About this trial
This study aims to evaluate the effectiveness of a physiotherapy program incorporating visual biofeedback compared to a conventional physiotherapy program in improving shoulder function in women following breast cancer surgery.
Breast cancer survivors frequently experience shoulder dysfunction, including reduced range of motion, decreased strength, altered neuromuscular activity, and impaired scapulohumeral control. While conventional physiotherapy is effective, there is growing interest in interventions targeting motor control and neuromuscular coordination through biofeedback strategies.
Participants will be randomly assigned to either a control group receiving conventional physiotherapy or an experimental group receiving the same program supplemented with visual biofeedback using the MotionGuidance system. Outcomes will include shoulder strength, range of motion, functional performance, electromyographic activity, and muscle oxygen saturation.
Eligibility criteria
Qualifiers
Women aged 18 years or older
History of breast cancer surgery (mastectomy or breast-conserving surgery within the last 6 months)
Presence of shoulder pain, reduced range of motion, strength deficit, or functional limitation
Ability to understand and follow study instructions
Disqualifiers
Presence of metastasis
Post-surgical complications contraindicating exercise
Severe lymphedema (Stage III or IV)
Neurological disorders affecting the upper limb
Trial design
Treatments tested in this trial
- Experimental Group: Physiotherapy + Visual Biofeedback