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Compares treatment options for Breast Cancer
Official title Effectiveness of a Visual Biofeedback Program Versus Conventional Physiotherapy on Shoulder Mobility, Strength, and Function in Women After Breast Cancer Surgery
ClinicalTrials.gov ID: NCT07542106
What this study is testing
- What it's testing
- 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.
- Time commitment: about 8 weeks
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older, women only. Healthy volunteers may be eligible.
You may be able to join if
- 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
You likely can't join if
- Presence of metastasis
- Post-surgical complications contraindicating exercise
- Severe lymphedema (Stage III or IV)
- Neurological disorders affecting the upper limb
- Severe musculoskeletal shoulder conditions unrelated to breast cancer
- Participation in other rehabilitation programs
The study team makes the final eligibility decision.
Where it's taking place
- Badajoz, Badajoz, Spain
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The study runs about 8 weeks per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.
Who can join this trial?
This study is enrolling female, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Badajoz, Badajoz, Spain. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.