This single institution, multi-site, single arm prospective study will enroll patients with a history of OA and assess changes in pain and function after treatment with LDRT as measured by patient-reported outcomes.
Inclusion Criteria:
Exclusion Criteria:
Marlowe.Estioko@Pennmedicine.upenn.edu
Participants will complete study intervention which consists of the BPI-SF, PROMIS Global v1.2, UEFI (for those with joint pain of the upper extremity) and/or LEFS (for those joint pain of the lower extremity) at baseline, 3-month and 1-year follow-up following 1 or 2 courses of standard of care LDRT.
Sonya.George@PennMedicine.upenn.edu267-760-7636
Philadelphia, Pennsylvania 19104, United States
Marlowe.Estioko@Pennmedicine.upenn.edu267-343-6483
Sonya.George@PennMedicine.upenn.edu267-760-7636
Marlowe.Estioko@Pennmedicine.upenn.edu267-343-6483
Sonya.George@PennMedicine.upenn.edu267-760-7636
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