Actively Recruiting
Breast Cancer BRAs Study (Breast Cancer Biomechanics of Radiotherapy And Surgery): Effects of Breast Surgery and Radiotherapy on Breast Movement and Support Needs in Women Treated for Breast Cancer
Led by Portsmouth Hospitals NHS Trust · Updated on 2025-08-22
45
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
P
Portsmouth Hospitals NHS Trust
Lead Sponsor
U
University of Portsmouth
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating breast biomechanics in women who have undergone surgery with or without radiotherapy for breast cancer. This study aims to assess whether it is possible to test breast biomechanics in this population. Breast cancer affects over 56,000 women yearly in the UK, and treatments like surgery and radiotherapy can change the breast's structure and movement, which may impact the type of bra support needed for comfort and tissue protection. Participants in this observational study will attend the biomechanics testing laboratory at the University of Portsmouth after their surgery and/or radiotherapy, and optionally before surgery. The study uses 3D scans and sensors to evaluate breast structure and movement. Women will also share their views on the testing methods, bra support needs, and exercise habits before and after treatment. The findings could help design better bras for women treated for breast cancer and inform treatment decisions based on expected changes in breast movement. Participants will be asked to attend assessments involving 3D scanning and sensor measurements of their breasts. Researchers will collect data on breast biomechanics as well as participant feedback on bras and exercise. The main goal is to determine if recruitment and data collection for this type of study are feasible. The study period averages about one year from enrollment to completion, with ongoing monitoring and analysis during this time.
CONDITIONS
Brief Title
Breast Cancer BRAs Study (Breast Cancer Biomechanics of Radiotherapy And Surgery)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female
- 18 years of age or above
- Early or locally advanced breast cancer classified as B5a or B5b (radical treatment intent)
- Unilateral breast cancer (contralateral breast used as control)
- Receiving or has received breast cancer surgery
- May have received adjuvant radiotherapy
- Able to travel to the University of Portsmouth Breast biomechanics laboratory
- Participant has capacity to consent
You will not qualify if you...
- Diagnosis of metastatic breast cancer
- Less than 2 weeks post-operative
- Less than 4 weeks post-radiotherapy
- Active post-operative breast infection
- Requires ongoing breast dressings
- Previous breast surgery to the opposite breast
- Bilateral breast cancer
- Epilepsy (due to strobe on 3D scanner)
- Pregnancy or less than 6 weeks post-partum
- Breastfeeding
- Rockwood Frailty score greater than 5 or unable to walk unassisted
- Requires interpreter
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 year
Participants undergo 3D scans and sensor assessments to evaluate breast structure and movement before and after breast cancer treatment.
1 to 3 visits depending on treatment timing
Duration - Up to 1 year
Participants provide feedback on bra requirements, exercise habits, and views on testing methods over the course of their treatment and recovery.
Periodic visits during the study period
Trial Site Locations
Total: 1 location
1
Queen Alexandra Hospital
Portsmouth, United Kingdom, PO6 3LY
Actively Recruiting
Research Team
A
Amy Huseyin
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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