Patient Priority Framework
PRIORITY-BASED SCALES FOR CHILDREN’S OUTCOMES – RESEARCH & EVALUATION (PSCORE)
1. To understand and define the priorities of children (and their parents) living with musculoskeletal conditions;
2. To inform the development of meaningful outcome measures; and
3. To use these measures to evaluate the effectiveness of interventions for these children and their parents.
PI: Dr. Unni Narayanan
We have developed and validated patient and parent-reported outcome measures that incorporate priorities arising from families’ experience living with a chronic condition.
Register for a license to use one of our outcome measures. There is no cost to using these tools for the purpose of non-commercial research, academic or clinical practice.
Get involved. There are opportunities available for students, research collaborators, patients and their families.