A Breast Support Intervention for Women With Breast Pain
Not Applicable
Completed
- Conditions
- Mastodynia
- Interventions
- Other: Standard CareOther: Bra prescription
- Registration Number
- NCT02515253
- Lead Sponsor
- University of Portsmouth
- Brief Summary
The purpose of this study is to assess whether prescribing a bra to participants results in an improvement in the Patient Global Impression of Change (PGIC) compared to participants who receive standard care alone.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 33
Inclusion Criteria
- Female, aged 18 years of age and above.
- Experiencing breast pain of any severity.
- Participants must be able to speak and read English fluently
- Participants must be a resident within the local area and not planning to move out of the area within the study timeline
- Participant must have attended the Queen Alexandra (QA) hospital for an assessment of their breast pain.
- Participant is willing and able to give informed consent for participation in the study.
- Participant is self-reported to be between a 34 and 40 under band size and a DD to G bra cup size.
- Able to walk on a treadmill for up to two minutes unaided and be able to walk unaided up and down a small set of steps (assessed verbally by the clinicians at QA hospital)
- Participants must be able to comply with the study procedures
Exclusion Criteria
- Participants are receiving any additional treatment for their breast pain that is not part of standard care (recommendation for a bra fit, topical ibuprofen, breast pain leaflet) including any cancer treatment
- Participants have had any surgery to the breasts within the last year
- Participants are currently pregnant or have been pregnant or breast fed in the past year
- Planning to undertake any activities or lifestyle changes which may affect their levels of breast pain e.g. trying for a baby, changing oral contraceptive, having breast surgery.
- Participant's data will be excluded from the analysis if they do not complete either survey at four or eight weeks (at least one follow up survey needs to be completed).
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Standard care group Standard Care Participants in this group will receive the standard care for benign breast pain sufferers administered by the Queen Alexandra Hospital in Portsmouth. Prescription group Bra prescription Participants in this group will receive the standard care for benign breast pain sufferers (administered by the Queen Alexandra Hospital in Portsmouth) and will also attend the Department of Sport and Exercise Science at the University of Portsmouth for an individual bra prescription. Participants will be prescribed an appropriate bra to wear over an eight week intervention period. Prescription group Standard Care Participants in this group will receive the standard care for benign breast pain sufferers (administered by the Queen Alexandra Hospital in Portsmouth) and will also attend the Department of Sport and Exercise Science at the University of Portsmouth for an individual bra prescription. Participants will be prescribed an appropriate bra to wear over an eight week intervention period.
- Primary Outcome Measures
Name Time Method Patient Global Impression of Change (PGIC) eight weeks post intervention Participants will complete the PGIC as part of a questionnaire eight weeks after receiving their treatment for benign breast pain
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
Department of Sport and Exercise Science, University of Portsmouth
🇬🇧Portsmouth, United Kingdom
Breast Care Services, Queen Alexandra Hospital
🇬🇧Portsmouth, United Kingdom