RECONJOINT: A patient-friendly decision tool to help choosing breast reconstruction options with your doctor
Official title: RECONJOINT: A Preference Elicitation Tool to Improve Shared Decision Making for Breast Reconstruction Surgery
Funded at Sloan-Kettering Inst Can Research · NIH-11286428 · Data updated 2026-11-12
A digital tool helps you share your preferences so your breast reconstruction choices align with what matters most to you during breast cancer care.
Quick facts
| Grant type | R21 grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | Sloan-Kettering Inst Can Research NIH-funded |
| Lab location | 1 site (New York, United States) |
| Project start | June 10, 2026 |
| Project end | May 31, 2028 |
| Funding year | 2026 |
| Award (this year) | $457,252 |
| NIH project number | 1R21CA309323-01 |
| Project ID | NIH-11286428 on NIH RePORTER |
Who could benefit from this research
✓Could help
Women considering breast reconstruction after mastectomy who want their personal goals and concerns reflected in the treatment plan.
✕Less likely to help
Individuals not planning to pursue breast reconstruction or not engaged in decision making around reconstruction might derive less direct benefit.
What this research studies
This project will adapt and implement a web-based decision tool that collects your personal preferences for breast reconstruction using an adaptive choice-based method, and creates an integrated toolkit for use in clinic. Researchers will test how feasible and acceptable it is to use the tool and toolkit during real appointments, with input from patients, doctors, and advocates to tailor it to clinical workflows. The goal is to make shared decision making smoother and ensure your treatment choices reflect your values and goals after mastectomy.
Why it matters
Potential benefit: If successful, patients could experience clearer, more collaborative decisions about reconstruction that better match their preferences and improve satisfaction with care.
How similar studies have gone: Preliminary work shows the tool is acceptable and usable, with patients wanting to see results and use it in clinic, but full clinical integration was not yet implemented.
Where this research is happening
-
Sloan-Kettering Inst Can Research
New York, United States Active
Researchers
- Principal investigator: Matros, Evan — Sloan-Kettering Inst Can Research
- Study coordinator: Matros, Evan
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About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page.