Effectiveness of a Visual Biofeedback Program Versus Conventional Physiotherapy on Shoulder Mobility, Strength, and Function in Women After Breast Cancer Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of Extremadura

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

This trial accepts healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • Experimental Group: Physiotherapy + Visual Biofeedback

    Procedure/Surgery

    Participants will receive a structured physiotherapy program combined with visual biofeedback using the MotionGuidance system. The intervention includes guided exercises with laser-based visual feedback to improve motor control and movement accuracy.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Experimental Group: Physiotherapy + Visual BiofeedbackActive comparator 1 intervention
Group B: Control Group: Conventional PhysiotherapyNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Shoulder Strength (kg)

Measured using handheld dynamometry (isometric strength in flexion, abduction, and external rotation).

Time frame
Baseline and 8 weeks

Secondary outcomes

1

Range of Motion (degrees)

Measured using goniometry (flexion, abduction, internal and external rotation).

Time frame
Baseline and 8 weeks
2

Muscle Activity (EMG-microvolts)

Surface electromyography analysis (RMS-Root mean square, and activation timing of shoulder muscles)

Time frame
Baseline and 8 weeks
3

Muscle Oxygen Saturation (SmO₂)

Measured using near-infrared spectroscopy (Moxy Monitor).

Time frame
Baseline and 8 weeks
4

Handgrip Strength (kg)

Measured using a digital dynamometer.

Time frame
Baseline and 8 weeks

Other outcomes

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