillar and axilla-inguinal anastomosis collectors and the arm region (up to the elbow) lymph collectors.

  • Myofascial relasing

    Other intervention

    it will be done with the thumb or 3rd finger from the acu points of the superficial arm-anterior myofascial chain. 6-8 seconds with thumb to these points. pressure will be applied and vibration will be given clockwise.

Treatment groups

48 Participants
are divided into 4 treatment groups
Group A: control groupActive comparator 1 intervention
Group B: Manual lymphatic drainage groupExperimental treatment 2 interventions
Group C: Myofascial relasing groupExperimental treatment 2 interventions
Group D: Lymphatic drainage and myofascial releasing groupExperimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

measurement of tissue stiffness (N/m)

Stiffness values will be measured with myotonPro on centers of coordination located along the myofascial chain .

Time frame
changes from baseline stiffness values will be measured at 6 week and 10 week
2

measurement of passive muscle tone (Hz)

muscle tones will be measured with myotonPro on centers of coordination located along the myofascial chain

Time frame
changes from baseline tone values will be measured at 6 week and 10 week
3

measurement of creep of tissue

creep of tissue will be measured with myotonPro on centers of coordination located along the myofascial chain

Time frame
changes from baseline creep values will be measured at 6 week and 10 week
4

measurement of the range of shoulder joint motion

The range of shoulder flexion, abduction, extension and external-internal rotation movements will be measured with a universal goniometer.

Time frame
changes from baseline range of the shoulder joint motion values will be measured at 6 week and 10 week

Secondary outcomes

1

measurement of skin temperature

measurements will be taken from the area covering 3 cm of the surgical incision with a P45 thermographic camera with high thermal sensitivity (Flir Sistem, ThermaCAM, Sweden).

Time frame
changes from baseline skin temperature values will be measured at 6 week and 10 week
2

measurement of pain

Pain will be evaluated by visual analog scale (VAS). In the scale, the patient is asked to mark the most appropriate pain intensity on a scale ranging from 0 (no pain) to 10 (tolerable pain). The higher the score, the greater the pain intensity.

Time frame
changes from baseline pain values will be measured at 6 week and 10 week
3

measurement of pain pressure threshold

Pain pressure threshold will be evaluated by a digital algometer (Algometer Commander, Jtech Medical, MM036\_K, 2016).

Time frame
changes from baseline pain pressure threshold values will be measured at 6 week and 10 week
4

measurement of grip strength

The grip strength of both hand will be evaluated by "hand-held" dynamometer.

Time frame
changes from baseline grip strength values will be measured at 6 week and 10 week

Other outcomes

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