Risk Factors for Shoulder Joint Motion Restriction
- Conditions
- Breast Cancer Survivors
- Interventions
- Other: measurement of tissue stiffness (N/m)Other: measurement of passive muscle tone (Hz)Other: measurement of creep of tissueOther: measurement of the range of shoulder joint motionOther: measurement of skin temperatureOther: measurement of painOther: measurement of pain pressure thresholdOther: measurement of grip strength
- Registration Number
- NCT05386641
- Lead Sponsor
- Istanbul Medeniyet University
- Brief Summary
In breast cancer patients, limitation of shoulder joint movement may occur following cancer treatment. Shoulder limitation causes a significant decrease in the patient's participation in activities of daily living. The aim of the study is to define these limitations, to evaluate in detail all the structures that cause the problem, and to determine the causes of the limitations in patients with shoulder joint movement limitation developed after breast cancer survivors.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- Female
- Target Recruitment
- 72
- Women between the ages of 30-60
- Having breast cancer treatment within 5 years
- Not having agreed to participate in the study
- Presence of additional orthopedic (scoliosis, etc.), neurological (multiple sclerosis, stroke, etc.) and rheumatological diseases (ankylosing spondylitis, rheumatoid arthritis, etc.) that will affect upper extremity functions
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Experimental Group measurement of pain Breast cancer survivors with shoulder joint motion restriction Control group measurement of skin temperature Breast cancer survivors without shoulder joint motion restriction Experimental Group measurement of creep of tissue Breast cancer survivors with shoulder joint motion restriction Experimental Group measurement of the range of shoulder joint motion Breast cancer survivors with shoulder joint motion restriction Experimental Group measurement of tissue stiffness (N/m) Breast cancer survivors with shoulder joint motion restriction Experimental Group measurement of passive muscle tone (Hz) Breast cancer survivors with shoulder joint motion restriction Control group measurement of tissue stiffness (N/m) Breast cancer survivors without shoulder joint motion restriction Control group measurement of pain Breast cancer survivors without shoulder joint motion restriction Control group measurement of pain pressure threshold Breast cancer survivors without shoulder joint motion restriction Experimental Group measurement of grip strength Breast cancer survivors with shoulder joint motion restriction Experimental Group measurement of skin temperature Breast cancer survivors with shoulder joint motion restriction Experimental Group measurement of pain pressure threshold Breast cancer survivors with shoulder joint motion restriction Control group measurement of the range of shoulder joint motion Breast cancer survivors without shoulder joint motion restriction Control group measurement of passive muscle tone (Hz) Breast cancer survivors without shoulder joint motion restriction Control group measurement of creep of tissue Breast cancer survivors without shoulder joint motion restriction Control group measurement of grip strength Breast cancer survivors without shoulder joint motion restriction
- Primary Outcome Measures
Name Time Method measurement of the range of shoulder joint motion Baseline The range of shoulder flexion, abduction, extension and external-internal rotation movements will be measured with a universal goniometer.
measurement of tissue stiffness (N/m) Baseline Stiffness values will be measured with myotonPro on centers of coordination located along the myofascial chain
measurement of passive muscle tone (Hz) Baseline muscle tones will be measured with myotonPro on centers of coordination located along the myofascial chain
measurement of creep of tissue Baseline creep of tissue will be measured with myotonPro on centers of coordination located along the myofascial chain
- Secondary Outcome Measures
Name Time Method measurement of grip strength Baseline The grip strength of both hand will be evaluated by "hand-held" dynamometer.
measurement of pain Baseline 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.
measurement of skin temperature Baseline measurements will be taken from the area covering 3 cm of the surgical incision with a P45 thermographic camera with high thermal sensitivity
measurement of pain pressure threshold Baseline Pain pressure threshold will be evaluated by a digital algometer
Trial Locations
- Locations (1)
İstanbul Medeniyet University
🇹🇷Istanbul, Turkey