A Study of the BREAST-Q REACT Tool for People Having Breast Surgery
- Conditions
- Mastectomy With ReconstructionBreast Conserving Surgery
- Interventions
- Other: QuickDASHOther: BREAST-Q Physical Well-Being
- Registration Number
- NCT06550401
- Lead Sponsor
- Memorial Sloan Kettering Cancer Center
- Brief Summary
The researchers are doing this study to find out whether it is practical (feasible) to conduct a larger study looking at the effects of the BREAST-Q Real-time Engagement and Communication Tool (REACT) on people's quality of life, interactions with their doctors, and medical interventions after undergoing routine breast conserving surgery or mastectomy. The BREAST-Q REACT tool shows scores from standard questionnaires completed before and after breast surgery about overall physical wellbeing, arm pain or tightness, the ability to move the arms and perform everyday tasks, and any symptoms related to the arms, and provides feedback including recommendations and detailed information that help explain these scores and guide topics for people and their doctor to discuss.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 80
- Scheduled to undergo BCS or mastectomy followed by breast reconstruction with tissue expander, autologous tissues, or direct-to-implant, regardless of neoadjuvant chemotherapy or radiation history
- Female sex
- Able to speak and understand English
- ≥18 years of age
- Able to access the patient portal online
- Patient is male
- Younger than 18 years of age
- Cannot communicate in English
- Recurrent breast cancer
- Patients without access to the internet.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Control group QuickDASH Participants in the control group will receive the usual feedback from questionnaires completed before and after routine surgery by discussing it with their surgeon Intervention group BREAST-Q Physical Well-Being Participants in the intervention group will receive feedback using the BREAST-Q REACT tool from questionnaires completed before and after routine surgery, in addition to the usual way by discussing it with their surgeon.
- Primary Outcome Measures
Name Time Method feasibility of recruitment up to 3 months assessed by frequency data from initial eligibility screening to enrollment
- Secondary Outcome Measures
Name Time Method feasibility of protocol delivery up to 3 months by evaluating survey completion rates and proportion of patients who are being referred to medical interventions.
Trial Locations
- Locations (6)
Memorial Sloan Kettering Nassau (All Protocol Activities)
🇺🇸Uniondale, New York, United States
Memorial Sloan Kettering Commack (All Protocol Activities)
🇺🇸Commack, New York, United States
Memorial Sloan Kettering Westchester (All Protocol Activities)
🇺🇸Harrison, New York, United States
Memorial Sloan Kettering Monmouth (All Protocol Activities)
🇺🇸Middletown, New Jersey, United States
Memorial Sloan Kettering at Basking Ridge (All Protocol Activities)
🇺🇸Basking Ridge, New Jersey, United States
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
🇺🇸New York, New York, United States